id|nct_id|document_id|document_type|url|comment
3173682|NCT00197210|444563/028/029/030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178064|NCT01323946|109825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173683|NCT00197210|444563/028/029/030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173684|NCT00197210|444563/028/029/030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173685|NCT00197210|444563/028/029/030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 444563/028 are summarised with studies 444563/029, 444563/030, 107070, 107072, and 107076 on the GSK Clinical Study Register.
3173686|NCT00197210|444563/028/029/030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173687|NCT00197210|444563/028/029/030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178065|NCT01323946|109825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178066|NCT01323946|109825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178067|NCT01323946|109825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178068|NCT01323946|109825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180254|NCT03343197||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3173688|NCT01030965|113589|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173689|NCT01030965|113589|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173690|NCT01030965|113589|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173691|NCT01030965|113589|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175874|NCT01192178|113872|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175875|NCT01192178|113872|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175876|NCT01192178|113872|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175877|NCT01192178|113872|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175878|NCT01192178|113872|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175879|NCT01192178|113872|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175880|NCT01192178|113872|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175881|NCT01706328|116974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175882|NCT01706328|116974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175883|NCT01706328|116974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175884|NCT01706328|116974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175885|NCT01706328|116974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175886|NCT01706328|116974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175887|NCT01706328|116974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175888|NCT01405859||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983677/|Final Study Results, Published in Tremor and Other Hyperkinetic Disorders
3175889|NCT04744181||Individual Participant Data Set|https://redcap-irccs.policlinicogemelli.it/|
3175890|NCT01014091|113810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175891|NCT01014091|113810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175892|NCT01014091|113810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175893|NCT01014091|113810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178069|NCT01323946|109825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180255|NCT03343197||Study Protocol|https://clinicaltrials.servier.com/|
3171497|NCT00684515||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05005&kw=P05005&tab=access|
3171498|NCT01209026|102936|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173692|NCT01030965|113589|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173693|NCT01030965|113589|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173694|NCT01030965|113589|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173695|NCT00993187||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-202&kw=NCT00993187&tab=access|
3173696|NCT00076934|SDY661|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661|ImmPort study identifier is SDY661
3173697|NCT00076934|SDY661|Study protocol synopsis, -summary, -design, -adverse events, -medications,-demographics, - lab tests, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661|ImmPort study identifier is SDY661
3173698|NCT00076934|ITN006AI/NMS02|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN006AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
3173699|NCT00076934|ITN006AI/NMS02|Study protocol synopsis; -schedule of assessments; data and reports; adverse event(s); -specimens availability; -manuscripts and abstracts|http://www.itntrialshare.org/project/Studies/ITN006AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
3173700|NCT00358449|MEE103219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173701|NCT00358449|MEE103219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175894|NCT01014091|113810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175895|NCT01014091|113810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175896|NCT01014091|113810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175897|NCT07258888||Individual Participant Data Set|https://dishekimligi.ksu.edu.tr/|Data sharing will follow institutional policies and ethical guidelines to ensure participant confidentiality.
3175898|NCT00765076|112147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178070|NCT01323946|109825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178071|NCT03272230||Study Protocol|https://data.mendeley.com/datasets/mv8hndcd95/2|The ECOCAPTURE ethograms: apathy ethogram and disinhibition ethogram
3180256|NCT03343197||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3180257|NCT03343197||Informed Consent Form|https://clinicaltrials.servier.com/|
3180258|NCT03343197||Clinical Study Report|https://clinicaltrials.servier.com/|
3180259|NCT03343197||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3180260|NCT01607372|116392|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180261|NCT01607372|116392|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180262|NCT01607372|116392|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180263|NCT01607372|116392|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173702|NCT00358449|MEE103219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173703|NCT00358449|MEE103219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173704|NCT00358449|MEE103219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178072|NCT03272230||Individual Participant Data Set|https://data.mendeley.com/datasets/vdrstwp5xx/1|ECOCAPTURE Dataset - Behavioral coding from video - 17 bvFTD and 18 HC - 28.04.2022
3180264|NCT01607372|116392|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180265|NCT01607372|116392|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180266|NCT01607372|116392|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180267|NCT00529516|109821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180268|NCT00529516|109821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180269|NCT00529516|109821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180270|NCT00529516|109821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180271|NCT00529516|109821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173705|NCT00358449|MEE103219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180272|NCT00529516|109821|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180273|NCT00529516|109821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173706|NCT00358449|MEE103219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173707|NCT03044171|57655916.3.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
3171499|NCT01209026|102936|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171500|NCT01209026|102936|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173708|NCT03579303|123|Individual Participant Data Set|http://bethesda.org?data-id=123|De-identified data for primary and secondary outcome measures
3175899|NCT00765076|112147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175900|NCT00765076|112147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175901|NCT00765076|112147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180274|NCT00687011||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3173709|NCT00979303||Archived consent, protocol and analytic plan.|http://www.childrenshospital.org/|Study completed prior to change in common rule. Requests should be directed to the investigation team at Boston Children's Hospital through mark.alexander@cardio.chboston.org
3173710|NCT01954264|200187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173711|NCT01954264|200187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180275|NCT05489250||Informed Consent Form|https://platon-network.de/contact|
3180276|NCT05489250||See Use & Access Regulation|https://platon-network.de/contact|
3180277|NCT04641741|FGBMEP202001|Study Protocol|https://www.idisantiago.es/|The study protocol was added to clinicaltrials.gov
3180278|NCT06972433||Study Protocol|http://www.scd.edu.pk|
3173712|NCT01954264|200187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173713|NCT01954264|200187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173714|NCT01954264|200187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175902|NCT00765076|112147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175903|NCT00765076|112147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175904|NCT00386698|104887|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175905|NCT00386698|104887|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175906|NCT00386698|104887|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175907|NCT00386698|104887|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175908|NCT00386698|104887|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175909|NCT00386698|104887|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178073|NCT03272230||Individual Participant Data Set|https://data.mendeley.com/datasets/p88gtz8wdz/4|ECOCAPTURE Dataset - Behavioral coding from video - 20 bvFTD and 18 HC - 21.03.2022
3178074|NCT03272230||Individual Participant Data Set|https://data.mendeley.com/datasets/6n7p3y3j58/2|ECOCAPTURE Dataset - Behavioral coding from video - 23 bvFTD and 24 HC - 28.11.2022
3180279|NCT06973135||Statistical Analysis Plan|https://dent.alexu.edu.eg/index.php/ar/|
3180280|NCT00126997|104020|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171501|NCT01209026|102936|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171502|NCT01209026|102936|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171503|NCT01209026|102936|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171504|NCT01209026|102936|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180281|NCT00126997|104020|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180282|NCT00126997|104020|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180283|NCT00126997|104020|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180284|NCT00126997|104020|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180285|NCT00126997|104020|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175910|NCT07130370|fabatool@numl.edu.pk|Informed Consent Form|https://pakjmcr.com/index.php/1/article/view/67|It is not applicable at this time.
3180286|NCT03419325||Individual Participant Data Set|http://dx.doi.org/10.17632/5t3d5wtvm3.1|Dataset and descriptive statistics of relevant clinical and demographic data, as well as individual genotypes at several candidate genes and genetically inferred ancestry measures for the pharmacogenomic study of clopidogrel in Caribbean Hispanics.
3180287|NCT02439827||Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-015-2543-2|Study design paper
3180288|NCT02439827||Individual Participant Data Set|http://www.scielo.br/scielo.php?pid=S1980-00372016000200207&script=sci_arttext|Instrument validation study
3180289|NCT02439827||Individual Participant Data Set|http://journals.humankinetics.com/doi/abs/10.1123/jpah.2016-0113|Intervention results
3180290|NCT01000597|113477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180291|NCT01000597|113477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180292|NCT01000597|113477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180293|NCT01000597|113477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180294|NCT01000597|113477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180295|NCT01000597|113477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171505|NCT03552341||Individual Participant Data Set|https://borninbradford.nhs.uk/|Submit expressions of interest on a short proforma. All suggestions will be reviewed by the BiB Executive Group.
3171506|NCT03276611||Statistical Analysis Plan|http://www.ncbi.nlm.nih.gov/|
3171507|NCT01353742|114957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171508|NCT01353742|114957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171509|NCT01353742|114957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171510|NCT01353742|114957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171511|NCT01353742|114957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171512|NCT01353742|114957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171513|NCT01353742|114957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171514|NCT00982904||Publication of results|http://www.dndi.org/wp-content/uploads/2009/06/ClinicalPK_Tarral_FexinidazoleHAT_2014.pdf|Publication of results
3175911|NCT00000935|SDY355|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
3175912|NCT00000935|SDY355|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
3175913|NCT00000935|SDY355|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
3171515|NCT00368576|LPL107629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171516|NCT00368576|LPL107629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171517|NCT00368576|LPL107629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171518|NCT00368576|LPL107629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171519|NCT00368576|LPL107629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178075|NCT02826850||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
3178076|NCT02826850||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
3178077|NCT00371007||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171520|NCT00368576|LPL107629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175914|NCT05704309|DPPOS|Individual Participant Data Set|https://repository.niddk.nih.gov/studies/dppos/|
3175915|NCT05704309||Individual Participant Data Set|https://naccdata.org/requesting-data/data-request-process|will be available in 2025
3175916|NCT05104346|COVID and acute appendicitis|Study Protocol|http://www.mans.edu.eg/|
3178078|NCT00290277|104951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178079|NCT00290277|104951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178080|NCT00290277|104951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178081|NCT00290277|104951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178082|NCT00290277|104951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178083|NCT00290277|104951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178084|NCT00290277|104951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178085|NCT00887406|104865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178086|NCT00887406|104865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178087|NCT00887406|104865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171521|NCT00368576|LPL107629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171522|NCT01017952|102970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171523|NCT01017952|102970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171524|NCT01017952|102970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171525|NCT01017952|102970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173715|NCT01954264|200187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173716|NCT00454909|109377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173717|NCT00454909|109377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173718|NCT00454909|109377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178088|NCT00887406|104865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178089|NCT00887406|104865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178090|NCT00887406|104865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178091|NCT05648071|[ PMID ]31560378|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31560378/|
3178092|NCT05648071|PMID:30285222|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30285222/|
3178093|NCT05648071|PMID:31378236|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31378236/|
3178094|NCT05648071|PMID:32997907|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32997907/|
3178095|NCT05648071|PMID:30955977|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30955977/|
3178096|NCT05648071|PMID:31402780|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31402780/|
3178097|NCT05648071|PMID:32781263|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32781263/|
3178098|NCT05648071|PMID: 34358724|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34358724/|
3171526|NCT01017952|102970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173719|NCT00454909|109377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175917|NCT00005123|HHP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hhp/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175918|NCT00005123||Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/hhp/|
3175919|NCT00536835|PLK107427|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175920|NCT00536835|PLK107427|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178099|NCT05648071|PMID: 29229461|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29229461/|
3178100|NCT05648071|PMID: 30119083|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30119083/|
3178101|NCT05749770||Individual Participant Data Set|https://zenodo.org/records/5913009|
3178102|NCT02848053||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=Chinese+Herbal+Medicine+Tianqi+Reduces+Progression+From+Impaired+Glucose+Tolerance+to+Diabetes%3A+A+Double-Blind%2C+Randomized%2C+Placebo-Controlled%2C+Multicenter+Trial|This is the original study, the registration study is the follow-up study aimed at Tianqi capsule
3178103|NCT03075046||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
3178104|NCT00101829|SDY961|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
3178105|NCT00101829|SDY961|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
3178106|NCT00101829|SDY961|Study summary, -design, -adverse event(s), - assessments, -medications, -demographics, -files , -laboratory tests, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
3178107|NCT01036061|108414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178108|NCT01036061|108414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178109|NCT01036061|108414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178110|NCT01036061|108414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178111|NCT01036061|108414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178112|NCT01036061|108414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178113|NCT06933992||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|
3178114|NCT01039974|112648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178115|NCT01039974|112648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178116|NCT01039974|112648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180296|NCT01000597|113477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180297|NCT00704184||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-007&kw=7009-007&tab=access|
3180298|NCT04649008||Individual Participant Data Set|https://www.ieeg.org/|
3180299|NCT03181711||Study Protocol|http://mah.se|can be requested by mail Karin.Ridell@mah.se
3180300|NCT00000936|SDY354|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
3180301|NCT00000936|SDY354|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
3180302|NCT00000936|SDY354|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
3180303|NCT02627469||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed?otool=karolib|"The study is reported in the paper:~Effect of 12-month weekly professional oral hygiene care on the composition of the oral flora in dentate, dependent elderly residents: A prospective study.~Wikström M, Kareem KL, Almståhl A, Palmgren E, Lingström P, Wårdh I.~Gerodontology. 2017 Jun;34(2):240-248"
3180304|NCT00802464|112077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180305|NCT00802464|112077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180306|NCT00802464|112077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180307|NCT00802464|112077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171527|NCT01017952|102970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171528|NCT01017952|102970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173720|NCT00454909|109377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173721|NCT00454909|109377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178117|NCT01039974|112648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178118|NCT01039974|112648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178119|NCT01039974|112648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178120|NCT01039974|112648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178121|NCT00136604|104727 (Booster - 15-24 mths)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178122|NCT00136604|104727 (Booster - 15-24 mths)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180308|NCT00802464|112077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180309|NCT00802464|112077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180310|NCT00802464|112077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180311|NCT03997916||Individual Participant Data Set|http://redcap.uhhospitals.org/redcap|
3180312|NCT05313529|10.6084/m9.figshare.30994510|Statistical Analysis Plan|https://figshare.com|
3180313|NCT07289971|PMID: 35852013|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35852013/|https://pubmed.ncbi.nlm.nih.gov/
3180314|NCT05571488|10.16909-dataset-46|Individual Participant Data Set|https://data.unisante.ch/catalog/63|
3178123|NCT00136604|104727 (Booster - 15-24 mths)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178124|NCT00136604|104727 (Booster - 15-24 mths)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178125|NCT00136604|104727 (Booster - 15-24 mths)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173722|NCT00454909|109377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178126|NCT00136604|104727 (Booster - 15-24 mths)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175921|NCT00536835|PLK107427|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175922|NCT00536835|PLK107427|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178127|NCT00023244|SDY133|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
3178128|NCT00023244|SDY133|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
3178129|NCT00023244|SDY133|Study summary, -design,-demographics, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
3175923|NCT00536835|PLK107427|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175924|NCT00536835|PLK107427|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178130|NCT06707064|2022-K205|Study Protocol|https://www.sydyy.com/|The study protocol includes detailed methods, intervention description, and outcome measures. It is available upon reasonable request from the corresponding author.
3178131|NCT03238742|2|Clinical Review& Education|http://www.ncbi.nlm.nih.gov/pubmed/26903338|Singer M, Deutschman CS, Seymour CW, Shankar-Hari M, Annane D, Bauer M, Bellomo R, Bernard GR, Chiche JD, Coopersmith CM, Hotchkiss RS, Levy MM, Marshall JC, Martin GS, Opal SM, Rubenfeld GD, van der Poll T, Vincent JL, Angus DC.The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA. 2016;315(8):801-10.
3178132|NCT00135564|711202/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178133|NCT00135564|711202/008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178134|NCT00135564|711202/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178135|NCT00135564|711202/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178136|NCT00135564|711202/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178137|NCT00135564|711202/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178138|NCT05377203|PMID: 37276913|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/37276913|
3180315|NCT01808339|117156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180316|NCT01808339|117156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173723|NCT01376167|112582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180317|NCT01808339|117156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180318|NCT01808339|117156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180319|NCT01808339|117156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180320|NCT01808339|117156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180321|NCT01808339|117156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180322|NCT03238313||Information on publicly available dataset|https://documentcloud.adobe.com/link/review?uri=urn:aaid:scds:US:a6e30fe6-fb70-4d4a-9ab5-7a98da6084bb|For any individuals interested in accessing a copy of this public use dataset, please email info@policyandresearch.com with your inquiry.
3180323|NCT07320430||Study Protocol|https://www.mediafire.com/file/szzzndzizgwklut/mohamed_talat_MD_protocol.docx/file|
3180324|NCT07320430||Informed Consent Form|https://www.mediafire.com/file/i75sevydp2nuygr/consent-.docx/file|
3180325|NCT07320430||Analytic Code|https://www.mediafire.com/file/5g7dd95o0kd399p/5-ponts_likert_scale_for_patient_satisfaction.docx/file|
3173724|NCT01376167|112582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173725|NCT01376167|112582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173726|NCT01376167|112582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173727|NCT01376167|112582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173728|NCT01376167|112582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180326|NCT07320443||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/39044827/|
3173729|NCT01171989|113978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171529|NCT01475734|108372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171530|NCT01475734|108372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173730|NCT01171989|113978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173731|NCT01171989|113978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171531|NCT01475734|108372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171532|NCT01475734|108372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173732|NCT01171989|113978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173733|NCT01171989|113978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173734|NCT01171989|113978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173735|NCT01171989|113978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175925|NCT00536835|PLK107427|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173736|NCT00693966|580299/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173737|NCT00693966|580299/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173738|NCT00693966|580299/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173739|NCT00693966|580299/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173740|NCT00693966|580299/005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173741|NCT00693966|580299/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173742|NCT02605395|201528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173743|NCT02605395|201528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173744|NCT02605395|201528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175926|NCT07011264||Study Protocol|https://reporter.nih.gov/search/xHobiVLiPU68u-6wSogmsA/project-details/11052906|
3175927|NCT06864273||Informed Consent Form|https://www.openicpsr.org/openicpsr/|Informed consent document can also be directly requested from the Principal Investigator, Marcia Hay-McCutcheon at mhaymccu@ua.edu
3178139|NCT00679055||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0736-006&kw=0736-006&tab=access|
3178140|NCT06934850||Clinical Study Report|https://etik.inonu.edu.tr/panel/index|
3178141|NCT01926015||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-060&kw=V260-060&tab=access|
3178142|NCT00857883|111314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178143|NCT00857883|111314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180327|NCT06357091||results can be obtained from principal investigator|https://www.kh-schwaz.at/|results can be obtained from the principle investigator
3180328|NCT05179200||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08035-7|
3180329|NCT00123903|COR103560|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180330|NCT00123903|COR103560|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180331|NCT00123903|COR103560|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180332|NCT00123903|COR103560|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180333|NCT00123903|COR103560|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173745|NCT02605395|201528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178144|NCT00857883|111314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175928|NCT01610388|113376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178145|NCT00857883|111314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180334|NCT00123903|COR103560|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180335|NCT00123903|COR103560|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180336|NCT01673555|116008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173746|NCT00379600|ARA102198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173747|NCT00379600|ARA102198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175929|NCT01610388|113376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175930|NCT01610388|113376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173748|NCT00379600|ARA102198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173749|NCT00379600|ARA102198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173750|NCT00379600|ARA102198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173751|NCT00379600|ARA102198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173752|NCT00379600|ARA102198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173753|NCT07025395|28 May 2025|Study Protocol|https://youtu.be/ql8SD07abnI|Core Training Protocol by Ioannis Tsartsapakis Ph.D.
3178146|NCT00857883|111314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180337|NCT01673555|116008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180338|NCT01673555|116008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180339|NCT01673555|116008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173754|NCT00624065|COR111096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173755|NCT00624065|COR111096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173756|NCT00624065|COR111096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173757|NCT00624065|COR111096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173758|NCT00624065|COR111096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173759|NCT00624065|COR111096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173760|NCT00624065|COR111096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173761|NCT01536405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V221-027&kw=V221-027&tab=access|
3173762|NCT01472341||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-113&kw=0000-113&tab=access|
3178147|NCT00857883|111314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178148|NCT00857883|111314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178149|NCT00543543||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-001&kw=V503-001&tab=access|
3178150|NCT03955380||Bibliografic References|http://ipb.hhu.de/publikationen-ipb.html|"1. Leithold et al., Pharm Res. 33, 328-336 (2016).~2. van Groen et al., Sci Rep 7, 16275 (2017).~3. Schemmert et al., Mol Neurobiol 56, 2211 (2019).~4. Kutzsche et al., Molecules 22, 1693 (2017).~5. Schemmert et al., Neurobiol Dis 124, 36 (2019)."
3180340|NCT01673555|116008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173763|NCT01171963|113808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173764|NCT01171963|113808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173765|NCT01171963|113808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180341|NCT01673555|116008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180342|NCT01673555|116008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180343|NCT05936177|World Health Organization|Health education concepts and strategies|https://apps.who.int/iris/bitstream/handle/10665/119953/EMRPUB_2012_EN_1362.pdf?sequence=1&isAllowed=y|
3173766|NCT01171963|113808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175931|NCT01610388|113376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171533|NCT01475734|108372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171534|NCT01475734|108372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171535|NCT01475734|108372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171536|NCT02000804|117326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173767|NCT01171963|113808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180344|NCT03701113|2018_04_05_EHS|Study Protocol|http://www.ul.ie/ehs/research-ethics|Contact The EHS Research Ethics Contact Point of the Education and Health Sciences Research Ethics Committee, Room E1003, University of Limerick, Limerick, Ireland
3180345|NCT05909618||Nature Communications manuscript|https://www.nature.com/articles/s41467-021-22186-0|
3180346|NCT07048717||General information about the study plus information about application for data|https://www.umu.se/en/research/groups/the-mauritius-study/|
3180347|NCT03172468||Informed Consent Form|https://box.medunigraz.at/s/QuTYym3xsqXybWI|
3180348|NCT03172468||Study Protocol|https://box.medunigraz.at/s/YbufqAn3DBI1f4Q|
3173768|NCT01171963|113808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173769|NCT01171963|113808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173770|NCT04752592||Study Protocol|https://www.seroselecttb.org/resources|
3173771|NCT04391933|CPR|Informed Consent Form|https://komite.regionsyddanmark.dk/wm258128|
3173772|NCT00302952|SDY473|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473. Participant level data is available.
3173773|NCT00302952|SDY473|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473
3173774|NCT00302952|SDY473|Study summary, -design, -adverse events, -medications, -demographics, -lab tests, -mechanistic assays, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473
3173775|NCT02578953|204646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175932|NCT01610388|113376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178151|NCT00699764|208141/017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175933|NCT01610388|113376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175934|NCT01610388|113376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175935|NCT01245933||general information|http://www.asconet.net|
3175936|NCT00385840|108708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178152|NCT00699764|208141/017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178153|NCT00699764|208141/017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178154|NCT00699764|208141/017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178155|NCT00699764|208141/017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180349|NCT00976105|111849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180350|NCT00976105|111849|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180351|NCT00976105|111849|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180352|NCT00976105|111849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180353|NCT00976105|111849|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171537|NCT02000804|117326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171538|NCT02000804|117326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173776|NCT02578953|204646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173777|NCT02578953|204646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175937|NCT00385840|108708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175938|NCT00385840|108708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175939|NCT00385840|108708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180354|NCT00976105|111849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180355|NCT05782231|VIV0001019|Individual Participant Data Set|https://doi.org/10.25934/PR00010109|
3180356|NCT00314860|101468/204|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171539|NCT02000804|117326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171540|NCT02000804|117326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173778|NCT04238767|10.5281/zenodo.6654462|Individual Participant Data Set|https://zenodo.org/record/6654462|"Dataset relating to:~Brown JA, Nsakala BL, Mokhele K, et al. Dolutegravir in real life: Self-reported mental and physical health outcomes after transitioning from efavirenz- to dolutegravir-based antiretroviral therapy in a prospective cohort study in Lesotho. HIV Med. Published online June 22, 2022. doi:10.1111/hiv.13352"
3180357|NCT00314860|101468/204|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180358|NCT00314860|101468/204|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180359|NCT00314860|101468/204|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180360|NCT00314860|101468/204|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180361|NCT00314860|101468/204|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180362|NCT00314860|101468/204|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180363|NCT01017146|114575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180364|NCT01017146|114575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171541|NCT02000804|117326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171542|NCT02000804|117326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171543|NCT01462266||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-260&kw=0431-260&tab=access|
3171544|NCT05506397||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/|
3171545|NCT03194984|27045285|Metanalysis, systematic review|https://www.ncbi.nlm.nih.gov/pubmed/?term=27045285|
3171546|NCT03194984|21740236|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21740236|
3173779|NCT04238767||Individual Participant Data Set|https://zenodo.org/record/5948369|"Dataset relating to:~Brown JA, Nsakala BL, Mokhele K, et al. Viral suppression after transition from nonnucleoside reverse transcriptase inhibitor- to dolutegravir-based antiretroviral therapy: A prospective cohort study in Lesotho (DO-REAL study). HIV Med. 2022;23(3):287-293. doi:10.1111/hiv.13189"
3173780|NCT02841488||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
3173781|NCT01639092|25596179|Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25596179|Publication for the primary study results
3173782|NCT03306394||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3173783|NCT03306394||Study Protocol|https://clinicaltrials.servier.com/|
3175940|NCT00385840|108708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175941|NCT00385840|108708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180365|NCT01017146|114575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180366|NCT01017146|114575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180367|NCT01017146|114575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171547|NCT03194984|21488723|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21488723|
3171548|NCT03194984|27007348|Informed Consent Form|https://www.ncbi.nlm.nih.gov/pubmed/?term=27007348|
3171549|NCT01827631|116416|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171550|NCT01827631|116416|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171551|NCT01827631|116416|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171552|NCT01827631|116416|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171553|NCT01827631|116416|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171554|NCT01827631|116416|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171555|NCT01827631|116416|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171556|NCT01552681|SDY823|Study Protocol|http://www.immport.org/immport-open/public/home/home|ImmPort study identifier is SDY823.
3171557|NCT01552681|SDY823|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/home|ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public.
3171558|NCT00379951||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171559|NCT00920660|113161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178156|NCT00699764|208141/017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180368|NCT01017146|114575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180369|NCT01017146|114575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180370|NCT07065084|dilek.cecen@cbu.edu.tr|Clinical Study Report|https://cdn.clinicaltrials.gov/large-docs/02/NCT04069702/ICF_000.pdf|
3180371|NCT04119284||Informed Consent Form|http://irbnet.org|The Informed consent form can be obtained while the patient is seen for scoliosis at Nemours-AIDHC.
3180372|NCT03111290||Summary Data Set|http://dx.doi.org/10.5281/zenodo.45811|Dataset supporting Alagapan et al. 2016 PLoS Biology
3171560|NCT00920660|113161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171561|NCT00920660|113161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171562|NCT00920660|113161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171563|NCT00920660|113161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171564|NCT00920660|113161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171565|NCT00920660|113161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171566|NCT02698098||Study Protocol|http://dx.doi.org/10.7910/DVN/RO34OK|
3171567|NCT02698098||Individual Participant Data Set|http://dx.doi.org/10.7910/DVN/RO34OK|
3171568|NCT02698098||Analytic Code|http://dx.doi.org/10.7910/DVN/RO34OK|
3171569|NCT06960408|sleep quality|Informed Consent Form|https://etikkurullar.gazi.edu.tr/Dosya/Formlar|This study will be conducted in a randomized controlled and statistician blinded prospective design. During the blinding phase of the statistician; after the individuals are recruited to the study, the individuals will not be informed about which group they are in; 1 (Group 2: Control group), 2 (Group 1: Experimental group), and a coding will be created with the numbers 1 (Group 2: Control group), 2 (Group 1: Experimental group). The intervention and control groups will be assigned with simple random randomization. The individuals will be assigned numbers and the intervention and control groups will be assigned using the random number table. The analysis of the coded data by the groups will be done by a statistician. The coded groups will be delivered to the researcher in a sealed envelope by the statistician. Which code will be taken as the experimental and control groups will be determined by drawing lots.
3171570|NCT05521737||Protocol reapproval report|https://drive.google.com/file/d/1P3sbgleW3murWJq_FIaerBlFU12aga9z/view?usp=sharing|
3180373|NCT00611559|110478|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180374|NCT00611559|110478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180375|NCT00611559|110478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171571|NCT00137917|710158/002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171572|NCT00137917|710158/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171573|NCT00137917|710158/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171574|NCT00137917|710158/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171575|NCT00137917|710158/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171576|NCT04887493|Misoprostol|Study Protocol|https://www.researchgate.net/publication/351331713_Efficacy_and_Safety_of_Sublingual_versus_Vaginal_Misoprostol_for_Induction_of_Labor_at_Term_and_Post_Term_Pregnancies_A_Randomized_Clinical_Trial_Efficacy_and_Safety_of_Sublingual_versus_Vaginal_Misop|
3171577|NCT00783393||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175942|NCT06855810|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
3175943|NCT07105761|15862065|Study Protocol|https://zenodo.org/records/15862065|The de-identified individual participant data (IPD) and supporting documents will be available to qualified researchers upon request, following review and approval by a data access committee. Data will be shared via a secure institutional repository beginning 6 months after study completion, for up to 3 years.
3178157|NCT00289718|100556 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180376|NCT00611559|110478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180377|NCT00611559|110478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175944|NCT02836769||Study Protocol|http://www.implementationscience.com/content/10/1/6|Publication of the initial project protocol
3175945|NCT02836769||Clinical Study Report|http://link.springer.com/article/10.1007%2Fs00520-015-3021-1|Publication based on findings from focus groups used to create the intervention in this study
3180378|NCT00611559|110478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180379|NCT00611559|110478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180380|NCT07214896|De-identified biometric audit|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
3180381|NCT07214896|ESG compliance logs|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
3180382|NCT07214896|Wage token minting and transfe|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
3180383|NCT07214896|SHA-256 notarized study protoc|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3171578|NCT02899858|140503|Study Protocol|https://www4.vanderbilt.edu/irb/|
3171579|NCT01097629||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-029&kw=4305-029&tab=access|
3171580|NCT00600171|B2C109575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180384|NCT07214896|Statistical analysis plan (SAP|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3180385|NCT07214896|Informed consent form (ICF)|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3180386|NCT07214896|Clinical study report (CSR)|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3171581|NCT00600171|B2C109575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171582|NCT00600171|B2C109575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171583|NCT00600171|B2C109575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171584|NCT00600171|B2C109575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171585|NCT00600171|B2C109575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171586|NCT00600171|B2C109575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171587|NCT00976144|113208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171588|NCT00976144|113208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171589|NCT00976144|113208|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171590|NCT00976144|113208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171591|NCT00976144|113208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171592|NCT00976144|113208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171593|NCT00976144|113208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173784|NCT03306394||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3175946|NCT00127010|103388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171594|NCT04719351||Individual Participant Data Set|https://osf.io/uz3b7/?view_only=ba37189d0b594529b159ba27564dfb81|
3171595|NCT01879410|114951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180387|NCT07214896|Analytic code for biometric sc|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3171596|NCT01879410|114951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171597|NCT01879410|114951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173785|NCT03306394||Informed Consent Form|https://clinicaltrials.servier.com/|
3173786|NCT03306394||Clinical Study Report|https://clinicaltrials.servier.com/|
3173787|NCT03306394||study-level clinical trial data|https://clinicaltrials.servier.com/|
3173788|NCT01421277||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-076&kw=0974-076&tab=access|
3173789|NCT01037114|112266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173790|NCT01037114|112266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173791|NCT01037114|112266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175947|NCT00127010|103388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180388|NCT07217600||Study Protocol|https://www.chictr.org.cn/showproj.html?proj=253510|
3180389|NCT03739450|602d|Individual Participant Data Set|https://www.tbindsc.org/StaticFiles/SOP/602d%20-%20External%20Use%20TBIMS%20National%20Database%20Notification.pdf|
3180390|NCT02073994||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3171598|NCT01879410|114951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171599|NCT01879410|114951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180391|NCT00792636|110948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180392|NCT00792636|110948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180393|NCT00792636|110948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171600|NCT01879410|114951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171601|NCT01879410|114951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180394|NCT00792636|110948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180395|NCT00792636|110948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180396|NCT00792636|110948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180397|NCT00792636|110948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180398|NCT07078721|TMI in AA|Study Protocol|https://clinicaltrials.gov/|Efficacy and Safety Study of Umbilical Cord Blood Transplantation (UCBT) with Total Marrow Irradiation (TMI)-Based Conditioning Regimen for Adults with Refractory/Relapsed Aplastic Anemia (AA)
3180399|NCT07078721|TMI in AA|Informed Consent Form|https://clinicaltrials.gov/|Efficacy and Safety Study of Umbilical Cord Blood Transplantation (UCBT) with Total Marrow Irradiation (TMI)-Based Conditioning Regimen for Adults with Refractory/Relapsed Aplastic Anemia (AA)
3180400|NCT07078721|TMI in AA|Clinical Study Report|https://clinicaltrials.gov/|Efficacy and Safety Study of Umbilical Cord Blood Transplantation (UCBT) with Total Marrow Irradiation (TMI)-Based Conditioning Regimen for Adults with Refractory/Relapsed Aplastic Anemia (AA)
3180401|NCT07076381|https://doi.org/10.17605/OSF.I|Individual Participant Data Set|https://osf.io/dashboard|Open Science Framework website for Principal Investigator, which includes public access to de-identified data set
3171602|NCT04106622||Pubmed|https://www.ncbi.nlm.nih.gov/pubmed/|
3171603|NCT00849017|112756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171604|NCT00849017|112756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171605|NCT00849017|112756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173792|NCT01037114|112266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173793|NCT01037114|112266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175948|NCT00127010|103388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178158|NCT00289718|100556 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171606|NCT00849017|112756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171607|NCT00849017|112756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171608|NCT00849017|112756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171609|NCT00849017|112756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171610|NCT04067518||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3171611|NCT04067518||Study Protocol|https://clinicaltrials.servier.com/|
3171612|NCT04067518||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3171613|NCT04067518||Informed Consent Form|https://clinicaltrials.servier.com/|
3171614|NCT04067518||Clinical Study Report|https://clinicaltrials.servier.com/|
3171615|NCT04067518||study-level clinical trial data|https://clinicaltrials.servier.com/|
3171616|NCT00348140|AVA102670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171617|NCT00348140|AVA102670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171618|NCT00348140|AVA102670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178159|NCT00289718|100556 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178160|NCT00289718|100556 (Y11)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100556 are summarised with studies 100557, 100558, 100559, and 100560 on the GSK Clinical Study Register.
3178161|NCT00289718|100556 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180402|NCT03136042||references|https://www.ncbi.nlm.nih.gov/pubmed/|GINA. Global Strategy for Asthma Management and Prevention NHLBI/WHO Workshop Report 2012. 2012 ISAAC. Worldwide variations in the prevalence of asthma symptoms: the International Study of Asthma and Allergies in Childhood (ISAAC). Eur Respir J 1998; 12:315-335 Solé D, Wandalsen GF, Camelo-Nunes IC, et al. Prevalence of symptoms of asthma, rhinitis, and atopic eczema among Brazilian children and adolescents identified by the International Study of Asthma and Allergies in Childhood (ISAAC) - Phase 3. J Pediatr (Rio J) 2006; 82:341-346 Barnabé V, Saraiva B, Stelmach R, et al. Chest physiotherapy does not induce bronchospasm in stable asthma. Physiotherapy 2003; 89:714-719 ATS. Standardization of Spirometry - American Thoracic Society. Am J Respir Crit Care Med 1995; 152:1107-1136 Saraiva-Romanholo BM, Barnabe V, Carvalho AL, et al. Comparison of three methods for differential cell count in induced sputum. Chest 2003; 124:1060-1066
3180403|NCT06795880||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/33062451/|
3180404|NCT06791993||Individual Participant Data Set|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op
3180405|NCT03423303||Statistical Analysis Plan|https://bmjopen.bmj.com/content/bmjopen/14/1/e075595.full.pdf|
3180406|NCT02306096|GSE60789|RNA-seq Processed Gene Expression Data and Annotations (n=49 patients)|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE60789|SuperSeries: GSE60789 SubSeries: GSE60785, GSE60788
3171619|NCT00348140|AVA102670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171620|NCT00348140|AVA102670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171621|NCT00348140|AVA102670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171622|NCT00348140|AVA102670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171623|NCT00868790||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3577-009&kw=3577-009&tab=access|
3171624|NCT00609596|ARI111402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171625|NCT00609596|ARI111402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173794|NCT01037114|112266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173795|NCT01037114|112266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173796|NCT04967794|CAAE 39685920.7.0000.5419|Informed Consent Form|https://plataformabrasil.saude.gov.br/|Through this address it is possible to identify the information about acceptance by the ethics committee of Univerdade São Paulo and also the consent form
3173797|NCT05355883||Informed Consent Form|https://epirate.ecu.edu/App/app/portal/smartform/read?project=com.webridge.entity.Entity%5BOID%5B21688D0E003911ECFE80AAA590565000%5D%5D&projectEditorView=com.webridge.entity.Entity%5BOID%5BDB15548F56BE6942A0B8A537449C64C3%5D%5D|
3180407|NCT02306096|GSE81540|RNA-seq Processed Gene Expression Data and Annotations (n=3678 patients)|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE81540|SuperSeries: GSE81540 SubSeries: GSE81538, GSE96058
3175949|NCT00127010|103388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103388 are summarised with followup study 104690 on the GSK Clinical Study Register.
3180408|NCT06846294||Protocol and ethics can be shared on request|https://medicine.exeter.ac.uk/phss/research/foodnutrition/clinical/|Information will be shared following ethical approval on relevant websites
3180409|NCT05150860||COVID Rapid Acceleration of Diagnostics (RADx) Data Hub|https://radx-hub.nih.gov/home|Data from this study is available on the RADx Data Hub
3180410|NCT05147155|10.1183/23120541.00939-2024|Clinical Study Report|https://publications.ersnet.org/content/erjor/early/2024/11/21/2312054100939-2024|Kotsiou Ourania S., Kirgou Paraskevi, Siachpazidou Dimitra, Bartziokas Konstantinos, Tourlakopoulos Konstantinos, Malli Foteini, Pinaka Maria, Daniil Zoe, Gourgoulianis Konstantinos I. Early benefit of mepolizumab on small airways in severe asthma: insights from IMPOSE study. ERJ Open Research 2024 00939-2024; DOI: https://doi.org/10.1183/23120541.00939-2024
3171626|NCT00609596|ARI111402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171627|NCT00609596|ARI111402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175950|NCT00127010|103388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175951|NCT00127010|103388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175952|NCT07121348|END-7-25-3400|Study Protocol|http://www.tanta.edu.eg|
3175953|NCT07080528||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2024-515545-41-00|
3178162|NCT01453725||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07642&kw=8259-006&tab=access|
3171628|NCT00609596|ARI111402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173798|NCT00609674|FFU111439|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173799|NCT00609674|FFU111439|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173800|NCT00609674|FFU111439|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173801|NCT00609674|FFU111439|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173802|NCT00609674|FFU111439|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173803|NCT00609674|FFU111439|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175954|NCT01248975|114387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178163|NCT00334607|107531|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178164|NCT00334607|107531|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178165|NCT00334607|107531|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178166|NCT00334607|107531|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178167|NCT00334607|107531|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178168|NCT00334607|107531|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178169|NCT00968890|113525|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178170|NCT00968890|113525|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178171|NCT00968890|113525|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180411|NCT05385718||Informed Consent Form|https://ezrapublic.blob.core.windows.net/staticassets/EzraFasterScanStudy-InformedConsentForm(L).pdf|This link will download the informed consent document for the Faster Scan Study. In this document potential participants will find additional information about the study.
3180412|NCT06987331||Statistical Analysis Plan|https://www.ibm.com/support/pages/downloading-ibm-spss-amos-24|https://www.ibm.com/support/pages/downloading-ibm-spss-amos-24
3180413|NCT06447519||Study Protocol|https://ikee.lib.auth.gr|https://ikee.lib.auth.gr
3171629|NCT00609596|ARI111402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173804|NCT00609674|FFU111439|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178172|NCT00968890|113525|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171630|NCT00609596|ARI111402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178173|NCT00968890|113525|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178174|NCT00968890|113525|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178175|NCT00968890|113525|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178176|NCT07278141|Study Protocol ACTIVAM|Study Protocol|https://alumnossantotomas-my.sharepoint.com/:b:/g/personal/ivonnejorquera_santotomas_cl/EeBXjIa_2FBMivQW63r3zkQBXK4j0X4-TiOdpAqmw_w2sg?e=Fh6PcR|The study protocol is accessible to anyone with the link
3178177|NCT07278141|Ethics Committee Approval|Data Monitoring Committee Charter|https://alumnossantotomas-my.sharepoint.com/:b:/g/personal/ivonnejorquera_santotomas_cl/EfT4D7DeqWJKg0G9BoL0JEIBgmCcMobhIPrQMe2MeCZu0g?e=QlrDDK|The file is publicly available via link
3178178|NCT07278141|INFORMED CONSENT|Informed Consent Form|https://alumnossantotomas-my.sharepoint.com/:b:/g/personal/ivonnejorquera_santotomas_cl/ETTRNyC4tIpKgXo3bKwcG-EBWanx328fkqIPiudt0LoMvA?e=m8mMB6|
3178179|NCT01254032|114169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178180|NCT01254032|114169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171631|NCT03311048|Sistema Nacional de Informação|Informed Consent Form|http://portal2.saude.gov.br/sisnep/pesquisador|
3180414|NCT02240472||Study Protocol|http://senomac.se/Home/study%20protocol.html|Study protocol and patient information (English)
3171632|NCT01648231|116797|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173805|NCT00385320|444563/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178181|NCT01254032|114169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180415|NCT02132936||Clinical Study Report|https://www.leopharmatrials.com/en|Clinical Trials at LEO Pharma
3173806|NCT00385320|444563/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173807|NCT00385320|444563/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175955|NCT01248975|114387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175956|NCT01248975|114387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178182|NCT01254032|114169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178183|NCT01254032|114169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175957|NCT01248975|114387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175958|NCT01248975|114387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178184|NCT06667661||NIH Reporter Information|https://reporter.nih.gov/search/w2y2LWuI50aTEgDfuqR7lg/project-details/11017278|Final Data set will be deposited into NICHD DASH database.
3178185|NCT00851344|110163|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178186|NCT00851344|110163|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180416|NCT06830330||ethics committee approval|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
3180417|NCT06786429||Clinical Study Report|https://www.nust.ac.zw|
3178187|NCT00851344|110163|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180418|NCT06786429|tba|Clinical Study Report|https://www.nust.ac.zw|
3180419|NCT04522375||Study Protocol|http://clinicaltrials.gov|clinicaltrials.gov
3171633|NCT01648231|116797|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171634|NCT01648231|116797|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171635|NCT01648231|116797|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173808|NCT00385320|444563/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173809|NCT00385320|444563/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173810|NCT00385320|444563/006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173811|NCT02197481|PMID:25925431|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25925431|
3173812|NCT03192163||Survey|http://j.mp/2qdz7P2|This is the RedCap survey that subjects will take.
3173813|NCT01231906||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3173814|NCT01929863|200185|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178188|NCT00851344|110163|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180420|NCT04522375||Statistical Analysis Plan|http://clinicaltrials.gov|clinicaltrials.gov
3180421|NCT06266806||Article|https://dergipark.org.tr/tr/pub/egehemsire/issue/66449/637342|Kilci Erciyas, Ş., Sevil, Ü. (2021). Laktasyonu Arttıran Yöntemler: Hipnoemzirme. Ege Üniversitesi Hemşirelik Fakültesi Dergisi, 37(3), 229-234.
3173815|NCT01929863|200185|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173816|NCT01929863|200185|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173817|NCT01929863|200185|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173818|NCT01929863|200185|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171636|NCT01648231|116797|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171637|NCT01648231|116797|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171638|NCT01648231|116797|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173819|NCT01929863|200185|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173820|NCT01929863|200185|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173821|NCT01899755|116987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180422|NCT06266806||Article|https://jurnal.unw.ac.id/index.php/ijm/article/view/267|Sofiyanti, I., Astuti, F. P., \& Windayanti, H. (2019). Penerapan Hypnobreastfeeding pada Ibu Menyusui. Indonesian Journal of Midwifery (IJM), 2(2): 84-9.
3171639|NCT01154101|114296|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180423|NCT06266806||Article|https://jmscr.igmpublication.org/home/index.php/archive/143-volume-05-issue-10-october-2017/3436-the-effect-of-hypnobreastfeeding-and-oxytocin-massage-on-breastmilk-production-in-postpartum|Dini, P.R., Suwondo, A., Hardjanti, T.S., Hadisaputro, S. (2017). The effect of hypnobreastfeeding and oxytocin massage on breastmilk production in postpartum. Journal of Medical Science and Clinical Research, 5(10), 28600-4. doi:https://dx.doi.org/10.18535/jmscr/v5i10.19.
3180424|NCT06266806||Article|https://thejmch.com/index.php/thejmch/article/view/40|Sari, L., Salimo, H., Budihastuti, U.R. (2017). Optimizing the combination of oxytocin massage and hypnobreastfeeding for breast milk production among post-partum mothers. Journal of Maternal and Child Health, 1(1), 20-29.
3180425|NCT06266806||Thesis|http://abakus.inonu.edu.tr/xmlui/bitstream/handle/11616/56418/689894.pdf?sequence=1&isAllowed=y|Altıparmak S. (2021). Hipnoemzirme ve Oksitosin Masajının Primiparlarda Emzirme Motivasyonu, Yetersiz Süt Algısı, Bağlanma ve Uterus İnvolüsyon Sürecine Etkisi. İnönü Üniversitesi Sağlık Bilimleri Enstitüsü Ebelik Anabilim Dalı, Doktora Tezi, Malatya.
3180426|NCT06266806||Article|https://dergipark.org.tr/en/pub/tjfmpc/issue/68782/977380|Duman FN, Gölbaşı Z. Türkiye'de Emzirme Eğitiminin Annelerin Emzirme Öz-Yeterlilik Düzeyine Etkisinin İncelenmesi. TJFMPC. 2022;16(1):140-5.
3171640|NCT01154101|114296|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171641|NCT01154101|114296|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171642|NCT01154101|114296|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171643|NCT01154101|114296|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171644|NCT01154101|114296|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171645|NCT05788939||Informed Consent Form|https://dergipark.org.tr/tr/download/article-file/820404|Dogan ES, Caydam OD. Investigation of Studies Conducted with Health Belief Model in Skin Cancer. Izmir Democracy University Health Sciences Journal.2019; 2(2):66-75.
3171646|NCT05788939||Statistical Analysis Plan|https://saudijournals.com/media/articles/SJNHC_48_205-213.pdf|Dogan ES, Caydam OD. A Scale Development Study: Health Belief Model Scale in Skin Cancer among Turkish University Students. Saudi Journal of Nursing and Health Care. 2021; 4(8): 205- 213. https://doi.org/10.36348/sjnhc.2021.v04i08.001.
3171647|NCT04523532||Study Protocol|http://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s13148-017-0407-6|
3171648|NCT01086436|113552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171649|NCT01086436|113552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171650|NCT01086436|113552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171651|NCT01086436|113552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171652|NCT01086436|113552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171653|NCT01086436|113552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171654|NCT01428466|114849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171655|NCT01428466|114849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171656|NCT01428466|114849|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171657|NCT01428466|114849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171658|NCT00851071||Publication|http://link.springer.com/article/10.1007%2Fs10840-015-9990-7|A prospective study of anxiety in ICD patients with a pilot randomized controlled trial of cognitive behavioral therapy for patients with moderate to severe anxiety Mohammed Qintar \& Jason J. George \& Melanie Panko \& Scott Bea \& Karen A. Broer \& Julie St. John \& Kecia-Ann Blissett \& Elizabeth Ching \& Samuel F. Sears \& Susanne S. Pedersen \& Leopoldo Pozuelo \& Mina K. Chung
3173822|NCT01899755|116987|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175959|NCT01248975|114387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178189|NCT00851344|110163|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178190|NCT00851344|110163|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178191|NCT00851344|110163|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178192|NCT02714907||Study Protocol|http://cortrium.com|In Danish language
3178193|NCT00397215|108251|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178194|NCT00397215|108251|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178195|NCT00397215|108251|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178196|NCT00397215|108251|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178197|NCT00397215|108251|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175960|NCT01248975|114387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175961|NCT01899703|117213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180427|NCT06266806||Article|https://jag.journalagent.com/behcetuz/pdfs/BUCHD_4_1_31_36.pdf|Yalçınöz Baysal, H, Türkoğlu, N., \& Küçükoğlu, S. Sağlıklı ve Hasta Bebeği Olan Annelerin Emzirme Öz-Yeterlilik Algılarının Karşılaştırılması. İzmir Dr. Behçet Uz Çocuk Hast. Dergisi, 2014; 4(1):31-36.
3180428|NCT03060421||Study Protocol|http://www.parkerinst.dk|
3180429|NCT05534802|28537661|Clinical Study Report|https://www.europeanreview.org/article/12702|Ulinastatin can effectively regulate the inflammatory cytokines and provide protection for organ function during cardiopulmonary bypass surgery, which is conducive to promote the recovery of patients.
3171659|NCT00537719|GLP107030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171660|NCT00537719|GLP107030|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171661|NCT00537719|GLP107030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178198|NCT00397215|108251|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 108251 are summarised with studies 108252, 111275, and 111276 on the GSK Clinical Study Register.
3175962|NCT01899703|117213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175963|NCT01899703|117213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175964|NCT01899703|117213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175965|NCT01899703|117213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178199|NCT00318058|104540|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178200|NCT00318058|104540|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178201|NCT00318058|104540|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180430|NCT06188754||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/38762486/|
3175966|NCT01899703|117213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180431|NCT03839940||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3180432|NCT00085735||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3180433|NCT05459688||Trial Results Summary|https://www.trialsummaries.com/Study/StudyDetails?id=25790&tenant=MT_MED_9011|Trial Results Summary
3175967|NCT01899703|117213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178202|NCT00318058|104540|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178203|NCT00318058|104540|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178204|NCT00318058|104540|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180434|NCT04979351||Review|https://dergipark.org.tr/tr/download/article-file/117117|
3171662|NCT00537719|GLP107030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171663|NCT00537719|GLP107030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178205|NCT00354536|GLP106073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178206|NCT00354536|GLP106073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178207|NCT00354536|GLP106073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178208|NCT00354536|GLP106073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180435|NCT04979351||Clinical Study Report|https://dergipark.org.tr/tr/download/article-file/29524|
3180436|NCT07323472|Multicare: Bed for protocol|Study Protocol|https://drive.google.com/file/d/1tTjIHQ18FQa7SDYQpLIKStPNh8LqN09o/view?usp=sharing|The Multicare: Bed for Protocol is used to standardize therapeutic positioning, ensuring precision and safety in evaluating the postural effects on lung aeration and respiratory drive
3180437|NCT07320794|fundacnr20@gmail.com|Clinical Study Report|https://earsiv.odu.edu.tr/jspui/bitstream/11489/3915/1/10435776.pdf|https://earsiv.odu.edu.tr/jspui/bitstream/11489/3915/1/10435776.pdf
3180438|NCT07320794|https://earsiv.odu.edu.tr/jspu|Clinical Study Report|https://earsiv.odu.edu.tr/jspui/bitstream/11489/3915/1/10435776.pdf|
3180439|NCT06852430|042025201171|Study Protocol|https://docs.google.com/document/d/18-WWwL8l_EB2nHv4wr1-Q1cslJ1VUYUf/edit?usp=drivesdk&ouid=111849282554145262325&rtpof=true&sd=true|
3180440|NCT07300137|comparison of 2 dressings|comparison between two types of dressings|https://pjmhsonline.com/index.php/pjmhs/article/view/3992|Mean duration of healing with sodium Carboxylic methyl-cellulose silver dressing was less than petroleum gauze dressing for management of second-degree burns.
3180441|NCT07321236||Study Protocol|https://jhrlmc.com/index.php/home/article/view/850|
3171664|NCT00537719|GLP107030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175968|NCT00335075||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175969|NCT01371682|112771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175970|NCT01371682|112771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175971|NCT01371682|112771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175972|NCT01371682|112771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175973|NCT01371682|112771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175974|NCT01371682|112771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175975|NCT01371682|112771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175976|NCT01996995||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/s13063-015-0622-4|
3175977|NCT00729001|444563/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175978|NCT00729001|444563/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175979|NCT00729001|444563/005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175980|NCT00729001|444563/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175981|NCT00729001|444563/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175982|NCT00729001|444563/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175983|NCT06389461||Castilloa, A. R. G. L., Recondob, R., Asbahrc, F. R. & Manfrod, G. G. (2000).|https://doi.org/10.1590/S1516-44462000000600006|Transtornos de ansiedade. Revista Brasileira de Psiquiatria. 22(2), 20-23.
3178209|NCT00354536|GLP106073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178210|NCT00354536|GLP106073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180442|NCT06899438||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/tezDetay.jsp?id=ojJkM_gxQRaH4Sn9fMdQWw&no=8WIZbpBlZOGWvkUUwksxFg|
3180443|NCT06907472||Individual Participant Data Set|https://redcap.uniabuja.edu.ng/redcap_v13.0.1/index.php?pid=203&__record_cache_complete=1|University of Abuja REDCap link to participant data set.
3180444|NCT06272903|MBRU IRB-2023-228|Study Protocol|http://www.mbru.ac.ae|
3180445|NCT06836700|10.7759/cureus|Clinical Study Report|https://www.cureus.com/publish/articles/342384-comparison-of-trifecta-analysis-of-standard-versus-mini-percutaneous-nephrolithotomy-in-the-management-of-urolithiasis/preview#!/|Further information including data sheets will be provided upon request
3180446|NCT02733159||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/PePS2/index.aspx|
3180447|NCT06836102|drmostafanasr1988@gmail.com|Study Protocol|https://doi.org/10.1016/j.hermed.2021.100468|
3171665|NCT00537719|GLP107030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171666|NCT03289130||Individual Participant Data Set|https://pcap.bioinf.unc.edu/|
3171667|NCT04091347|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
3171668|NCT04091347|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
3173823|NCT01899755|116987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180448|NCT07063940||Study Protocol|http://www.birmingham.ac.uk/ExaLT|
3180449|NCT07063940||Informed Consent Form|http://www.birmingham.ac.uk/ExaLT|
3180450|NCT06821919|2022-09-22_012059|Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
3180451|NCT01385189||Clinical Study Report|http://smhs.gwu.edu/mitm-crg/clinical-trials|
3178211|NCT00354536|GLP106073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180452|NCT05989685||Statistical Analysis Plan|https://osf.io/dmyuq/files/osfstorage/67cb0a2098ee14b2b7fd7157|Statistical Analysis Plan available in OSF.
3171669|NCT00792298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-006&kw=4305-006&tab=access|
3171670|NCT02706938|Clinical Trial Protocol|Study Protocol|https://drive.google.com/open?id=0B6Uam9x9PtiiV2xUcDBKU3RHYU0|
3171671|NCT00707798|111651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180453|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/25735317|"Passardi A et al. Effectiveness of bevacizumab added to gold standard chemotherapy in metastatic colorectal cancer: final results of first-line from the ITACa randomized clinical trial.~Ann Oncol 2015 Jun;26(6):1201-7"
3171672|NCT00707798|111651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171673|NCT00707798|111651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171674|NCT00707798|111651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171675|NCT00707798|111651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171676|NCT00358813|NKT102783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171677|NCT00358813|NKT102783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171678|NCT00358813|NKT102783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171679|NCT00358813|NKT102783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171680|NCT00358813|NKT102783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171681|NCT00358813|NKT102783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171682|NCT00358813|NKT102783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171683|NCT06896929|permethrin|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/21860157/|Comparison of permethrin and ivermectin in scabies was done
3171684|NCT07236723||Data Monitoring Committee Charter|https://pmc.ncbi.nlm.nih.gov/articles/PMC7571449/|https://pmc.ncbi.nlm.nih.gov/articles/PMC7571449/
3175984|NCT06389461||Abenavoli, A., Badi, F., Barbieri, M., Bianchi, M., Biglione, G., Dealessi, C., Grandini, M., Lavazza, C., Mapelli, L., Milano, V., Monti, L., Seppia, S., Tresoldi, M. & Maggiani, A. (2020).|http://doi.org/10.1016/j.jbmt.2020.07.017|Cranial osteopathic treatment and stress-related effects on autonomic nervous system measured by salivary markers: A pilot study. Journal of Bodywork and Movement Therapies. 24(4), 215-221.
3175985|NCT01059851||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-023&kw=4305-023&tab=access|
3175986|NCT01039675|113120|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175987|NCT01039675|113120|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175988|NCT01039675|113120|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175989|NCT01039675|113120|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175990|NCT01039675|113120|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178212|NCT03979612||Individual Participant Data Set|https://www.iuct-oncopole.fr/information-sur-les-donnees-de-sante|General information on our web site about investigations from patients data
3180454|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/26244985|"Passardi A et al. Impact of Pre-Treatment Lactate Dehydrogenase Levels on Prognosis and Bevacizumab Efficacy in Patients with Metastatic Colorectal Cancer.~PLoS One 2015; 10(8): e0134732"
3171685|NCT01495026|115708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171686|NCT01495026|115708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171687|NCT01495026|115708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171688|NCT01495026|115708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171689|NCT01495026|115708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175991|NCT01039675|113120|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175992|NCT01039675|113120|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175993|NCT06882057|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
3175994|NCT07301775||Individual Participant Data Set|http://www.eyecon.pk|
3175995|NCT00567580|NCT00567580|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3175996|NCT00134719|102370 (primary study)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178213|NCT00000488|LRC-CPPT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3178214|NCT00000488||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|
3171690|NCT01495026|115708|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175997|NCT00134719|102370 (primary study)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173824|NCT01899755|116987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173825|NCT01899755|116987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173826|NCT01899755|116987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173827|NCT01899755|116987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173828|NCT01818024|116343|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173829|NCT01818024|116343|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173830|NCT01818024|116343|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173831|NCT01818024|116343|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173832|NCT01818024|116343|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173833|NCT01818024|116343|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173834|NCT01818024|116343|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173835|NCT03119025||Clinical Study Report|https://doi.org/10.1007/s12026-017-8967-2|Chernykh E., Leplina O., Oleynik E., Tikhonova M., Tyrinova T., Starostina N., Ostanin A. Immunotherapy with interferon-α-induced dendritic cells for chronic HCV infection (the results of pilot clinical trial) // Immunologic Research.- 2017
3173836|NCT00268203|BEX104545|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173837|NCT00268203|BEX104545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173838|NCT00268203|BEX104545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173839|NCT00268203|BEX104545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173840|NCT00005292|AADR|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/aadr|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180455|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/27120807|"Passardi A et al. Inflammatory indexes as predictors of prognosis and bevacizumab efficacy in patients with metastatic colorectal cancer.~Oncotarget 2016 May 31;7(22):33210-9"
3173841|NCT00005292||Study Forms|https://biolincc.nhlbi.nih.gov/studies/aadr/Forms/|
3171691|NCT01495026|115708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171692|NCT01499290|D4280C00001 Revised CSP|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1448&filename=RECLAIM%201%20(D4280C00001)%20Protocol.pdf|RECLAIM 1 (D4280C00001) Revised Clinical Study Protocol
3171693|NCT07199218||Study Protocol|https://osf.io/f69ds/files/osfstorage|Study protocol, statistical analysis plan, and parental informed consent form are available in the OSF repository: https://osf.io/f69ds/files/osfstorage (Updated September 2025)
3171694|NCT07199218||Statistical Analysis Plan|https://osf.io/f69ds/files/osf|Study protocol, statistical analysis plan, and parental informed consent form are available in the OSF repository: https://osf.io/f69ds/files/osfstorage (Updated September 2025)
3173842|NCT00789308|Accession ID: SDY1437|Individual Participant Data Set|https://www.immport.org/shared/study/SDY1437|Digital object identifier (DOI): 10.21430/M3YZY4PXCS. Location of data: Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts.
3173843|NCT00789308|Accession ID: SDY1437|Study Protocol|https://www.immport.org/shared/study/SDY1437|Digital object identifier (DOI): 10.21430/M3YZY4PXCS. Location of data: Immunology Database and Analysis Portal (ImmPort).
3173844|NCT00789308|Accession ID: SDY1437|Statistical Analysis Plan|https://www.immport.org/shared/study/SDY1437|Digital object identifier (DOI): 10.21430/M3YZY4PXCS. Location of data: Immunology Database and Analysis Portal (ImmPort).
3173845|NCT00789308|Accession ID: SDY1437|Informed Consent Form|https://www.immport.org/shared/study/SDY1437|Digital object identifier (DOI): 10.21430/M3YZY4PXCS. Location of data: Immunology Database and Analysis Portal (ImmPort).
3173846|NCT00363077|107975|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173847|NCT00363077|107975|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173848|NCT00363077|107975|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173849|NCT00363077|107975|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173850|NCT00363077|107975|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178215|NCT00118690|SFA100316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171695|NCT07199218||Informed Consent Form|https://osf.io/f69ds/files/osf|
3171696|NCT00996840|111592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171697|NCT00996840|111592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171698|NCT00996840|111592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178216|NCT00118690|SFA100316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178217|NCT00118690|SFA100316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178218|NCT00118690|SFA100316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180456|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/26259598|"Ulivi P et al. eNOS polymorphisms as predictors of efficacy of bevacizumab-based chemotherapy in metastatic colorectal cancer: data from a randomized clinical trial.~J Transl Med 2015;11(3): 258"
3180457|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/26848624|"Casadei Gardini A et al. Prognostic role of serum concentrations of high-sensitivity C-reactive protein in patients with metastatic colorectal cancer: results from the ITACa trial.~Oncotarget 2016 Mar 1;7(9):10193-202"
3180458|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/28465540|"Marisi G et al Circulating VEGF and eNOS variations as predictors of outcome in metastatic colorectal cancer patients receiving bevacizumab.~Sci Rep 2017 May 2;7(1):1293"
3180459|NCT06814223||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
3180460|NCT06817746||Study Protocol|https://www.fsm.unipi.it|
3180461|NCT06876051|10.47363/JPRRR/2024(6)163|Peer-reviewed journal publication related to the study|https://onlinescientificresearch.com/articles/greek-validation-of-the-questionnaire-prenatal-breastfeeding-self-efficacy-scale.pdf|"Greek Validation of the Questionnaire Prenatal Breast-Feeding Self Efficacy Scale July 2024Journal of Pediatrics Research Reviews \& Reports"
3180462|NCT06876051|PMID: 28043180|Peer-reviewed journal publication related to the study|https://pubmed.ncbi.nlm.nih.gov/28043180/|Title: The effect of body and mind stress-releasing techniques on the breastfeeding of full term babies; a critical analysis of published interventional studies
3180463|NCT06805448|2024-516715-25-00|Study Protocol|https://euclinicaltrials.eu/|
3171699|NCT00996840|111592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171700|NCT00996840|111592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171701|NCT00996840|111592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171702|NCT00996840|111592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173851|NCT01039961|113022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173852|NCT01039961|113022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173853|NCT01039961|113022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173854|NCT01039961|113022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173855|NCT01039961|113022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173856|NCT01039961|113022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173857|NCT01039961|113022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173858|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/31353554/|
3175998|NCT00134719|102370 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175999|NCT00134719|102370 (primary study)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 102370 are summarised with study 102371 on the GSK Clinical Study Register.
3176000|NCT00134719|102370 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180464|NCT03114072||Study Protocol|https://helseforskning.etikkom.no/prosjekterirek/prosjektregister/prosjekt?p_document_id=742253&p_parent_id=755398&_ikbLanguageCode=n|This is a brief description of the Project published at the web site of The Regional Ethics Committee (REC West).
3171703|NCT02069002||Study Protocol|http://bmjopen.bmj.com/content/6/6/e011003.full.pdf+html|
3171704|NCT01164878||Individual Participant Data Set|https://dfzljdn9uc3pi.cloudfront.net/2016/2483/1/SPSS_repa_et_al.sav|SPSS Data Set for Analysis
3171705|NCT01471327|115705|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171706|NCT01471327|115705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171707|NCT01471327|115705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171708|NCT01471327|115705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173859|NCT07067515||PMC article.|https://pubmed.ncbi.nlm.nih.gov/30734608/|
3173860|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/35508275/|
3178219|NCT00118690|SFA100316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171709|NCT01471327|115705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173861|NCT01934205|116666|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173862|NCT01934205|116666|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173863|NCT01934205|116666|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173864|NCT01934205|116666|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173865|NCT01934205|116666|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176001|NCT03496675||Individual Participant Data Set|https://osf.io/tpdhu/|
3176002|NCT04976725||Statistical Analysis Plan|https://doi.org/10.1016/J.JCM.2019.12.001|
3176003|NCT07233525||Study Protocol|https://osf.io/ryq6k/overview?view_only=82691366adfe4dd3999bfba95ce6466d|The full study protocol
3178220|NCT01622231|116365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178221|NCT01622231|116365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178222|NCT01622231|116365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178223|NCT01622231|116365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178224|NCT02809612||Study Protocol|http://www.kbh.uu.se|
3178225|NCT02747875|Pr 7364|Study Protocol|http://www.irbear.org|The Effect of Methadone vs. Fentanyl Administration on Postoperative Pain Control in Pediatric Patients Undergoing Cardiac Surgery. A Randomized, Double-Blinded Controlled Trial
3178226|NCT06462885||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
3178227|NCT00347360|CFD105453|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178228|NCT00347360|CFD105453|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180465|NCT06884007|https://tez.yok.gov.tr/UlusalT|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp
3180466|NCT05591924||C3RP Laboratory Website|https://c3rp.org/leligdowiczlab|
3180467|NCT06824558|Fear of Childbirth Scale|Individual Participant Data Set|https://gcris.pau.edu.tr/bitstream/11499/6124/1/7ba3f584-23f9-4af0-9a4a-56f72570f94d.pdf|https://gcris.pau.edu.tr/bitstream/11499/6124/1/7ba3f584-23f9-4af0-9a4a-56f72570f94d.pdf
3180468|NCT06824558|Fear of Childbirth Scale|Individual Participant Data Set|https://gcris.pau.edu.tr/bitstream/11499/6124/1/7ba3f584-23f9-4af0-9a4a-56f72570f94d.pdf|
3173866|NCT01934205|116666|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180469|NCT06824922|Protocolo_ECA_piloto|Study Protocol|https://drive.google.com/file/d/1PhNe1G9PVs2FkOmKeyXazMLW3l-sxRR7/view?usp=sharing|
3180470|NCT06863207||Individual Participant Data Set|https://vivli.org/|
3173867|NCT01934205|116666|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173868|NCT05866263||Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/23405164/|
3173869|NCT05866263||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/23405164/|
3180471|NCT05334355||Individual Participant Data Set|https://digitalcommons.montclair.edu/data/10|Complete individual participant data set is publicly available on the Montclair State University Digital Commons.
3173870|NCT00197249|270362/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176004|NCT07301047|No individual participant data|No individual participant data (IPD) or supporting documents will be shared. Only aggregated study results may be published in journals or presented at conferences.|https://www.cgmh.org.tw/|No individual participant data (IPD) or supporting documents will be shared. Only aggregated study results may be published in journals or presented at conferences.
3180472|NCT06883916|Ethics Committee Approval|Informed Consent Form|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
3180473|NCT02415933||Study Protocol|https://knowledge.uchicago.edu/handle/11417/69|
3171710|NCT01471327|115705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173871|NCT00197249|270362/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176005|NCT01996540||study publication|https://www.ncbi.nlm.nih.gov/pubmed/27472648|"Maltoni M et al Systematic versus on-demand early palliative care: results from a multicentre, randomised clinical trial.~Eur J Cancer 2016 Sep;65:61-8"
3178229|NCT00347360|CFD105453|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180474|NCT06997874|COMBAT trial|Study Protocol|https://nictu.hscni.net/service/combat/|
3180475|NCT06778889||Study Protocol|https://orcid.org/0009-0009-6142-6201|Data and supporting documents, including the study protocol, statistical analysis plan, and anonymized data set, will be available upon request to the corresponding author (email: nazeermed313@gmail.com) starting \[insert date\]. Requests will be reviewed based on a valid research purpose and agreement to use data ethically
3180476|NCT06886594||Study Protocol|https://bap.ksu.edu.tr/|
3180477|NCT06744946|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3180478|NCT04098276|10.1186/s12889-021-11930-2|Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-021-11930-2|
3180479|NCT06881381||Study Protocol|https://docs.google.com/document/d/19ZwAv6y0UUaSa_Hjb3jlzuhMfTro0Y6p/edit?usp=drive_link&ouid=101334879348395838064&rtpof=true&sd=true|STUDY PROTOKOL DIAGRAM
3171711|NCT01471327|115705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173872|NCT00197249|270362/006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173873|NCT00197249|270362/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173874|NCT00197249|270362/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173875|NCT02045849|117349|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173876|NCT02045849|117349|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173877|NCT02045849|117349|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173878|NCT02045849|117349|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176006|NCT01996540||study publication|https://www.ncbi.nlm.nih.gov/pubmed/27821313|"Maltoni M et al Systematic versus on-demand early palliative care: A randomised clinical trial assessing quality of care and treatment aggressiveness near the end of life.~Eur J Cancer 2016 Dec;69:110-118."
3176007|NCT01996540||study publication|https://doi.org/10.1007/s00520-018-4517-2|"Scarpi E. et al~Systematic vs. on-demand early palliative care in gastric cancer patients:~a randomized clinical trial assessing patient and healthcare service outcomes"
3176008|NCT00496327||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176009|NCT00002874|NCT00002874|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3176010|NCT00976391|108486|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176011|NCT00976391|108486|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176012|NCT00976391|108486|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176013|NCT00976391|108486|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176014|NCT00976391|108486|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176015|NCT00976391|108486|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176016|NCT00976391|108486|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176017|NCT00005133|CHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/chs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176018|NCT04967703||Full Paper|http://www.europeanreview.org/article/32287|
3176019|NCT00705965||treatment manual and supplemental content|http://links.lww.com/PSYMED/A275|
3176020|NCT01894360|117100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176021|NCT01894360|117100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180480|NCT06951308|PhD2-2025|Study Protocol|https://docs.google.com/document/d/1IpRJsfgeH_tvSrji9ydietlVCuID47xq/edit?usp=sharing&ouid=106245773366942496306&rtpof=true&sd=true|Open to enyone with link
3180481|NCT06746389|201021/B/03|Protocol and ethics can be shared on request|https://www.exeter.ac.uk/departments/cgr/researchethics/|Ethics documents and study protocol can be shared on request. Please contact PI Dr Raquel Revuelta Iniesta at r.revuelta-iniesta@exeter.ac.uk or the PHSS Ethics Committee at a.guy@exeter.ac.uk
3180482|NCT06692621|Yöktez|Individual Participant Data Set|https://tez.yok.gov.tr/UlusalTezMerkezi/tezlerim.jsp?sira=0|You can reach us at harunzengin71@gmail.com
3180483|NCT07039682|EKSTRIM study protocol|Study Protocol|https://drive.google.com/file/d/18K8ImooxCYP9CJ7Vpxg1NBH6ySyYy1Tr/view?usp=sharing|This study does not plan to share individual participant data (IPD) due to the involvement of minors and the sensitive nature of HIV-related information. The protocol prioritizes adolescent privacy, confidentiality, and protection of digital health data in accordance with national regulations and institutional ethical standards. Sharing of IPD, even in de-identified form, may risk re-identification, especially in small or specific community samples. All collected data will be stored securely and accessed only by authorized study personnel. Aggregated results may be shared in publications and presentations, but raw IPD will remain confidential.
3171712|NCT00312013|FRX106365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173879|NCT02045849|117349|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173880|NCT02045849|117349|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173881|NCT02045849|117349|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173882|NCT00429481|444563/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173883|NCT00429481|444563/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173884|NCT00429481|444563/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173885|NCT00429481|444563/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173886|NCT00429481|444563/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173887|NCT00429481|444563/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173888|NCT00985751|113171|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173889|NCT00985751|113171|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173890|NCT00985751|113171|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173891|NCT00985751|113171|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173892|NCT00985751|113171|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176022|NCT01894360|117100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176023|NCT01894360|117100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176024|NCT01894360|117100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176025|NCT01894360|117100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178230|NCT00347360|CFD105453|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178231|NCT00347360|CFD105453|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171713|NCT00312013|FRX106365|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171714|NCT00312013|FRX106365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178232|NCT00347360|CFD105453|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171715|NCT00312013|FRX106365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171716|NCT00312013|FRX106365|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171717|NCT00312013|FRX106365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171718|NCT00312013|FRX106365|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171719|NCT00265941|NCT00265941|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3171720|NCT00684177|TOC110977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173893|NCT00294047|104820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173894|NCT00294047|104820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173895|NCT00294047|104820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173896|NCT00294047|104820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173897|NCT00294047|104820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173898|NCT00294047|104820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176026|NCT01894360|117100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176027|NCT00985790|113237|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176028|NCT00985790|113237|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171721|NCT00684177|TOC110977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171722|NCT00684177|TOC110977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171723|NCT00684177|TOC110977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176029|NCT00985790|113237|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176030|NCT00985790|113237|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176031|NCT00985790|113237|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178233|NCT00347360|CFD105453|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176032|NCT00985790|113237|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176033|NCT00676052|AC2110664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176034|NCT00676052|AC2110664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176035|NCT00676052|AC2110664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176036|NCT00676052|AC2110664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178234|NCT06652529||Study Protocol|https://www.aromics.es/en/|
3178235|NCT01254071|114694|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178236|NCT01254071|114694|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176037|NCT00676052|AC2110664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176038|NCT00676052|AC2110664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178237|NCT01254071|114694|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178238|NCT01254071|114694|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178239|NCT01254071|114694|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178240|NCT01254071|114694|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178241|NCT01254071|114694|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180484|NCT07039682|EKSTRIM_ICF|Informed Consent Form|https://drive.google.com/file/d/1cnEfDqkpzy54F8jV8atQ161KA-9C9gwW/view?usp=sharing|The EKSTRIM Informed Consent Form is clearly structured and comprehensive, addressing all essential components of ethical research. It outlines the study's objectives, procedures, risks, benefits, and rights of participants in a language that is accessible and age-appropriate for adolescents. It emphasizes voluntary participation and the right to withdraw at any time without consequence. The form includes detailed information on data confidentiality, compensation, and peer educator support, enhancing participant protection and engagement. The inclusion of contact information offers transparency and accessibility. However, the form could be strengthened by explicitly stating how long data will be retained and whether participants will receive feedback on study findings. Overall, the ICF demonstrates ethical rigor and appropriateness for adolescent involvement in HIV-related digital health research.
3180485|NCT06762756||Individual Participant Data Set|https://researchdata.bath.ac.uk|The datasets generated and/or analysed during the current study are available in the University of Bath repository.
3171724|NCT00684177|TOC110977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176039|NCT00676052|AC2110664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178242|NCT01893203|25109244|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/|
3178243|NCT00109122||CSR Synopsiis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178244|NCT00094172|SDY547|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY547|ImmPort study identifier is SDY547. ImmPort is the long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts.
3178245|NCT00094172|SDY547|Study summary, -design with synopsis, -adverse events, -medications, -demographics, -lab tests, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY547|ImmPort study identifier is SDY547
3178246|NCT00094172|ITN020AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN020AI
3180486|NCT06762756||Analytic Code|https://osf.io/v5deq/?view_only=d5dd1f5903a0480d94402c7c6528c6a4|Scripts are available on Open Science Framework
3178247|NCT00094172|ITN020AI|Study overview with synopsis, -navigator, -schedule of assessments, data and reports, -manuscripts and abstracts et al.|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare is the research portal of the Immune Tolerance Network (ITN) that makes data from the consortium's studies publicly available.
3178248|NCT01471678|115707|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180487|NCT06744270|Inonu University Clinical Rese|Clinical Study Report|https://www.inonu.edu.tr/klinik.etik|https://www.inonu.edu.tr/klinik.etik
3180488|NCT06781047|gulevdali@hotmail.com|Statistical Analysis Plan|https://www.akademikredaksiyon.com/|The study data is shared with the official at the website https://www.akademikredaksiyon.com/ for statistical analysis and evaluation of the results.
3180489|NCT06764238|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
3180490|NCT06950970|tetinstitute.rn@gmail.com|Informed Consent Form|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
3180491|NCT06950970|tetinstitute.rn@gmail.com|Statistical Analysis Plan|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
3171725|NCT00684177|TOC110977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171726|NCT00684177|TOC110977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171727|NCT02740309|Sala Institute|Sala Institute for Child & Family Centered Care|http://nyulangone.org/locations/hassenfeld-childrens-hospital/sala-institute-for-child-family-centered-care|
3171728|NCT00818259||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=0869-134&kw=0869-134&tab=access|
3171729|NCT00291343|105239 (mth24-30)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171730|NCT00291343|105239 (mth24-30)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171731|NCT00291343|105239 (mth24-30)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171732|NCT00291343|105239 (mth24-30)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171733|NCT00291343|105239 (mth24-30)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 105239 are summarised with study 105245 on the GSK Clinical Study Register.
3171734|NCT00291343|105239 (mth24-30)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171735|NCT03088501|PMID: PMC5065083|Protocol of the birth cohort|https://bmcpregnancychildbirth.biomedcentral.com/articles/10.1186/s12884-016-1088-4|The proposed randomized controlled trial is nested within the MAASTHI Birth cohort in order to improve the follow-up rates.
3171736|NCT02184637|200951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171737|NCT02184637|200951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171738|NCT02184637|200951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171739|NCT02184637|200951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171740|NCT02184637|200951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171741|NCT02184637|200951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171742|NCT02184637|200951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171743|NCT03094247||Individual Participant Data Set|https://openscholarship.wustl.edu/data/101/|
3171744|NCT00473694||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171745|NCT01772134|116135|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171746|NCT01772134|116135|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171747|NCT01772134|116135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171748|NCT01772134|116135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173899|NCT00196963|103532|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173900|NCT00196963|103532|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173901|NCT00196963|103532|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176040|NCT00120848|580299/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176041|NCT00120848|580299/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176042|NCT00120848|580299/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176043|NCT00120848|580299/007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176044|NCT00120848|580299/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180492|NCT06762743||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|registered clinical trial about Brivaracetam oral solution on Chinese website
3173902|NCT00196963|103532|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173903|NCT00196963|103532|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176045|NCT00120848|580299/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176046|NCT00120848|580299/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176047|NCT01266980|113970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176048|NCT01266980|113970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176049|NCT01266980|113970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176050|NCT01266980|113970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176051|NCT01266980|113970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176052|NCT01266980|113970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176053|NCT01266980|113970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176054|NCT05872945||Individual Participant Data Set|https://github.com/dradolfomunoz/PF12RED|
3176055|NCT01064284|NEJM2016;374:2054-206|Article|http://www.nejm.org/doi/full/10.1056/NEJMoa1516437?af=R&rss=currentIssue&|
3176056|NCT07055932||Study Protocol|https://theses.gla.ac.uk/1017/|
3176057|NCT01934231|117150|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176058|NCT01934231|117150|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176059|NCT01934231|117150|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176060|NCT01934231|117150|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176061|NCT01934231|117150|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176062|NCT01934231|117150|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176063|NCT01934231|117150|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176064|NCT01379937|115115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173904|NCT00268216|SCO30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173905|NCT00268216|SCO30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173906|NCT00268216|SCO30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173907|NCT00268216|SCO30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173908|NCT00268216|SCO30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173909|NCT00268216|SCO30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173910|NCT00268216|SCO30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173911|NCT01494532|111569|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173912|NCT01494532|111569|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173913|NCT01494532|111569|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173914|NCT01494532|111569|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176065|NCT01379937|115115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171749|NCT01772134|116135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173915|NCT01494532|111569|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173916|NCT01494532|111569|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176066|NCT01379937|115115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176067|NCT01379937|115115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178249|NCT01471678|115707|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178250|NCT01471678|115707|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178251|NCT01471678|115707|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178252|NCT01471678|115707|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178253|NCT01471678|115707|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178254|NCT01471678|115707|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178255|NCT00369824|107682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178256|NCT00369824|107682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178257|NCT00369824|107682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178258|NCT00369824|107682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178259|NCT00369824|107682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171750|NCT01772134|116135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171751|NCT01772134|116135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171752|NCT03322358||Individual Participant Data Set|https://www.sleepdata.org/datasets/urbanpoor|
3171753|NCT02690896||Study-related materials|http://psychology.cos.ucf.edu/older/|Please contact the UCF OLDeR Lab for any questions regarding the study and/or study materials.
3171754|NCT06935851||Study Protocol|https://osf.io|signing a data agreement
3171755|NCT00942162|111476|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180493|NCT01128595|113126|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180494|NCT01128595|113126|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180495|NCT01128595|113126|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180496|NCT01128595|113126|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180497|NCT01128595|113126|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180498|NCT01128595|113126|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180499|NCT01128595|113126|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180500|NCT06776536||institutional review board|https://camsakurasehir.saglik.gov.tr/|
3180501|NCT06828367|not necessary|Study Protocol|https://docs.google.com/document/d/1hvjyp_RfCDDpHWkrTv_s7qhztM4Pqw9T/edit|is a public document
3171756|NCT00942162|111476|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173917|NCT01989884||Clinical Study Report|https://doi.org/10.1007/s11060-019-03116-z|
3176068|NCT01379937|115115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178260|NCT00369824|107682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178261|NCT01148472|2004-005069-39|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2004-005069-39/results|
3178262|NCT06934993||Study Protocol|https://docs.google.com/document/d/18BaS1fHrkVkHIiYzNlN0CmgH7mLS9MH2H82qL_TXMsA/edit?tab=t.0|The data will be uploaded three months after the publication of the study. The data is not currently available at the provided address.
3171757|NCT00942162|111476|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173918|NCT01573819|115719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180502|NCT00857766|112355|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180503|NCT00857766|112355|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180504|NCT00857766|112355|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180505|NCT00857766|112355|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180506|NCT00857766|112355|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180507|NCT00857766|112355|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176069|NCT01379937|115115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176070|NCT00552279|109179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176071|NCT00552279|109179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176072|NCT00552279|109179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176073|NCT00552279|109179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176074|NCT00552279|109179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176075|NCT00552279|109179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176076|NCT00552279|109179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176077|NCT00000603|COBLT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/coblt/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176078|NCT00000603||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coblt/|
3176079|NCT00000603||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coblt/|
3176080|NCT00000603||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coblt/|
3176081|NCT00000544|DASH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/dash/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176082|NCT00000544||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dash/|
3176083|NCT00000544||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/dash/|
3176084|NCT03755154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3176085|NCT03755154||Study Protocol|https://clinicaltrials.servier.com/|
3178263|NCT06934993||Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1wNK5vDSm42LuTVoIUTiuYG_Yg_b2tGHBi1PKytJVMNw/edit?usp=sharing|The data will be uploaded three months after the publication of the study. The data is not currently available at the provided address.
3178264|NCT06934993||Informed Consent Form|https://docs.google.com/document/d/1F8ermx5WFwjpxtn4MubaZDkew90csOJMbjbKOXvCgC0/edit?usp=sharing|The data will be uploaded three months after the publication of the study. The data is not currently available at the provided address.
3178265|NCT06934993||Statistical Analysis Plan|https://docs.google.com/document/d/1nG06s9_mVy9alLULhhv0LBmW4YkqVBX1RBXj8GoaGXQ/edit?usp=sharing|The data will be uploaded three months after the publication of the study. The data is not currently available at the provided address.
3178266|NCT06934993||Clinical Study Report|https://docs.google.com/document/d/17UWmXMrss0xVXFFsI-ulf6aGNU3tHCWMr34yhpWYiNA/edit?usp=sharing|The data will be uploaded three months after the publication of the study. The data is not currently available at the provided address.
3173919|NCT01573819|115719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173920|NCT01573819|115719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173921|NCT01573819|115719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176086|NCT03755154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178267|NCT00508365|CFD109701|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176087|NCT03755154||Informed Consent Form|https://clinicaltrials.servier.com/|
3176088|NCT03755154||Clinical Study Report|https://clinicaltrials.servier.com/|
3176089|NCT03755154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3176090|NCT01313676|113782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176091|NCT01313676|113782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176092|NCT01313676|113782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173922|NCT01573819|115719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176093|NCT01313676|113782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176094|NCT01313676|113782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176095|NCT01313676|113782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176096|NCT01313676|113782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176097|NCT01691482|114956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176098|NCT01691482|114956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176099|NCT01691482|114956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178268|NCT00508365|CFD109701|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178269|NCT00508365|CFD109701|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178270|NCT00508365|CFD109701|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178271|NCT00508365|CFD109701|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178272|NCT00508365|CFD109701|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178273|NCT00508365|CFD109701|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178274|NCT00043901|LAM40097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178275|NCT00043901|LAM40097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171758|NCT00942162|111476|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171759|NCT00942162|111476|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171760|NCT00942162|111476|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171761|NCT00942162|111476|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176100|NCT01691482|114956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176101|NCT01691482|114956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176102|NCT01691482|114956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176103|NCT01691482|114956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176104|NCT01370642||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-043&kw=7009-043&tab=access|
3176105|NCT02477046||Statistical Analysis Plan|https://idmod.sharepoint.com/projects/_layouts/15/guestaccess.aspx?guestaccesstoken=3%2bxJO%2bcBwXx6PfMuzCQmu8ESB0X7mhLPtowTTLaYTmY%3d&docid=02ab39752ccb14c10bdfd61c0a731e6ff&rev=1|
3176106|NCT00480025|109493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176107|NCT00480025|109493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176108|NCT00480025|109493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176109|NCT00480025|109493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176110|NCT00480025|109493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176111|NCT00480025|109493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176112|NCT00480025|109493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178276|NCT00043901|LAM40097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178277|NCT00043901|LAM40097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178278|NCT00043901|LAM40097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171762|NCT06329388||Clinical Study Report|https://www.truheightvitamins.com/pages/clinical-study|Submit your email to have a copy of the Clinical Trial sent to you.
3171763|NCT00463437|109507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171764|NCT00463437|109507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171765|NCT00463437|109507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171766|NCT00463437|109507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171767|NCT00463437|109507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171768|NCT00463437|109507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171769|NCT00463437|109507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171770|NCT03184948||Statistical Analysis Plan|http://ketkisheth.weebly.com/|
3176113|NCT00132912||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171771|NCT01583036|116216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176114|NCT03142451||Study Protocol|http://foamix.co.il/|
3176115|NCT00871000|111815|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176116|NCT00871000|111815|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176117|NCT00871000|111815|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176118|NCT00871000|111815|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176119|NCT00871000|111815|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176120|NCT00871000|111815|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178279|NCT00043901|LAM40097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178280|NCT00043901|LAM40097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178281|NCT00289783|103813|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178282|NCT00289783|103813|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178283|NCT00289783|103813|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178284|NCT00289783|103813|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178285|NCT00289783|103813|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103813 are summarised with study 105067 on the GSK Clinical Study Register.
3178286|NCT01773733||published data|https://www.omet-endojournals.ru/jour/article/view/7988|The observation program allow to implement the principles of active monitoring of the efficacy and safety of the drug in the current clinical practice and to develop a skill of reasonable prescribing. In Primavera program it was shown that the use of Reduxine® (sibutramine+ microcrystalline cellulose) leads to loss of body weight and doesn't lead to serious adverse effect
3178287|NCT03733470|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
3178288|NCT05930912||Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
3178289|NCT05930912|zenodo.7382529|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7382529|
3178290|NCT05930912|zenodo.6942208|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6942208|
3178291|NCT05930912|zenodo.7188211|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7188211|
3178292|NCT05930912|zenodo.6941906|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6941906|
3178293|NCT05930912|zenodo.6952516|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6952516|
3178294|NCT05930912|zenodo.7022873|Analytic Code|http://doi.org/10.5281/zenodo.7022873|The technological-psychoanalytic mass psychological observation and analysis schemes.
3178295|NCT00043914|LAM40013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178296|NCT00043914|LAM40013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178297|NCT00043914|LAM40013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178298|NCT00043914|LAM40013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178299|NCT00043914|LAM40013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178300|NCT00043914|LAM40013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178301|NCT00043914|LAM40013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178302|NCT00963937|111035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178303|NCT00963937|111035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178304|NCT00963937|111035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178305|NCT00963937|111035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171772|NCT01583036|116216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176121|NCT00871000|111815|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176122|NCT00459550|106006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176123|NCT00459550|106006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180508|NCT00857766|112355|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180509|NCT07038772|EAT-40|Study Protocol|https://www.eat-26.com/|
3180510|NCT05018143|GUID|Individual Participant Data Set|https://nda.nih.gov/|
3176124|NCT00459550|106006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178306|NCT00000557|ENRICHD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/enrichd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176125|NCT00459550|106006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176126|NCT00459550|106006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176127|NCT00459550|106006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178307|NCT00000557||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
3176128|NCT02100644|200776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178308|NCT00000557||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
3178309|NCT01762878|116617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178310|NCT01762878|116617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178311|NCT01762878|116617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178312|NCT01762878|116617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178313|NCT01762878|116617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178314|NCT01762878|116617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178315|NCT01762878|116617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180511|NCT06662136||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3180512|NCT05201599|zxt4|Study Protocol|https://pan.baidu.com/s/1PNKfPWrpeJtodX1RwH8k-w|
3180513|NCT01702376|113789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180514|NCT01702376|113789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180515|NCT01702376|113789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180516|NCT01702376|113789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180517|NCT01702376|113789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180518|NCT01702376|113789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180519|NCT01702376|113789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176129|NCT02100644|200776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176130|NCT02100644|200776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176131|NCT02100644|200776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176132|NCT02100644|200776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176133|NCT00202852||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176134|NCT06791044||Study Protocol|https://eka-hosp.gr/|
3176135|NCT03495635|osf.io/8ukfv|Individual Participant Data Set|https://osf.io/|
3180520|NCT02677766|TOEFFI15_14|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/30250407|"Titolo dello studio: Terapia occupazionale nei pazienti complessi : studio pilota.~Codice protocollo TOEFFI15\_14 Data di rilascio: 16/09/15"
3176136|NCT00970710||Study Protocol|http://bmcpediatr.biomedcentral.com/articles/10.1186/1471-2431-12-93|
3176137|NCT00970710||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=mustila+taina+vacopp|
3180521|NCT03956628||stay safe programme|http://www.staysafe.ie|data can be accessed by approaching the above specified cite as it has programme that was used in the study.
3180522|NCT00756067|111652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180523|NCT00756067|111652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180524|NCT00756067|111652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180525|NCT00756067|111652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180526|NCT00756067|111652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180527|NCT00979121|ARDSNet-SAILS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/sails/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180528|NCT00979121||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/sails/|
3171773|NCT01583036|116216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180529|NCT00979121||Study Forms|http://biolincc.nhlbi.nih.gov/studies/sails/|
3180530|NCT00309166|580299/011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180531|NCT00309166|580299/011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180532|NCT00309166|580299/011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180533|NCT00309166|580299/011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180534|NCT00309166|580299/011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180535|NCT00309166|580299/011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180536|NCT00449774|LBI108617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180537|NCT00449774|LBI108617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180538|NCT00449774|LBI108617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180539|NCT00449774|LBI108617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180540|NCT00449774|LBI108617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180541|NCT00449774|LBI108617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180542|NCT00449774|LBI108617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180543|NCT01119651|114574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180544|NCT01119651|114574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180545|NCT01119651|114574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180546|NCT01119651|114574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180547|NCT01119651|114574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180548|NCT01119651|114574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180549|NCT01119651|114574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180550|NCT06861205||Study Protocol|https://doi.org/10.3389/fnut.2024.1438740|
3180551|NCT06753526|ahmed-mahmoud@sohag.med.edu.eg|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/9008325/|
3180552|NCT03019835||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/7880668|
3180553|NCT06750744|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3180554|NCT01332552|115040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180555|NCT01332552|115040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180556|NCT01332552|115040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180557|NCT01332552|115040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180558|NCT01332552|115040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180559|NCT01332552|115040|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180560|NCT01332552|115040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180561|NCT02798900||Statistical Analysis Plan|https://uredu-my.sharepoint.com/personal/rosy_cardenas_urosario_edu_co/_layouts/15/guestaccess.aspx?guestaccesstoken=QcFnsRtAu0sL3C3BykRoRmzup56%2fKS1U50PYsgfCPaQ%3d&docid=180e16d39085f4beda2f90ff3f40398ad|
3180562|NCT02798900||Informed Consent Form|https://uredu-my.sharepoint.com/personal/rosy_cardenas_urosario_edu_co/_layouts/15/guestaccess.aspx?guestaccesstoken=22KPPvsG5ChMhU6k%2bwtjMT9u%2b72A2ABD0JwYpY0D7p8%3d&docid=1b012eb2a38df4685b5d63e2429ba5bcf|
3180563|NCT01491815||Study Protocol|http://www.biomedcentral.com/search?query=glinatsi&searchType=publisherSearch|Publication of the protocol. Glinatsi et al. Trials (2017) 18:161
3180564|NCT00489554|109661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171774|NCT01583036|116216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171775|NCT01583036|116216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171776|NCT01583036|116216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171777|NCT01583036|116216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173923|NCT01573819|115719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173924|NCT01573819|115719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173925|NCT04748991||Product monograph - Vernakalant|https://pdf.hres.ca/dpd_pm/00038441.PDF|
3173926|NCT04748991||Product monograph - Amiodarone|https://pdf.hres.ca/dpd_pm/00035425.PDF|
3173927|NCT03045458||Clinical Study Report|http://mc.manuscriptcentral.com/jperio|
3173928|NCT01717950||Clinical Study Report|https://smhs.gwu.edu/mitm-crg/|
3173929|NCT07138755||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/39489090/|
3173930|NCT05341453||Study Protocol|https://www.chmirakl.cz/aktuality/study-protokol|
3173931|NCT05341453||Statistical Analysis Plan|https://www.chmirakl.cz/aktuality/statistical-analysis-plan|
3173932|NCT05341453||Informed Consent Form|https://www.chmirakl.cz/aktuality/type-informed-consent-form|
3173933|NCT07309094||Statistical Analysis Plan|http://osf.io/|
3173934|NCT07309094||Analytic Code|http://osf.io|
3173935|NCT00533507|109861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173936|NCT00533507|109861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176138|NCT01316900|113360|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176139|NCT01316900|113360|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176140|NCT01316900|113360|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173937|NCT00533507|109861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173938|NCT00533507|109861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173939|NCT00533507|109861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173940|NCT00533507|109861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173941|NCT00533507|109861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173942|NCT07254182||Individual Participant Data Set|https://zenodo.org/records/17255092|
3173943|NCT07254182||Study Protocol|https://zenodo.org/records/17255092|
3173944|NCT07254182||Statistical Analysis Plan|https://zenodo.org/records/17255092|
3173945|NCT03065699|DIALIVE CSR summary 20210319|Clinical Study Report|http://yaqrit.com|"A summary of the final Clinical Study Report can be obtained through request to:~1. YAQRIT Ltd, attention of Daniel Green, CEO (daniel.green@yaqrit.com) or Carrie Morgan (carrie.morgan@yaqrit.com)~2. FAKKEL bvba, attention of Jaak Minten, CEO (info@fakkel-bvba.com)"
3173946|NCT00452348|ADA109057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173947|NCT00452348|ADA109057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176141|NCT01316900|113360|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173948|NCT00452348|ADA109057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173949|NCT00452348|ADA109057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173950|NCT00452348|ADA109057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173951|NCT00452348|ADA109057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173952|NCT00452348|ADA109057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173953|NCT03141216||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|"Search for buscar pesquisas aprovadas and fill the the blanks with research title and investigator's full name"
3173954|NCT00139815|103420|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173955|NCT00139815|103420|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173956|NCT00139815|103420|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176142|NCT01316900|113360|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173957|NCT00139815|103420|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173958|NCT00139815|103420|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173959|NCT00139815|103420|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176143|NCT01316900|113360|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176144|NCT01316900|113360|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176145|NCT01703221||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-020&kw=3102-020&tab=access|
3176146|NCT01362530||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-208&kw=0869-208&tab=access|
3176147|NCT02592655||Primary Outcome Ultrasound Images|https://doi.org/10.5281/zenodo.236263|NCT02592655 Primary Outcome Tourniquet Study
3173960|NCT00139815|103420|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173961|NCT05895435||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/12841881/|
3173962|NCT03221972||Study Protocol|http://www.chinanutri.cn/gzrw_132/zgjmyyyjkzkjcxm/201412/t20141229_108493.html|
3173963|NCT00377572|SDY211|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
3176148|NCT02592655||Individual Participant Data Set|https://doi.org/10.5281/zenodo.237773|NCT02592655 Individual level data set
3176149|NCT02592655||Informed Consent Form|https://doi.org/10.5281/zenodo.245150|Informed consent form containing description of study and procedures.
3173964|NCT00377572|SDY211|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
3173965|NCT00377572|SDY211|Study summary, -design, -adverse event(s), -interventions, -medications, -demographics, -study files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
3173966|NCT01873339|115678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173967|NCT01873339|115678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173968|NCT01873339|115678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173969|NCT01873339|115678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173970|NCT01873339|115678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173971|NCT01873339|115678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173972|NCT01873339|115678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173973|NCT01192776||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25536254|
3173974|NCT00307541|105554|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173975|NCT00307541|105554|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173976|NCT00307541|105554|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176150|NCT02074839||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3171778|NCT05446675|EC/EH/220608-SK|Individual Participant Data Set|https://ehs-hernia-registry.com|
3173977|NCT00307541|105554|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173978|NCT00307541|105554|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173979|NCT00307541|105554|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173980|NCT01119625|113266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176151|NCT02074839||Study Protocol|https://clinicaltrials.servier.com/|
3176152|NCT02074839||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3176153|NCT02074839||Informed Consent Form|https://clinicaltrials.servier.com/|
3176154|NCT02074839||Clinical Study Report|https://clinicaltrials.servier.com/|
3176155|NCT02074839||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3176156|NCT00289900||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-024&kw=0524B-024&tab=access|
3173981|NCT01119625|113266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173982|NCT01119625|113266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173983|NCT01119625|113266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173984|NCT01119625|113266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173985|NCT01119625|113266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173986|NCT01119625|113266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173987|NCT02941159||Study Protocol|http://www.tdrc.org.zm|Data documents can be requested from at info@tdrc.org.zm using the above given website contact page
3173988|NCT00633022|PM1111138|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173989|NCT00633022|PM1111138|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173990|NCT00633022|PM1111138|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176157|NCT02988076|CNSR012 Protocol|Study Protocol|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of the protocol
3176158|NCT02988076|CNSR012 ICD|Informed Consent Form|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of ICD
3176159|NCT02233088|PMC6589338|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/30234352|A manuscript summarizing the development of the intervention.
3176160|NCT02233088|11111701-IRB01|Informed Consent Form|https://rrp.rush.edu/researchportal/sd/ResourceAdministration/Project/PrintSmartForms?Project=com.webridge.entity.Entity%5BOID%5B4B88F935265BF94D8A92A0BD5A70A202%5D%5D&rootEntity=com.webridge.entity.Entity%5BOID%5B4B88F935265BF94D8A92A0BD5A70A202%5D%5D&PrintBySection=False&PrintHeaderView=True&PrintHeaderInfo=True&PrintPageBreak=True&PrintLogo=True&showHiddenData=False&showCDTFormsAtEnd=True|The informed consent is available through RuMC IRB portal.
3176161|NCT00298155||Paper with attached protocol and outcomes|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887479/|
3176162|NCT01101555|113299|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176163|NCT01101555|113299|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176164|NCT01101555|113299|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176165|NCT01101555|113299|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176166|NCT01101555|113299|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176167|NCT01101555|113299|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176168|NCT01101555|113299|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176169|NCT05646173||data|http://pubmed.ncbi.nlm.nih.gov/30311715/|Chakravarthy KV, Xing F, Bruno K, Kent AR, Raza A, Hurlemann R, Kinfe TM. A Review of Spinal and Peripheral Neuromodulation and Neuroinflammation: Lessons Learned Thus Far and Future Prospects of Biotype Development. Neuromodulation. 2019 Apr;22(3):235-243. doi: 10.1111/ner.12859. Epub 2018 Oct 12. PMID: 30311715.
3176170|NCT00078195|SDY1|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
3180565|NCT00489554|109661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176171|NCT00078195|SDY1|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
3176172|NCT00078195|SDY1|Study design, -summary, -files, -interventions, participant schedule of events, -demographics, et al.|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|ImmPort study identifier is SDY1
3176173|NCT00078195|CASALE ITN019AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
3176174|NCT00078195|CASALE ITN019AD|Study protocol synopsis; -schedule of assessments; -data and reports; -specimens availability et al.|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
3176175|NCT00979407|113535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176176|NCT00979407|113535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176177|NCT00979407|113535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176178|NCT00979407|113535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173991|NCT00633022|PM1111138|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176179|NCT00979407|113535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176180|NCT00979407|113535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176181|NCT06694064||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/36464977/|
3176182|NCT01302834|NCT01302834|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3176188|NCT07163195|Protocol_V1_2025|Individual Participant Data Set|https://u.podiatricare.my.id/|The de-identified IPD underlying primary and secondary outcomes, along with the study protocol and SAP, will be available upon reasonable request to the Principal Investigator via email. Access requires a data sharing agreement.
3171779|NCT00920543|SAM40086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171780|NCT00920543|SAM40086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178316|NCT01323959|113060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178317|NCT01323959|113060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178318|NCT01323959|113060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178319|NCT01323959|113060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178320|NCT01323959|113060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178321|NCT01323959|113060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178322|NCT00758836||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-046&kw=0974-046&tab=access|
3178323|NCT01648101|114855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178324|NCT01648101|114855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178325|NCT01648101|114855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178326|NCT01648101|114855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178327|NCT01648101|114855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178328|NCT01648101|114855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178329|NCT01648101|114855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178330|NCT01168167|01168167|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT01168167|
3178331|NCT00169546|SAM40100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178332|NCT00169546|SAM40100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178333|NCT00169546|SAM40100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178334|NCT00169546|SAM40100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178335|NCT00169546|SAM40100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178336|NCT00169546|SAM40100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178337|NCT00169546|SAM40100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178338|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/auad/issue/60075/826745|
3178339|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/411491|
3178340|NCT06253572||Review|http://journalofomepturkey.org/index.php/eccd/article/view/78|
3180566|NCT00489554|109661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180567|NCT00489554|109661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180568|NCT00489554|109661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180569|NCT00489554|109661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180570|NCT01767688||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-031&kw=3102-031&tab=access|
3180571|NCT06950320||Study Protocol|https://ethikkommission.meduniwien.ac.at|studyplan/studyprotocol/patient informed consent form/timeline are available on homepage of ethics committee of the medical university of Vienna
3180572|NCT06952582|doi.org/10.17605/OSF.IO/SE8M7|Individual Participant Data Set|https://osf.io/puxgw/|
3180573|NCT00057499|SDY568|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY568|ImmPort study identifier is SDY568.
3180574|NCT00057499|SDY568|Study summary, -schematic, -design, medications,-demographics, - lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY568|ImmPort study identifier is SDY568.
3180575|NCT00057499|ITN012AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN012AIPUBLIC/Study%20Data/begin.view?|TrialShare is the Immune Tolerance Network (ITN) portal that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3180576|NCT00057499|ITN012AI|Study protocol synopsis, -navigator, -schedule of events,-data &reports, -specimens et al.|http://www.itntrialshare.org/project/Studies/ITN012AIPUBLIC/Study%20Data/begin.view?|TrialShare is the Immune Tolerance Network (ITN) portal that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3171781|NCT00920543|SAM40086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171782|NCT00920543|SAM40086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171783|NCT00920543|SAM40086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171784|NCT00920543|SAM40086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171785|NCT00920543|SAM40086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171786|NCT04457921|Mary Colleen Simonelli|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/30102886/|web site is provided
3171787|NCT01672892|NCT01672892-D1|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3171788|NCT00499707|712753/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171789|NCT00499707|712753/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171790|NCT00499707|712753/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171791|NCT00499707|712753/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171792|NCT00499707|712753/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171793|NCT00499707|712753/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171794|NCT00499707|712753/007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171795|NCT00814710|111188|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171796|NCT00814710|111188|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171797|NCT00814710|111188|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171798|NCT00814710|111188|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171799|NCT00814710|111188|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171800|NCT00814710|111188|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171801|NCT00814710|111188|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171802|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
3171803|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
3171804|NCT07107542||Study Protocol|https://sites.google.com/view/femhrehab/%E6%9C%AC%E7%A7%91%E4%BB%8B%E7%B4%B9/%E9%86%AB%E7%99%82%E5%9C%98%E9%9A%8A%E4%BB%8B%E7%B4%B9|This document contains the study protocol and statistical analysis plan for the cross-sectional study assessing Mini-CEX and EPAs in occupational therapy interns.
3171805|NCT00693706|110127|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171806|NCT00693706|110127|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171807|NCT00693706|110127|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171808|NCT00693706|110127|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171809|NCT00693706|110127|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171810|NCT00693706|110127|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171811|NCT00693706|110127|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171812|NCT01362322|114778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171813|NCT01362322|114778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171814|NCT01362322|114778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171815|NCT01362322|114778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171816|NCT01362322|114778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171817|NCT01362322|114778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171818|NCT01009463|102871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171819|NCT01009463|102871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173992|NCT00633022|PM1111138|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173993|NCT00633022|PM1111138|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173994|NCT00633022|PM1111138|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173995|NCT00224484|208141/040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180577|NCT01772199|116477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180578|NCT01772199|116477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180579|NCT01772199|116477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171820|NCT01009463|102871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171821|NCT01009463|102871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171822|NCT01009463|102871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171823|NCT01009463|102871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173996|NCT00224484|208141/040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173997|NCT00224484|208141/040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173998|NCT00224484|208141/040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173999|NCT00224484|208141/040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174000|NCT00224484|208141/040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174001|NCT06793592||More information on IPD sharing|https://osf.io/preprints/osf/6pwxe|
3174002|NCT00279045|49653/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174003|NCT00279045|49653/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174004|NCT00279045|49653/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174005|NCT00279045|49653/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174006|NCT00279045|49653/048|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174007|NCT00279045|49653/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174008|NCT00279045|49653/048|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174009|NCT00346892|444563/014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174010|NCT00346892|444563/014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174011|NCT00346892|444563/014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174012|NCT00346892|444563/014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174013|NCT00346892|444563/014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174014|NCT00346892|444563/014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174015|NCT01706263|114551|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174016|NCT01706263|114551|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174017|NCT01706263|114551|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174018|NCT01706263|114551|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174019|NCT01706263|114551|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176189|NCT07163195|SAP_V1_2025|Statistical Analysis Plan|https://u.podiatricare.my.id/|The statistical analysis plan (SAP) describes predefined methods for analyzing the primary and secondary outcomes, including sample size justification, handling of missing data, and statistical tests. Available upon request to the PI
3176190|NCT07163195|Code_V1_2025|Analytic Code|https://u.podiatricare.my.id/|Analytic code used for data processing and statistical analyses, including scripts for wound area measurement (ImageJ) and outcome analyses (SPSS/R). The code will be available by request to the PI and requires a data sharing agreement
3178341|NCT06253572||master's thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|Tahta, N. (2022). Creation of a program for training of military trainers. (Unpublished master's thesis). İstanbul: National Defence University.
3178342|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/199140|
3178343|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/rep/issue/63330/827844|
3178344|NCT05085652||Clinical Study Report|https://doi.org/10.1007/s12630-020-01630-7|Chen R, Zhang Y, Huang L, Cheng B, Xia Z, Meng Q. Safety and efﬁcacy of different anesthetic regimens for parturients with COVID-19 undergoing cesarean delivery: a case series of 17 patients. Can J Anesth. 2020. DOI: https://doi.org/10.1007/s12630-020-01630-7
3178345|NCT05085652||Clinical Study Report|https://dx.doi.org/10.3389%2Ffmed.2021.713733|12- Zhang Y, Chen R, Cao C, et al. The Risk of Neuraxial Anesthesia-Related Hypotension in COVID-19 Parturients Undergoing Cesarean Delivery: A Multicenter, Retrospective, Propensity Score Matched Cohort Study. Front Med (Lausanne). 2021;8:713733. Published 2021 Aug 19. doi:10.3389/fmed.2021.713733
3178346|NCT05792709||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788277/|
3178347|NCT01606800||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8908B-059&kw=8908B-059&tab=access|
3178348|NCT04329871||Individual Participant Data Set|http://Metabolic-institute.com|
3178349|NCT05695209|VIV00009027|Individual Participant Data Set|https://vivli.org|https://doi.org/10.25934/PR00009027
3178350|NCT00907777|112807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178351|NCT00907777|112807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178352|NCT00907777|112807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178353|NCT00907777|112807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178354|NCT00907777|112807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178355|NCT00907777|112807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178356|NCT00617123||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05183&kw=P05183&tab=access|
3178357|NCT04213079||Study Protocol|http://mdds.nyc/|
3178358|NCT01262911|115083|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178359|NCT01262911|115083|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178360|NCT01262911|115083|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178361|NCT01262911|115083|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178362|NCT01262911|115083|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178363|NCT01262911|115083|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178364|NCT01262911|115083|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178365|NCT00684593||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04481&kw=7123-009&tab=access|
3178366|NCT02696603||Data description|http://www.nature.com/articles/sdata201611|Here we present data from mPower, a clinical observational study about Parkinson disease conducted purely through an iPhone app interface. The study interrogated aspects of this movement disorder through surveys and frequent sensor-based recordings from participants with and without Parkinson disease. Benefitting from large enrollment and repeated measurements on many individuals, these data may help establish baseline variability of real-world activity measurement collected via mobile phones, and ultimately may lead to quantification of the ebbs-and-flows of Parkinson symptoms. App source code for these data collection modules are available through an open source license for use in studies of other conditions. We hope that releasing data contributed by engaged research participants will seed a new community of analysts working collaboratively on understanding mobile health data to advance human health.
3178367|NCT01577680|114637|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178368|NCT01577680|114637|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178369|NCT01577680|114637|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178370|NCT01577680|114637|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178371|NCT01577680|114637|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178372|NCT01577680|114637|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178373|NCT01577680|114637|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176191|NCT05600517|10.1016/j.ebiom.2017.11.019|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832611/|
3176192|NCT02732145|ISBN:978-1-63484-507-6|Chapter/Commentary|https://novapublishers.com/shop/cryosurgery-and-colposcopy-practices-outcomes-and-potential-complications/|"Harni V, Babic D, Barisic D. Three Rings Vulvoscopy - A New Approach to the Vulva. In: Cryosurgery and Colposcopy: Practices, Outcomes and Potential Complications, Editor: Lillian Watson. Publisher: Nova Science Publishers Inc, NewYork, USA, 2016."
3176193|NCT04292496||Study Protocol|https://doi.org/10.1007/s00464-023-10025-w|
3176194|NCT00911157|111436|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176195|NCT00911157|111436|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176196|NCT00911157|111436|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176197|NCT02842671||Study Protocol|http://irb.psu.edu|
3176198|NCT02842671||Informed Consent Form|http://irb.psu.edu|for participants
3176199|NCT02842671||Accommodation Survey|http://irb.psu.edu|
3176200|NCT02842671||Patient Satisfaction Survey|http://irb.psu.edu|
3176201|NCT02842671||Medical Student Survey|http://irb.psu.edu|
3176202|NCT02842671||Summary Explanation of Research|http://irb.psu.edu|for medical students
3176203|NCT00434811|SDY1178|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study ID is SDY1178.
3176204|NCT00434811|SDY1178|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/studySearch|ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public.
3176205|NCT01817777|116086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176206|NCT01817777|116086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176207|NCT01817777|116086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176208|NCT01817777|116086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176209|NCT01817777|116086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176210|NCT01817777|116086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176211|NCT01817777|116086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176212|NCT01051661|114000|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176213|NCT01051661|114000|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176214|NCT01051661|114000|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176215|NCT01051661|114000|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176216|NCT01051661|114000|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176217|NCT01051661|114000|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176218|NCT04164186|NSCLC Radiomics Interobserver|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics-Interobserver1|
3176219|NCT04164186|NSCLC Radiomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics|
3176220|NCT04164186|NSCLC Radiogenomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC+Radiogenomics|
3176221|NCT01916226|200165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176222|NCT01916226|200165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176223|NCT01916226|200165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176224|NCT01916226|200165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176225|NCT01916226|200165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176226|NCT01916226|200165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176227|NCT01916226|200165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176228|NCT00680914|110808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176229|NCT00680914|110808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180580|NCT01772199|116477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180581|NCT01772199|116477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180582|NCT01772199|116477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180583|NCT01772199|116477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171824|NCT01009463|102871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178374|NCT00783003|112146|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178375|NCT00783003|112146|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178376|NCT00783003|112146|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178377|NCT00783003|112146|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178378|NCT00783003|112146|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178379|NCT00783003|112146|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178380|NCT00783003|112146|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178381|NCT01916720|480848/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178382|NCT01916720|480848/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180584|NCT00910962|111810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180585|NCT00910962|111810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180586|NCT00910962|111810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180587|NCT00910962|111810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180588|NCT00910962|111810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180589|NCT00910962|111810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180590|NCT00910962|111810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180591|NCT00985088|113440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180592|NCT00985088|113440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180593|NCT00985088|113440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180594|NCT00985088|113440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180595|NCT00985088|113440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180596|NCT00985088|113440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180597|NCT00985088|113440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180598|NCT04352400|GPR (PI)|Individual Participant Data Set|https://ncov.medsci.ox.ac.uk|The link https://ncov.medsci.ox.ac.uk allows connection to EDCap database, a secure web platform for building and managing online databases and surveys. Data collection will use the WHO Case Record Form.
3180599|NCT05847257|10.5281/zenodo.|Individual Participant Data Set|https://zenodo.org/records/8191740|data of impact of coenzyme Q10 as an adjuvant therapy to letrozole on spermiogram results and sex hormone levels in Iraqi men with infertility; randomized open label comparative study
3180600|NCT00907933|111610|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180601|NCT00907933|111610|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180602|NCT00907933|111610|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180603|NCT00907933|111610|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180604|NCT00907933|111610|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180605|NCT00907933|111610|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180606|NCT00907933|111610|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180607|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32532623/|Study scientific background
3180608|NCT05075499|PMID|Study Protocol|http://apps.who.int/iris/handle/10665/338671|Study scientific background. World Health Organization 2021. Background document on mRNA vaccine BNT162b2 (Pfizer-BioNTech) against COVID-19.
3180609|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32727835/|Study scientific background.
3180610|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32769063/|Study scientific background.
3180611|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/25636714/|Study scientific background.
3180612|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/24444048/|Alemtuzumab medication
3180613|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/27766281/|Alemtuzumab medication
3180614|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31898276/|Alemtuzumab medication
3171825|NCT06961422|0009-0009-61|Individual Participant Data Set|https://orcid.org/0009-0009-6142-6201|
3171826|NCT07030387||Study Protocol|https://www.precis-2.org/Help/Documentation/Help|
3171827|NCT07228520|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
3180615|NCT05075499|PMID|Study Protocol|http://products.sanofi.us/aubagio/aubagio.html|Aubagio (teriflunomide) \[prescribing information\]. Cambridge (MA): Genzyme Corporation; September 2012.
3180616|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/31898276/|Aubagio (teriflunomide) medication
3180617|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/29275977/|Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria.
3180618|NCT01074242||CSR Synopsis|http://www.merck.com/clinical-trials/search.html?kw=V260-037|
3180619|NCT01957163|200109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180620|NCT01957163|200109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180621|NCT01957163|200109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180622|NCT01957163|200109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180623|NCT01957163|200109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180624|NCT01957163|200109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180625|NCT01957163|200109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180626|NCT01827839|116796|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180627|NCT01827839|116796|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180628|NCT01827839|116796|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180629|NCT01827839|116796|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180630|NCT01827839|116796|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180631|NCT01827839|116796|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180632|NCT01827839|116796|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180633|NCT00614614|110870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180634|NCT00614614|110870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180635|NCT00614614|110870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180636|NCT00614614|110870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180637|NCT00614614|110870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180638|NCT00614614|110870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180639|NCT00614614|110870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180640|NCT00972686|112826|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180641|NCT00972686|112826|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180642|NCT00972686|112826|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180643|NCT00972686|112826|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180644|NCT00972686|112826|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180645|NCT00972686|112826|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180646|NCT00972686|112826|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180647|NCT00273052|COR103561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180648|NCT00273052|COR103561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180649|NCT00273052|COR103561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180650|NCT00273052|COR103561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180651|NCT00273052|COR103561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180652|NCT00273052|COR103561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180653|NCT00273052|COR103561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180654|NCT00240994|SDY134|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
3180655|NCT00240994|SDY134|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
3180656|NCT00240994|SDY134|Study summary, - schedule of events, -download packages et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
3180657|NCT02236611|201315|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180658|NCT02236611|201315|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180659|NCT02236611|201315|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180660|NCT02236611|201315|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180661|NCT02236611|201315|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180662|NCT02236611|201315|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180663|NCT02236611|201315|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180664|NCT00718120|110584|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180665|NCT00718120|110584|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180666|NCT00718120|110584|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180667|NCT00718120|110584|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180668|NCT00718120|110584|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180669|NCT00718120|110584|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180670|NCT00718120|110584|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180671|NCT00929526|112949|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180672|NCT00929526|112949|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180673|NCT00929526|112949|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180674|NCT00929526|112949|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180675|NCT00929526|112949|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180676|NCT00929526|112949|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180677|NCT01072149|110946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180678|NCT01072149|110946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171828|NCT07228520|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
3180679|NCT01072149|110946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180680|NCT01072149|110946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180681|NCT01072149|110946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180682|NCT01072149|110946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180683|NCT01072149|110946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180684|NCT01911559|9433361|Clinical Study Report|http://www.biomedsearch.com/nih/Effectiveness-Standing-Frame-Constipation-in/24838311.html|Rivi, Elena \& Filippi, Mariacristina \& Fornasari, Elisa \& Mascia, Maria Teresa \& Ferrari, Adriano \& Costi, Stefania. (2014). Effectiveness of Standing Frame on Constipation in Children with Cerebral Palsy: A Single-Subject Study. Occupational therapy international.
3180685|NCT07013123|2025-521258-41-00|Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en|avalable after authorization of competent authorities
3180686|NCT07044193||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521375-31-00|
3180687|NCT05400525||Study Protocol|https://discoverthesecretofgoodhealth.weebly.com|
3180688|NCT01602900|116038|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180689|NCT01602900|116038|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180690|NCT01602900|116038|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180691|NCT01602900|116038|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180692|NCT01602900|116038|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180693|NCT01602900|116038|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180694|NCT01602900|116038|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180695|NCT03928665||DDLS - reference|https://www.sign.ac.uk/assets/sign144_disc_chart_colour.pdf|
3180696|NCT02521493||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3180697|NCT01316913|113374|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180698|NCT01316913|113374|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180699|NCT01316913|113374|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180700|NCT01316913|113374|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180701|NCT01316913|113374|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180702|NCT01316913|113374|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180703|NCT01316913|113374|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180704|NCT04205669||Individual Participant Data Set|https://www.kaggle.com/julianmatthewman/grattigratta-data|
3180705|NCT06477549|Protocol version 1.0|Study Protocol|https://cloud.mail.ru/public/wQ1q/8amGwZdMb|Study protocol signed
3180706|NCT00035048||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180707|NCT04526171||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/Q3P4WX|
3180708|NCT00424476|HGS1006-C1057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180709|NCT00424476|HGS1006-C1057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180710|NCT00424476|HGS1006-C1057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180711|NCT00424476|HGS1006-C1057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180712|NCT00424476|HGS1006-C1057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180713|NCT00424476|HGS1006-C1057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180714|NCT00424476|HGS1006-C1057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180715|NCT00346398|SDY545|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY545|ImmPort study identifier is SDY545.
3180716|NCT00346398|SDY545|Study summary, -design with synopsis, -adverse events, -assessment, -medications, -demographics, -lab tests, -files, et al.|http://www.itntrialshare.org/project/Studies/ITN025ADPUBLIC/Study%20Data/begin.view?|ImmPort study identifier is SDY545.
3180717|NCT00346398|ITN025AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN025ADPUBLIC/Study%20Data/begin.view?|TrialShare is the ITN clinical trials research portal available to the public.
3180718|NCT00346398|ITN025AD|Study overview with synopsis, -navigator, -schedule of events, -data and reports, biospecimens and availability.|http://www.itntrialshare.org/project/Studies/ITN025ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN025AD.
3180719|NCT06699511||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34847915/|
3180720|NCT04338568||Clinical Study Report|https://www.castoredc.com/|
3180721|NCT03543904||Pilot study|http://doi.org/10.1016/j.jpedsurg.2019.10.058|Preserving pulmonary function and functional capacity in children undergoing open abdominal surgery: A one group pretest-posttest, quasiexperimental pilot trial
3171829|NCT05966038|NeuroGUID/NeuroSTAmP|Individual Participant Data Set|https://www.data4cures.org/requestingdata|Anonymized data may be requested by submitting research proposal online. Data Access Committee will review the submission and upon its approval and execution of the Data Sharing Agreement, the dataset will be provided to the data requestor.
3180722|NCT03543904|Version 1|Individual Participant Data Set|http://dx.doi.org/10.17632/skkt9tsjd3.1|"Effect of Pre-operative physiotherapy education and Post-operative physiotherapy in children with abdominal surgery, Mendeley Data, v1 http://dx.doi.org/10.17632/skkt9tsjd3.1"
3180723|NCT03543904||Clinical Study Report|http://doi.org/10.1016/j.jpedsurg.2020.04.007|A randomized clinical trial in improving pulmonary function and functional capacity in paediatric open abdominal surgery
3180724|NCT00470483|TMT106386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180725|NCT00470483|TMT106386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180726|NCT00470483|TMT106386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180727|NCT00470483|TMT106386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180728|NCT00470483|TMT106386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180729|NCT00470483|TMT106386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180730|NCT00092378||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180731|NCT05214248||Study Protocol|https://doi.org/10.1097/JNR.0000000000000134|Article title: The Lived Experience of Jordanian Parents in a Neonatal Intensive Care Unit: A Phenomenological Study
3180732|NCT05214248||Study Protocol|https://doi.org/10.1017/S1463423619000021|Article Title: Stress and feelings in mothers and fathers in NICU: identifying risk factors for early interventions
3180733|NCT05214248||Study Protocol|https://doi.org/10.3389/fped.2019.00439|Article title: Parental Stress Experience and Age of Mothers and Fathers After Preterm Birth and Admission of Their Neonate to Neonatal Intensive Care Unit; A Prospective Observational Pilot Study
3180734|NCT05214248||Study Protocol|https://doi.org/10.4040/jkan.2012.42.7.936|Article Title: Development and Evaluation of a Video Discharge Education Program focusing on Mother-infant Interaction for Mothers of Premature Infants
3180735|NCT05214248||Study Protocol|https://doi.org/10.1016/j.jnn.2017.04.001|Article Title: A fathers' group in NICU: Recognising and responding to paternal stress, utilising peer support
3180736|NCT05214248||Study Protocol|https://doi.org/10.1016/S0377-1237(10)80131-5|Article Title: Meconium Aspiration Syndrome: An Insight
3180737|NCT03884478||Study Protocol|https://www.researchprotocols.org/2021/4/e24647|available open access at URL provided
3180738|NCT03875729||Individual Participant Data Set|https://www.vivli.org/|Qualified researchers can submit a research proposal that includes specific information about the purpose of the research, the objectives, the analysis plan, the publication plan, etc. Qualified researchers may request access to patient level data and related study documents. Patient level data will be anonymized, and study documents will be redacted to protect the privacy of trial participants.
3180739|NCT00103857||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180740|NCT00632736|101468/248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180741|NCT00632736|101468/248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180742|NCT00632736|101468/248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180743|NCT00632736|101468/248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180744|NCT00632736|101468/248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180745|NCT00632736|101468/248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180746|NCT00632736|101468/248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180747|NCT04883541||PhD thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
3180748|NCT02404012||Website|https://ngletsum.wixsite.com/nito|
3180749|NCT01381445|113435|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180750|NCT01381445|113435|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180751|NCT01381445|113435|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180752|NCT01381445|113435|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180753|NCT01381445|113435|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180754|NCT01381445|113435|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180755|NCT01381445|113435|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180756|NCT00879827|217744/049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180757|NCT00879827|217744/049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180758|NCT00879827|217744/049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180759|NCT00879827|217744/049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171830|NCT00005301|TSS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/tss/|Samples and characterization data. NHLBI provides controlled access to samples through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a materials use agreement.
3171831|NCT05957562|orcid.org/0000-0003-0558-6402|Study Protocol|http://orcid.org/0000-0003-0558-6402|
3171832|NCT01857895|200016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171833|NCT01857895|200016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171834|NCT01857895|200016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171835|NCT01857895|200016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171836|NCT01857895|200016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171837|NCT01857895|200016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171838|NCT01857895|200016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171839|NCT04160403||Study Protocol|https://www.ncbi.nlm.nih.gov/|
3171840|NCT04936672||Study Protocol|https://doi.org/10.1249/MSS.0b013e318213fefb|The protocol setting and data collection process is based on this reference
3171841|NCT03407391||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data is available for use by researchers on application through the website
3171842|NCT04406038|ID|Individual Participant Data Set|http://github.com/eusporg/spb_covid_study20|Please consult with the README.md for the repository.
3171843|NCT00971321|113462|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171844|NCT00971321|113462|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171845|NCT00971321|113462|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171846|NCT00971321|113462|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171847|NCT00971321|113462|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171848|NCT00971321|113462|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171849|NCT00971321|113462|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171850|NCT00196937|103514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171851|NCT00196937|103514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103514 are summarised with studies 105880 and 105881 on the GSK Clinical Study Register.
3171852|NCT00196937|103514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171853|NCT00196937|103514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171854|NCT00196937|103514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171855|NCT00196937|103514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171856|NCT00196937|103514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171857|NCT00410371|LBI108614|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171858|NCT00410371|LBI108614|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171859|NCT00410371|LBI108614|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171860|NCT00410371|LBI108614|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171861|NCT00410371|LBI108614|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171862|NCT00410371|LBI108614|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171863|NCT00410371|LBI108614|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171864|NCT01972425||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1442-x|
3171865|NCT00474253||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171866|NCT01873950|doi:10.13026/C2HP45|ECG, PK and clinical information database|https://physionet.org/physiobank/database/ecgrdvq/|This publicly available database contains raw and annotated ECG signals, PK measures as well as clinical information of this study.
3171867|NCT04752787||Study Protocol|http://files.eric.ed.gov/fulltext/EJ1086361.pdf|
3171868|NCT04752787||Study Protocol|https://mhealth.jmir.org/2018/4/e109/|
3171869|NCT00945750||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0208-144&kw=0208-144&tab=access|
3171870|NCT02525224|DOI: 10.1111/jocd.12295|Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1111/jocd.12295/full|
3171871|NCT01516450|116119|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171872|NCT01516450|116119|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171873|NCT01516450|116119|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171874|NCT01516450|116119|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171875|NCT01516450|116119|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171876|NCT01516450|116119|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171877|NCT01516450|116119|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171878|NCT00984659|112989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171879|NCT00984659|112989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171880|NCT00984659|112989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171881|NCT00984659|112989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171882|NCT00984659|112989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171883|NCT00984659|112989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171884|NCT00984659|112989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171885|NCT05700344||Summary of Product Characteristics|https://www.ema.europa.eu/en/documents/product-information/bavencio-epar-product-information_en.pdf|Summary of Product Characteristics
3171886|NCT05700344||Burki TK. Erdafitinib for advanced urothelial carcinoma|http://dx.doi.org/10.1016/S1470-2045(19)30522-4|Burki TK. Erdafitinib for advanced urothelial carcinoma. Lancet Oncology Vol.20 September 2019. Published Online August 1, 2019
3171887|NCT00440128|NKV100781|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171888|NCT00440128|NKV100781|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171889|NCT00440128|NKV100781|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171890|NCT00440128|NKV100781|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171891|NCT00440128|NKV100781|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171892|NCT00440128|NKV100781|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171893|NCT00440128|NKV100781|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171894|NCT02680067||Arthritis Research & Therapy Publication|http://arthritis-research.biomedcentral.com/articles/10.1186/s13075-016-1092-0|Lymphatic imaging to assess rheumatoid flare: mechanistic insights and biomarker potential.
3171895|NCT00000530|RTS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/rts/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3171896|NCT00000530||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rts/|
3180760|NCT00879827|217744/049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180761|NCT00866619|110021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171897|NCT00000530||Study Forms|http://biolincc.nhlbi.nih.gov/studies/rts/|
3171898|NCT00283712|SDY655|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|Participant level data and additional relevant materials are available to the public in the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. Data analysis tools are also available to researchers.
3171899|NCT00283712|SDY655|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|ImmPort study identifier is SDY655
3171900|NCT00283712|SDY655|Study summary, -design, -adverse event(s), -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -mechanistic Assays, -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|ImmPort study identifier is SDY655
3180762|NCT00866619|110021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171901|NCT03136705|STU00089165|Study Protocol|https://irb.northwestern.edu/contact|
3171902|NCT03136705|STU00089165|Informed Consent Form|https://irb.northwestern.edu/contact|
3171903|NCT01097616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-028&kw=4305-028&tab=access|
3171904|NCT01367743||Statistical Analysis Plan|http://cic-p-nancy.fr/wp-content/uploads/2019/01/revUS_SAP_OPTIMA_CC_KD_NG.pdf|
3171905|NCT02345161|116853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171906|NCT02345161|116853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171907|NCT02345161|116853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174020|NCT01706263|114551|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174021|NCT05583097||Study Protocol|https://www.gu.se/forskning/tyreoideacancer|
3174022|NCT00000555|WAVE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/wave/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174023|NCT00000555||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/wave/|
3171908|NCT02345161|116853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171909|NCT02345161|116853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171910|NCT02345161|116853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171911|NCT02345161|116853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171912|NCT00169494|580299/012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171913|NCT00169494|580299/012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171914|NCT00169494|580299/012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171915|NCT00169494|580299/012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171916|NCT00169494|580299/012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171917|NCT00169494|580299/012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171918|NCT00169494|580299/012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 580299/012 are summarised with studies 107476 (M18), 107477 (M24), and 107479 (M36) on the GSK Clinical Study Register.
3171919|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/33842036/|Athletes must have a high level of fitness, strength, coordination, agility, speed and motor control to perform at an elite level with minimal injury risk
3171920|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/22607780/|Dysfunctional movement patterns are directly related to the mechanism of injury
3171921|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/27215935/|In addition, the improvement of motor control is directly related to the prevention of injury
3171922|NCT06344520||Clinical Study Report|https://acikerisim.gelisim.edu.tr/xmlui/handle/11363/323|Sport has become a necessity for a healthy and balanced life today. Children who play sports regularly at a young age become adults who do sports later in their lives. Swimming is one of the sports branches that includes many factors such as aerobic and anaerobic endurance, strength, flexibility, speed, quickness, rhythm, coordination as well as sportive performance and technical skills. Swimming is not only a sport, but also provides a symmetrical and balanced development of some muscles as well as making use of free time, gaining strength and rehabilitation.
3171923|NCT06344520||Clinical Study Report|https://www.researchgate.net/publication/356845509_Comparative_upper-quarter_posture_analysis_of_female_adolescent_freestyle_swimmers_and_non-swimmers|Repetitive upper extremity movements imposed by freestyle swimming may lead to changes in muscle length and tension by paving the way for postural misalignment in adolescent swimmers . Botha et al. (2022), in their study, revealed that there were great differences in sagittal stance angles of freestyle swimming female adolescent athletes compared to their non-swimming peers, and adolescent athletes engaged in swimming sports had far from the desired angles in sagial stance
3171924|NCT06344520||Clinical Study Report|https://research.usc.edu.au/esploro/outputs/99449442202621|One of the parameters affecting swimming sport is muscle strength. While four techniques are used as freestyle, backstroke, breaststroke and butterfly, swimming speed is considered to be the most important performance indicator in all
3171925|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/20664366/|Lower extremity strength is also accepted as an important criterion in terms of starting swimming and especially completing the first 15 meters
3171926|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/20699426/|Intrinsic and extrinsic factors are effective in the prevention of acute, subacute and chronic injuries in sports
3171927|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/19442581/|The sensorymotor system, on the other hand, is defined as the system that provides sensory, motor and central integration to ensure functional joint stability
3171928|NCT06344520||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164311/|Swimming; It is a sport branch that includes many factors such as high level aerobic and anaerobic endurance, strength, flexibility, speed, quickness, rhythm, coordination, sportive performance and technical skills
3171929|NCT06344520||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851131/|As can be seen in the studies, young swimmers who are preparing for the competition have postural disorders and injuries related to use, such as decreased posture, shoulder joint range of motion and subacromial distance
3174024|NCT00000555||Study Forms|http://biolincc.nhlbi.nih.gov/studies/wave/|
3174025|NCT00000555||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/wave/|
3174026|NCT02416180|201909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171930|NCT06344520||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857441/|Mi-Kyoung et al. (2018) observed the effects of shoulder stabilization exercises and pectoralis minor stretching exercises on balance and maximal shoulder strength in a study conducted on healthy young people with a rounded shoulder posture.
3180763|NCT00866619|110021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180764|NCT00866619|110021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180765|NCT00866619|110021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180766|NCT00866619|110021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171931|NCT06344520|D.A. Neumann,|Book|https://shop.elsevier.com/books/kinesiology-of-the-musculoskeletal-system/neumann/978-0-323-28753-1|An effective factor in acceleration during swimming is the force of the arm while pulling the water. The lower trapezius, latismus dorsi pectoralis minor, and the supclavius muscle work as the scapula-thoracic depressor. The lower trapezius and pectoralis minor muscles directly affect the scapula, while the latismus dorsi muscle helps by pushing the humerus inferiorly. While the pectoralis minor muscle pulls the crocoid process forward, it lowers its posterolateral corner, which helps the latismus dorsi to extend and the lower trapezius to depress the scapula
3171932|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/14573714/|In the shortness of the pectoralis minor muscle, the full function cannot be revealed, thus preventing the maximum extension of the arm. The shortness of the pectoralis minor muscle causes a postural disorder called the round shoulder. It is important to increase the mobility of the shoulder by stretching this muscle in terms of the smoothness of the posture. Since the depressed scapula increases the backward thrust of the arm, it is thought that it will directly affect the acceleration in swimming sports
3171933|NCT00126451||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171934|NCT00404768||Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171935|NCT00404768||Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171936|NCT00404768||Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171937|NCT00404768||Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171938|NCT00404768||Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171939|NCT00404768||Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171940|NCT00404768||Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171941|NCT01614769||CSR Snyposis Link|http://www.merck.com/clinical-trials/study.html?id=0000-253&kw=0000-253&tab=access|
3171942|NCT02124798|200339|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171943|NCT02124798|200339|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171944|NCT02124798|200339|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171945|NCT02124798|200339|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171946|NCT02124798|200339|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171947|NCT02124798|200339|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171948|NCT02124798|200339|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171949|NCT03246035|CODIM-MBM-17-052|Study Protocol|http://www.ladydavis.ca/en/jonathanafilalo|Pilot study protocol
3171950|NCT03246035|CODIM-MBM-17-052|Informed Consent Form|http://www.ladydavis.ca/en/jonathanafilalo|Patient consent Caregiver consent French and English available
3171951|NCT01101568|113506|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180767|NCT03151694||Peer-Reviewed Article|http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12646/full|
3180768|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529982|
3180769|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529983|
3180770|NCT00787371||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180771|NCT00227422|102394|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180772|NCT00227422|102394|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180773|NCT00227422|102394|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180774|NCT00227422|102394|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180775|NCT00227422|102394|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180776|NCT00227422|102394|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180777|NCT07013162||Study Protocol|http://www.ust.edu.ye|De-identified data including patient demographics, treatment allocation (scaling only, scaling + high-power diode laser, scaling + low-power diode laser), changes in periodontal pocket depth, and levels of cytokines (IL-1β, IL-6, IL-8, TNF-α) will be made available. Data access will be granted upon reasonable request submitted to the corresponding author via email at: aamanialsharani.aa@gmail.com.
3180778|NCT06694441||Study Overview and Intial Screening Eligibility Form|https://redcap.nubic.northwestern.edu/redcap/surveys/?s=WK7CDXRNNTLCWEEK|Full protocol available via email request: CCSMresearch@northwestern.edu
3180779|NCT00197262|FFR104861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180780|NCT00197262|FFR104861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180781|NCT00197262|FFR104861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180782|NCT00197262|FFR104861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180783|NCT00197262|FFR104861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180784|NCT00197262|FFR104861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180785|NCT00197262|FFR104861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180786|NCT04985994||Study Protocol|https://bmjopen.bmj.com/content/12/6/e058463.full|Complete study protocol has been published and can be accessed through the URL given above.
3180787|NCT02907489||Study Protocol|https://www.scribd.com/document/328018560/Protocol-Omaia-Repaired-Autosaved|
3180788|NCT00000492|BHAT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/bhat/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180789|NCT00000492||Study Forms|http://biolincc.nhlbi.nih.gov/studies/bhat/|
3180790|NCT04419571|285260|Individual Participant Data Set|https://www.myresearchproject.org.uk/|Data collection template available on IRAS (Integrated Research Application System) registration
3180791|NCT04419571|285260|Statistical Analysis Plan|https://www.myresearchproject.org.uk/|Statistical analysis plan as part of protocol available on IRAS (Integrated Research Application System) registration
3180792|NCT04419571|285260|Study Protocol|https://www.myresearchproject.org.uk/|Protocol available on IRAS (Integrated Research Application System) registration
3180793|NCT04503434||Informed Consent Form|https://enquesta.clinic.cat/index.php/admin/survey/sa/view/surveyid/818692|
3180794|NCT00475436|AC4106889|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180795|NCT00475436|AC4106889|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180796|NCT00475436|AC4106889|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180797|NCT00475436|AC4106889|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180798|NCT00475436|AC4106889|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180799|NCT00475436|AC4106889|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180800|NCT00475436|AC4106889|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180801|NCT02384122|27619827|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27619827|
3180802|NCT05144659|orcid.org/0000-0002-6328-6419|Study Protocol|http://orcid.org/0000-0002-6328-6419|Upon request of data, any researcher can e-mail the investigators at daboosmohammad@gmail.com or mohamedhafez\_82@yahoo.com and the investigators will share the required data with the researchers and will be happy for any support.
3180803|NCT06700161|Study Protocol|Study Protocol|https://tipfakultesi.ksu.edu.tr/Default.aspx?SId=24451|
3180804|NCT00352963|217744/097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180805|NCT00352963|217744/097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180806|NCT00352963|217744/097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180807|NCT00352963|217744/097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180808|NCT00352963|217744/097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180809|NCT00352963|217744/097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180810|NCT00092365||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180811|NCT00197119|100566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100566 are summarised with studies 100567, 100568, 100569, and 100570 on the GSK Clinical Study Register.
3180812|NCT00197119|100566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180813|NCT00197119|100566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180814|NCT00197119|100566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180815|NCT00197119|100566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180816|NCT00197119|100566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180817|NCT00733551|MOT109681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180818|NCT00733551|MOT109681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180819|NCT00733551|MOT109681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180820|NCT00733551|MOT109681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180821|NCT00733551|MOT109681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180822|NCT00733551|MOT109681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180823|NCT00733577|111829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180824|NCT00733577|111829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180825|NCT00733577|111829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180826|NCT00733577|111829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180827|NCT00733577|111829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180828|NCT00733577|111829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180829|NCT00733577|111829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180830|NCT00434577|108494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180831|NCT00434577|108494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180832|NCT00434577|108494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180833|NCT00434577|108494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180834|NCT00434577|108494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180835|NCT00434577|108494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180836|NCT00434577|108494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180837|NCT05680597||Study Protocol|http://octri.ohsu.edu/redcap/redcap_v12.5.12/DataEntry/index.php?pid=3056&id=EI254&event_id=105878&page=demographics|Data will be gathered from questionnaires and instrumented assessments, and entered into the web-based Research Electronic Data Capture system (REDCap) and into the OHSU Balance Disorders database. REDCap is a secure electronic database administered by OHSU. Hard copies of these records will be stored behind a locked office in a locked cabinet at OHSU. The de-identified Mobility Lab data will be collected on a password-protected and data-encrypted laptop computer and uploaded after each test session to an OHSU secure server, where the Balance Disorders database is located.
3180838|NCT01809691||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3180839|NCT06200480|NorHead|Study Protocol|https://www.ntnu.no/norhead/om|English Study protocol available by request to the Norwegian Centre of Headache Research (NorHead)
3180840|NCT06200480|NorHead|Statistical Analysis Plan|https://www.ntnu.no/norhead/om|English SAP available by request to the the Norwegian Centre of Headache Research (NorHead)
3180841|NCT02214017|doi: 10.1177/1357633X15608984|publication|https://www.ncbi.nlm.nih.gov/pubmed/26468213|
3171952|NCT01101568|113506|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171953|NCT01101568|113506|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171954|NCT01101568|113506|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171955|NCT01101568|113506|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171956|NCT01101568|113506|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171957|NCT01101568|113506|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171958|NCT01254604||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=2452-002&kw=2452-002&tab=access|
3171959|NCT06253286||Study Protocol|https://drive.google.com/file/d/1edivKccFOAyt3_A6aNnNROe7JQnRmp4C/view?usp=sharing|
3171960|NCT06253286||Informed Consent Form|https://drive.google.com/file/d/1gA2nThyz6di3bSZKJQ7aQ_Usy1_wpOrR/view?usp=sharing|
3171961|NCT00866294|112810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171962|NCT00866294|112810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171963|NCT00866294|112810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171964|NCT00866294|112810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171965|NCT00866294|112810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171966|NCT01702363|115361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171967|NCT01702363|115361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171968|NCT01702363|115361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171969|NCT01702363|115361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171970|NCT01702363|115361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171971|NCT01702363|115361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171972|NCT01702363|115361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171973|NCT00000567|HIFI|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hifi/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3171974|NCT00000567||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/hifi/|
3171975|NCT00000567||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hifi/|
3171976|NCT00000567||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hifi/|
3171977|NCT00875784|103629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171978|NCT00875784|103629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171979|NCT00875784|103629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171980|NCT00875784|103629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171981|NCT00875784|103629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171982|NCT00875784|103629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171983|NCT00875784|103629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171984|NCT03102775||final report (Norwegian)|https://skriftserien.hioa.no/index.php/skriftserien/article/view/649|
3171985|NCT01165203|112673|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171986|NCT01165203|112673|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171987|NCT01165203|112673|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171988|NCT01165203|112673|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171989|NCT01165203|112673|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171990|NCT01165203|112673|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171991|NCT01165203|112673|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180842|NCT07311967||Study Protocol|https://uofi.box.com/s/3vs1mzdcyzsbafojrytxk3d1n6ed45z8|
3171992|NCT01147731|111681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171993|NCT01147731|111681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171994|NCT01147731|111681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171995|NCT01147731|111681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171996|NCT01147731|111681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171997|NCT01147731|111681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171998|NCT01147731|111681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171999|NCT01323673|115054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172000|NCT01323673|115054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172001|NCT01323673|115054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172002|NCT01323673|115054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172003|NCT01323673|115054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172004|NCT01323673|115054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172005|NCT01323673|115054|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172006|NCT00726323|MET111644|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172007|NCT00726323|MET111644|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172008|NCT00726323|MET111644|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172009|NCT00726323|MET111644|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172010|NCT00726323|MET111644|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172011|NCT00726323|MET111644|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172012|NCT04552236||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
3172013|NCT03731416||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27283920|
3172014|NCT00933335|393229/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172015|NCT00933335|393229/023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172016|NCT00933335|393229/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172017|NCT00933335|393229/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172018|NCT00933335|393229/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172019|NCT00933335|393229/023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172020|NCT00933335|393229/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172021|NCT00828867|111341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172022|NCT00828867|111341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172023|NCT00828867|111341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172024|NCT00828867|111341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172025|NCT00828867|111341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172026|NCT00828867|111341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172027|NCT00828867|111341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172028|NCT06011005|MBRU IRB-2022-174|Study Protocol|http://www.mbru.ac.ae|
3172029|NCT06527274||Study Protocol|https://nagano.umontreal.ca/login|Protocol and other documentation available upon request to the principal investigator email
3172030|NCT01299597|109652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172031|NCT01299597|109652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176230|NCT00680914|110808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176231|NCT00680914|110808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176232|NCT00680914|110808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176233|NCT00680914|110808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176234|NCT00680914|110808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176235|NCT00005479||NCBI website|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724776/|
3176236|NCT00734032|LPL110118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176237|NCT00734032|LPL110118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176238|NCT00734032|LPL110118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176239|NCT00734032|LPL110118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176240|NCT00734032|LPL110118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176241|NCT00734032|LPL110118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176242|NCT01353729|114346|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176243|NCT01353729|114346|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176244|NCT01353729|114346|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176245|NCT01353729|114346|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176246|NCT01353729|114346|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176247|NCT01353729|114346|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176248|NCT01353729|114346|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176249|NCT02743221||Individual Participant Data Set|http://clinicaltrials.servier.com/|
3176250|NCT02743221||Study Protocol|https://clinicaltrials.servier.com/|
3176251|NCT02743221||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3176252|NCT02743221||Informed Consent Form|https://clinicaltrials.servier.com/|
3176253|NCT02743221||Clinical Study Report|https://clinicaltrials.servier.com/|
3176254|NCT02743221||study-level clinical trial data|https://clinicaltrials.servier.com/|
3176255|NCT00086515||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176256|NCT03044899||Study Protocol|http://www.asos.org.za/|ASOS Protocol version 1.0
3176257|NCT00323622|104297|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176258|NCT00323622|104297|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176259|NCT00323622|104297|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176260|NCT00323622|104297|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176261|NCT00323622|104297|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176262|NCT00323622|104297|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176263|NCT00492544|110168|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176264|NCT00492544|110168|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176265|NCT00492544|110168|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176266|NCT00492544|110168|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176267|NCT00492544|110168|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176268|NCT00492544|110168|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176269|NCT00492544|110168|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176270|NCT02738463||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/pubmed|
3176271|NCT00140920||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176272|NCT01706315|116778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174027|NCT02416180|201909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174028|NCT02416180|201909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174029|NCT02416180|201909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174030|NCT02416180|201909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174031|NCT02416180|201909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174032|NCT00296530|ADA103578|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174033|NCT00296530|ADA103578|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174034|NCT00296530|ADA103578|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174035|NCT00296530|ADA103578|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174036|NCT00296530|ADA103578|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174037|NCT00296530|ADA103578|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174038|NCT00296530|ADA103578|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175809|NCT00706563|111631|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175810|NCT00706563|111631|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175811|NCT00706563|111631|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175812|NCT07155863||Study Protocol|https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-024-06091-6|
3175813|NCT06956586|Research|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37330438/|"There is no additional information."
3175814|NCT00689741|580299/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175815|NCT00689741|580299/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175816|NCT00689741|580299/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175817|NCT00689741|580299/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175818|NCT00689741|580299/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175819|NCT00689741|580299/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175820|NCT07265245|MREC APPROVAL LETTER|IPD Approval letter|https://osf.io/v26ku/files/yskbz|
3175821|NCT01524835|SDY294|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
3175822|NCT01524835|SDY294|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294. The study protocol is available in the Design tab section.
3172032|NCT01299597|109652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172033|NCT01299597|109652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172034|NCT01299597|109652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172035|NCT01299597|109652|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172036|NCT01299597|109652|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172037|NCT00139334|103992|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172038|NCT00139334|103992|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172039|NCT00139334|103992|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172040|NCT00139334|103992|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172041|NCT00139334|103992|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172042|NCT00139334|103992|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172043|NCT00861484|111155|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172044|NCT00861484|111155|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172045|NCT00861484|111155|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172046|NCT00861484|111155|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172047|NCT00861484|111155|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172048|NCT00861484|111155|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172049|NCT00861484|111155|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172050|NCT01425190||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07614&kw=P07614&tab=access|
3172051|NCT01245426|114749|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172052|NCT01245426|114749|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172053|NCT01245426|114749|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172054|NCT01245426|114749|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172055|NCT01245426|114749|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172056|NCT01245426|114749|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172057|NCT01245426|114749|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172058|NCT01640990|115387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172059|NCT01640990|115387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172060|NCT01640990|115387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172061|NCT01640990|115387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180843|NCT07311967||Informed Consent Form|https://uofi.box.com/s/5g14s3norggukhl3oyrh6vy6mm8f1vpp|
3180844|NCT07311967||Recruitment Email|https://uofi.box.com/s/sr3cztrcr8av6ydub4s76kxo7co5slck|
3180845|NCT07311967||Screening Materials|https://uofi.box.com/s/0ixpcy9goxx5ggguo8vurdb6ncq3lne7|
3180846|NCT05147662|2023-504388-18-00|CTIS Summary of Results|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2023-504388-18-00|
3180847|NCT05147662|2023-504388-18-00|Layperson Summary of Results|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2023-504388-18-00|
3180848|NCT00356564|106744|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180849|NCT00356564|106744|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180850|NCT00356564|106744|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180851|NCT00356564|106744|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180852|NCT00356564|106744|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178383|NCT01916720|480848/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178384|NCT01916720|480848/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178385|NCT01916720|480848/010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178386|NCT01916720|480848/010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178387|NCT01916720|480848/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178388|NCT00318630|104385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178389|NCT00318630|104385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174039|NCT04404907||Clinical Study Report|http://doi.org/10.3886/ICPSR37603.v1|Mustanski, Brian. Multilevel Influences on HIV and Substance Use in a YMSM Cohort (RADAR) - Visit #1, Chicago Metropolitan Area, 2015-2018. Inter-university Consortium for Political and Social Research \[distributor\], 2020-03-19.
3174040|NCT00363857|101468/249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174041|NCT00363857|101468/249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174042|NCT00363857|101468/249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174043|NCT00363857|101468/249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174044|NCT00363857|101468/249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174045|NCT00363857|101468/249|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174046|NCT00363857|101468/249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174047|NCT00000516|SOLVD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/solvd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174048|NCT00000516||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/solvd/|
3174049|NCT00000516||Study Forms|http://biolincc.nhlbi.nih.gov/studies/solvd/|
3174050|NCT00000516||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/solvd/|
3174051|NCT00333450|106623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172062|NCT01640990|115387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172063|NCT01640990|115387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172064|NCT01640990|115387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172065|NCT00441441|SFA106484|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172066|NCT00441441|SFA106484|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174052|NCT00333450|106623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174053|NCT00333450|106623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174054|NCT00333450|106623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178390|NCT00318630|104385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178391|NCT00318630|104385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178392|NCT00318630|104385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178393|NCT00318630|104385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178394|NCT00318630|104385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178395|NCT02446483|201527|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178396|NCT02446483|201527|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178397|NCT02446483|201527|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178398|NCT02446483|201527|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178399|NCT02446483|201527|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172067|NCT00441441|SFA106484|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180853|NCT00356564|106744|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180854|NCT01031186|113324|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180855|NCT01031186|113324|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180856|NCT01031186|113324|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180857|NCT01031186|113324|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180858|NCT01031186|113324|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180859|NCT01031186|113324|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180860|NCT01031186|113324|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180861|NCT00938041|393229/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180862|NCT00938041|393229/010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180863|NCT00938041|393229/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180864|NCT00938041|393229/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180865|NCT00938041|393229/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180866|NCT00938041|393229/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180867|NCT00938041|393229/010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180868|NCT01503515||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3180869|NCT02033668|116891|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180870|NCT02033668|116891|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180871|NCT02033668|116891|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180872|NCT02033668|116891|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180873|NCT02033668|116891|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180874|NCT02033668|116891|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180875|NCT02033668|116891|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180876|NCT00383903|444563/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180877|NCT00383903|444563/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180878|NCT00383903|444563/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180879|NCT00383903|444563/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180880|NCT00383903|444563/013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180881|NCT00383903|444563/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176273|NCT01706315|116778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176274|NCT01706315|116778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176275|NCT01706315|116778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180882|NCT01697592||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=3102-015&kw=3102-015&tab=access|
3180883|NCT00603278|FFA109685|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180884|NCT00603278|FFA109685|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180885|NCT00603278|FFA109685|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180886|NCT00603278|FFA109685|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180887|NCT00603278|FFA109685|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180888|NCT00603278|FFA109685|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180889|NCT00603278|FFA109685|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180890|NCT01772147|116136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180891|NCT01772147|116136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180892|NCT01772147|116136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180893|NCT01772147|116136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180894|NCT01772147|116136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180895|NCT01772147|116136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180896|NCT01772147|116136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180897|NCT02071680||Published article|http://www.heartrhythmjournal.com/article/S1547-5271(16)30735-4/fulltext|DOI: http://dx.doi.org/10.1016/j.hrthm.2016.08.038
3180898|NCT00684203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04772&kw=P04772&tab=access|
3180899|NCT01742234|SDY292|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292|ImmPort study identifier is SDY292
3180900|NCT01742234|SDY292|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292|ImmPort study identifier is SDY292. The study protocol is available in the Design tab section.
3180901|NCT04018547||Individual Participant Data Set|http://www.oxitone.com|De-identified data for primary and secondary outcome measures
3180902|NCT03116672|UABC|Clinical Study Report|http://www.uabc.mx|Clinical trial that evaluate drug and placebo
3176276|NCT01706315|116778|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176277|NCT01706315|116778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176278|NCT01706315|116778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178400|NCT00530309|GLP107865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178401|NCT00530309|GLP107865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178402|NCT00530309|GLP107865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178403|NCT00530309|GLP107865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178404|NCT00530309|GLP107865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178405|NCT00530309|GLP107865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178406|NCT00530309|GLP107865|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178407|NCT01802931|117016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178408|NCT01802931|117016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178409|NCT01802931|117016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180903|NCT03116672|protocol guide|Individual Participant Data Set|http://www.uabc.mx|Clinical Guide
3178410|NCT01802931|117016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178411|NCT01802931|117016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178412|NCT01802931|117016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178413|NCT01802931|117016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178414|NCT07221565|IPD|Study Protocol|https://www.truwayhealth.com|The Truway Health ClinicalChain repository will host de-identified datasets, full study protocol, and statistical analysis plan following publication. Access will be provided through blockchain-verified credentials to ensure compliance and auditability.
3178415|NCT01366521|114092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178416|NCT01366521|114092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178417|NCT01366521|114092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178418|NCT01366521|114092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178419|NCT01366521|114092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178420|NCT01366521|114092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178421|NCT01366521|114092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178422|NCT07001969||Individual Participant Data Set|https://t.me/drmassoud77/24301|Book of author about technique
3178423|NCT02877615||Study Protocol|https://clinicaltrials.servier.com/|
3178424|NCT02877615||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178425|NCT02877615||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178426|NCT02877615||Informed Consent Form|https://clinicaltrials.servier.com/|
3178427|NCT02877615||Clinical Study Report|https://clinicaltrials.servier.com/|
3178428|NCT02877615||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3178429|NCT00843024|107979|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178430|NCT00843024|107979|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178431|NCT00843024|107979|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178432|NCT00843024|107979|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178433|NCT00843024|107979|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178434|NCT00843024|107979|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178435|NCT00843024|107979|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178436|NCT00197132|49653/375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178437|NCT00197132|49653/375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178438|NCT00197132|49653/375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178439|NCT00197132|49653/375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178440|NCT00197132|49653/375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180904|NCT03391583||Individual Participant Data Set|http://project-redcap.org/|"The Applied Health Research Centre (AHRC), an academic research organization based at St Michael's Hospital, will use software called REDCap to create the web-based electronic CRF (eCRF).~Authorized personnel receive a username and password which is unique, and database access is controlled by the DCC in collaboration with the Principal Investigator."
3178441|NCT00197132|49653/375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180905|NCT00591409||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180906|NCT03013725||Study Protocol|http://husk.b.uib.no/prototest/|Protocol
3180907|NCT00522678|HZA102928|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180908|NCT00522678|HZA102928|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180909|NCT00522678|HZA102928|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180910|NCT00522678|HZA102928|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180911|NCT00522678|HZA102928|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172068|NCT00441441|SFA106484|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176279|NCT00157872||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176280|NCT02989857||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3176281|NCT02989857||Study Protocol|https://clinicaltrials.servier.com/|
3176282|NCT02989857||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3176283|NCT02989857||Informed Consent Form|https://clinicaltrials.servier.com/|
3176284|NCT02989857||Clinical Study Report|https://clinicaltrials.servier.com/|
3176285|NCT02989857||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3176286|NCT04458766||MMAS-8 with permission from Dr Donald Morisky. as written below:|http://www.moriskyscale.com|The MMAS-8 Scale, content, name, and trademarks are protected by US copyright and trademark laws. Permission for use of the scale and its coding is required. A license agreement is available from MMAR, LLC.
3176287|NCT00332566|106602|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176288|NCT00332566|106602|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176289|NCT00332566|106602|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176290|NCT00332566|106602|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176291|NCT00332566|106602|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176292|NCT00332566|106602|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176293|NCT05698498||CDSS Waiver Request Approval Letter|http://tinyurl.com/SVGIP|California Department of Social Services (CDSS) approval letter in response to Silicon Valley Guaranteed Income Project (SVGIP) waiver request to exclude SVGIP guaranteed income payments from CalWORKS and CalFresh eligibility determination, re-determination, and benefit amount
3180912|NCT00522678|HZA102928|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180913|NCT00522678|HZA102928|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180914|NCT00721812|111406|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180915|NCT00721812|111406|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180916|NCT00721812|111406|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180917|NCT00721812|111406|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180918|NCT00721812|111406|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180919|NCT00721812|111406|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172069|NCT00441441|SFA106484|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176294|NCT00140686|102247/036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176295|NCT00140686|102247/036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176296|NCT00140686|102247/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176297|NCT00140686|102247/036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176298|NCT00140686|102247/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176299|NCT00140686|102247/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176300|NCT00140686|102247/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176301|NCT06250257||Individual Participant Data Set|https://kf.kobotoolbox.org/#/forms/aSWyWhEb2TmCqshx54qTW7|
3176302|NCT01999530||Publication|https://www.ncbi.nlm.nih.gov/pubmed/28233334|
3176303|NCT03141970|CTRI/2015/06/005939|Study Protocol|http://ctri.nic.in/Clinicaltrials/login.php|Contains details of registration of clinical trial prior to recruiting patients in India, at website of Clinical Trials Registry of India
3176304|NCT07004348|PROM link|Statistical Analysis Plan|https://livenorthumbriaac-my.sharepoint.com/:w:/g/personal/frank_lai_northumbria_ac_uk/EbKJJ3cbnk5Ikr-NpppTxHoBmGuJLYpePT6qQ1ZnXA4P-w?e=ZZuX7U|
3176305|NCT01702298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-312&kw=0431D-312&tab=access|
3176306|NCT00373542|RRL103660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176307|NCT00373542|RRL103660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176308|NCT00373542|RRL103660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176309|NCT00373542|RRL103660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176310|NCT00373542|RRL103660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176311|NCT00373542|RRL103660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176312|NCT00373542|RRL103660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176313|NCT06835959|Informed consent form|Informed Consent Form|https://drive.google.com/file/d/1q09u34SVFOO2TXC7vXuDAE0MAjJfgVyA/view?usp=drive_link|
3176314|NCT00005121|FHS-Cohort|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/framcohort/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval, and completion of a data use agreement.
3176315|NCT00005121|FHS-Cohort|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
3176316|NCT00005121|FHS-Cohort|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
3176317|NCT00005121|FHS-Cohort|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
3176318|NCT00005121|FHS-OS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval, and completion of a data use agreement.
3176319|NCT00005121|FHS-OS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
3176320|NCT00005121|FHS-OS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
3176321|NCT00005121|FHS-OS|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
3176322|NCT00005121|FHS-Gen III|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/gen3/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval, and completion of a data use agreement.
3176323|NCT00005121|FHS-Gen III|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/gen3/|
3176324|NCT00005121|FHS-Gen III|Study Forms|http://biolincc.nhlbi.nih.gov/studies/gen3/|
3176325|NCT00005121|FHS-Gen III|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/gen3/|
3176326|NCT04831229|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
3176327|NCT02870426||Individual Participant Data Set|http://www.stgeorges.nhs.uk|The project documents will be available directly from the research team. Please e-mail Dr Florence Hogg fhogg@sgul.ac.uk
3176328|NCT06379828||Study Protocol|https://newborn-health-standards.org/about/project-overview/|
3176329|NCT00317122|759346/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176330|NCT00317122|759346/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176331|NCT00317122|759346/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176332|NCT00317122|759346/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176333|NCT00317122|759346/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176334|NCT00317122|759346/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176335|NCT07161297||Study Protocol|https://www.humanitas-research.com/|Requests should be submitted to: ibd@humanitas.it Subject: REMI-IBD
3176336|NCT05162755||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3176337|NCT05162755||Study Protocol|https://clinicaltrials.servier.com/|
3176338|NCT05162755||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3176339|NCT05162755||Informed Consent Form|https://clinicaltrials.servier.com/|
3176340|NCT05162755||Clinical Study Report|https://clinicaltrials.servier.com/|
3176341|NCT05162755||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3176342|NCT01697085||Clinical Study Report|http://www.maturitas.org/article/S0378-5122%2814%2900239-4/abstract?cc=y=|
3176343|NCT00730756|FFR111158|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176344|NCT00730756|FFR111158|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176345|NCT00730756|FFR111158|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176346|NCT00730756|FFR111158|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176347|NCT00730756|FFR111158|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176348|NCT00730756|FFR111158|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176349|NCT00730756|FFR111158|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176350|NCT00320606|SDY662:WISP-R ITN029ST|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY662|ImmPort study identifier is Study ID is SDY662:WISP-R ITN029ST
3176351|NCT00320606|SDY662:WISP-R ITN029ST|Study summary, -schematic, -detailed description, -download packages et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY662|ImmPort study identifier is Study ID is SDY662:WISP-R ITN029ST
3172070|NCT00441441|SFA106484|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172071|NCT00441441|SFA106484|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172072|NCT03167580||Study Protocol|https://sites.google.com/view/relaxtrial/study-details-and-documents/protocol|
3172073|NCT00606697|NKI110334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172074|NCT00606697|NKI110334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172075|NCT00606697|NKI110334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172076|NCT00606697|NKI110334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172077|NCT00606697|NKI110334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172078|NCT00606697|NKI110334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172079|NCT00606697|NKI110334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172080|NCT00048594||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172081|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172082|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
3172083|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Forms|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
3172084|NCT00000579|ARDSNet-LASRS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lasrs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172085|NCT00000579|ARDSNet-LASRS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
3172086|NCT00000579|ARDSNet-LASRS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
3172087|NCT00000579|ARDSNet-ALVEOLI|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/alveoli/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172088|NCT00000579|ARDSNet-ALVEOLI|Study Forms|http://biolincc.nhlbi.nih.gov/studies/alveoli/|
3172089|NCT00000579|ARDSNet-FACTT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/factt/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172090|NCT00000579|ARDSNet-FACTT|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/factt/|
3172091|NCT00000579|ARDSNet-FACTT|Study Forms|http://biolincc.nhlbi.nih.gov/studies/factt/|
3172092|NCT00256867|AVS101946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172093|NCT00256867|AVS101946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172094|NCT00256867|AVS101946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172095|NCT00256867|AVS101946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172096|NCT00256867|AVS101946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172097|NCT00256867|AVS101946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172098|NCT00256867|AVS101946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172099|NCT01258530|115096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172100|NCT01258530|115096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172101|NCT01258530|115096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172102|NCT01258530|115096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172103|NCT01258530|115096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172104|NCT01258530|115096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172105|NCT01258530|115096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172106|NCT01954251|117036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172107|NCT01954251|117036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172108|NCT01954251|117036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176352|NCT00320606|WISP-R ITN029ST|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN029STJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3176353|NCT00320606|WISP-R ITN029ST|Study protocol synopsis, -navigator, abstracts and manuscripts, datasets et al.|https://www.itntrialshare.org/project/Studies/ITN029STJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3176354|NCT03150264||Study Protocol|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161575/|
3176355|NCT01128569|113090|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176356|NCT01128569|113090|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176357|NCT01128569|113090|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176358|NCT01128569|113090|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176359|NCT01128569|113090|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176360|NCT01128569|113090|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176361|NCT01128569|113090|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176362|NCT07003204|msabry776@yahoo.com|Clinical Study Report|https://pmc.ncbi.nlm.nih.gov/articles/PMC8075197/|very good
3172109|NCT01954251|117036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172110|NCT01954251|117036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176363|NCT06616610||Individual Participant Data Set|https://idus.us.es/|The idUS repository is part of the digital infrastructures for open science guaranteed by the National Strategy for Open Science (ENCA). It allows authors from the University of Seville (US) to deposit their publications in open access and manage their research data according to FAIR principles (Findable, Accessible, Interoperable, and Reusable).
3176364|NCT06680583||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/34812069/|Physical indicators with shock index relatives are used in the prediction of prognosis on cirrhosis with gastrointestinal bleeding
3176365|NCT01110057|113049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176366|NCT01110057|113049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176367|NCT01110057|113049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176368|NCT01110057|113049|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176369|NCT01110057|113049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176370|NCT01110057|113049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176371|NCT01110057|113049|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176372|NCT00325143|217744/100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176373|NCT00325143|217744/100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176374|NCT00325143|217744/100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176375|NCT00325143|217744/100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176376|NCT00325143|217744/100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176377|NCT00325143|217744/100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176378|NCT01495013|115317|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176379|NCT01495013|115317|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176380|NCT01495013|115317|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176381|NCT01495013|115317|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176382|NCT01495013|115317|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176383|NCT01495013|115317|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176384|NCT00652743|111443|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176385|NCT00652743|111443|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 111470 are summarised with studies 111443, 111471, and 111472 on the GSK Clinical Study Register.
3176386|NCT00652743|111443|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176387|NCT00652743|111443|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176388|NCT00652743|111443|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176389|NCT00652743|111443|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176390|NCT00538057|HZA105871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176391|NCT00538057|HZA105871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176392|NCT00538057|HZA105871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176393|NCT00538057|HZA105871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176394|NCT00538057|HZA105871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176395|NCT00538057|HZA105871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176396|NCT00538057|HZA105871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176397|NCT04748692||Individual Participant Data Set|https://vub-my.sharepoint.com/:f:/g/personal/aldo_scafoglieri_vub_be/EspOeK0bPk9JgvUpkobVcZEB-fPjar_48PO4_aIq-JhsIw?e=Wsu4DC|Access can be granted by the participant data set holder: Prof dr Aldo Scafoglieri
3176398|NCT00335881|106745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176399|NCT00335881|106745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176400|NCT00335881|106745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176401|NCT00335881|106745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176402|NCT00335881|106745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176403|NCT00335881|106745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176404|NCT07150442||Study Protocol|https://bit.ly/45NuVGB|https://bit.ly/45NuVGB
3176405|NCT01978145|115646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176406|NCT01978145|115646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176407|NCT01978145|115646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176408|NCT01978145|115646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176409|NCT01978145|115646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176410|NCT01978145|115646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176411|NCT01978145|115646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176412|NCT00445094||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176413|NCT00688467||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05363&kw=P05363&tab=access|
3176414|NCT03750019|10.5255/UKDA-SN-853370|Individual Participant Data Set|http://dx.doi.org/10.5255/UKDA-SN-853370|
3176415|NCT03750019|10.17605/OSF.IO/WYCKJ|Study Protocol|https://doi.org/10.17605/OSF.IO/WYCKJ|
3176416|NCT01436110|115285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176417|NCT01436110|115285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176418|NCT01436110|115285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176419|NCT01436110|115285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176420|NCT01436110|115285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176421|NCT01436110|115285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176422|NCT01436110|115285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176423|NCT00225862|100310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176424|NCT00225862|100310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176425|NCT00225862|100310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176426|NCT00225862|100310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176427|NCT00225862|100310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176428|NCT00225862|100310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176429|NCT00225862|100310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176430|NCT01000506|112997|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176431|NCT01000506|112997|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178442|NCT00197132|49653/375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178443|NCT01372137|doi: 10.1111/bph.13433|Manuscript|http://onlinelibrary.wiley.com/doi/10.1111/bph.13433/abstract;jsessionid=E657A6C9667BB70DE92E5B69B86B1D3F.f01t01|
3178444|NCT01366560|114639|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178445|NCT01366560|114639|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178446|NCT01366560|114639|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178447|NCT01366560|114639|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178448|NCT01366560|114639|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178449|NCT01366560|114639|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178450|NCT01366560|114639|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178451|NCT00694993|HHI110157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178452|NCT00694993|HHI110157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180920|NCT00721812|111406|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178453|NCT00694993|HHI110157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178454|NCT00694993|HHI110157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178455|NCT00694993|HHI110157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178456|NCT00694993|HHI110157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178457|NCT00694993|HHI110157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178458|NCT04221009||Informed Consent Form|https://arc.research.usf.edu/Prod/sd/Doc/0/DDRU7K2KMHLK9ECT12FPTMA60B/3S78A88933BKN7869JO1NSMT62.pdf|
3178459|NCT04221009||Study Protocol|https://arc.research.usf.edu/Prod/sd/Doc/0/06USV5NTK2VKJ06CUK3TQJR578/Protocol%20v01%202019-10-24.docx|
3178460|NCT00609492|109621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178461|NCT00609492|109621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178462|NCT00609492|109621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178463|NCT00609492|109621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178464|NCT00609492|109621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178465|NCT00609492|109621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178466|NCT00609492|109621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178467|NCT03134287||Textbook|http://onlinelibrary.wiley.com/doi/10.1111/j.1742-6723.2004.00655.x/full|Samuels LE, Roberts JR, Hedges JR. Nasogastric and Feeding Tube Placement, In: Clinical Procedures in Emergency Medicine. 4th ed. WB Saunders; 2004. p784-804.
3178468|NCT03134287||Textbook|https://books.google.co.id/books?id=ooH1nH81_h4C&pg=PR4&lpg=PR4&dq=Irwin+and+Rippe%27s+Intensive+Care+Medicine+2008&source=bl&ots=43X9QRBshe&sig=Y3ycuRyss2vYHzN3q0WFtrSdPRM&hl=en&sa=X&ved=0ahUKEwjk_6TIo8LTAhWMvY8KHSvTDo8Q6AEIRzAG#v=onepage&q=Irwin%20and%20Rippe's%20Intensive%20Care%20Medicine%202008&f=false|Irwin RS, Rippe JM. Irwin and Rippe's Intensive Care Medicine: Endoscopic Placement of Feeding Tubes. 6th ed. Lippincott Williams \& Wilkins; 2008. p145-150.
3176432|NCT01000506|112997|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176433|NCT01000506|112997|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178469|NCT03134287||Textbook|https://books.google.co.id/books/about/The_ICU_Book.html?id=OWEmVx9MS74C&redir_esc=y|Marino PL. Enteral Tube Feeding. In: The ICU Book. 3rd ed. Lippincott Williams \& Wilkins; 2007. p842-855.
3178470|NCT00811798|111712|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178471|NCT00811798|111712|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178472|NCT00811798|111712|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178473|NCT00811798|111712|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178474|NCT00811798|111712|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178475|NCT00811798|111712|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178476|NCT00811798|111712|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178477|NCT01018186|106839|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178478|NCT01018186|106839|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178479|NCT01018186|106839|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178480|NCT01018186|106839|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178481|NCT01018186|106839|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178482|NCT01018186|106839|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178483|NCT01018186|106839|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178484|NCT01411111|112362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178485|NCT01411111|112362|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178486|NCT01411111|112362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178487|NCT01411111|112362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178488|NCT01411111|112362|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178489|NCT01411111|112362|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178490|NCT01411111|112362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176434|NCT01000506|112997|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176435|NCT01000506|112997|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176436|NCT01000506|112997|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176437|NCT00363311|AVO105948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176438|NCT00363311|AVO105948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176439|NCT00363311|AVO105948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176440|NCT00363311|AVO105948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178491|NCT01077856||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-033&kw=V501-033&tab=access|
3176441|NCT00363311|AVO105948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176442|NCT00363311|AVO105948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176443|NCT00363311|AVO105948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176444|NCT06187857||Study Protocol|https://osf.io/cavkf/?view_only=cc219af15f614756b43742875b6b0b39|
3178492|NCT00372112|B2C108562|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176445|NCT06246747||Study Protocol|https://drive.google.com/file/d/1F2ZuHApDf800Q9Tox-sujdf0sHmctTO0/view?usp=sharing|The protocol can be accessed by clicking the Google Drive link above. For any additional questions or an issue with opening the link, please contact bella@wizecare.com
3176446|NCT01644643|D4280C00006|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1452&filename=Clinical%20Study%20Protocol_3%20Redacted%20amended.pdf|D4280C00006 Clinical Study Protocol
3176447|NCT01644643|D4280C00006|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1452&filename=Clinical%20Study%20Protocol%20Amendment%202%20Redacted%20amended.pdf|D4280C00006 Clinical Study Protocol Amendment 2 Redacted amended
3176448|NCT01644643|D4280C00006|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1452&filename=Clinical%20Study%20Protocol%20Amendment%203%20Redacted%20amended.pdf|D4280C00006 Clinical Study Protocol Amendment 3 Redacted amended
3176449|NCT00421148||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176450|NCT01030822|112909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176451|NCT01030822|112909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176452|NCT01030822|112909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176453|NCT01030822|112909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176454|NCT01030822|112909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176455|NCT01030822|112909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176456|NCT01030822|112909|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176457|NCT00400855|SIG103337|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176458|NCT00400855|SIG103337|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176459|NCT00400855|SIG103337|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176460|NCT00400855|SIG103337|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176461|NCT00400855|SIG103337|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176462|NCT00400855|SIG103337|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176463|NCT00400855|SIG103337|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176464|NCT00488514|TXA107977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176465|NCT00488514|TXA107977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176466|NCT00488514|TXA107977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176467|NCT00488514|TXA107977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176468|NCT00488514|TXA107977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176469|NCT00488514|TXA107977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176470|NCT00488514|TXA107977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176471|NCT00289172|103792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176472|NCT00289172|103792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176473|NCT00289172|103792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176474|NCT00289172|103792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176475|NCT00289172|103792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176476|NCT00289172|103792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176477|NCT01073293||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-007&kw=V503-007&tab=access|
3172111|NCT01954251|117036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176478|NCT01475721|115359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172112|NCT01954251|117036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176479|NCT01475721|115359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172113|NCT00444509|HZA108799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172114|NCT00444509|HZA108799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172115|NCT00444509|HZA108799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180921|NCT05662683|Journal of Continuing Medical|REVIEW|https://dergipark.org.tr/en/pub/sted/issue/52715/466811|Ozturk, Y. (2020). Barriers to Women Having Pap Smear Screening Test .29 (1), 61-68. DOI: 10.17942/sted.466811
3180922|NCT05405322||podcasts|https://www.ird.fr/positifs-une-collection-de-podcasts-pour-un-nouveau-regard-sur-les-jeunes-vivant-avec-le-vih-en|Experiences of participatoy research with the participants included in the Transitions Study and their peers.
3180923|NCT00064428|103413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180924|NCT00064428|103413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180925|NCT00064428|103413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180926|NCT00064428|103413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174055|NCT00333450|106623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174056|NCT00333450|106623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174057|NCT00396630|106260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174058|NCT00396630|106260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174059|NCT00396630|106260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174060|NCT00396630|106260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174061|NCT00396630|106260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174062|NCT00396630|106260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174063|NCT00396630|106260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174064|NCT03211039|37114|Individual Participant Data Set|http://view.ncbi.nlm.nih.gov/dbgap-controlled|
3174065|NCT03211039|37114|Summary level phenotype data|http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs002094.v1.p1|
3174066|NCT03211039|37114|Subject Sample Telemetry Report (SSTR) for Subject and Sample IDs, consents, summary counts, processing status, and molecular and sequence sample uses|http://www.ncbi.nlm.nih.gov/gap/sstr/report/phs002094.v1.p1|
3174067|NCT00108082|COR100216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180927|NCT00064428|103413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180928|NCT00064428|103413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180929|NCT00064428|103413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180930|NCT03037814|26161601|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/26161601|
3172116|NCT00444509|HZA108799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172117|NCT00444509|HZA108799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172118|NCT00444509|HZA108799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172119|NCT00444509|HZA108799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172120|NCT00377611|107564|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172121|NCT00377611|107564|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172122|NCT00377611|107564|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172123|NCT00377611|107564|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172124|NCT00377611|107564|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172125|NCT00377611|107564|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172126|NCT00310388|VRX-RET-E22-304|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172127|NCT00310388|VRX-RET-E22-304|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180931|NCT03037814|19953810|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/19953810|
3176480|NCT01475721|115359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176481|NCT01475721|115359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176482|NCT01475721|115359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176483|NCT01475721|115359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176484|NCT01475721|115359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172128|NCT00310388|VRX-RET-E22-304|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172129|NCT00310388|VRX-RET-E22-304|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172130|NCT00310388|VRX-RET-E22-304|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172131|NCT00310388|VRX-RET-E22-304|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172132|NCT00310388|VRX-RET-E22-304|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172133|NCT04987853|BR10965164|Study Protocol|https://is.ncste.kz/login|
3172134|NCT04987853|BR10965164|Informed Consent Form|https://is.ncste.kz/login|
3172135|NCT04987853|BR10965164|Clinical Study Report|https://is.ncste.kz/login|
3172136|NCT01000727|480848/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172137|NCT01000727|480848/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172138|NCT01000727|480848/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172139|NCT01000727|480848/033|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176485|NCT05711875|Sridhar A, Shiliang Z, Woodson|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/33140989/|web site is provided
3176486|NCT04588636|10.17605/OSF.IO/9XTMD|Study Protocol|https://osf.io/9xtmd/|Supporting information for this study is available in the open science framework (OSF): the data set of individual participants, study protocol, statistical analysis plan, and informed consent form.
3176487|NCT05173376||Study Protocol|https://osf.io/scjn6/|Protocol on the Open Science Framework (OSF)
3176488|NCT05173376||Statistical Analysis Plan|https://osf.io/scjn6/|
3176489|NCT05173376||Individual Participant Data Set|https://osf.io/scjn6/|The study protocol and statistical analysis plan were pre-registered on the OSF prior to starting recruitment. Participant dataset (anonymised) will be made available when results are published.
3180932|NCT03037814|12542617|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/12542617|
3172140|NCT01000727|480848/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172141|NCT01000727|480848/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172142|NCT06459622||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29337030/|
3172143|NCT00120289|AIM-HIGH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172144|NCT00120289|AIM-HIGH|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
3172145|NCT00120289|AIM-HIGH|Study forms|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
3172146|NCT00718666|112021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172147|NCT00718666|112021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172148|NCT00718666|112021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176490|NCT02747758||Clinical Study Report|https://www.frontiersin.org/articles/10.3389/fneur.2023.1069434/full|"The research report is published open access:~ORIGINAL RESEARCH article Front. Neurol., 01 March 2023, Volume 14 - 2023 \| https://doi.org/10.3389/fneur.2023.1069434"
3176491|NCT00412191|LAM105379|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172149|NCT00718666|112021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176492|NCT00412191|LAM105379|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176493|NCT00412191|LAM105379|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176494|NCT00412191|LAM105379|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176495|NCT00412191|LAM105379|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176496|NCT00412191|LAM105379|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174068|NCT00108082|COR100216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174069|NCT00108082|COR100216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174070|NCT00108082|COR100216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174071|NCT00108082|COR100216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174072|NCT00108082|COR100216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174073|NCT00108082|COR100216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174074|NCT01190930||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Available IPD/Information: Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3174075|NCT07254273|The individual participant dat|Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1ZN1TbLb_kPid_fZNsQVWYNu02qO5s-mv/edit?usp=sharing&ouid=107542558214893941575&rtpof=true&sd=true|https://docs.google.com/spreadsheets/d/1ZN1TbLb\_kPid\_fZNsQVWYNu02qO5s-mv/edit?usp=sharing\&ouid=107542558214893941575\&rtpof=true\&sd=true
3174076|NCT00743860|LPL112498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174077|NCT00743860|LPL112498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174078|NCT00743860|LPL112498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174079|NCT00743860|LPL112498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174080|NCT00743860|LPL112498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174081|NCT00743860|LPL112498|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174082|NCT00743860|LPL112498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174083|NCT00139932||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3174084|NCT02724826||Clinical Study Report|http://resolver.ebscohost.com/openurl?sid=Entrez%3aPubMed&id=pmid%3a18090079&site=ftf-live|
3174085|NCT01039454|109710|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174086|NCT01039454|109710|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174087|NCT01039454|109710|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174088|NCT01039454|109710|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174089|NCT01039454|109710|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174090|NCT01039454|109710|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174091|NCT01077505|107032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174092|NCT01077505|107032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174093|NCT01077505|107032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174094|NCT01077505|107032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174095|NCT01077505|107032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174096|NCT01077505|107032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174097|NCT01077505|107032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174098|NCT01098539|114130|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174099|NCT01098539|114130|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174100|NCT01098539|114130|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174101|NCT01098539|114130|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174102|NCT01098539|114130|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174103|NCT01098539|114130|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174104|NCT01098539|114130|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180933|NCT01274559||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0524A-133&kw=0524A-133&tab=access|
3176497|NCT00412191|LAM105379|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176498|NCT01484496|112341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176499|NCT01484496|112341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176500|NCT01484496|112341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176501|NCT01484496|112341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180934|NCT03315234|NCT03150680|Clinical Study Report|https://clinicaltrials.gov/ct2/show/NCT03150680|"GESS trial \[ClinicalTrials.gov Identifier: NCT03150680\] was designed exclusively based on the protocol of the study Correlation of Genetic Polymorphisms and Clinical Parameters With the Complexity of Coronary Artery Disease \[CIP\_PhD Rampidis Georgios\_1.1\]"
3180935|NCT00372255|106252|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180936|NCT00372255|106252|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180937|NCT00372255|106252|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180938|NCT00372255|106252|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180939|NCT00372255|106252|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180940|NCT00372255|106252|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180941|NCT02991781|neurofeedback-auth|Individual Participant Data Set|http://ckan.smokefreebrain.eu/|
3180942|NCT00005541|HEIRS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/heirs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180943|NCT00005541||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/heirs/|
3180944|NCT00005541||Study Forms|http://biolincc.nhlbi.nih.gov/studies/heirs/|
3180945|NCT00005541||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/heirs/|
3180946|NCT00144846|SB030002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176502|NCT01484496|112341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176503|NCT01484496|112341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176504|NCT01484496|112341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176505|NCT00005739||Abstract|http://ajph.aphapublications.org/doi/pdf/10.2105/AJPH.86.8_Pt_1.1146|
3176506|NCT06694246||Study Protocol|https://drive.google.com/drive/folders/1KXhFMWnU8LAIEVoOEpM2C4iXiE02_8-7?usp=share_link|The above link for inspecting the study protocol and the evidence for a timely study progress.
3176507|NCT01999842|201072|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176508|NCT01999842|201072|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176509|NCT01999842|201072|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176510|NCT01999842|201072|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176511|NCT01999842|201072|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176512|NCT01999842|201072|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176513|NCT01999842|201072|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176514|NCT01453491|115951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176515|NCT01453491|115951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176516|NCT01453491|115951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176517|NCT01453491|115951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176518|NCT01453491|115951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176519|NCT01453491|115951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176520|NCT01453491|115951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176521|NCT00920556|113222|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180947|NCT00144846|SB030002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180948|NCT00144846|SB030002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180949|NCT00144846|SB030002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172150|NCT00718666|112021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172151|NCT00718666|112021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172152|NCT01842620|117219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172153|NCT01842620|117219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172154|NCT01842620|117219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172155|NCT01842620|117219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172156|NCT01842620|117219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172157|NCT01842620|117219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172158|NCT01842620|117219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172159|NCT00380211|IDB-200-001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172160|NCT00380211|IDB-200-001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172161|NCT00380211|IDB-200-001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172162|NCT00380211|IDB-200-001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172163|NCT00380211|IDB-200-001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172164|NCT00757770|444563/033|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172165|NCT00757770|444563/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172166|NCT00757770|444563/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172167|NCT00757770|444563/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172168|NCT00757770|444563/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172169|NCT00757770|444563/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172170|NCT01098461|110932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172171|NCT01098461|110932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172172|NCT01098461|110932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172173|NCT01098461|110932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172174|NCT01098461|110932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172175|NCT01098461|110932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172176|NCT01098461|110932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172177|NCT02640144||Study Protocol|http://www.nr-ortho.com|Original study protocol is written in Hebrew. protocol is available at the Ziv Medical Center, Institutional Review Board (IRB) , or in direct request via the website address posted above.
3172178|NCT00992784|113094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180950|NCT00144846|SB030002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172179|NCT00992784|113094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172180|NCT00992784|113094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172181|NCT00992784|113094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172182|NCT00992784|113094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172183|NCT00992784|113094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172184|NCT00992784|113094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176522|NCT00920556|113222|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176523|NCT00920556|113222|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176524|NCT00920556|113222|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176525|NCT00920556|113222|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178493|NCT00372112|B2C108562|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178494|NCT00372112|B2C108562|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178495|NCT00372112|B2C108562|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178496|NCT00372112|B2C108562|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178497|NCT00372112|B2C108562|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178498|NCT00372112|B2C108562|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178499|NCT01428453|114458|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178500|NCT01428453|114458|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178501|NCT01428453|114458|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178502|NCT01428453|114458|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178503|NCT01428453|114458|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178504|NCT01428453|114458|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178505|NCT01428453|114458|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178506|NCT00044278|LAM20007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178507|NCT00044278|LAM20007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178508|NCT00044278|LAM20007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178509|NCT00044278|LAM20007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178510|NCT00044278|LAM20007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178511|NCT00044278|LAM20007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178512|NCT00044278|LAM20007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178513|NCT03944460||Bibliografic References|http://www.ipb.hhu.de/publikationen-ipb.html|"1. Leithold et al., Pharm Res. 33, 328-336 (2016).~2. van Groen et al., Sci Rep 7, 16275 (2017).~3. Schemmert et al., Mol Neurobiol 56, 2211 (2019).~4. Kutzsche et al., Molecules 22, 1693 (2017).~5. Schemmert et al., Neurobiol Dis 124, 36 (2019)."
3178514|NCT03012802||Study Protocol|http://www.grupogerm.es/power|
3178515|NCT03012802||Statistical Analysis Plan|http://www.grupogerm.es/power|
3178516|NCT03012802||Clinical Study Report|http://www.grupogerm.es/power|
3180951|NCT00144846|SB030002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180952|NCT00144846|SB030002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180953|NCT04882748||Individual Participant Data Set|https://www.frontiersin.org/articles/10.3389/fnbot.2021.715632/full#supplementary-material|
3180954|NCT05907317||Study Protocol|https://www.rigshospitalet.dk/english/departments/juliane-marie-centre/department-of-neonatology/research/safeboosc-iiiv/Pages/protocol.aspx|
3180955|NCT06244693|aparral|Individual Participant Data Set|http://www.redcap.med.uchile.cl|Data registry online system provided by sponsor
3180956|NCT00118703|FFR30007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180957|NCT00118703|FFR30007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180958|NCT00118703|FFR30007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180959|NCT00118703|FFR30007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174105|NCT00725764|MET111646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180960|NCT00118703|FFR30007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178517|NCT00356369|107386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178518|NCT00356369|107386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178519|NCT00356369|107386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178520|NCT00356369|107386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178521|NCT00356369|107386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178522|NCT00356369|107386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178523|NCT01124422|113877|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178524|NCT01124422|113877|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178525|NCT01124422|113877|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178526|NCT01124422|113877|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178527|NCT01124422|113877|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178528|NCT01124422|113877|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178529|NCT01124422|113877|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178530|NCT01607086|111649|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178531|NCT01607086|111649|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178532|NCT01607086|111649|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178533|NCT01607086|111649|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178534|NCT01607086|111649|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178535|NCT01607086|111649|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178536|NCT01607086|111649|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178537|NCT00369993|SAS104449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178538|NCT00369993|SAS104449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178539|NCT00369993|SAS104449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178540|NCT00369993|SAS104449|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178541|NCT00369993|SAS104449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178542|NCT00369993|SAS104449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178543|NCT00369993|SAS104449|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178544|NCT01702454|116023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178545|NCT01702454|116023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178546|NCT01702454|116023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178547|NCT01702454|116023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178548|NCT01702454|116023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178549|NCT01702454|116023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178550|NCT01702454|116023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178551|NCT01030939|112861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178552|NCT01030939|112861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178553|NCT01030939|112861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178554|NCT01030939|112861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176526|NCT00920556|113222|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176527|NCT01366573|115256|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176528|NCT01366573|115256|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180961|NCT00118703|FFR30007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180962|NCT00118703|FFR30007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180963|NCT00038961|103414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180964|NCT00038961|103414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180965|NCT00038961|103414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180966|NCT00038961|103414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180967|NCT00038961|103414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180968|NCT00038961|103414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180969|NCT00005278|REDS-GSR/GLPR|Operations Manual|http://biolincc.nhlbi.nih.gov/studies/gsrglpr/|Samples and characterization data. NHLBI provides controlled access to samples through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a materials use agreement.
3180970|NCT00005278|REDS-HTLV|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/reds/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180971|NCT00005278|REDS-HTLV|Study Forms|http://biolincc.nhlbi.nih.gov/studies/reds/|
3180972|NCT00005278|REDS-RADAR|Operations Manual|http://biolincc.nhlbi.nih.gov/studies/radar/|Samples and characterization data. NHLBI provides controlled access to samples through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a materials use agreement.
3180973|NCT04629443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3180974|NCT04629443||Study Protocol|https://clinicaltrials.servier.com/|
3180975|NCT04629443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3180976|NCT04629443||Informed Consent Form|https://clinicaltrials.servier.com/|
3180977|NCT04629443||Clinical Study Report|https://clinicaltrials.servier.com/|
3180978|NCT04629443||study-level clinical trial data|https://clinicaltrials.servier.com/|
3180979|NCT01316887|113359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180980|NCT01316887|113359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180981|NCT01316887|113359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180982|NCT01316887|113359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180983|NCT01316887|113359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180984|NCT01316887|113359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180985|NCT01316887|113359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180986|NCT01086384|106837|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180987|NCT01086384|106837|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180988|NCT01086384|106837|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180989|NCT01086384|106837|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180990|NCT01086384|106837|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180991|NCT01086384|106837|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180992|NCT01086384|106837|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180993|NCT06254755||Individual Participant Data Set|http://competetrials@gmail.com|
3180994|NCT00197223|104438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180995|NCT00197223|104438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180996|NCT00197223|104438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180997|NCT00197223|104438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176529|NCT01366573|115256|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176530|NCT01366573|115256|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176531|NCT01366573|115256|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176532|NCT01366573|115256|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176533|NCT01366573|115256|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176534|NCT02272946||Clinical Study Report|https://drive.google.com/open?id=1n47RTe3nB2_aPQTCXkkTfYodX-gnWKLE|The link above shows the current enrollment table of the Canakinumab study as of March 2, 2020.
3176535|NCT02272946||IL-1B inhibition [by way of Canakinumab] Reduces Atherosclerotic Inflammation in HIV Infection - Journal of the American College of Cardiology|https://linkinghub.elsevier.com/retrieve/pii/S0735-1097(18)38665-0|The link above is the research publication written by Dr. Hsue (Primary Investigator) about how IL-1B inhibition \[by way of Canakinumab\] reduces atherosclerotic inflammation in the setting of HIV.
3176536|NCT02771405||Informed Consent Form|http://www.megafileupload.com/f3sT/Attachments_201656.zip|
3176537|NCT05223673||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3176538|NCT05223673||Study Protocol|https://clinicaltrials.servier.com/|
3176539|NCT05223673||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3176540|NCT05223673||Informed Consent Form|https://clinicaltrials.servier.com/|
3176541|NCT05223673||Clinical Study Report|https://clinicaltrials.servier.com/|
3176542|NCT05223673||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3176543|NCT00292071||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176544|NCT03202433||Clinical Study Report|http://www.researchgate.net/publication/287542931_Psychological_coping_with_invasive_and_painful_medical_procedures_in_the_treatment_of_childhood_and_adolescent_cancer_The_cognitive-behavioural_approach|
3176545|NCT03202433|ISSN 0124-8146|Study Protocol|http://scielo.org.co/scielo.php?script=sci_arttext&pid=S0124-81462013000200010|
3176546|NCT03202433||Clinical Practice Guide|http://www.criscancer.org|
3176547|NCT00127855|792014/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176548|NCT00127855|792014/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176549|NCT00127855|792014/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176550|NCT00127855|792014/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176551|NCT00127855|792014/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176552|NCT06085235||Individual Participant Data Set|https://osf.io/y8e2r/|
3176553|NCT00943761||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-028&kw=7009-028&tab=access|
3176554|NCT04200794||Individual Participant Data Set|https://yareta.unige.ch|The data of this study are deposited on a YARETA, a FAIR digital solution for long-term preservation of research data for all Geneva Universities (https://yareta.unige.ch). DOI: 10.26037/yareta:dhglarpzdfcgzefx4pky7sua3m
3176555|NCT00906178||Intervention website|http://www.cybersenga.com|
3176556|NCT02789085||Reference|http://www.psy.unsw.edu.au/research/research-tools/depression-anxiety-stress-scales-dass|UNSW Australia SoP. Depression \& Anxiety Stress Scales (DASS): UNSW Australia; 2011
3176557|NCT02052661|106793|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176558|NCT02052661|106793|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176559|NCT02052661|106793|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176560|NCT02052661|106793|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176561|NCT02052661|106793|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176562|NCT02052661|106793|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176563|NCT02052661|106793|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176564|NCT01277705|711866/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176565|NCT01277705|711866/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174106|NCT00725764|MET111646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176566|NCT01277705|711866/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176567|NCT01277705|711866/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176568|NCT01277705|711866/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176569|NCT01277705|711866/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174107|NCT00725764|MET111646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174108|NCT00725764|MET111646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174109|NCT00725764|MET111646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174110|NCT00725764|MET111646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174111|NCT00725764|MET111646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174112|NCT00129116|792014/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174113|NCT00129116|792014/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174114|NCT00129116|792014/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174115|NCT00129116|792014/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174116|NCT00129116|792014/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174117|NCT05562648||data|https://pubmed.ncbi.nlm.nih.gov/21943614/|Rozzi, P., Bongiorno, D., \& Vitturini, C. (2011). Fascial release effects on patients with non-specific cervical or lumbar pain. Journal of bodywork and movement therapies, 15(4), 405-416.
3174118|NCT00476307|110221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174119|NCT00476307|110221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174120|NCT00476307|110221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174121|NCT00476307|110221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174122|NCT00476307|110221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174123|NCT00476307|110221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174124|NCT00476307|110221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174125|NCT01956487|116371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174126|NCT01956487|116371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174127|NCT01956487|116371|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174128|NCT01956487|116371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174129|NCT01956487|116371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174130|NCT01956487|116371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174131|NCT01956487|116371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174132|NCT00197080|101468/205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174133|NCT00197080|101468/205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174134|NCT00197080|101468/205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174135|NCT00197080|101468/205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174136|NCT00197080|101468/205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174137|NCT00197080|101468/205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174138|NCT00197080|101468/205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174139|NCT00489099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3174140|NCT00480324|107625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174141|NCT00480324|107625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174142|NCT00480324|107625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174143|NCT00480324|107625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174144|NCT00480324|107625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178555|NCT01030939|112861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178556|NCT01030939|112861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178557|NCT01030939|112861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178558|NCT00877877|111375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178559|NCT00877877|111375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178560|NCT00877877|111375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178561|NCT00877877|111375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178562|NCT00877877|111375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178563|NCT00877877|111375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178564|NCT00877877|111375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178565|NCT01949051|200285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178566|NCT01949051|200285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178567|NCT01949051|200285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178568|NCT01949051|200285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178569|NCT01949051|200285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178570|NCT01949051|200285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178571|NCT01949051|200285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178572|NCT01777256|115919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178573|NCT01777256|115919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178574|NCT01777256|115919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178575|NCT01777256|115919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178576|NCT01777256|115919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178577|NCT01777256|115919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178578|NCT01777256|115919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178579|NCT00412854|104567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178580|NCT00412854|104567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178581|NCT00412854|104567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178582|NCT00412854|104567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178583|NCT00412854|104567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178584|NCT00412854|104567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178585|NCT00412854|104567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178586|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/4psc_clabscurrent.pdf|Bloodstream Infection Event (Central Line-Associated Bloodstream Infection and non-central line-associated Bloodstream Infection)
3178587|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf|CDC/NHSN Surveillance Definitions for Specific Types of Infections
3178588|NCT03019133|201609843|Informed Consent Form|http://hawkirb.research.uiowa.edu|
3178589|NCT04464369|LPDSItopride study|Study Protocol|http://www.targid.eu|
3178590|NCT00256893|ROF102100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178591|NCT00256893|ROF102100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178592|NCT00256893|ROF102100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178593|NCT00256893|ROF102100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178594|NCT00256893|ROF102100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178595|NCT00256893|ROF102100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178596|NCT00256893|ROF102100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178597|NCT03715166||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178598|NCT03715166||Study Protocol|https://clinicaltrials.servier.com/|
3178599|NCT03715166||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178600|NCT03715166||Informed Consent Form|https://clinicaltrials.servier.com/|
3178601|NCT03715166||Clinical Study Report|https://clinicaltrials.servier.com/|
3178602|NCT03715166||study-level clinical trial data|https://clinicaltrials.servier.com/|
3178603|NCT00496093||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178604|NCT03577743|BMTN|Study Protocol|http://clinicaltrials.gov/NCT03577743|Phase 2 study to evaluate the effect of bevacizumab in metastatic triple negative breast cancer patients
3178605|NCT00268996|SB-480848/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178606|NCT00268996|SB-480848/026|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178607|NCT00268996|SB-480848/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178608|NCT00268996|SB-480848/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178609|NCT00268996|SB-480848/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178610|NCT00268996|SB-480848/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178611|NCT00268996|SB-480848/026|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178612|NCT02982967||Individual Participant Data Set|https://figshare.com/s/8f238bd02ca631cfe5fd|
3178613|NCT00102882|SFA100062|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178614|NCT00102882|SFA100062|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178615|NCT00102882|SFA100062|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178616|NCT00102882|SFA100062|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178617|NCT00102882|SFA100062|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178618|NCT00102882|SFA100062|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178619|NCT00102882|SFA100062|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178620|NCT01792674||Clinical Study Report|http://ncbi.nlm.nih.gov/pmc/articles/PMC4611309/pdf/bmjopen-2015-008344.pdf|Sørensen JL, van der Vleuten C, Rosthøj S, Østergaard D, LeBlanc V, Johansen M, Ekelund K, Starkopf L, Lindschou J, Gluud C, Weikop P, Ottesen B.Simulation-based multiprofessional obstetric anaesthesia training conducted in situ versus off-site leads to similar individual and team outcomes: a randomised educational trial. BMJ Open 2015;5: e008344
3178621|NCT01792674||Qualitative study based on the study population from randomised trial.|http://ncbi.nlm.nih.gov/pmc/articles/PMC4608174/pdf/bmjopen-2015-008345.pdf|Sørensen JL, Navne LE, Martin HM, Ottesen B, Albrectsen CK, Pedersen BW. Clarifying the learning experiences of healthcare professionals with in situ versus off site simulation-based medical education: a qualitative study. BMJ Open 2015;5:e008345
3178622|NCT02045797|116704|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178623|NCT02045797|116704|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178624|NCT02045797|116704|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178625|NCT02045797|116704|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178626|NCT02045797|116704|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178627|NCT02045797|116704|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178628|NCT02045797|116704|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178629|NCT05069454||Study Protocol|http://www.isim.az|
3178630|NCT04631081||Individual Participant Data Set|https://www.project-redcap.org/|
3178631|NCT00503009|HZA109895|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178632|NCT00503009|HZA109895|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178633|NCT00503009|HZA109895|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174145|NCT00480324|107625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178634|NCT00503009|HZA109895|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178635|NCT00503009|HZA109895|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178636|NCT00503009|HZA109895|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178637|NCT00451321|115493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178638|NCT00451321|115493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178639|NCT00451321|115493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178640|NCT00451321|115493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178641|NCT00451321|115493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178642|NCT00451321|115493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178643|NCT00451321|115493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178644|NCT02028065||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-101&kw=8616-101&tab=access|
3178645|NCT01686633|116863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178646|NCT01686633|116863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178647|NCT01686633|116863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178648|NCT01686633|116863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178649|NCT01686633|116863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178650|NCT01686633|116863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178651|NCT01686633|116863|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178652|NCT01847417|116498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178653|NCT01847417|116498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178654|NCT01847417|116498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178655|NCT01847417|116498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176570|NCT01018017|114010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176571|NCT01018017|114010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176572|NCT01018017|114010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176573|NCT01018017|114010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176574|NCT01018017|114010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176575|NCT01018017|114010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176576|NCT01018017|114010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176577|NCT02397915|201474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176578|NCT02397915|201474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176579|NCT02397915|201474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176580|NCT02397915|201474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176581|NCT02397915|201474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176582|NCT02397915|201474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176583|NCT02397915|201474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176584|NCT02833129||Study Protocol|http://arxiv.org/abs/1607.01756|
3176585|NCT00540592|110847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176586|NCT00540592|110847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176587|NCT00540592|110847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178656|NCT01847417|116498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178657|NCT01847417|116498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178658|NCT02369341|201959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178659|NCT02369341|201959|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178660|NCT02369341|201959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178661|NCT02369341|201959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178662|NCT02369341|201959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178663|NCT02369341|201959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178664|NCT02369341|201959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178665|NCT00527943||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04736&kw=P04736&tab=access|
3178666|NCT00056407|ARI40006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178667|NCT00056407|ARI40006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178668|NCT00056407|ARI40006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178669|NCT00056407|ARI40006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178670|NCT00056407|ARI40006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178671|NCT00056407|ARI40006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176588|NCT00540592|110847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176589|NCT00540592|110847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176590|NCT00540592|110847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176591|NCT00540592|110847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176592|NCT02726464||Patient Brochure|http://www.lightintegra.com/prism-study|
3176593|NCT02993627|18039384|Clinical Study Report|http://lipidworld.biomedcentral.com/articles/10.1186/1476-511X-6-33/|
3176594|NCT00742131|MET111647|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176595|NCT00742131|MET111647|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176596|NCT00742131|MET111647|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176597|NCT00742131|MET111647|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176598|NCT00742131|MET111647|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176599|NCT00742131|MET111647|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176600|NCT00742131|MET111647|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176601|NCT03160456|IPG598|"NICE guidance Hypoglossal Nerve Stimulation"|https://www.nice.org.uk/guidance/ipg598|National Institute for Health and Care Excellence
3176602|NCT03511508||Study Protocol|http://doi.org/10.1186/s13063-019-3405-5|Study Protocol
3176603|NCT00883948|ARDSNet-EDEN|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/eden/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176604|NCT00883948||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/eden/|
3176605|NCT00883948||Study Forms|http://biolincc.nhlbi.nih.gov/studies/eden/|
3178672|NCT00056407|ARI40006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178673|NCT04742101||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178674|NCT04742101||Study Protocol|https://clinicaltrials.servier.com/|
3178675|NCT04742101||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178676|NCT04742101||Informed Consent Form|https://clinicaltrials.servier.com/|
3178677|NCT04742101||Clinical Study Report|https://clinicaltrials.servier.com/|
3178678|NCT04742101||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3178679|NCT00608283|SDY289|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
3178680|NCT00608283|SDY289|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
3178681|NCT00608283|SDY289|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
3172185|NCT00377585|104888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study104888 are summarised with study 107509 on the GSK Clinical Study Register.
3172186|NCT00377585|104888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172187|NCT00377585|104888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172188|NCT00377585|104888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172189|NCT00377585|104888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172190|NCT00377585|104888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172191|NCT01062074||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-059&kw=V501-059&tab=access|
3172192|NCT00289185|104298|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172193|NCT00289185|104298|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176606|NCT01165125|105548|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176607|NCT01165125|105548|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178682|NCT00873509||Individual Participant Data Set|https://ndar.nih.gov|
3178683|NCT02626520||Study Protocol|https://docs.google.com/viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxyZWFsd29ybGRvbmNvbG9neXxneDo2OGI0ZDgxMzdkZDIxYWJh|
3178684|NCT05883930||Scales Validity and Reliability|https://tr-scales.arabpsychology.com/wp-content/uploads/pdf/uluslararasi-fiziksel-aktivite-anketi-toad.pdf|Ozturk, M. (2005). The validity and reliability of the international physical activity questionnaire and the determination of physical activity level in university students. Unpublished master thesis. Hacettepe University, Institute of Health Sciences, Ankara.
3178685|NCT00197041|257049/026|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180998|NCT00197223|104438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180999|NCT00197223|104438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181000|NCT00197223|104438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181001|NCT00157898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181002|NCT04498988||Official study group website|https://tu-dresden.de/bereichsuebergreifendes/sfb940/|
3181003|NCT04498988||English description of the Collaborative Research Centre|https://gepris.dfg.de/gepris/projekt/178833530|The study is conducted within the Collaborative Research Centre 940 funded by the Deutsche Forschungsgemeinschaft (DFG).
3181004|NCT02348372|115385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181005|NCT02348372|115385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181006|NCT02348372|115385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181007|NCT02348372|115385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181008|NCT02348372|115385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181009|NCT02348372|115385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181010|NCT02348372|115385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181011|NCT03034850||Study Protocol|https://drive.google.com/open?id=0B0qo2hDQpXhncWZFZkNfZXhZMjVuUGcxc0IzZll5TEtjaXdn|
3181012|NCT03034850|eudract/B-nr B37120154199|Advice Ethical Committee|https://drive.google.com/open?id=0B0qo2hDQpXhnU3AzRHY0d1NtVmlsSmx1cFhKOGtKLTVscno0|
3181013|NCT01015677||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6913-004&kw=6913-004&tab=access|
3181014|NCT01841697||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-026&kw=3102-026&tab=access|
3181015|NCT01138098|113954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181016|NCT01138098|113954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181017|NCT01138098|113954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181018|NCT01138098|113954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181019|NCT01138098|113954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181020|NCT01138098|113954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181021|NCT01648153|116378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181022|NCT01648153|116378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181023|NCT01648153|116378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181024|NCT01648153|116378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181025|NCT01648153|116378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181026|NCT01648153|116378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181027|NCT01648153|116378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174146|NCT00480324|107625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174147|NCT00784134|Data repository-VISTA|Data repository-VISTA|http://vista.gla.ac.uk|when available
3174148|NCT00784134||Study Protocol|http://vista.gla.ac.uk|when available
3174149|NCT00784134||Statistical Analysis Plan|http://vista.gla.ac.uk|when available
3174150|NCT02940678|10.6084/m9.figshare.4042572.v1|Study Protocol|https://dx.doi.org/10.6084/m9.figshare.4042572.v1|
3174151|NCT00792623|208133/178|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174152|NCT00792623|208133/178|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174153|NCT00792623|208133/178|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174154|NCT00792623|208133/178|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174155|NCT00792623|208133/178|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174156|NCT00792623|208133/178|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174157|NCT02502734|107112|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174158|NCT02502734|107112|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174159|NCT02502734|107112|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174160|NCT02502734|107112|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174161|NCT02502734|107112|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174162|NCT02502734|107112|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174163|NCT02502734|107112|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174164|NCT00964106|112684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174165|NCT00964106|112684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174166|NCT00964106|112684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174167|NCT00964106|112684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174168|NCT00964106|112684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174169|NCT00964106|112684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174170|NCT00964106|112684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174171|NCT02369120||Study Protocol|http://www.biomedcentral.com/1472-6947/15/97|
3174172|NCT00749411|DB1111581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174173|NCT00749411|DB1111581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174174|NCT00749411|DB1111581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174175|NCT00749411|DB1111581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174176|NCT00749411|DB1111581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174177|NCT00749411|DB1111581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174178|NCT00749411|DB1111581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174179|NCT03980028||Individual Participant Data Set|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|All the information is provided on this web page in accordance with the RGPD regulations
3174180|NCT00240617|TRX103635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174181|NCT00240617|TRX103635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174182|NCT00240617|TRX103635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174183|NCT00240617|TRX103635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174184|NCT00240617|TRX103635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174185|NCT00240617|TRX103635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172194|NCT00289185|104298|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181028|NCT02075619|200561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181029|NCT02075619|200561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181030|NCT02075619|200561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174186|NCT00240617|TRX103635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174187|NCT00109486|FFR101747|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174188|NCT00109486|FFR101747|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174189|NCT00109486|FFR101747|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174190|NCT00109486|FFR101747|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174191|NCT00109486|FFR101747|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174192|NCT00109486|FFR101747|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174193|NCT00109486|FFR101747|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174194|NCT06290219||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
3174195|NCT07279909||Main reference|https://diabetes.org/|it is the main reference used to identify definitions of the Diabetes \& its complications
3174196|NCT01043926||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-017&kw=4305-017&tab=access|
3174197|NCT02682147|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
3174198|NCT04828434||International Cognitive Stimulation Therapy Centre Website|http://www.ucl.ac.uk/international-cognitive-stimulation-therapy|
3174199|NCT01294566|114422|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174200|NCT01294566|114422|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174201|NCT01294566|114422|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174202|NCT01294566|114422|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174203|NCT01294566|114422|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174204|NCT01294566|114422|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174205|NCT01294566|114422|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174206|NCT01797926|116799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174207|NCT01797926|116799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174208|NCT01797926|116799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181031|NCT02075619|200561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181032|NCT02075619|200561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172195|NCT00289185|104298|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172196|NCT00289185|104298|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172197|NCT00289185|104298|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172198|NCT04183842||Protocol, Validation of Ethic Comitee, Informed consent form, D2 test of attention, Hangover severity scale, Randomization chart|https://hidrive.ionos.com/share/bv7z7738u3|Password will be provided by Administrator. Please ask for it at : bommelaer@shadeline.com
3172199|NCT00430521|107495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172200|NCT00430521|107495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172201|NCT00430521|107495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172202|NCT00430521|107495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172203|NCT00430521|107495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172204|NCT00430521|107495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174209|NCT01797926|116799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181033|NCT02075619|200561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181034|NCT02075619|200561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181035|NCT01006616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05575&kw=7123-019&tab=access|
3181036|NCT00516139|LEP105972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181037|NCT00516139|LEP105972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181038|NCT00516139|LEP105972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181039|NCT00516139|LEP105972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181040|NCT00516139|LEP105972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181041|NCT00516139|LEP105972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181042|NCT00516139|LEP105972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181043|NCT00719043|110624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181044|NCT00719043|110624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181045|NCT00719043|110624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181046|NCT00719043|110624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181047|NCT00719043|110624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181048|NCT00719043|110624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181049|NCT00749359|PCR111656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181050|NCT00749359|PCR111656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181051|NCT00749359|PCR111656|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181052|NCT00749359|PCR111656|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181053|NCT00749359|PCR111656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181054|NCT00749359|PCR111656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181055|NCT00749359|PCR111656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181056|NCT00823836|106066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181057|NCT00823836|106066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181058|NCT00823836|106066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181059|NCT00823836|106066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181060|NCT00823836|106066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181061|NCT01777334|117115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181062|NCT01777334|117115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181063|NCT01777334|117115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181064|NCT01777334|117115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181065|NCT01777334|117115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181066|NCT01777334|117115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181067|NCT01777334|117115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181068|NCT02446613|204509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181069|NCT02446613|204509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172205|NCT00430521|107495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176608|NCT01165125|105548|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176609|NCT01165125|105548|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176610|NCT01165125|105548|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176611|NCT01165125|105548|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176612|NCT01165125|105548|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176613|NCT00456625|108984|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176614|NCT00456625|108984|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176615|NCT00456625|108984|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176616|NCT00456625|108984|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176617|NCT00456625|108984|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176618|NCT00456625|108984|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176619|NCT00456625|108984|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176620|NCT00097929||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176621|NCT00140712|101468/253|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176622|NCT00140712|101468/253|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176623|NCT00140712|101468/253|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176624|NCT00140712|101468/253|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176625|NCT00140712|101468/253|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176626|NCT00140712|101468/253|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176627|NCT00140712|101468/253|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176628|NCT01536561|104728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176629|NCT01536561|104728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176630|NCT01536561|104728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176631|NCT01536561|104728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176632|NCT01536561|104728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176633|NCT01536561|104728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176634|NCT01536561|104728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176635|NCT00329576|106640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176636|NCT00329576|106640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176637|NCT00329576|106640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176638|NCT00329576|106640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172206|NCT05532995||Informed Consent Form|https://drive.google.com/file/d/1qiU0UgEzvPBntfA0lLWFe_AzOGngacl9/view?usp=sharing|
3176639|NCT00329576|106640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176640|NCT00703846|114568|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176641|NCT00703846|114568|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176642|NCT00703846|114568|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172207|NCT00838916|112754|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178686|NCT00197041|257049/026|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178687|NCT00197041|257049/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178688|NCT00197041|257049/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178689|NCT00197041|257049/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178690|NCT00197041|257049/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178691|NCT00197041|257049/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178692|NCT00060476||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178693|NCT03141281|https://osf.io/dp8n5/|Statistical Analysis Plan|https://osf.io/kq8yz/register/565fb3678c5e4a66b5582f67|Open Science Foundation registration of Data Analysis Plan
3178694|NCT01641692|116402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178695|NCT01641692|116402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178696|NCT01641692|116402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178697|NCT01641692|116402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178698|NCT01641692|116402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178699|NCT01641692|116402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178700|NCT01641692|116402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178701|NCT01984775|117191|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178702|NCT01984775|117191|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178703|NCT01984775|117191|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178704|NCT01984775|117191|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178705|NCT01984775|117191|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178706|NCT01984775|117191|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178707|NCT04999150|B0710118|Study Protocol|https://irbrcm.rcm.upr.edu/|
3178708|NCT01107587|113518|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178709|NCT01107587|113518|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178710|NCT01107587|113518|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178711|NCT01107587|113518|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178712|NCT01107587|113518|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178713|NCT01107587|113518|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178714|NCT04644614||Study Protocol|https://doi.org/10.1016/j.urols.2015.06.286|
3178715|NCT01756495|116628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178716|NCT01756495|116628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178717|NCT01756495|116628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178718|NCT01756495|116628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178719|NCT01756495|116628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178720|NCT01756495|116628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181070|NCT02446613|204509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178721|NCT01756495|116628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178722|NCT00000586|MSH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/MSH/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3178723|NCT00000586||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/MSH/|
3178724|NCT00000586||Study Forms|http://biolincc.nhlbi.nih.gov/studies/MSH/|
3178725|NCT03578081||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|
3178726|NCT04608500||Study Protocol|http://foamix.co.il/|
3178727|NCT01010906||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-005&kw=7009-005&tab=access|
3178728|NCT01948739||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25570900|
3178729|NCT04187560||Clinical Study Report|http://lbpharma.us/wp-content/uploads/2020/12/lb-102-001-clinical-study-report-final.pdf|
3178730|NCT00000560|BEST|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/best/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3178731|NCT00000560||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/best/|
3178732|NCT00000560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/best/|
3178733|NCT07188935|rUTI_T2DM_2025|Individual Participant Data Set|https://doi.org/10.1016/0163-4453(92)92876-K|De-identified participant-level data, including demographics, glycemic status, UTI recurrence, antimicrobial therapy, adherence (MARS), and clinical outcomes. Available upon request for research purposes.
3178734|NCT00779012||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178735|NCT03134560||Textbook|https://books.google.co.id/books/about/Pediatric_Anesthesia.html?id=RYe4GBD6LrQC&redir_esc=y|Hannallah RS , Verghese ST. Peripheral vascular access. In: Bissonnette B, Anderson BJ, Bosenberg A, Engelhardt T, Mason LJ, Tobias JD, editors. Pediatric Anesthesia. Connecticut: People's Medical Publishing House USA, 2011.p. 1097-102.
3178736|NCT01782664|116679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178737|NCT01782664|116679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178738|NCT01782664|116679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178739|NCT01782664|116679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178740|NCT01782664|116679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178741|NCT01782664|116679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178742|NCT01782664|116679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178743|NCT01462669|115860|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178744|NCT01462669|115860|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178745|NCT01462669|115860|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178746|NCT01462669|115860|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178747|NCT01462669|115860|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178748|NCT01462669|115860|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178749|NCT01462669|115860|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178750|NCT00048607||CSR Synospis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178751|NCT00454987|109664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178752|NCT00454987|109664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178753|NCT00454987|109664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178754|NCT00454987|109664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178755|NCT00454987|109664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181071|NCT02446613|204509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181072|NCT02446613|204509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181073|NCT02446613|204509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181074|NCT02446613|204509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181075|NCT01691547|116415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181076|NCT01691547|116415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172208|NCT00838916|112754|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172209|NCT00838916|112754|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172210|NCT00838916|112754|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172211|NCT00838916|112754|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172212|NCT00838916|112754|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172213|NCT00838916|112754|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172214|NCT01021852||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6096-011&kw=6096-011&tab=access|
3172215|NCT01153893|113199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172216|NCT01153893|113199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172217|NCT01153893|113199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178756|NCT07171762||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/18166260/|
3181077|NCT01691547|116415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181078|NCT01691547|116415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181079|NCT01691547|116415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181080|NCT01691547|116415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181081|NCT01691547|116415|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181082|NCT02242643|201234|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181083|NCT02242643|201234|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181084|NCT02242643|201234|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181085|NCT02242643|201234|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178757|NCT01147861|114187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178758|NCT01147861|114187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178759|NCT01147861|114187|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178760|NCT01147861|114187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178761|NCT01147861|114187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178762|NCT01147861|114187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178763|NCT01147861|114187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178764|NCT01330485||Individual Participant Data Set|https://osf.io/426pd|
3178765|NCT01330485||All study files|https://osf.io/uhwnb|
3178766|NCT00751348|110876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178767|NCT00751348|110876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178768|NCT00751348|110876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178769|NCT00751348|110876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178770|NCT00751348|110876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181086|NCT02242643|201234|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181087|NCT02242643|201234|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181088|NCT02242643|201234|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181089|NCT07267559||Study Protocol|https://osf.io/8mvn6|
3181090|NCT07267559||Informed Consent Form|https://osf.io/5kuyn|
3181091|NCT00379769|BRL-049653/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181092|NCT00379769|BRL-049653/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181093|NCT00379769|BRL-049653/231|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181094|NCT00379769|BRL-049653/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172218|NCT01153893|113199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178771|NCT00751348|110876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178772|NCT00228917|103812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178773|NCT00228917|103812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103812 are summarised with study 104727 on the GSK Clinical Study Register.
3178774|NCT00228917|103812|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178775|NCT00228917|103812|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178776|NCT00228917|103812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178777|NCT00228917|103812|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178778|NCT01075698||Study Protocol|https://prsinfo.clinicaltrials.gov/definitions.html|
3178779|NCT01391065||Published article|https://doi.org/10.1016/j.ijrobp.2019.10.037|
3178780|NCT00129129|101858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178781|NCT00129129|101858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178782|NCT00129129|101858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178783|NCT00129129|101858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 101858 are summarised with study 102015 on the GSK Clinical Study Register.
3178784|NCT00129129|101858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178785|NCT00451386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178786|NCT00322335|106672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178787|NCT00322335|106672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178788|NCT00322335|106672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 106672 are summarised with studies 106673, 106675, 106679, and 106680 on the GSK Clinical Study Register.
3178789|NCT00322335|106672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178790|NCT00322335|106672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178791|NCT00322335|106672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178792|NCT00380393|106464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178793|NCT00380393|106464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178794|NCT00380393|106464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178795|NCT00380393|106464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178796|NCT00380393|106464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178797|NCT00380393|106464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178798|NCT00907985|112676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178799|NCT00907985|112676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178800|NCT00907985|112676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178801|NCT00907985|112676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178802|NCT00907985|112676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178803|NCT00907985|112676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178804|NCT00907985|112676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178805|NCT06906133||Information site for participants (in Icelandic)|https://www.unak.is/is/rannsoknir/rannsoknir-vid-ha/svefn|
3178806|NCT07181772|gsatir@biruni.edu.tr|virtual escape room link for students|https://docs.google.com/forms/d/1IGzEsuxfcY0aDEJ5_3JbotdJqtI4fq0K5o06ETrlRm4/edit|virtual escape room for triage education
3178807|NCT07180485|t780927t@yahoo.com.tw|Study Protocol|https://orcid.org/0000-0002-8823-6901|t780927t@yahoo.com.tw
3178808|NCT02319031|PMID: 26822022|Primary Publication|http://www.ncbi.nlm.nih.gov/pubmed/26822022|
3176643|NCT00703846|114568|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176644|NCT00703846|114568|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176645|NCT00703846|114568|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176646|NCT00703846|114568|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176647|NCT02947802||Study Instrument (Online Survey)|https://hbs.qualtrics.com/SE/?SID=SV_1LdkKR5P4DyCevH|This is the online survey participants will complete.
3176648|NCT00104416|LAM100036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176649|NCT00104416|LAM100036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176650|NCT00104416|LAM100036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176651|NCT00104416|LAM100036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176652|NCT00104416|LAM100036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178809|NCT00133874|TOC100224|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178810|NCT00133874|TOC100224|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178811|NCT00133874|TOC100224|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178812|NCT00133874|TOC100224|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178813|NCT00133874|TOC100224|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178814|NCT00133874|TOC100224|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178815|NCT00133874|TOC100224|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178816|NCT07110649|VR_Shoulder_Rehab_2024|Individual Participant Data Set|https://translate.google.com/|This dataset includes the shoulder range of motion (ROM) and visual analogue scale (VAS) pain scores for 45 collegiate female basketball players. The data were collected over a 9-week period as part of a randomized controlled trial evaluating the effectiveness of virtual reality-assisted rehabilitation for shoulder injuries. The dataset is anonymized and can be shared upon request for non-commercial academic research purposes only
3178817|NCT07110649|VR_Shoulder_Rehab_2024|Study Protocol|https://translate.google.com/|This study aims to evaluate the effect of virtual reality (VR)-assisted rehabilitation training on shoulder range of motion (ROM) and pain relief in college women's basketball players. Forty-five college women's basketball players with shoulder injuries were randomly divided into three groups: VR-assisted rehabilitation group, traditional rehabilitation group, and control group. The VR group underwent 9 weeks of immersive training, the traditional group received conventional physical therapy, and the control group did not receive any intervention. The primary evaluation index was shoulder ROM (flexion, abduction, internal rotation, and external rotation), and the secondary evaluation index was pain intensity (VAS). All assessments will be performed at baseline and after the intervention, and the data will be analyzed using SPSS statistical software. The study hypothesized that VR rehabilitation methods can improve shoulder range of motion, reduce pain, and increase athlete participatio
3178818|NCT07110649|VR_Shoulder_Rehab_2024|Statistical Analysis Plan|https://translate.google.com/|This study used a randomized controlled method and all randomly assigned participants were included. Data analysis was performed using SPSS or R software. Baseline characteristics will be described using descriptive statistics, with continuous variables expressed as mean ± standard deviation (SD) and categorical variables expressed as frequency/percentage. The primary outcome was shoulder range of motion (ROM), and the difference before and after the intervention was compared using paired t-test (if the data did not conform to normal distribution). The differences between the groups were analyzed using MANOVA, and if the data did not conform to normal distribution, the Kruskal-Wallis test was used. The secondary outcome was pain intensity (VAS), and independent sample t-test or Mann-Whitney U test was used to compare continuous data. Missing data were handled using multiple imputation. The statistical significance level was set at p \< 0.05, and 95% confidence intervals and effect sizes
3178819|NCT07110649|VR_Shoulder_Rehab_2024|Informed Consent Form|https://translate.google.com/|To explore the effect of virtual reality technology on improving the range of motion of the shoulder joints of Chinese college women's basketball players and provide a basis for future sports rehabilitation training. The study has been approved by the Ethics Committee of Sanming Medical Science and Technology Vocational College. Participants will receive 9 weeks of shoulder rehabilitation training, including traditional rehabilitation or virtual reality intervention. During the study, we will collect data on the participants' shoulder range of motion (ROM) and pain scores (VAS), which will only be used for statistical analysis of this study. All personal information and data will be strictly confidential, limited to research purposes, and will not be used for other purposes. Participation in this study is completely voluntary, and participants can withdraw without reason at any stage, and withdrawal will not be affected or punished in any way.
3178820|NCT07110649|SMMAPVC16042024|Data Monitoring Committee Charter|https://translate.google.com/|This dataset includes data from a 9-week study on VR-assisted rehabilitation for shoulder mobility in female basketball players. The study was approved by the Ethics Review Committee of Sanming Medical and Polytechnic Vocational College (SMMAPVC), with written informed consent obtained from all participants. Data is available for academic research purposes only.
3181095|NCT00379769|BRL-049653/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181096|NCT00379769|BRL-049653/231|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181097|NCT00379769|BRL-049653/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181098|NCT05394090||Individual Participant Data Set|http://www.pum.edu.pl|
3181099|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFNnVaQWlTakh5dEU|
3181100|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFazRhT1hZVm41RzA|05.01.2017 updated because of an amendment of ethnic proposal.
3181101|NCT01245140|117221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181102|NCT01245140|117221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181103|NCT01245140|117221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181104|NCT01245140|117221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181105|NCT01245140|117221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181106|NCT01245140|117221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181107|NCT01245140|117221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181108|NCT00443209||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-012&kw=0974-012&tab=access|
3181109|NCT07267637|https://doi.org/10.1111/clr.14|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/39132806/|This data includes radiographic changes from the clinical trial involving alveolar ridge preservation using autogenous tooth particles and xenograft materials.
3181110|NCT07267637|https://doi.org/10.1186/s40729|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/28361377/|"This study explores the use of autologous particulated dentin as a novel approach for alveolar ridge preservation. The intervention involves the patient's own extracted tooth, which is processed into dentin particles and used as a bone graft material. The study demonstrates successful outcomes in terms of bone regeneration and subsequent implant placement, suggesting that autologous dentin may be a promising alternative to traditional grafting materials."
3181111|NCT07267000||Individual Participant Data Set|https://project-redcap.org/|IPD will be collected in the REDCap database. Since enrolment of patients has not started yet, no data has yet been entered. We are undecided on whether to share IPD with other researchers in future.
3181112|NCT01381575|114700|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181113|NCT01381575|114700|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181114|NCT01381575|114700|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181115|NCT01381575|114700|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181116|NCT01381575|114700|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181117|NCT01381575|114700|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181118|NCT02224469|k9f10|Individual Participant Data Set|http://datadryad.org/resource/doi:10.5061/dryad.k9f10|
3181119|NCT00092183||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181120|NCT01407276||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-009&kw=3102-009&tab=access|
3181121|NCT01431950|114496|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181122|NCT01431950|114496|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181123|NCT01431950|114496|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181124|NCT01431950|114496|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181125|NCT01431950|114496|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181126|NCT01431950|114496|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181127|NCT01431950|114496|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181128|NCT00725712|MET111643|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181129|NCT00725712|MET111643|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181130|NCT00725712|MET111643|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181131|NCT00725712|MET111643|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176653|NCT00104416|LAM100036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176654|NCT00104416|LAM100036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176655|NCT01534351||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0906A-149&kw=0906A-149&tab=access|
3176656|NCT00758069||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176657|NCT00434993|ARDSNet-ALTA|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/alta/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176658|NCT00434993||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/alta/|
3176659|NCT00434993||Study Forms|http://biolincc.nhlbi.nih.gov/studies/alta/|
3176660|NCT02218697|117276|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176661|NCT02218697|117276|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176662|NCT02218697|117276|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176663|NCT02218697|117276|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176664|NCT02218697|117276|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176665|NCT02218697|117276|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176666|NCT02218697|117276|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176667|NCT01899638|115380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176668|NCT01899638|115380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176669|NCT01899638|115380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176670|NCT01899638|115380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176671|NCT01899638|115380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176672|NCT01899638|115380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176673|NCT01899638|115380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176674|NCT00972517|113638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176675|NCT00972517|113638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176676|NCT00972517|113638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176677|NCT00972517|113638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176678|NCT00972517|113638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176679|NCT00972517|113638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176680|NCT00972517|113638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176681|NCT00875485|110699|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176682|NCT00875485|110699|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176683|NCT00875485|110699|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176684|NCT00875485|110699|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176685|NCT00875485|110699|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176686|NCT02060344|HCHS-SOL|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hchssol/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176687|NCT02060344||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
3174210|NCT01797926|116799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176688|NCT02060344||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
3181132|NCT00725712|MET111643|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181133|NCT00725712|MET111643|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181134|NCT00725712|MET111643|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181135|NCT01453023|112777|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181136|NCT01453023|112777|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174211|NCT01797926|116799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174212|NCT01797926|116799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174213|NCT00296491|ADA103575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174214|NCT00296491|ADA103575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174215|NCT00296491|ADA103575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174216|NCT00296491|ADA103575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174217|NCT00296491|ADA103575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174218|NCT00296491|ADA103575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174219|NCT00296491|ADA103575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174220|NCT01577693|115148|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174221|NCT01577693|115148|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174222|NCT01577693|115148|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174223|NCT01577693|115148|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174224|NCT01577693|115148|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174225|NCT01577693|115148|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174226|NCT01577693|115148|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174227|NCT07280546||Study Protocol|https://www.vghtpe.gov.tw/Index.action|The study protocol describing the methodology of electronic auscultation of breath sounds during anesthesia will be available. De-identified respiratory sound data and related analysis scripts may be shared upon reasonable request to the principal investigator.
3174228|NCT01267006|114922|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174229|NCT01267006|114922|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174230|NCT01267006|114922|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176689|NCT06660966||Statistical Analysis Plan|https://bmcanesthesiol.biomedcentral.com/articles/10.1186/s12871-022-01866-4|The conformity of numerical data to normal distribution will be tested with the ShaphiroWilk test. Student t test will be used to compare variables that comply with normal distribution in 2 groups, and Mann Whitney U test will be used to compare variables that do not distribute normally in 2 groups. Relationships between categorical variables will be tested with the Chi-square test. Relationships between numerical variables will be tested with the correlation coefficient. SPSS 22.0 package program will be used in the analyses. A P value of less than 0.05 will be considered statistically significant.
3176690|NCT00633074|111454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176691|NCT00633074|111454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176692|NCT00633074|111454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176693|NCT00633074|111454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176694|NCT00633074|111454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176695|NCT00633074|111454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176696|NCT00633074|111454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176697|NCT00365105|NCT00365105|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3176698|NCT00466947|109563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176699|NCT00466947|109563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181137|NCT01453023|112777|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172219|NCT01153893|113199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172220|NCT01153893|113199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172221|NCT00043875|LAM20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172222|NCT00043875|LAM20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176700|NCT00466947|109563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176701|NCT00466947|109563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176702|NCT00466947|109563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176703|NCT00466947|109563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176704|NCT01822899|116134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176705|NCT01822899|116134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176706|NCT01822899|116134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176707|NCT01822899|116134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176708|NCT01822899|116134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176709|NCT01822899|116134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176710|NCT01822899|116134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176711|NCT03030352||Pilot Study of the How-to trial|http://link.springer.com/article/10.1007/s10826-013-9751-0|
3176712|NCT00344318|107007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176713|NCT00344318|107007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176714|NCT00344318|107007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176715|NCT00344318|107007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176716|NCT00344318|107007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176717|NCT00344318|107007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176718|NCT00404378|NKV105093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176719|NCT00404378|NKV105093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176720|NCT00404378|NKV105093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176721|NCT00404378|NKV105093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176722|NCT00404378|NKV105093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176723|NCT00404378|NKV105093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176724|NCT00404378|NKV105093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176725|NCT00500461|AC2106213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176726|NCT00500461|AC2106213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176727|NCT00500461|AC2106213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176728|NCT00500461|AC2106213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176729|NCT00500461|AC2106213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176730|NCT00500461|AC2106213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176731|NCT00500461|AC2106213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172223|NCT00043875|LAM20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174231|NCT01267006|114922|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176732|NCT01762774|114068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176733|NCT01762774|114068|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176734|NCT01762774|114068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176735|NCT01762774|114068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176736|NCT01762774|114068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176737|NCT01762774|114068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176738|NCT01762774|114068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176739|NCT00306293|VLX105832|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176740|NCT00306293|VLX105832|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176741|NCT00306293|VLX105832|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176742|NCT00306293|VLX105832|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176743|NCT00306293|VLX105832|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176744|NCT00306293|VLX105832|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176745|NCT00306293|VLX105832|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176746|NCT02679872||Study Protocol|http://www.regionh.dk/CAMES|Possible to request full protocol, inclusive full reference list, in pdf from first investigator Kirsten Gjeraa, MD, email: kirsten.gjeraa@regionh.dk
3176747|NCT05896098||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/14616599/|
3176748|NCT01431937|114347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181138|NCT01453023|112777|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181139|NCT01453023|112777|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181140|NCT01453023|112777|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172224|NCT00043875|LAM20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172225|NCT00043875|LAM20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172226|NCT00043875|LAM20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172227|NCT00043875|LAM20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172228|NCT00135486|711202/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172229|NCT00135486|711202/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172230|NCT00135486|711202/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172231|NCT00135486|711202/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172232|NCT00135486|711202/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172233|NCT00135486|711202/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172234|NCT01299610|113434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172235|NCT01299610|113434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172236|NCT01299610|113434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172237|NCT01299610|113434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172238|NCT01299610|113434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172239|NCT01299610|113434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172240|NCT01299610|113434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176749|NCT01431937|114347|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176750|NCT01431937|114347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176751|NCT01431937|114347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176752|NCT01431937|114347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176753|NCT01431937|114347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176754|NCT01431937|114347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176755|NCT00473668|104977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176756|NCT00473668|104977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176757|NCT00473668|104977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176758|NCT00473668|104977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176759|NCT00473668|104977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176760|NCT00473668|104977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176761|NCT04569136|DOI：10.6315/2009.37(4)06|Clinical Study Report|http://www.airitilibrary.com/Publication/alDetailedMesh?DocID=10253009-200912-201002050027-201002050027-261-268|
3176762|NCT03257202|HS-17-00319|Study Protocol|http://istar.usc.edu|
3176763|NCT03257202|HS-17-00319|Informed Consent Form|http://istar.usc.edu|
3176764|NCT00758264|111393|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176765|NCT00758264|111393|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176766|NCT00758264|111393|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176767|NCT00758264|111393|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176768|NCT00758264|111393|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176769|NCT00758264|111393|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176770|NCT00758264|111393|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176771|NCT00625196|HZA102940|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176772|NCT00625196|HZA102940|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176773|NCT00625196|HZA102940|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176774|NCT00625196|HZA102940|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176775|NCT00625196|HZA102940|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176776|NCT00625196|HZA102940|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176777|NCT00625196|HZA102940|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176778|NCT05446792||Approval of the Ethics Committee for Research with Human Beings in Brazil|https://plataformabrasil.saude.gov.br/login.jsf|
3176779|NCT00697866|208129/037|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176780|NCT00697866|208129/037|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176781|NCT00697866|208129/037|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176782|NCT00697866|208129/037|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176783|NCT00697866|208129/037|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176784|NCT00697866|208129/037|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174232|NCT01267006|114922|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176785|NCT00519376|B2C110165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176786|NCT00519376|B2C110165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174233|NCT01267006|114922|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174234|NCT01267006|114922|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174235|NCT01466322|114919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174236|NCT01466322|114919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174237|NCT01466322|114919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174238|NCT01466322|114919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174239|NCT01466322|114919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174240|NCT01466322|114919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174241|NCT01466322|114919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174242|NCT05917691||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
3174243|NCT00333723|49653/143|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174244|NCT00333723|49653/143|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174245|NCT00333723|49653/143|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174246|NCT00333723|49653/143|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174247|NCT00333723|49653/143|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174248|NCT00333723|49653/143|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174249|NCT00333723|49653/143|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174250|NCT00289757|100576 (Y11)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174251|NCT00289757|100576 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181141|NCT01453023|112777|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181142|NCT07260201|no identifier available|Individual participant data will not be shared because the study is retrospective and based on anonymized medical records.|https://www.hisarhospital.com|This publication provides background evidence supporting the evaluation of triglyceride-glucose-based indices as markers of insulin resistance.
3181143|NCT00546078|109628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181144|NCT00546078|109628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181145|NCT00546078|109628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181146|NCT00546078|109628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181147|NCT00546078|109628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181148|NCT00546078|109628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181149|NCT00546078|109628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181150|NCT00383123|104858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181151|NCT00383123|104858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181152|NCT00383123|104858|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181153|NCT00383123|104858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181154|NCT00383123|104858|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178821|NCT07110649|VR_Shoulder_Rehab_2024|Clinical Study Report|https://translate.google.com/|The VR group showed an increase in ROM in flexion from 157.24° to 171.64°, abduction from 157.93° to 173.21°, internal rotation from 57.94° to 67.43°, and external rotation from 71.17° to 84.16° (p \< 0.001). The pain score in the VR group also decreased significantly, with the VAS score for flexion decreasing from 6.2 to 3.5, abduction from 6.0 to 3.3, and internal rotation from 5.8 to 3.9 (p \< 0.001). In contrast, the traditional rehabilitation group showed some improvement, but the effect was smaller than that of the VR group, and no significant change was observed in the control group. Statistical analysis showed that VR-assisted rehabilitation was superior to traditional methods in improving the range of motion of the shoulder joint and reducing pain, and showed higher rehabilitation participation and motivation. Therefore, VR technology has great application potential in sports rehabilitation for shoulder injuries.
3178822|NCT00116831|AVD100521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178823|NCT00116831|AVD100521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178824|NCT00116831|AVD100521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178825|NCT00116831|AVD100521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178826|NCT00116831|AVD100521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178827|NCT00116831|AVD100521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178828|NCT00116831|AVD100521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178829|NCT03672435||Individual Participant Data Set|http://www.abcd-vision.org/OCR/OCR%20proparacaine%20de-identified.pdf|deidentified OCR topical anesthetic recovery outcomes
3178830|NCT04164901||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178831|NCT02735083||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178832|NCT02735083||Study Protocol|https://clinicaltrials.servier.com/|
3178833|NCT02735083||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178834|NCT02735083||Informed Consent Form|https://clinicaltrials.servier.com/|
3178835|NCT02735083||Clinical Study Report|https://clinicaltrials.servier.com/|
3178836|NCT02735083||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3178837|NCT00896558|112668|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178838|NCT00896558|112668|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178839|NCT00896558|112668|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178840|NCT00896558|112668|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178841|NCT00896558|112668|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178842|NCT00896558|112668|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178843|NCT00896558|112668|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178844|NCT00578175|110058|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178845|NCT00578175|110058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178846|NCT00578175|110058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178847|NCT00578175|110058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178848|NCT00578175|110058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178849|NCT00578175|110058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178850|NCT00578175|110058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178851|NCT01165138|106827|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178852|NCT01165138|106827|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178853|NCT01165138|106827|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178854|NCT01165138|106827|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178855|NCT01165138|106827|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178856|NCT01165138|106827|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178857|NCT01165138|106827|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178858|NCT00603746|FFA109684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178859|NCT00603746|FFA109684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178860|NCT00603746|FFA109684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178861|NCT00603746|FFA109684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178862|NCT00603746|FFA109684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178863|NCT00603746|FFA109684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178864|NCT00603746|FFA109684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178865|NCT04962815||Individual Participant Data Set|https://eeg.ceribell.com|This website is password protected and the de-identified individual participant data is only available to participating research sites.
3178866|NCT00394030|GLP107724|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178867|NCT00394030|GLP107724|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178868|NCT00394030|GLP107724|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178869|NCT00394030|GLP107724|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178870|NCT00394030|GLP107724|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178871|NCT00394030|GLP107724|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178872|NCT00394030|GLP107724|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178873|NCT03068299|63133316.4.0000.5504|Ethics Acceptance letter|http://plataformabrasil.saude.gov.br/login.jsf|Enter with number CAAE box (63133316.4.0000.5504) and access the official document of ethics acceptance letter of study.
3178874|NCT00196950|134612/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178875|NCT00196950|134612/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178876|NCT00196950|134612/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 134612/003 are summarised with studies 102252, 102253, and 102254 on the GSK Clinical Study Register.
3178877|NCT00196950|134612/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178878|NCT00196950|134612/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178879|NCT00196950|134612/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178880|NCT01934153|117157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178881|NCT01934153|117157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178882|NCT01934153|117157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178883|NCT01934153|117157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178884|NCT01934153|117157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178885|NCT01934153|117157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178886|NCT01934153|117157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178887|NCT07044180||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521373-13-00|
3178888|NCT00000514|SHEP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/shep/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3178889|NCT00000514||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/shep/|
3178890|NCT00000514||Study Forms|http://biolincc.nhlbi.nih.gov/studies/shep/|
3178891|NCT00000514||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/shep/|
3178892|NCT00519649|110474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178893|NCT00519649|110474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178894|NCT00519649|110474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176787|NCT00519376|B2C110165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176788|NCT00519376|B2C110165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176789|NCT00519376|B2C110165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176790|NCT00519376|B2C110165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176791|NCT00519376|B2C110165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176792|NCT01792817||Publication|http://onlinelibrary.wiley.com/doi/10.1111/head.12896/full|Non-Invasive Vagus Nerve Stimulation for the ACute Treatment of Cluster Headache: Findings From the Randomized, Double-Blind, Sham-Controlled ACT1 Study Stephen D. Silberstein, MD; Laszlo L. Mechtler, MD; David B. Kudrow, MD; Anne H. Calhoun, MD; Candace McClure, PhD; Joel R. Saper, MD; Eric J. Liebler; Emily Rubenstein Engel, MD; Stewart J. Tepper, MD; on Behalf of the ACT1 Study Group
3176793|NCT01245738||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-204&kw=0000-204&tab=access|
3176794|NCT00000593|VATS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/vats/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176795|NCT00000593||Study Forms|http://biolincc.nhlbi.nih.gov/studies/vats/|
3176796|NCT03192020||Study Protocol|http://bmjopen.bmj.com/content/8/3/e019054|Protocol in BMJ Open access
3176797|NCT02998203||Manuscript and supplementary files|https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0219420|
3174252|NCT00289757|100576 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174253|NCT00289757|100576 (Y11)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100576 are summarised with studies 100577, 100578, 100579, 100580, 111028, 111029, 111030, 111031, and 111032 on the GSK Clinical Study
3174254|NCT00289757|100576 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174255|NCT00289757|100576 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174256|NCT02339740||Individual Participant Data Set|http://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3174257|NCT02662231||Study Protocol|http://globalsurg.org/globalsurg-2-protocol/|GlobalSurg-II Study Protocol: available in multiple languages
3174258|NCT02119286|200110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174259|NCT02119286|200110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174260|NCT02119286|200110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174261|NCT02119286|200110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174262|NCT02119286|200110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174263|NCT02119286|200110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174264|NCT02119286|200110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174265|NCT03272282|prospective auther of journals|Study Protocol|http://www.iiste.org/journals/|All the journals articles are amiable online to the reader all over the world without financially legal barriers
3172241|NCT00989404|113625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172242|NCT00989404|113625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172243|NCT00989404|113625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172244|NCT00989404|113625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172245|NCT00989404|113625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172246|NCT00989404|113625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172247|NCT00989404|113625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172248|NCT00880763||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-016&kw=7009-016&tab=access|
3176798|NCT00908115|208355/128|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176799|NCT00908115|208355/128|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176800|NCT00908115|208355/128|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176801|NCT00908115|208355/128|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181155|NCT00383123|104858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181156|NCT00383123|104858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181157|NCT05688618||Study Protocol|https://drive.google.com/drive/u/0/folders/1JG22lkEchQULxW79ktlsVcM5uGNB4iVh|
3181158|NCT04240249||Individual Participant Data Set|https://github.com/hmep/r2fu/|
3181159|NCT04240249||Analytic Code|https://github.com/hmep/r2fu/|
3181160|NCT00334334|107005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181161|NCT00334334|107005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181162|NCT00334334|107005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181163|NCT00334334|107005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181164|NCT00334334|107005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181165|NCT00334334|107005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181166|NCT02656667|22116795|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Vivodtzev I, Debigaré R, Gagnon P, and al. Vivodtzev I, Debigaré R, Gagnon P, Mainguy V, Saey D, Dubé A, Paré MÈ, Bélanger M, Maltais F. Functional and muscular effects of neuromuscular electrical stimulation in patients with severe COPD: a randomized clinical trial. Chest. 2012 Mar;141(3):716-25.
3181167|NCT02656667|24418570|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Vieira PJ, Chiappa AM, Cipriano G Jr, Umpierre D, Arena R, Chiappa GR. Neuromuscular electrical stimulation improves clinical and physiological function in COPD patients.Respir Med. 2014 Apr;108(4):609-20.
3181168|NCT02656667|23440837|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Maddocks M, Gao W, Higginson IJ, Wilcock A.Neuromuscular electrical stimulation for muscle weakness in adults with advanced disease. Cochrane Database Syst Rev. 2013 Jan 31;1.
3181169|NCT02656667|16806873|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Ozalevli S, Ozden A, Itil O, Akkoclu A. Comparison of the Sit-to-Stand Test with 6 min walk test in patients with chronic obstructive pulmonary disease. Respir Med 2007;101(2):286-93.
3181170|NCT06611696||Study Protocol|https://www.m.chiba-u.jp/dept/allergy-clin-immunol/researcher/clinical/|Regarding deidentified patient data, please request to Dr Shunsuke Furuta at shfuruta@chiba-u.jp or Dr Masayoshi Harigai at mharigai@iuhw.ac.jp after publishing pre-defined trial results.
3181171|NCT07049211||Individual Participant Data Set|https://zenodo.org/records/15672312|Method of obtaining the raw data: If there are reasonable requests, the related raw data to support the research results can be obtained from the corresponding authors or the first authors. Data sharing website: https://zenodo.org/records/15080604 Time of making the raw data public: the research raw data will be publicly shared six months after the publication of the research paper.
3176802|NCT00908115|208355/128|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176803|NCT00908115|208355/128|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176804|NCT01155466||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04938&kw=P04938&tab=access|
3176805|NCT00500058|ILI105618|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176806|NCT00500058|ILI105618|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176807|NCT00500058|ILI105618|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176808|NCT00500058|ILI105618|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176809|NCT00500058|ILI105618|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176810|NCT00500058|ILI105618|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176811|NCT00500058|ILI105618|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176812|NCT00316693|104798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176813|NCT00316693|104798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176814|NCT00316693|104798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176815|NCT00316693|104798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176816|NCT00316693|104798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176817|NCT00316693|104798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176818|NCT01165320||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0991-074&kw=0991-074&tab=access|
3181172|NCT07049211||Study Protocol|https://zenodo.org/records/15672312|Method of obtaining the raw data: If there are reasonable requests, the related raw data to support the research results can be obtained from the corresponding authors or the first authors. Data sharing website: https://zenodo.org/records/15080604 Time of making the raw data public: the research raw data will be publicly shared six months after the publication of the research paper.
3181173|NCT07049211||Analytic Code|https://zenodo.org/records/15672312|Method of obtaining the raw data: If there are reasonable requests, the related raw data to support the research results can be obtained from the corresponding authors or the first authors. Data sharing website: https://zenodo.org/records/15080604 Time of making the raw data public: the research raw data will be publicly shared six months after the publication of the research paper.
3181174|NCT00390260||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181175|NCT00968526|113459|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181176|NCT00968526|113459|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181177|NCT00968526|113459|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181178|NCT00968526|113459|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181179|NCT00968526|113459|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181180|NCT00968526|113459|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181181|NCT00968526|113459|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181182|NCT06509360||Individual Participant Data Set|https://www.castoredc.com/|Individual participant data is collected anonymously in Castor EDC.
3181183|NCT00479882||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-063&kw=0524B-063&tab=access|
3181184|NCT01160237|114454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181185|NCT01160237|114454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176819|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27179664|
3181186|NCT01160237|114454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181187|NCT01160237|114454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181188|NCT01160237|114454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181189|NCT01160237|114454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181190|NCT01160237|114454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181191|NCT00263653|103954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181192|NCT00263653|103954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181193|NCT00263653|103954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181194|NCT00263653|103954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181195|NCT00263653|103954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181196|NCT00263653|103954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181197|NCT03260478||Study Protocol|https://bmjopen.bmj.com/content/12/10/e067117.info|
3181198|NCT05555745||Statistical Analysis Plan|https://osf.io/zw5cq|
3181199|NCT00344032|104479|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181200|NCT00344032|104479|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181201|NCT00344032|104479|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181202|NCT00344032|104479|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181203|NCT00344032|104479|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181204|NCT00344032|104479|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181205|NCT00090155||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181206|NCT00678301|110521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181207|NCT00678301|110521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181208|NCT00678301|110521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176820|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27629371|
3176821|NCT00964340|113312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176822|NCT00964340|113312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176823|NCT00964340|113312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176824|NCT00964340|113312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176825|NCT00964340|113312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176826|NCT00964340|113312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176827|NCT01691885|116601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176828|NCT01691885|116601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176829|NCT01691885|116601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176830|NCT01691885|116601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176831|NCT01691885|116601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176832|NCT01691885|116601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176833|NCT01691885|116601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176834|NCT06660953||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37971133/|
3176835|NCT00896363|109035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176836|NCT00896363|109035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176837|NCT00896363|109035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176838|NCT00896363|109035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176839|NCT00896363|109035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181209|NCT00678301|110521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181210|NCT00678301|110521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181211|NCT00678301|110521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181212|NCT00678301|110521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181213|NCT03266926||Study Protocol|https://www.scribd.com/document/344597619/Study-Protocol|
3176840|NCT00896363|109035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176841|NCT00896363|109035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176842|NCT00559468||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176843|NCT01953549||Statistical Analysis Plan|https://doi.org/10.6084/m9.figshare.5375026.v1|Statistical Analysis Plan of PHYS-Stroke Trial. If download path is offline please contact torsten.rackoll@charite.de
3178895|NCT00519649|110474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178896|NCT00519649|110474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178897|NCT00519649|110474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178898|NCT00519649|110474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178899|NCT01494610|114334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178900|NCT01494610|114334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178901|NCT01494610|114334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178902|NCT01494610|114334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181214|NCT03266926||Informed Consent Form|https://www.scribd.com/document/344597523/Consent-Form|
3172249|NCT01656317|DOI: 10.2340/16501977-2121|Article|https://www.ncbi.nlm.nih.gov/pubmed/27494170|"Impact of early mobilization and rehabilitation on global functional outcome one year after aneurysmal subarachnoid hemorrhage.~Karic T1,2, Røe C1,3, Nordenmark TH1, Becker F4,3, Sorteberg W2, Sorteberg A2,3."
3176844|NCT00871117|111852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176845|NCT00871117|111852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176846|NCT00871117|111852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176847|NCT00871117|111852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176848|NCT00871117|111852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176849|NCT00871117|111852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176850|NCT00871117|111852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176851|NCT03104972||similar protocol|http://www.ncbi.nlm.nih.gov/pubmed/27339019|Looi CY, Cohen Kadosh R. Brain stimulation, mathematical, and numerical training: Contribution of core and noncore skills. Prog Brain Res. 2016;227:353-88. doi: 10.1016/bs.pbr.2016.04.009.
3176852|NCT06896500|Ethics Committee Application|Clinical Study Report|https://drive.google.com/file/d/19dj7wMiq4mPOobklxuHQObULyObAOvgc/view?usp=sharing|
3176853|NCT06896500|informed consent form|Informed Consent Form|https://docs.google.com/document/d/1PuTtTRr_LxSuZvbzWyvw3EQZYQ0VyA7b/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
3176854|NCT06896500|Vaginal flatus status form|Forms|https://docs.google.com/document/d/1kFejPnvwa_N52yM8A2UKoAgZ3s1uPYuw/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
3176855|NCT06896500|study main data|Study Protocol|https://drive.google.com/file/d/1yPsrrEh2E2eVLPD-_QtWy8F0rgT0dM9g/view?usp=sharing|
3176856|NCT01224821|104731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176857|NCT01224821|104731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176858|NCT01224821|104731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176859|NCT01224821|104731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176860|NCT01224821|104731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176861|NCT01224821|104731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176862|NCT01224821|104731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176863|NCT03207321||Individual Participant Data Set|http://apcaps.lshtm.ac.uk/|
3176864|NCT06891469|https://doi.org/10.6084/m9.fig|Individual Participant Data Set|https://figshare.com|figshare
3176865|NCT02014480|116132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176866|NCT02014480|116132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176867|NCT02014480|116132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176868|NCT02014480|116132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176869|NCT02014480|116132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176870|NCT02014480|116132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176871|NCT02014480|116132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176872|NCT00549900|107336|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176873|NCT00549900|107336|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176874|NCT00549900|107336|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176875|NCT00549900|107336|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176876|NCT00549900|107336|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176877|NCT00549900|107336|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176878|NCT00937404|112581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174266|NCT00000607||NHLBI website|http://www.nhlbi.nih.gov/news/press-releases/2001/nhlbi-funded-study-finds-heart-assist-device-extends-and-improves-lives-of-patients-with-end-stage-heart-failure|
3176879|NCT00937404|112581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174267|NCT05905263||Clinical Study Report|https://clinicaltrials.gov/ProvidedDocs/58/NCT04444258/Prot_SAP_ICF_000.pdf|DEVELOPMENT AND USAGE OF VIRTUAL REALITY APPLICATION IN TEACHING FETAL DEVELOPMENT
3174268|NCT00158756|104021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174269|NCT00158756|104021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174270|NCT00158756|104021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174271|NCT00158756|104021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174272|NCT00158756|104021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174273|NCT00158756|104021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174274|NCT01195792|111850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174275|NCT01195792|111850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174276|NCT01195792|111850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174277|NCT01195792|111850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174278|NCT01195792|111850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174279|NCT01195792|111850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174280|NCT01195792|111850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174281|NCT00306943|104745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174282|NCT00306943|104745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174283|NCT00306943|104745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174284|NCT00306943|104745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174285|NCT00306943|104745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174286|NCT00316147|104005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174287|NCT00316147|104005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174288|NCT00316147|104005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174289|NCT00316147|104005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174290|NCT00316147|104005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174291|NCT00316147|104005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174292|NCT01849016|Version 7.0 - 5/31/2016|Statistical Analysis Plan|http://www2.hematologie-amc.nl/nac_studie|
3174293|NCT02006537|117023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174294|NCT02006537|117023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174295|NCT02006537|117023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174296|NCT02006537|117023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174297|NCT02006537|117023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174298|NCT02006537|117023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174299|NCT02006537|117023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174300|NCT03182582||Study Protocol|https://eprotocol.stanford.edu/|
3174301|NCT03237949|NCT02571244|Study Protocol|https://clinicaltrials.gov|This protocol is an extension of a previous research:Telephone Counseling and Text Messaging for Supporting Post-discharge Quit Attempts Among Hospitalized Smokers in Brazil, a feasibility study.
3174302|NCT00169481|103488|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174303|NCT00169481|103488|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176880|NCT00937404|112581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181215|NCT03266926||Individual Participant Data Set|https://www.scribd.com/document/344597573/Data-Collection-Spreadsheet|
3174304|NCT00169481|103488|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174305|NCT00169481|103488|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174306|NCT00169481|103488|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174307|NCT00307034|105539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174308|NCT00307034|105539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174309|NCT00307034|105539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174310|NCT00307034|105539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174311|NCT00307034|105539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174312|NCT00307034|105539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174313|NCT00929331|110586|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174314|NCT00929331|110586|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174315|NCT00929331|110586|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174316|NCT00929331|110586|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174317|NCT00929331|110586|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174318|NCT00929331|110586|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174319|NCT00929331|110586|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174320|NCT00048204|NKD20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174321|NCT00048204|NKD20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174322|NCT00048204|NKD20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174323|NCT00048204|NKD20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174324|NCT00048204|NKD20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174325|NCT00048204|NKD20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174326|NCT00048204|NKD20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174327|NCT00144911|SCO40043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174328|NCT00144911|SCO40043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174329|NCT00144911|SCO40043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174330|NCT00144911|SCO40043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174331|NCT00144911|SCO40043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174332|NCT00144911|SCO40043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174333|NCT00144911|SCO40043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174334|NCT00069836|712753/009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174335|NCT00069836|712753/009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174336|NCT00069836|712753/009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174337|NCT00069836|712753/009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174338|NCT00069836|712753/009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174339|NCT00069836|712753/009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174340|NCT00069836|712753/009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175823|NCT01524835|SDY294|Study summary, -design, -demographics, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
3174341|NCT06357663|Pro00071128|Study Protocol|https://www.advarra.com/review-services/institutional-review-board/canadian-review-services/|"Upon request, ADVARRA (IRB) can provide your with Study Protocol + Statistical Plan, Informed Consent Form, and any other reviewed and approved documents of the study.~Should you require any more information, please contact me on email sharesearchfoundation@yahoo.ca and I will provide you with any documents relevant to the study.~Peter Hudoba De Badyn FRCS"
3181216|NCT03266926||Participant Documents|https://www.scribd.com/document/344597424/Participant-Documents|
3181217|NCT02718261|NCT02467621|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT02467621?term=SUP-ICU&rank=1|SUP-ICU Website
3174342|NCT00197288|104437|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174343|NCT00197288|104437|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174344|NCT00197288|104437|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174345|NCT00197288|104437|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174346|NCT00197288|104437|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174347|NCT00197288|104437|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174348|NCT00197288|104437|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174349|NCT03324321||Funder|http://dunhillmedical.org.uk/|Dunhill RTF Grant (RTF97/0117)
3174350|NCT00763438|2007-002160-10|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-002160-10/results|
3174351|NCT00117325|FFR30006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174352|NCT00117325|FFR30006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174353|NCT00117325|FFR30006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174354|NCT00117325|FFR30006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174355|NCT00117325|FFR30006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174356|NCT00117325|FFR30006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174357|NCT00117325|FFR30006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174358|NCT00548171|110804|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174359|NCT00548171|110804|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174360|NCT00548171|110804|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174361|NCT00548171|110804|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174362|NCT00548171|110804|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174363|NCT00548171|110804|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174364|NCT00548171|110804|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174365|NCT00541970|110659|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176881|NCT00937404|112581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176882|NCT00937404|112581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174366|NCT00541970|110659|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174367|NCT00541970|110659|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174368|NCT00541970|110659|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174369|NCT00541970|110659|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174370|NCT00541970|110659|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174371|NCT00541970|110659|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176883|NCT00937404|112581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176884|NCT03760016|424597|Individual Participant Data Set|https://dash.nichd.nih.gov/study/424597|
3181218|NCT00770744|2008-000479-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-000479-11/results|
3181219|NCT00632502||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05365&kw=7123-017&tab=access|
3181220|NCT00388440|209762/147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181221|NCT00388440|209762/147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181222|NCT00388440|209762/147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181223|NCT00388440|209762/147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181224|NCT00388440|209762/147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181225|NCT03567629||Individual Participant Data Set|https://en.wikipedia.org/wiki/United_States_National_Library_of_Medicine|
3181226|NCT01132443|115902|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181227|NCT01132443|115902|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181228|NCT01132443|115902|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181229|NCT01132443|115902|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181230|NCT01132443|115902|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181231|NCT01132443|115902|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181232|NCT01132443|115902|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181233|NCT01939353||Poster Abstracts|https://apsard.org/wp-content/uploads/2016/11/Poster-Abstracts-Compiled1.pdf|Poster number 25
3181234|NCT04954326||Individual Participant Data Set|https://clinicaltrials.servier.com|
3181235|NCT04954326||Study Protocol|https://clinicaltrials.servier.com|
3181236|NCT04954326||Statistical Analysis Plan|https://clinicaltrials.servier.com|
3181237|NCT04954326||Informed Consent Form|https://clinicaltrials.servier.com|
3181238|NCT04954326||Clinical Study Report|https://clinicaltrials.servier.com|
3181239|NCT04954326||Study-level clinical trial data|https://clinicaltrials.servier.com|
3172250|NCT01656317|DOI: 10.3171/2015.12.JNS151744|Article|https://www.ncbi.nlm.nih.gov/pubmed/27058204|"J Neurosurg. 2017 Feb;126(2):518-526. doi: 10.3171/2015.12.JNS151744. Epub 2016 Apr 8.~Effect of early mobilization and rehabilitation on complications in aneurysmal subarachnoid hemorrhage.~Karic T1,2, Røe C1,3, Nordenmark TH1, Becker F4,3, Sorteberg W2, Sorteberg A2,3."
3174372|NCT00273039|NKF100110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181240|NCT05059184||Individual Participant Data Set|https://figshare.com/articles/dataset/Analysis_of_COVID-19_Patients_Symptoms_and_Vaccine_Impact_Using_Deep_Learning_Approach_and_Development_Machine_Learning_Based_Risk_Calculator_A_Multicentric_Collaborative_Study/25585452|Open Code and Dataset
3181241|NCT01734239||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V110-018&kw=V110-018&tab=access|
3181242|NCT04728139||Study Protocol|http://rehamhany809@gmail.com|
3181243|NCT04110704|IRAS 261294|Study Protocol|http://preview-kcl.cloud.contensis.com/Preview/1/research/project?id=478a6e61-4446-4a12-945e-c41a3879371d|
3181244|NCT00972322||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8245-012&kw=8245-012&tab=access|
3181245|NCT01333813|112688|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181246|NCT01333813|112688|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181247|NCT01333813|112688|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181248|NCT01333813|112688|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181249|NCT01333813|112688|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181250|NCT01333813|112688|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181251|NCT01376232|113634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181252|NCT01376232|113634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181253|NCT01376232|113634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181254|NCT01376232|113634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181255|NCT01376232|113634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181256|NCT01376232|113634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181257|NCT01376232|113634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181258|NCT01725126|116623|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181259|NCT01725126|116623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181260|NCT01725126|116623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181261|NCT01725126|116623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181262|NCT01725126|116623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181263|NCT01725126|116623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181264|NCT01725126|116623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181265|NCT02145468|116197|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181266|NCT02145468|116197|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181267|NCT02145468|116197|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181268|NCT02145468|116197|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181269|NCT02145468|116197|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181270|NCT02145468|116197|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181271|NCT02145468|116197|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176885|NCT00624819|111345 (Mth 12)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176886|NCT00624819|111345 (Mth 12)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176887|NCT00624819|111345 (Mth 12)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181272|NCT00635128|110947|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181273|NCT00635128|110947|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181274|NCT00635128|110947|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181275|NCT00635128|110947|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181276|NCT00635128|110947|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181277|NCT00635128|110947|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181278|NCT00635128|110947|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181279|NCT07124052|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
3181280|NCT00586612|110215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study are summarised with 110217 on the GSK Clinical Study Register.
3181281|NCT00586612|110215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181282|NCT00586612|110215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181283|NCT00586612|110215|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176888|NCT00624819|111345 (Mth 12)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176889|NCT00624819|111345 (Mth 12)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176890|NCT00624819|111345 (Mth 12)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176891|NCT05455008||Individual Participant Data Set|https://iro.uiowa.edu/esploro/outputs/dataset/9984236057502771|
3176892|NCT03630744||web page|http://fluidday.com|
3176893|NCT03029078||Study Protocol|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003048-11/FR|
3176894|NCT00343915|101695 Ext. Mth30|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176895|NCT00343915|101695 Ext. Mth30|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176896|NCT00343915|101695 Ext. Mth30|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176897|NCT00343915|101695 Ext. Mth30|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 101695 (Ext HBV-280 M30) are summarised with studies 103860/280 (HBV-280), 101696 (Ext HBV-280 M42), 101697 (Ext HBV-280 M54) and 101698
3176898|NCT00343915|101695 Ext. Mth30|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176899|NCT00035360||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176900|NCT01357135||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-201&kw=0431-201&tab=access|
3176901|NCT00379977|106345|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176902|NCT00379977|106345|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176903|NCT00379977|106345|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176904|NCT00379977|106345|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176905|NCT00379977|106345|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176906|NCT00379977|106345|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176907|NCT01360398|114378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176908|NCT01360398|114378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176909|NCT01360398|114378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176910|NCT01360398|114378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176911|NCT01360398|114378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176912|NCT01360398|114378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176913|NCT01360398|114378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176914|NCT04859244||Individual Participant Data Set|https://osf.io/am5s8/|Supplementary Table 1: Blood chemistry (CBC, CMP) results. Supplementary Table 2: Plasma concentrations of GS-441524 at indicated timepoints.
3172251|NCT01656317|10.3109/09638288.2014.966162|Article|https://www.ncbi.nlm.nih.gov/pubmed/25264735|"Disabil Rehabil. 2015;37(16):1446-54. doi: 10.3109/09638288.2014.966162. Epub 2014 Sep 29.~Early rehabilitation in patients with acute aneurysmal subarachnoid hemorrhage.~Karic T1, Sorteberg A, Haug Nordenmark T, Becker F, Roe C."
3172252|NCT00671216|DB1111509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172253|NCT00671216|DB1111509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172254|NCT00671216|DB1111509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172255|NCT00671216|DB1111509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172256|NCT00671216|DB1111509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172257|NCT00671216|DB1111509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172258|NCT00671216|DB1111509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172259|NCT01615796|115198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172260|NCT01615796|115198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172261|NCT01615796|115198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178903|NCT01494610|114334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178904|NCT01494610|114334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178905|NCT01494610|114334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178906|NCT03672695||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178907|NCT03672695||Study Protocol|https://clinicaltrials.servier.com/|
3178908|NCT03672695||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178909|NCT03672695||Informed Consent Form|https://clinicaltrials.servier.com/|
3178910|NCT03672695||Clinical Study Report|https://clinicaltrials.servier.com/|
3178911|NCT00812929|112025|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178912|NCT00812929|112025|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178913|NCT00812929|112025|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178914|NCT00812929|112025|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178915|NCT00812929|112025|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178916|NCT00812929|112025|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178917|NCT00812929|112025|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178918|NCT02016963|HGS1021-C1069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178919|NCT02016963|HGS1021-C1069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178920|NCT02016963|HGS1021-C1069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178921|NCT02016963|HGS1021-C1069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178922|NCT02016963|HGS1021-C1069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178923|NCT02016963|HGS1021-C1069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178924|NCT02016963|HGS1021-C1069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178925|NCT06876779||Study Protocol|https://www.ugc.edu.hk/eng/rgc/funding_opport/fds/funded%20research/fds2425.html|
3178926|NCT07110077|vanesssatob@gmail.com|Study Protocol|https://drive.google.com/drive/folders/1oaz8ewLKW--cX5Nm7Y0I_j0jPhJzwzVS?usp=sharing|
3178927|NCT04126785|CAAE 96882818.3.0000.5398|Brazil Research Ethics Committees|http://plataformabrasil.saude.gov.br/|
3178928|NCT05706688||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|American College of Surgeons National Surgical Quality Improvement Program and the hospitals participating in the ACS NSQIP are the source of the data used herein. The Participant Use Data File (PUF) is a Health Insurance Portability and Accountability Act (HIPAA)-compliant data file containing cases submitted to the American College of Surgeons National Surgical Quality Improvement Program®. To request a copy of the PUF, individuals (data recipients) must agree to comply with the terms and conditions set forth in the Data Use Agreement, provide contact information, and complete a short online questionnaire. Once the information provided by the data recipient is received and processed by ACS NSQIP staff, a website address will be submitted electronically to the data recipient. The data recipient will then have 10 days (240 hours) to visit the website and download the data file.
3178929|NCT00637195|111567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178930|NCT00637195|111567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178931|NCT00637195|111567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178932|NCT00637195|111567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178933|NCT00637195|111567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178934|NCT00637195|111567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178935|NCT00637195|111567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181284|NCT00586612|110215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181285|NCT00586612|110215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181286|NCT00586612|110215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181287|NCT02963025||Study Protocol|http://prothor.info|
3181288|NCT04340791||Study Protocol|https://osf.io/kq9c8/|
3181289|NCT04340791||Statistical Analysis Plan|https://osf.io/kq9c8/|
3176915|NCT00642148|MKI102428|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176916|NCT00642148|MKI102428|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176917|NCT00642148|MKI102428|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176918|NCT00642148|MKI102428|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176919|NCT00642148|MKI102428|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176920|NCT00642148|MKI102428|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176921|NCT00642148|MKI102428|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176922|NCT00000558|PEACE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/peace/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3176923|NCT00000558||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/peace/|
3176924|NCT00000558||Study Forms|http://biolincc.nhlbi.nih.gov/studies/peace/|
3176925|NCT00355342|SCO40041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176926|NCT00355342|SCO40041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176927|NCT00355342|SCO40041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176928|NCT00355342|SCO40041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172262|NCT01615796|115198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172263|NCT01615796|115198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176929|NCT00355342|SCO40041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176930|NCT00355342|SCO40041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181290|NCT04340791||Informed Consent Form|https://osf.io/kq9c8/|
3172264|NCT01615796|115198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172265|NCT01615796|115198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172266|NCT01245764||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-046&kw=V501-046&tab=access|
3172267|NCT00989612|113519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172268|NCT00989612|113519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172269|NCT00989612|113519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181291|NCT04340791||Individual Participant Data Set|https://osf.io/kq9c8/|When results will be published
3181292|NCT00989625|108504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181293|NCT00989625|108504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181294|NCT00989625|108504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181295|NCT00989625|108504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181296|NCT00989625|108504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181297|NCT00989625|108504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181298|NCT00989625|108504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181299|NCT00109330|776423/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181300|NCT00109330|776423/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181301|NCT00109330|776423/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181302|NCT00109330|776423/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181303|NCT00109330|776423/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181304|NCT00109330|776423/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181305|NCT00091559||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172270|NCT00989612|113519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172271|NCT00989612|113519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172272|NCT00989612|113519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172273|NCT00989612|113519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172274|NCT01293006||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-032&kw=4305-032&tab=access|
3172275|NCT01842607|115661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172276|NCT01842607|115661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172277|NCT01842607|115661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172278|NCT01842607|115661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172279|NCT01842607|115661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172280|NCT01842607|115661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172281|NCT01842607|115661|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172282|NCT02771652||Detailed intervention description|https://www.sport.fau.de/files/2016/05/ms-intakt-e-training-intervention-description.pdf|Detailed description of the processes of the e-training intervention (english language)
3172283|NCT02771652||Clinical Study Report|https://www.sport.fau.de/files/2015/05/ms-intakt-abschlussbericht-19_05_2015.pdf|Final report for funding foundation (german)
3172284|NCT01551758|115151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172285|NCT01551758|115151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172286|NCT01551758|115151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172287|NCT01551758|115151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172288|NCT01551758|115151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172289|NCT01551758|115151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172290|NCT01551758|115151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172291|NCT01231607|114263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172292|NCT01231607|114263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172293|NCT01231607|114263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172294|NCT01231607|114263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172295|NCT01231607|114263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172296|NCT01231607|114263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172297|NCT01231607|114263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172298|NCT00971425|113572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172299|NCT00971425|113572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172300|NCT00971425|113572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172301|NCT00971425|113572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172302|NCT00971425|113572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172303|NCT00971425|113572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172304|NCT00971425|113572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172305|NCT00731393|100351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172306|NCT00731393|100351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172307|NCT00731393|100351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181306|NCT05931913||Individual Participant Data Set|https://nda.nih.gov/|
3176931|NCT00355342|SCO40041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176932|NCT00363727|101468/228|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176933|NCT00363727|101468/228|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176934|NCT00363727|101468/228|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178936|NCT01573624|115938|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178937|NCT01573624|115938|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178938|NCT01573624|115938|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178939|NCT01573624|115938|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178940|NCT01573624|115938|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178941|NCT01573624|115938|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178942|NCT01573624|115938|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178943|NCT03900299||Study Protocol|http://www.med.alexu.edu.eg/ethics-committee/|
3178944|NCT00924911|112034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178945|NCT00924911|112034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178946|NCT00924911|112034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178947|NCT00924911|112034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178948|NCT00924911|112034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178949|NCT00924911|112034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178950|NCT00924911|112034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178951|NCT00689481|114742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178952|NCT00689481|114742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178953|NCT00689481|114742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178954|NCT00689481|114742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178955|NCT00689481|114742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178956|NCT00689481|114742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178957|NCT00945503|109731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178958|NCT00945503|109731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178959|NCT00945503|109731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178960|NCT00945503|109731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178961|NCT00945503|109731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178962|NCT00945503|109731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178963|NCT00945503|109731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178964|NCT02632708||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178965|NCT02632708||Study Protocol|https://clinicaltrials.servier.com/|
3178966|NCT02632708||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178967|NCT02632708||Informed Consent Form|https://clinicaltrials.servier.com/|
3178968|NCT02632708||Clinical Study Report|https://clinicaltrials.servier.com/|
3178969|NCT02632708||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3178970|NCT06893809|https://www.jscimedcentral.com|Clinical Study Report|https://www.jscimedcentral.com/public/assets/articles/anesthesiology-4-1050.pdf|Int J Clin Anesthesiol 4(1): 1050 (2016)
3178971|NCT07086157|PRJNA1112427|Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/sra|Raw 16S rRNA sequencing data are publicly available through the National Library of Medicine's Sequence Read Archive (SRA) under accession number PRJNA1112427.
3178972|NCT07171892||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/29447733/|Data were sourced from Ningbo University Affiliated First Hospital restricted Whole Disease Database Database (not publicly accessible).
3172308|NCT00731393|100351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176935|NCT00363727|101468/228|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176936|NCT00363727|101468/228|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176937|NCT00363727|101468/228|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176938|NCT00363727|101468/228|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176939|NCT00134732|103478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176940|NCT00134732|103478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176941|NCT00134732|103478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176942|NCT00134732|103478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176943|NCT00134732|103478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176944|NCT00134732|103478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176945|NCT01480609|115214|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176946|NCT01480609|115214|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176947|NCT01480609|115214|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176948|NCT01480609|115214|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176949|NCT01480609|115214|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176950|NCT01480609|115214|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176951|NCT01480609|115214|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176952|NCT03745183||Study Protocol|https://drive.google.com/open?id=1ial1puH4ar075LyGcoWIrU1AXclt3FO-|
3176953|NCT03745183||Tables 1-5|https://drive.google.com/open?id=1pmZyUhTfoOPWRDJgEFjMsa_K9bvQ_Lon|
3176954|NCT03745183||Figure 1. Flow chart of the study procedure|https://drive.google.com/open?id=1MpUGMeNkzeOlThYZ_Zur4xTgt5cOvQNN|
3176955|NCT03745183||Informed Consent Form|https://drive.google.com/open?id=1kV91jvmtUDi_BA2paf-iszXb7bCnKHZO|
3176956|NCT03745183||Individual Participant Data Set|https://drive.google.com/open?id=1n3y-FDFc63KGyGfbkNBlpLJ-6HE9BBUZ|
3176957|NCT03745183||Appendix E. Illustrated checklist for the T'boli|https://drive.google.com/open?id=1t2b-wyQsJaTEy6qqJCiL4Opg-Hdvdxzj|
3176958|NCT03745183||Appendix F. Illustrated instruction on Senna alata decoction preparation|https://drive.google.com/open?id=17hMRr2-GhROnq7Gdw0Skd1KFApCpCgzy|
3176959|NCT00474617||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3176960|NCT00320463|105910|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176961|NCT00320463|105910|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176962|NCT00320463|105910|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176963|NCT00320463|105910|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176964|NCT00320463|105910|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176965|NCT00320463|105910|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176966|NCT01669083|116741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176967|NCT01669083|116741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176968|NCT01669083|116741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176969|NCT01669083|116741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176970|NCT01669083|116741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176971|NCT01669083|116741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176972|NCT01669083|116741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176973|NCT00307567|105555|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176974|NCT00307567|105555|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178973|NCT03125265||Study Protocol|http://bmjopen.bmj.com/content/5/3/e006897.long|
3178974|NCT07024537|Statistical analysis|Analytic Code|http://www.Rproject.org|The Kaplan-Meier method was used to analyze OS and PFS in the overall population with estimated medians and 95% CIs presented. Survival curves were performed using R software version 4.2.2 (http://www.Rproject.org).
3178975|NCT01462357|115411|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178976|NCT01462357|115411|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178977|NCT01462357|115411|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178978|NCT01462357|115411|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178979|NCT01462357|115411|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178980|NCT01462357|115411|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178981|NCT01930058||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8876-003&kw=8876-003|
3178982|NCT07173842||"De-identified clinical, phenotypic, Genotypic Raw, and biospecimen metadata; laboratory quality control metrics; and data dictionaries describing collected variables"|https://www.neuropsybit.org/data-governance|
3174373|NCT00273039|NKF100110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174374|NCT00273039|NKF100110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174375|NCT00273039|NKF100110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174376|NCT00273039|NKF100110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174377|NCT00273039|NKF100110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174378|NCT00273039|NKF100110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176975|NCT00307567|105555|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176976|NCT00307567|105555|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176977|NCT00307567|105555|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176978|NCT00307567|105555|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176979|NCT01636713|114634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176980|NCT01636713|114634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176981|NCT01636713|114634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176982|NCT01636713|114634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176983|NCT01636713|114634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176984|NCT01636713|114634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176985|NCT01636713|114634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176986|NCT00289198|FFR106080|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176987|NCT00289198|FFR106080|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176988|NCT00289198|FFR106080|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176989|NCT00289198|FFR106080|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176990|NCT00289198|FFR106080|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176991|NCT00289198|FFR106080|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176992|NCT00289198|FFR106080|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176993|NCT04786418||Study Protocol|http://www.directclinicaltrial.org.uk|
3176994|NCT00354666|B2E101312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176995|NCT00354666|B2E101312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176996|NCT00354666|B2E101312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176997|NCT00354666|B2E101312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176998|NCT00354666|B2E101312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181307|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
3181308|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
3181309|NCT00056277|SCA30924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181310|NCT00056277|SCA30924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181311|NCT00056277|SCA30924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181312|NCT00056277|SCA30924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3176999|NCT00126984|104703 (Primary study)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177000|NCT00126984|104703 (Primary study)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174379|NCT03274882||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3174380|NCT03274882||Study Protocol|https://clinicaltrials.servier.com/|
3174381|NCT03274882||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3174382|NCT03274882||Informed Consent Form|https://clinicaltrials.servier.com/|
3174383|NCT03274882||Clinical Study Report|https://clinicaltrials.servier.com/|
3174384|NCT03274882||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3174385|NCT01711463|115199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174386|NCT01711463|115199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174387|NCT01711463|115199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174388|NCT01711463|115199|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174389|NCT01711463|115199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174390|NCT01711463|115199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174391|NCT01711463|115199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174392|NCT00655876|NCT00655876|Individual Participant Data Set|http://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3177001|NCT00126984|104703 (Primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177002|NCT00126984|104703 (Primary study)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177003|NCT00126984|104703 (Primary study)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 104703 are summarised with study 104704 on the GSK Clinical Study Register.
3177004|NCT00126984|104703 (Primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177005|NCT06980662||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/36072082/|The Effect of Happiness Training on Psychological Well-Being in Patients with Thalassaemia Major: A quasi-experimental study
3177006|NCT07041424||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28955539/|
3177007|NCT00353873|SAM104926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177008|NCT00353873|SAM104926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174393|NCT03762486||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/citmatch|
3174394|NCT01335997||CSR Synsopsi Link|http://www.merck.com/clinical-trials/study.html?id=0524B-143&kw=0524B-143&tab=access|
3174395|NCT02664935||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/lung-matrix/index.aspx|
3174396|NCT04838522||Breast Milk At the Dawn of New Discoveries|https://betterbeginnings.org/what-we-do/research/breast-milk/|
3174397|NCT00000476|DIG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/dig/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174398|NCT00000476||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dig/|
3174399|NCT00000476||Study Forms|http://biolincc.nhlbi.nih.gov/studies/dig/|
3174400|NCT00811356|111319|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174401|NCT00811356|111319|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174402|NCT00811356|111319|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174403|NCT00811356|111319|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177009|NCT00353873|SAM104926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177010|NCT00353873|SAM104926|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177011|NCT00353873|SAM104926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177012|NCT00353873|SAM104926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177013|NCT00353873|SAM104926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177014|NCT06979739||Informed Consent Form|https://www.hku.edu.tr/iletisim/|
3177015|NCT06367907|SM 68/6-1|Study Protocol|https://gepris.dfg.de/gepris/projekt/424869737|
3177016|NCT01762813||Study Protocol|http://translational-medicine.biomedcentral.com/articles/10.1186/s12967-016-0951-4|
3177017|NCT05936528||Individual Participant Data Set|https://drive.google.com/drive/folders/1CBAPVtAVYsi2x1iLQdWl48b9OowGSxw9|
3177018|NCT00422994|RRL103628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181313|NCT00056277|SCA30924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181314|NCT00056277|SCA30924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181315|NCT00056277|SCA30924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181316|NCT02755818||Informed Consent Form|https://www.irbnet.org/release/study/overview.do?ctx_id=0&spk_id=855867|for a copy of Approved Consent Form-please contact Study Coordinator -Tjien Dwyer at tlthio@ucdavis.edu
3181317|NCT00659178|ILI108621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181318|NCT00659178|ILI108621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181319|NCT00659178|ILI108621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181320|NCT00659178|ILI108621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181321|NCT00659178|ILI108621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181322|NCT00659178|ILI108621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181323|NCT00659178|ILI108621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181324|NCT04445727|vitamin c|Clinical Study Report|http://www.bonusan.es/vademecum/vitamina_c1000_complejo_de_ascorbatos.html|
3181325|NCT00537654|ARI109882|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181326|NCT00537654|ARI109882|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181327|NCT00537654|ARI109882|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181328|NCT00537654|ARI109882|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181329|NCT00537654|ARI109882|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181330|NCT00537654|ARI109882|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181331|NCT00537654|ARI109882|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174404|NCT00811356|111319|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174405|NCT00811356|111319|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174406|NCT00811356|111319|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174407|NCT02904824||Clinical Study Report|http://www.dynasolutions.com|CRO data base
3174408|NCT00196924|580299/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174409|NCT00196924|580299/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174410|NCT00196924|580299/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174411|NCT00196924|580299/013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 580299/013 are summarised with studies 104896 (M18), 104902 (M24), 104904 (M36) and 104918 (M48) on the GSK Clinical Study Register.
3181332|NCT01353768|115008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181333|NCT01353768|115008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181334|NCT01353768|115008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174412|NCT00196924|580299/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174413|NCT00196924|580299/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174414|NCT00196924|580299/013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174415|NCT00426361|108464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174416|NCT00426361|108464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174417|NCT00426361|108464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181335|NCT01353768|115008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181336|NCT01353768|115008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177019|NCT00422994|RRL103628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177020|NCT00422994|RRL103628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177021|NCT00422994|RRL103628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177022|NCT00422994|RRL103628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177023|NCT00422994|RRL103628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177024|NCT00422994|RRL103628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177025|NCT00475215||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177026|NCT00969436|109995|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177027|NCT00969436|109995|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177028|NCT00969436|109995|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177029|NCT00969436|109995|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177030|NCT00969436|109995|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177031|NCT00969436|109995|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177032|NCT00969436|109995|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177033|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/0310250742582348|
3177034|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/1823080587913061|
3177035|NCT00306644|49653/334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177036|NCT00306644|49653/334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177037|NCT00306644|49653/334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177038|NCT00306644|49653/334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177039|NCT00306644|49653/334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177040|NCT00306644|49653/334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177041|NCT00306644|49653/334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177042|NCT06103929||Individual Participant Data Set|https://le.ac.uk/people/sam-tromans|
3177043|NCT06103929||Study Protocol|https://le.ac.uk/people/sam-tromans|
3177044|NCT06103929||Statistical Analysis Plan|https://le.ac.uk/people/sam-tromans|
3177045|NCT06103929||Informed Consent Form|https://le.ac.uk/people/sam-tromans|
3177046|NCT02011490||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-105&kw=8616-105&tab=access|
3178983|NCT00263692|213503/047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178984|NCT00263692|213503/047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172309|NCT00731393|100351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178985|NCT00263692|213503/047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172310|NCT00731393|100351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172311|NCT00731393|100351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172312|NCT00083343||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172313|NCT00823940|111497|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172314|NCT00823940|111497|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177047|NCT00652951|110142|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 110142 are summarised with study 111053 on GSK Clinical Study Register
3177048|NCT00652951|110142|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177049|NCT00652951|110142|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178986|NCT00263692|213503/047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172315|NCT00823940|111497|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172316|NCT00823940|111497|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172317|NCT00823940|111497|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172318|NCT00823940|111497|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172319|NCT00823940|111497|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172320|NCT04744636||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3172321|NCT04744636||Study Protocol|https://clinicaltrials.servier.com/|
3172322|NCT04744636||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3172323|NCT04744636||Informed Consent Form|https://clinicaltrials.servier.com/|
3172324|NCT04744636||Clinical Study Report|https://clinicaltrials.servier.com/|
3172325|NCT04744636||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3172326|NCT01153841|113151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172327|NCT01153841|113151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172328|NCT01153841|113151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172329|NCT01153841|113151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172330|NCT01153841|113151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172331|NCT01153841|113151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174418|NCT00426361|108464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174419|NCT00426361|108464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174420|NCT00426361|108464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174421|NCT00426361|108464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174422|NCT00883909|103094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174423|NCT00883909|103094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174424|NCT00883909|103094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174425|NCT00883909|103094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174426|NCT00883909|103094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174427|NCT00883909|103094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174428|NCT00883909|103094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174429|NCT04599127|MU-CIRB 2019/206.06.08|Study Protocol|https://sp.mahidol.ac.th/eng/contact-mucirb.html|The data can be accessed by using the ethics committee of Mahidol University Central Institutional Review Board to see the ethics approval protocols with the code: MU-CIRB 2019/206.06.08 or using the email to feypqbd@yahoo.com
3174430|NCT05985629||Study Protocol|https://hsd.luc.edu/cro/|"Information about this study can be requested from the Clinical Research Office at Loyola University Chicago by calling 708-216-1153 or by mail at:~Loyola University Chicago Center for Translational Research and Education (CTRE) Bldg. 115, Suite 253, Rm 255 Maywood, IL 60153"
3174431|NCT06613204||data set|http://www.ohsu.edu/alzheimers-disease-research-center/data-resources|
3174432|NCT00258700|103974 (primary study)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174433|NCT00258700|103974 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174434|NCT00258700|103974 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174435|NCT00258700|103974 (primary study)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174436|NCT00258700|103974 (primary study)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174437|NCT00258700|103974 (primary study)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174438|NCT00474266|109670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174439|NCT00474266|109670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174440|NCT00474266|109670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181337|NCT01353768|115008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181338|NCT01353768|115008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174441|NCT00474266|109670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174442|NCT00474266|109670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174443|NCT00474266|109670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174444|NCT00474266|109670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174445|NCT06982014|lecturer|Individual Participant Data Set|https://kocaelisaglik.edu.tr/|
3174446|NCT02152605|201211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174447|NCT02152605|201211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174448|NCT02152605|201211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174449|NCT02152605|201211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174450|NCT02152605|201211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174451|NCT02152605|201211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174452|NCT02152605|201211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174453|NCT04815889||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35704376/|
3174454|NCT00871741|111761|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174455|NCT00871741|111761|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174456|NCT00871741|111761|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174457|NCT00871741|111761|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174458|NCT00871741|111761|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174459|NCT00871741|111761|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174460|NCT00871741|111761|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172332|NCT00240539|100449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174461|NCT01371812|114660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172333|NCT00240539|100449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172334|NCT00240539|100449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172335|NCT00240539|100449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172336|NCT00240539|100449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172337|NCT00044486||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172338|NCT00118729|FFR101816|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172339|NCT00118729|FFR101816|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172340|NCT00118729|FFR101816|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172341|NCT00118729|FFR101816|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172342|NCT00118729|FFR101816|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172343|NCT00118729|FFR101816|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172344|NCT00118729|FFR101816|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172345|NCT00438022|Study ID is SDY4|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
3172346|NCT00438022|Study ID is SDY4|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
3172347|NCT00438022|Study ID is SDY4|Study details, -download packages, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
3172348|NCT02979366||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3172349|NCT02979366||Study Protocol|https://clinicaltrials.servier.com/|
3172350|NCT02979366||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3172351|NCT02979366||Informed Consent Form|https://clinicaltrials.servier.com/|
3172352|NCT02979366||Clinical Study Report|https://clinicaltrials.servier.com/|
3172353|NCT02979366||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3172354|NCT00406211|208136/039|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172355|NCT00406211|208136/039|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172356|NCT00406211|208136/039|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172357|NCT00406211|208136/039|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172358|NCT00406211|208136/039|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172359|NCT00406211|208136/039|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172360|NCT00533611||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172361|NCT04798248||Information on publicly available dataset|https://acrobat.adobe.com/id/urn:aaid:sc:VA6C2:e0548c67-55a8-452d-9854-ade3876c29d8|For any individuals interested in accessing a copy of this public use dataset, please email info@policyandresearch.com with your inquiry.
3172362|NCT04392869|clinicaltrialsCRAFT|Summary and comparison of mindfulness based programs|https://drive.ugr.es/index.php/s/ytdazx47iReHMeu|This is not a comprehensive description of any of the programs, but rather a schematic outline with the most salient similarities and differences between them.
3172363|NCT04392869|clinicaltrialsCRAFT|Human Subjects Review|https://drive.ugr.es/index.php/s/DGKxnBhZfm058DA|Human Subjects Review approval and its translation into English
3172364|NCT04392869|clinicaltrialsCRAFT|Informed Consent Form|https://drive.ugr.es/index.php/s/10ptY8LrAdwdWTj|This document contains the welcome email, the informed consent form and the demographic survey. Please, bear in mind that this is the English version of the text in Spanish uploaded to the LimeSurvey platform.
3172365|NCT04392869|clinicaltrialsCRAFT|Official CRAFTftiugr logo|https://drive.ugr.es/index.php/s/zHklhje0InjZAF7|This is the official logo of the project. It represents a way of communication that goes beyond words. Earphones are a special reference to interpreters.
3172366|NCT00866515|112205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172367|NCT00866515|112205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172368|NCT00866515|112205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172369|NCT00866515|112205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172370|NCT00866515|112205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172371|NCT00866515|112205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172372|NCT00866515|112205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172373|NCT01376245|113684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172374|NCT01376245|113684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172375|NCT01376245|113684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172376|NCT01376245|113684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178987|NCT00263692|213503/047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178988|NCT00263692|213503/047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178989|NCT00779766|107638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178990|NCT00779766|107638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178991|NCT00779766|107638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178992|NCT00779766|107638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178993|NCT00779766|107638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172377|NCT01376245|113684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172378|NCT01376245|113684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172379|NCT01376245|113684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172380|NCT01357889|114856|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172381|NCT01357889|114856|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178994|NCT00779766|107638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178995|NCT00779766|107638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178996|NCT05007457|Benedetta Isani|Study Protocol|http://aosp.bo.it|
3178997|NCT01957189|200254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178998|NCT01957189|200254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178999|NCT01957189|200254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179000|NCT01957189|200254|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179001|NCT01957189|200254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172382|NCT01357889|114856|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172383|NCT01357889|114856|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172384|NCT01357889|114856|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172385|NCT01357889|114856|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172386|NCT01357889|114856|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172387|NCT01315847||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-067&kw=0974-067&tab=access|
3172388|NCT00546286||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172389|NCT01527110|115215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172390|NCT01527110|115215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172391|NCT01527110|115215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172392|NCT01527110|115215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172393|NCT01527110|115215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172394|NCT01527110|115215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172395|NCT02141217|117044|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172396|NCT02141217|117044|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172397|NCT02141217|117044|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172398|NCT02141217|117044|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172399|NCT02141217|117044|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172400|NCT02141217|117044|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172401|NCT07091838||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28179436/|
3179002|NCT01957189|200254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179003|NCT01957189|200254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179004|NCT01114841|114572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179005|NCT01114841|114572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179006|NCT01114841|114572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179007|NCT01114841|114572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179008|NCT01114841|114572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179009|NCT01114841|114572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179010|NCT01114841|114572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179011|NCT01310413|114464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179012|NCT01310413|114464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179013|NCT01310413|114464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179014|NCT01310413|114464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179015|NCT01310413|114464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179016|NCT01310413|114464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179017|NCT00482079||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179018|NCT02829359||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/28122361|Oncotarget. 2017 Feb 28;8(9):15047-15056. doi: 10.18632/oncotarget.14789.
3179019|NCT00075829|BMT CTN-0102|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local Institutional Review Board (IRB) approval or certification of exemption from IRB review, and completion of a data use agreement.
3179020|NCT00075829|BMT CTN-0102|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
3179021|NCT00075829|BMT CTN-0102|Study Forms|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
3179022|NCT01003418|113629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179023|NCT01003418|113629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179024|NCT01003418|113629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179025|NCT01003418|113629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179026|NCT01003418|113629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179027|NCT01003418|113629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172402|NCT00964158|113528|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179028|NCT06919185|2025-01028-01|Study Protocol|https://slmf.se/forskning/lungmedicinsk-forskning/sparc/|
3179029|NCT01837316|116592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179030|NCT01837316|116592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181339|NCT00599911|2007-001071-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001071-11/results|
3172403|NCT00964158|113528|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172404|NCT00964158|113528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172405|NCT00964158|113528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172406|NCT00964158|113528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172407|NCT00964158|113528|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172408|NCT00964158|113528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172409|NCT00092482||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179031|NCT01837316|116592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179032|NCT01837316|116592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181340|NCT01198756|113314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181341|NCT01198756|113314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172410|NCT00141037|SDY132|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
3172411|NCT00141037|SDY132|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
3172412|NCT00141037|SDY132|Study summary, -design,-demographics, -mechanistic assays, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
3172413|NCT01021813||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-009&kw=4305-009&tab=access|
3172414|NCT01319019|115032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172415|NCT01319019|115032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172416|NCT01319019|115032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172417|NCT01319019|115032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172418|NCT01319019|115032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172419|NCT01319019|115032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172420|NCT01319019|115032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172421|NCT00334152|NKT102552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172422|NCT00334152|NKT102552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172423|NCT00334152|NKT102552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172424|NCT00334152|NKT102552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172425|NCT00334152|NKT102552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172426|NCT00334152|NKT102552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172427|NCT00334152|NKT102552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172428|NCT02542813|201558|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172429|NCT02542813|201558|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172430|NCT02542813|201558|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172431|NCT02542813|201558|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172432|NCT02542813|201558|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172433|NCT02542813|201558|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172434|NCT02542813|201558|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172435|NCT06849427|sibelcynk@gmail.com|Individual Participant Data Set|https://www.antalya.edu.tr/tr|If online access is not available: instructions for how to obtain information
3172436|NCT05184309|Principle investigator|Statistical Analysis Plan|https://pubmed.ncbi.nlm.nih.gov/28446376/|
3172437|NCT03336827||Study design|http://pdf.lu/YtWd|
3172438|NCT03336827||List of questionnaires|http://pdf.lu/TJ4c|
3172439|NCT03336827||Informed Consent Form|http://pdf.lu/dN2P|
3172440|NCT03336827||Informed Consent Form|http://pdf.lu/07Xz|
3172441|NCT03909672||Study Protocol|http://facisa.ufrn.br|
3172442|NCT05885048||Study Protocol|https://www.researchprotocols.org/2024/1/e51145|
3172443|NCT00704431|LPL111814|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172444|NCT00704431|LPL111814|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172445|NCT00704431|LPL111814|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172446|NCT00704431|LPL111814|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172447|NCT00704431|LPL111814|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172448|NCT00704431|LPL111814|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172449|NCT00996593|104507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174462|NCT01371812|114660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174463|NCT01371812|114660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174464|NCT01371812|114660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174465|NCT01371812|114660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174466|NCT01371812|114660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174467|NCT01371812|114660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174468|NCT06989255|doi: 10.5281/zenodo.11371924|Study Protocol|https://zenodo.org/records/11371924|Study protocol including ICF
3174469|NCT00609180|ARDSNet-Omega|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/omega/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174470|NCT00609180||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/omega/|
3174471|NCT00609180||Study Forms|http://biolincc.nhlbi.nih.gov/studies/omega/|
3174472|NCT01160003|113209|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174473|NCT01160003|113209|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174474|NCT01160003|113209|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174475|NCT01160003|113209|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174476|NCT01160003|113209|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174477|NCT01160003|113209|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174478|NCT01160003|113209|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174479|NCT00678886|115495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174480|NCT00678886|115495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174481|NCT00678886|115495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174482|NCT00678886|115495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174483|NCT00678886|115495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174484|NCT00678886|115495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174485|NCT00678886|115495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174486|NCT02549027||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-003&kw=1064-003&tab=access|
3174487|NCT00385008|TRX105848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174488|NCT00385008|TRX105848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174489|NCT00385008|TRX105848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174490|NCT00385008|TRX105848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172450|NCT00996593|104507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172451|NCT00996593|104507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172452|NCT00996593|104507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172453|NCT00996593|104507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172454|NCT00996593|104507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172455|NCT00996593|104507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172456|NCT02800720||Embedded Qualitative Study|http://link.springer.com/article/10.1007/s12671-015-0458-8|
3172457|NCT00014911|SDY567|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY567|ImmPort study identifier is SDY567. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3172458|NCT00014911|SDY567|Study summary, -schematic, -design, -adverse event(s),-medications,-demographics, - lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY567|ImmPort study identifier is SDY567. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3172459|NCT00014911|ITN005CT|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN005CTPUBLIC/Study%20Data/begin.view?|TrialShare is the Immune Tolerance Network (ITN) portal that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3172460|NCT00014911|ITN005CT|Study overview & protocol synopsis, -navigator, -schedule of assessments, -data&reports, -specimens, etc.|http://www.itntrialshare.org/project/Studies/ITN005CTPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
3172461|NCT05981378||Study Protocol|https://drive.google.com/drive/folders/1SJk21vz3MOlaF8tSVnwPlwo9sxmmewZp?usp=drive_link|Google drive link to visualize the study protocol in Spanish and English
3172462|NCT02697058||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3179033|NCT01837316|116592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179034|NCT01837316|116592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179035|NCT01837316|116592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172463|NCT02697058||Study Protocol|https://clinicaltrials.servier.com/|
3172464|NCT02697058||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3172465|NCT02697058||Informed Consent Form|https://clinicaltrials.servier.com/|
3172466|NCT02697058||Clinical Study Report|https://clinicaltrials.servier.com/|
3172467|NCT02697058||study-level clinical trial data|https://clinicaltrials.servier.com/|
3172468|NCT00702910|B2C111401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172469|NCT00702910|B2C111401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172470|NCT00702910|B2C111401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172471|NCT00702910|B2C111401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172472|NCT00702910|B2C111401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172473|NCT00702910|B2C111401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172474|NCT00702910|B2C111401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172475|NCT00922974|NCT00922974|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3172476|NCT00290303|100478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172477|NCT00290303|100478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172478|NCT00290303|100478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172479|NCT00290303|100478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172480|NCT00290303|100478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179036|NCT01706250|114550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172481|NCT00290303|100478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172482|NCT01376388|115362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179037|NCT01706250|114550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179038|NCT01706250|114550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179039|NCT01706250|114550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179040|NCT01706250|114550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179041|NCT05262205||Study Protocol|http://irb.mans.edu.eg|
3179042|NCT00586469|111258|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179043|NCT00586469|111258|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179044|NCT00586469|111258|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179045|NCT00586469|111258|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179046|NCT00586469|111258|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179047|NCT00586469|111258|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179048|NCT00586469|111258|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179049|NCT00094380|SDY798|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY798|ImmPort study identifier is SDY798.
3179050|NCT00094380|SDY798|Study protocol synopsis; -Study summary; -design; -adverse event; -Assessment; -Medications, -demographics; -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY798|ImmPort study identifier is SDY798.
3179051|NCT00094380|ITN002AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN002AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
3179052|NCT00094380|ITN002AI|Informed Consent Form|http://www.itntrialshare.org/project/Studies/ITN002AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
3179053|NCT00094380|ITN002AI|Study synopsis, -schedule of events, -adverse events, et al.|http://www.itntrialshare.org/project/Studies/ITN002AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
3179054|NCT00338351|106208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179055|NCT00338351|106208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179056|NCT00338351|106208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179057|NCT00338351|106208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179058|NCT00338351|106208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179059|NCT00338351|106208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179060|NCT00812812|112487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179061|NCT00812812|112487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179062|NCT00812812|112487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179063|NCT00812812|112487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179064|NCT02696850|CGI scale|Questionnaire|https://www.psywellness.com.sg/docs/CGI.pdf|
3179065|NCT01181895|112060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179066|NCT01181895|112060|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179067|NCT01181895|112060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179068|NCT01181895|112060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179069|NCT01181895|112060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179070|NCT01181895|112060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179071|NCT01181895|112060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172483|NCT01376388|115362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177050|NCT00652951|110142|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177051|NCT00652951|110142|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177052|NCT00652951|110142|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177053|NCT00652951|110142|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177054|NCT01462617|115117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177055|NCT01462617|115117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177056|NCT01462617|115117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177057|NCT01462617|115117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177058|NCT01462617|115117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177059|NCT01462617|115117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177060|NCT01462617|115117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177061|NCT07060339|non-pharmacological methods|Individual Participant Data Set|https://dergipark.org.tr/tr/pub/ausbid/issue/38415/445612|https://dergipark.org.tr/tr/pub/ausbid/issue/38415/445612
3177062|NCT00231413|102115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177063|NCT00231413|102115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177064|NCT00231413|102115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177065|NCT00231413|102115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 102115 are summarised with studies 107919 and 108052 on the GSK Clinical Study Register.
3177066|NCT00231413|102115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177067|NCT00231413|102115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177068|NCT01116427|ACCLAIM ITN035AI|Study protocol synopsis, -navigator, -schedule of assessments, study schema, and manuscript(s) with overviews, data and reports, participant level data|https://www.itntrialshare.org/project/Studies/ITN035AIPRI/Study%20Data/begin.view?|ACCLAIM ITN035AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
3177069|NCT01426776|PMID: 24938583|published article|https://pubmed.ncbi.nlm.nih.gov/24938583|We found central sleep apnea was eliminated after cardiac valve replacement surgery, however, there was no change in obstructive sleep apnea.
3177070|NCT01147900|113055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177071|NCT01147900|113055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177072|NCT01147900|113055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177073|NCT01147900|113055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177074|NCT01147900|113055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177075|NCT01147900|113055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177076|NCT00945932|112851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177077|NCT00945932|112851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177078|NCT00945932|112851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177079|NCT00945932|112851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177080|NCT00945932|112851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177081|NCT00945932|112851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177082|NCT00945932|112851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177083|NCT00307554|105553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177084|NCT00307554|105553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177085|NCT00307554|105553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177086|NCT00307554|105553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177087|NCT00307554|105553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177088|NCT00307554|105553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177089|NCT01209078|113414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177090|NCT01209078|113414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177091|NCT01209078|113414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177092|NCT01209078|113414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177093|NCT01209078|113414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179072|NCT07078825|39085438|Publication|https://doi.org/10.1038/s41372-024-02077-0|This publication provides background data related to the current study's hypothesis and methodology.
3179073|NCT07086287|rhBNP|Study Protocol|https://www.chictr.org.cn/|China Clinical Trial Registration Center
3181342|NCT01198756|113314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181343|NCT01198756|113314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181344|NCT01198756|113314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181345|NCT01198756|113314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181346|NCT01198756|113314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181347|NCT01498679|113719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181348|NCT01498679|113719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181349|NCT01498679|113719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181350|NCT01498679|113719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181351|NCT01498679|113719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181352|NCT01498679|113719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181353|NCT01498679|113719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181354|NCT00640081||Clinical Study Report|http://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(14)70106-8/abstract|
3181355|NCT01978327|200592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181356|NCT01978327|200592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181357|NCT01978327|200592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181358|NCT01978327|200592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181359|NCT01978327|200592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181360|NCT01978327|200592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181361|NCT01978327|200592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181362|NCT01035645|110040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181363|NCT01035645|110040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181364|NCT01035645|110040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177094|NCT01209078|113414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181365|NCT01035645|110040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181366|NCT01035645|110040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181367|NCT01035645|110040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181368|NCT00225823|FFR103184|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181369|NCT00225823|FFR103184|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181370|NCT00225823|FFR103184|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181371|NCT00225823|FFR103184|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181372|NCT00225823|FFR103184|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181373|NCT00225823|FFR103184|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181374|NCT00225823|FFR103184|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181375|NCT00359983|107824|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181376|NCT00359983|107824|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181377|NCT00359983|107824|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181378|NCT00359983|107824|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181379|NCT00359983|107824|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181380|NCT00359983|107824|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181381|NCT00603252|111149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181382|NCT00603252|111149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181383|NCT00603252|111149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181384|NCT00603252|111149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181385|NCT00603252|111149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181386|NCT01805752|doi: 10.1016/S2352-3018(16)000|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/27126487|Aliyu MH, Blevins M, Audet CM, Kalish M, Gebi UI, Onwujekwe O, Lindegren ML, Shepherd BE, Wester CW, Vermund SH. Integrated prevention of mother-to-child HIV transmission services, antiretroviral therapy initiation, and maternal and infant retention in care in rural north-central Nigeria: a cluster-randomised controlled trial. Lancet HIV. 2016 May;3(5):e202-11. doi: 10.1016/S2352-3018(16)00018-7. PubMed PMID: 27126487; PubMed Central PMCID: PMC4852280.
3181387|NCT03091231|mpUS2016|Study Protocol|http://www.martini-klinik.de|to request an electronic copy send an email to a.renter@uke.de
3181388|NCT00806572|ITN007AI-NDB01|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN007AIPUBLIC/Study%20Data/begin.view?|TrialShare is a portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3181389|NCT00806572|ITN007AI-NDB01|Study protocol synopsis, -navigator, -schedule of events,-data &reports, -specimens et al.|http://www.itntrialshare.org/project/Studies/ITN007AIPUBLIC/Study%20Data/begin.view?|TrialShare is a portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3181390|NCT00806572|SDY569|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY569|ImmPort study identifier is SDY569. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3181391|NCT00806572|SDY569|Study summary, -design, -medications, -demographics, -lab tests, and -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY569|ImmPort study identifier is SDY569. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3181392|NCT04312334||Individual Participant Data Set|https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-015-0532-z|Our data will be suitable for sharing in anonymised form.Potential users will learn about the data on the websites of the collaborating institutes, and links to the relevant data repositories will be available on those websites.The link will contain information on how to apply to use the data. We aim to offer controlled access to study data. Potential users of the data will be invited to register and provide information on their aims and proposed analyses of the data. The PI and Co-Is will decide whether to grant release of the data based on these requests. Our intended policy will be to make data available to researchers, within 2 years of completion of the study. This is to make maximum use of data collected using public funding while protecting the intellectual property rights of the study team.Restrictions or delays to sharing, with planned actions to limit such restrictions We would like to retain exclusive use for 2 years
3181393|NCT00092352||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181394|NCT02615002||Study website|http://www.recognitionstudy.com|
3181395|NCT01139580|114743|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179074|NCT00432380|109216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179075|NCT00432380|109216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179076|NCT00432380|109216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179077|NCT00432380|109216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179078|NCT00432380|109216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179079|NCT00432380|109216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179080|NCT00432380|109216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179081|NCT00264615|LEP103944|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179082|NCT00264615|LEP103944|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181396|NCT01139580|114743|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181397|NCT01139580|114743|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181398|NCT01139580|114743|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181399|NCT01139580|114743|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181400|NCT01139580|114743|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181401|NCT01139580|114743|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181402|NCT02688218|STUDY00015452|Study Protocol|http://eirb.ohsu.edu|Institutionally reviewed and accepted protocol for this study.
3181403|NCT00306696|49653/342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181404|NCT00306696|49653/342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181405|NCT00306696|49653/342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181406|NCT00306696|49653/342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181407|NCT00306696|49653/342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181408|NCT00306696|49653/342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181409|NCT00306696|49653/342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181410|NCT03789448||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2128-8|
3181411|NCT00158860|HS2100275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181412|NCT00158860|HS2100275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181413|NCT00158860|HS2100275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181414|NCT00158860|HS2100275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181415|NCT00158860|HS2100275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181416|NCT00158860|HS2100275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181417|NCT00158860|HS2100275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181418|NCT00552929||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181419|NCT00852540|110978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181420|NCT00852540|110978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181421|NCT00852540|110978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181422|NCT00852540|110978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181423|NCT00852540|110978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181424|NCT00852540|110978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172484|NCT01376388|115362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174491|NCT00385008|TRX105848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174492|NCT00385008|TRX105848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174493|NCT00385008|TRX105848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174494|NCT02000765|115774|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174495|NCT02000765|115774|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174496|NCT02000765|115774|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174497|NCT02000765|115774|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174498|NCT02000765|115774|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174499|NCT02000765|115774|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174500|NCT02000765|115774|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174501|NCT00000620|ACCORD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/accord|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174502|NCT00000620||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/accord|
3174503|NCT00000620||Study Forms|http://biolincc.nhlbi.nih.gov/studies/accord|
3174504|NCT00000620||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/accord|
3174505|NCT01590797||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-254&kw=0431-254&tab=access|
3174506|NCT00224471|208141/042|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174507|NCT00224471|208141/042|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174508|NCT00224471|208141/042|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174509|NCT00224471|208141/042|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174510|NCT00224471|208141/042|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174511|NCT00224471|208141/042|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174512|NCT00086593|101464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174513|NCT00086593|101464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174514|NCT00086593|101464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174515|NCT00086593|101464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174516|NCT00086593|101464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174517|NCT00086593|101464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174518|NCT05088135||Clinical Study Report|https://doi.org/10.3389/fphys.2023.1215757|
3174519|NCT00323050|102547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174520|NCT00323050|102547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174521|NCT00323050|102547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174522|NCT00323050|102547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174523|NCT00323050|102547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174524|NCT00323050|102547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174525|NCT02105974|200820|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174526|NCT02105974|200820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174527|NCT02105974|200820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174528|NCT02105974|200820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174529|NCT02105974|200820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174530|NCT02105974|200820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177095|NCT01209078|113414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181425|NCT00852540|110978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181426|NCT02960750|4382156|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382156/?report=classic|
3181427|NCT02960750|4323230|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323230/?report=classic|
3181428|NCT02960750|4266209|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266209/|
3181429|NCT00662818||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-034&kw=0974-034&tab=access|
3181430|NCT03136445|PMC6792262|Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-019-3663-2|"The protocol was published in The Trials Journal, The TREATT Trial (TRial to EvaluAte Tranexamic acid therapy in Thrombocytopenia): safety and efficacy of tranexamic acid in patients with haematological malignancies with severe thrombocytopenia: study protocol for a double-blind randomised controlled trial.~Trials Free Article - Estcourt LJ, McQuilten Z, Powter G, Dyer C, Curnow E, Wood EM, Stanworth SJ, TREATT Trial Collaboration (provisional).~To request a protocol please contact the Trial Manager Gillian Powter gillian.powter@nhsbt.nhs.uk"
3181431|NCT01156792|114255|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181432|NCT01156792|114255|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181433|NCT01156792|114255|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181434|NCT01156792|114255|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181435|NCT01156792|114255|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181436|NCT01156792|114255|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181437|NCT01156792|114255|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181438|NCT00116883|FFR100012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181439|NCT00116883|FFR100012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181440|NCT00116883|FFR100012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181441|NCT00116883|FFR100012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181442|NCT00116883|FFR100012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181443|NCT00116883|FFR100012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181444|NCT00116883|FFR100012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181445|NCT02900066||Individual Participant Data Set|https://doi.org/10.1016/j.ijid.2018.10.010|The data supporting the findings of this study/publication are retained at the Institute of Tropical Medicine, Antwerp and will not be made openly accessible due to ethical and privacy concerns. Data can however be made available after approval of a motivated and written request to the Institute of Tropical Medicine at ITMresearchdataaccess@itg.be/.
3172485|NCT01376388|115362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172486|NCT05464472||BECK DEPRESSION INVENTORY|https://www.ismanet.org/doctoryourspirit/pdfs/Beck-Depression-Inventory-BDI.pdf|
3172487|NCT05464472||SF-36 QUESTIONNAIRE|https://clinmedjournals.org/articles/jmdt/jmdt-2-023-figure-1.pdf|
3172488|NCT05957588|Documents|Informed Consent Form|https://irbnet.org/release/study/designer.do?ctx_id=9&spk_id=1793612|This URL and identifier are used internally by Common Spirit Health IRB. The link is IRBNET.org and registration thru CSH is required. The link provides access to a digital document repository including the consent form.
3172489|NCT05957588|Protocol|Study Protocol|https://irbnet.org/release/study/designer.do?ctx_id=9&spk_id=1793612|This URL and identifier are used internally by Common Spirit Health IRB. The link is IRBNET.org and registration thru CSH is required. The link provides access to a digital document repository including the protocol document.
3172490|NCT00383227|208129/032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172491|NCT00383227|208129/032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172492|NCT00383227|208129/032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172493|NCT00383227|208129/032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172494|NCT00383227|208129/032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172495|NCT00383227|208129/032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177096|NCT00771615|111729|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172496|NCT01594749||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-031&kw=0517-031&tab=access|
3172497|NCT06120192|10.6084/m9.figshare.23994768|Informed Consent Form|https://doi.org/10.6084/m9.figshare.23994768|
3172498|NCT06120192|10.6084/m9.figshare.23994768|Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.23994768|
3172499|NCT01235728||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-022&kw=0873-022&tab=access|
3172500|NCT05752786||Study Protocol|https://osf.io/3gts8/|
3172501|NCT05752786||Statistical Analysis Plan|https://osf.io/3gts8/|
3172502|NCT05752786||Individual Participant Data Set|https://osf.io/3gts8/|
3172503|NCT00306241|106001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172504|NCT00306241|106001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172505|NCT00306241|106001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172506|NCT00306241|106001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172507|NCT00306241|106001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172508|NCT00306241|106001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172509|NCT04143425||Clinical Study Report|https://link-springer-com-ssl.libproxy.amc.seoul.kr/article/10.1007/s00330-022-09164-w|Vessel size and perfusion-derived vascular habitat refines prediction of treatment failure to bevacizumab in recurrent glioblastomas: validation in a prospective cohort
3172510|NCT00937326|113160|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172511|NCT00937326|113160|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172512|NCT00937326|113160|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172513|NCT00937326|113160|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172514|NCT00937326|113160|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172515|NCT00937326|113160|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172516|NCT00937326|113160|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172517|NCT00005306|NANB-TAH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172518|NCT00005306||Study Forms|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|
3172519|NCT03134612||Textbook|https://sydney.edu.au/medicine/pmri/pdf/Acute-pain-management-scientific-evidence-third-edition.pdf|Assessment and measurement of pain and its treatment. In: Macintyre PE SD, Schug SA, Visser EJ, Walker SM, editors. Acute pain management: scientific evidence. Melbourne: Australian and New Zealand College of Anaesthetists and Faculty of Pain Medicine; 2010.p. 35-43
3172520|NCT03134612||Textbook|http://accessanesthesiology.mhmedical.com/book.aspx?bookID=413|Candido KD, Winnie AP. Intravenous regional block for upper \& lower extremity surgery. In: Hadzic A, editor. Textbook of regional anesthesia and acute pain management. New York: McGraw-Hill; 2007. p. 565-78
3172521|NCT01031108|114089|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172522|NCT01031108|114089|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172523|NCT01031108|114089|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172524|NCT01031108|114089|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172525|NCT01031108|114089|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172526|NCT01031108|114089|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172527|NCT01031108|114089|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172528|NCT02197598|2014-000413-31|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-000413-31/results|
3181446|NCT02135354||Study Protocol|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
3172529|NCT00092404||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172530|NCT03427138|C2495|Individual Participant Data Set|http://ndar.nih.gov|
3172531|NCT01366534|114460|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172532|NCT01366534|114460|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172533|NCT01366534|114460|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172534|NCT01366534|114460|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172535|NCT01366534|114460|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181447|NCT02135354||Statistical Analysis Plan|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
3181448|NCT00005130|CARDIA|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/cardia/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3181449|NCT00005130||Study Protocol|http://www.cardia.dopm.uab.edu/exam-materials2/protocols|
3181450|NCT00005130||Informed Consent Form|http://www.cardia.dopm.uab.edu/exam-materials2/consent-forms|
3181451|NCT00005130||Data Collection Forms|http://www.cardia.dopm.uab.edu/exam-materials2/data-collection-forms|
3172536|NCT01366534|114460|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172537|NCT00329784|SDY660|Individual Participant Data Set|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
3172538|NCT00329784|SDY660|Study summary, -design, -adverse event(s), -demographics, -study files|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
3172539|NCT00329784|LEAP (ITN032AD)|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN032ADNEJM/Study%20Data/begin.view?pageId=study.PARTICIPANTS|TrialShare study identifier is LEAP (ITN032AD)
3172540|NCT00329784|LEAP (ITN032AD)|Overview, Date & Reports, Manuscripts et al.|https://www.itntrialshare.org/project/Studies/ITN032ADNEJM/Study%20Data/begin.view?|TrialShare study identifier is LEAP (ITN032AD)
3172541|NCT01177826|111426|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172542|NCT01177826|111426|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172543|NCT01177826|111426|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172544|NCT01177826|111426|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172545|NCT01177826|111426|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172546|NCT01177826|111426|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172547|NCT02798640||Informed Consent Form|https://mega.nz/#!C5U1HZwI!7XB2jar-JDElrnYOZTbwg0RD5T1WPQEv3HkzT0XPXz8|
3172548|NCT02798640||Clinical Investigation plan|https://mega.nz/#!3gEnFCDK!DK911mpjGBw_bAKdfsR4F2RgzCQG7mYR3oBqrVkRtpA|
3172549|NCT02798640||Clinical Study Report|https://mega.nz/#!S1tThKrL!gaWPII28P3I0BLBrLD9iZJYRqb2R1x-uZT5djgV4ML8|
3172550|NCT03612674||Analytic Code|http://www.epiclin.it|
3172551|NCT00750178||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172552|NCT00264667|ADG103440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172553|NCT00264667|ADG103440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172554|NCT00264667|ADG103440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172555|NCT00264667|ADG103440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172556|NCT00264667|ADG103440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172557|NCT00264667|ADG103440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172558|NCT00264667|ADG103440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172559|NCT00684463||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172560|NCT00911144|112933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172561|NCT00911144|112933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172562|NCT00911144|112933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172563|NCT00911144|112933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172564|NCT00911144|112933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172565|NCT00911144|112933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172566|NCT00911144|112933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181452|NCT00005130||Study Manuals|http://www.cardia.dopm.uab.edu/exam-materials2/manual-of-operations|
3181453|NCT06906354|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3172567|NCT00654420||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0646-007&kw=0646-007&tab=access|
3181454|NCT00321373|107022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172568|NCT05837000|MKSU 51- 2 _ 16|Study Protocol|http://kfs.edu.eg/engkfs/|
3172569|NCT00076856||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181455|NCT00321373|107022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177097|NCT00771615|111729|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177098|NCT00771615|111729|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177099|NCT00771615|111729|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177100|NCT00771615|111729|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177101|NCT00771615|111729|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177102|NCT00771615|111729|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177103|NCT04303299|Thai government data|Data references|https://ddc.moph.go.th|
3177104|NCT04303299||News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
3177105|NCT04303299||Reference review data set of DMS database|http://dx.doi.org/10.2139/ssrn.3633173|Preliminary Database result of prospective open study of 119 pneumonia ( another population)patient ( it is not data from this RCT)
3177106|NCT04303299||Reference News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
3177107|NCT01600092||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-035&kw=V260-035&tab=access|
3177108|NCT01381536|114243|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177109|NCT01381536|114243|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177110|NCT01381536|114243|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177111|NCT01381536|114243|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177112|NCT01381536|114243|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177113|NCT01381536|114243|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177114|NCT03696901|Xydalba|Study Protocol|https://awbdb.bfarm.de/ords/f?p=101:STARTSEITE::::::|BfArM AWB Datenbank
3177115|NCT01300455||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-036&kw=4305-036&tab=access|
3177116|NCT00778895|111635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177117|NCT00778895|111635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177118|NCT00778895|111635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177119|NCT00778895|111635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177120|NCT00778895|111635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172570|NCT00111891||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172571|NCT01431521||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4074-008&kw=4074-008&tab=access|
3172572|NCT04283773||Clinical Study Report|https://journals.lww.com/greenjournal/Fulltext/2006/05000/Malignant_Germ_Cell_Tumors_of_the_Ovary.19.aspx|Incidence and Survival Rates for Female Malignant Germ Cell Tumors
3172573|NCT04283773||Clinical Study Report|https://synapse.koreamed.org/DOIx.php?id=10.3802/jgo.2012.23.2.125|Early diagnosis of malignant-transformed ovarian mature cystic teratoma: fat-suppressed MRI findings
3172574|NCT05394363||GenV Protocol paper (open access)|https://doi.org/10.1186/s12889-024-21108-1|Hughes, E.K., Siero, W., Gülenç, A. et al. Generation Victoria (GenV): protocol for a longitudinal birth cohort of Victorian children and their parents. BMC Public Health 25, 20 (2025).
3172575|NCT05394363||Informed Consent Form|https://doi.org/10.25374/MCRI.16902154|Wake M, Goldfeld S, Saffery R; Siero W, Hughes E. Generation Victoria (GenV) Cohort 2020s Participant Information Statement and Consent Form In: Generation Victoria Figshare Project. Figshare 2021.
3172576|NCT05394363||Generation Victoria (GenV) Cohort 2020s Statement of Intent|https://doi.org/10.25374/MCRI.9962084|Wake M, Goldfeld S, Saffery R, Siero W, Lamb K, Stringer M, et al. Generation Victoria (GenV) Cohort 2020s Statement of Intent In: Generation Victoria Figshare Project. Figshare 2019.
3172577|NCT05394363||Generation Victoria (GenV) Cohort 2020s Synopsis|https://doi.org/10.25374/MCRI.9122522|Wake M, Goldfeld S, Saffery R, Siero W, Hourani D, Gulenc A, et al. Generation Victoria (GenV) Cohort 2020s Synopsis In: Generation Victoria Figshare Project. Figshare 2019.
3172578|NCT05394363||Guidance and expressions of interest for enquires and proposals to collaborate with GenV|https://genv.org.au/for-researchers/enquire-about-collaborating-with-genv/|
3172579|NCT05394363||Current GenV collaborations|https://www.genv.org.au/for-researchers/current-genv-collaborations/|
3172580|NCT05394363||Working Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/working-papers/|
3172581|NCT05394363||Published Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/published-papers/|
3172582|NCT04704206|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
3172583|NCT00783549|111596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172584|NCT00783549|111596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172585|NCT00783549|111596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172586|NCT00783549|111596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172587|NCT00783549|111596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172588|NCT00783549|111596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172589|NCT00783549|111596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177121|NCT00778895|111635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177122|NCT04892108||Study Protocol|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
3177123|NCT04892108||Statistical Analysis Plan|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
3177124|NCT04892108||Informed Consent Form|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
3177125|NCT01521377|114635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177126|NCT01521377|114635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177127|NCT01521377|114635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177128|NCT01521377|114635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177129|NCT01521377|114635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172590|NCT01962467|200284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177130|NCT01521377|114635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177131|NCT01521377|114635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177132|NCT07322081||Study Protocol|https://www.adu.edu.tr|No external links to the study data are publicly available at this time. Data requests can be made by contacting the corresponding author or the Community Mental Health Center at Aydın Adnan Menderes University.
3177133|NCT02747017||Study Protocol|http://insight.ccbr.umn.edu/official_documents/CDIFF/protocol_documents/I7-Protocol.pdf|
3177134|NCT00343707|NKP102280|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177135|NCT00343707|NKP102280|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172591|NCT01962467|200284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172592|NCT01962467|200284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174531|NCT02105974|200820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174532|NCT00366366|217744/075|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174533|NCT00366366|217744/075|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174534|NCT00366366|217744/075|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174535|NCT00366366|217744/075|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174536|NCT00366366|217744/075|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174537|NCT00366366|217744/075|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174538|NCT02872376||Study Protocol|https://sites.google.com/site/ridartstudy/|
3174539|NCT02872376||Informed Consent Form|https://sites.google.com/site/ridartstudy/|
3174540|NCT05382585||Mutation data|https://www.ncbi.nlm.nih.gov/clinvar/submitters/507417/|Data of 37 mutations identified till 2020 has been uploaded, more mutations will be uploaded soon
3174541|NCT05063708||Analytic Code|http://zenodo.org|
3177136|NCT00343707|NKP102280|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177137|NCT00343707|NKP102280|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177138|NCT00343707|NKP102280|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177139|NCT00343707|NKP102280|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177140|NCT01147848|113091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177141|NCT01147848|113091|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177142|NCT01147848|113091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177143|NCT01147848|113091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177144|NCT01147848|113091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177145|NCT01147848|113091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177146|NCT01147848|113091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177147|NCT02891382||Individual Participant Data Set|https://figshare.com/articles/REDEEM_Study_Feasibility_pilot_study/7180802|
3177148|NCT01000324|112267|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177149|NCT01000324|112267|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177150|NCT01000324|112267|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177151|NCT01000324|112267|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177152|NCT01000324|112267|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177153|NCT01000324|112267|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177154|NCT01000324|112267|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177155|NCT06507384||Study Protocol|https://drbukret.com/research-ipd-sharing/|To access the study protocol, please visit the provided URL and follow the instructions for requesting access.
3177156|NCT01183468|RETAIN ITN041AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN041AIPUBLIC/Study%20Data/begin.view?pageId=study.DATA_ANALYSIS|RETAIN ITN041AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
3177157|NCT00148941|213503/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177158|NCT00148941|213503/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177159|NCT00148941|213503/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177160|NCT00148941|213503/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177161|NCT00148941|213503/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177162|NCT00148941|213503/048|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177163|NCT04904848||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/25437107/|
3177164|NCT04657783||Study Protocol|https://drive.google.com/drive/my-drive|
3177165|NCT06583694||Clinical Study Report|https://www.bangkoknoimodel.com/stat.|
3177166|NCT05502510||Analytic Code|https://osf.io/bty8n/?view_only=f8bb6e5a7698443494d4c3788a45cc0f|The analytic code will be uploaded to OSF upon publishing the manuscript.
3177167|NCT01431963|115376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177168|NCT01431963|115376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177169|NCT01431963|115376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177170|NCT01431963|115376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177171|NCT01431963|115376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177172|NCT00954993||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-029&kw=7009-029&tab=access|
3177173|NCT01853878|116389|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174542|NCT05063708||Statistical Analysis Plan|http://zenodo.org|
3177174|NCT01853878|116389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177175|NCT01853878|116389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174543|NCT01499446|FFA20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174544|NCT01499446|FFA20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181456|NCT00321373|107022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181457|NCT00321373|107022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181458|NCT00321373|107022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181459|NCT00950586|110792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181460|NCT00950586|110792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181461|NCT00950586|110792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181462|NCT00950586|110792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181463|NCT00950586|110792|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181464|NCT00950586|110792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181465|NCT00950586|110792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181466|NCT01476098|114693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181467|NCT01476098|114693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174545|NCT01499446|FFA20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174546|NCT01499446|FFA20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174547|NCT01499446|FFA20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174548|NCT01499446|FFA20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174549|NCT01499446|FFA20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174550|NCT01890863|200260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181468|NCT01476098|114693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181469|NCT01476098|114693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181470|NCT01476098|114693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181471|NCT01476098|114693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181472|NCT01476098|114693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181473|NCT00196976|103533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181474|NCT00196976|103533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181475|NCT00196976|103533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181476|NCT00196976|103533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103533 are summarised with study 103534 on the GSK Clinical Study Register.
3181477|NCT00196976|103533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181478|NCT00196976|103533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181479|NCT01016977|114566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181480|NCT01016977|114566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181481|NCT01016977|114566|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181482|NCT01016977|114566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174551|NCT01890863|200260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177176|NCT01853878|116389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177177|NCT01853878|116389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177178|NCT01853878|116389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177179|NCT01853878|116389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172593|NCT01962467|200284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172594|NCT01962467|200284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172595|NCT01962467|200284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172596|NCT01962467|200284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172597|NCT01160224|114312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172598|NCT01160224|114312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172599|NCT01160224|114312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172600|NCT01160224|114312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172601|NCT01160224|114312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172602|NCT01160224|114312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172603|NCT01160224|114312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172604|NCT01899768|117270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172605|NCT01899768|117270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172606|NCT01899768|117270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172607|NCT01899768|117270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172608|NCT01899768|117270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172609|NCT01899768|117270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172610|NCT01899768|117270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177180|NCT00348309|AVA102672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172611|NCT02968966||Synopsis|http://www.medizin.uni-tuebingen.de/kinder/de/abteilungen/cpcs/projekte/|
3172612|NCT03582969||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
3172613|NCT00469040|B2C108784|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172614|NCT00469040|B2C108784|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172615|NCT00469040|B2C108784|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172616|NCT00469040|B2C108784|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172617|NCT00469040|B2C108784|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172618|NCT00469040|B2C108784|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172619|NCT00469040|B2C108784|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172620|NCT00748306|111834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172621|NCT00748306|111834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172622|NCT00748306|111834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172623|NCT00748306|111834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172624|NCT00748306|111834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172625|NCT00748306|111834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177181|NCT00348309|AVA102672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174552|NCT01890863|200260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174553|NCT01890863|200260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174554|NCT01890863|200260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174555|NCT01890863|200260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174556|NCT01890863|200260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174557|NCT02006602|201011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174558|NCT02006602|201011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174559|NCT02006602|201011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174560|NCT02006602|201011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174561|NCT02006602|201011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174562|NCT02006602|201011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174563|NCT02006602|201011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174564|NCT02257385|116961|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174565|NCT02257385|116961|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174566|NCT02257385|116961|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174567|NCT02257385|116961|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174568|NCT02257385|116961|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174569|NCT02257385|116961|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174570|NCT02257385|116961|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174571|NCT00315731|393229/027|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174572|NCT00315731|393229/027|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174573|NCT00315731|393229/027|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174574|NCT00315731|393229/027|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174575|NCT00315731|393229/027|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174576|NCT00315731|393229/027|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174577|NCT00315731|393229/027|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179083|NCT00264615|LEP103944|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179084|NCT00264615|LEP103944|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179085|NCT00264615|LEP103944|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179086|NCT00264615|LEP103944|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179087|NCT00264615|LEP103944|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179088|NCT00298831||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179089|NCT03112317|REC West (2016-2193)|Study Protocol|https://helseforskning.etikkom.no/komiteerogmoter/vest/sekretariat?region=10796&p_dim=34985&_ikbLanguageCode=us|Study protocol is available on request to Regional Committees for Medical and Health Research Ethics.
3179090|NCT00129259|SDY524|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY524|ImmPort study identifier is SDY524.
3179091|NCT00129259|SDY524|Study summary, -design (and protocol synopsis), adverse events, medications, demographics, lab tests, study files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY524|ImmPort study identifier is SDY524.
3179092|NCT00129259|AbaTE - ITN027AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN027AIDB/Study%20Data/begin.view|TrialShare is the Immune Tolerance Network (ITN) clinical trials research portal that makes data from their clinical trials publicly available without charge.
3179093|NCT00129259|AbaTE-ITN027AI|Study overview and synopsis, -data and reports, -schedule of assessments, -participant flow diagram, -abstracts and manuscripts|http://www.itntrialshare.org/project/Studies/ITN027AIDB/Study%20Data/begin.view|TrialShare is the Immune Tolerance Network (ITN) clinical trials research portal that makes data from their clinical trials publicly available without charge.
3179094|NCT03977844|doi.org/10.3886/E130842V1|Individual Participant Data Set|https://www.openicpsr.org/|Includes redacted, de-identified transcripts of interviews completed in Parts 1 and 3.
3179095|NCT00701389||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-026&kw=0974-026&tab=access|
3179096|NCT01978119|115645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179097|NCT01978119|115645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179098|NCT01978119|115645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179099|NCT01978119|115645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179100|NCT01978119|115645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179101|NCT01978119|115645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179102|NCT01814722||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-266&kw=0518-266&tab=access|
3179103|NCT03105362||Study Protocol|http://www.childrenshospital.org/research-and-innovation/research/research-administration/office-of-clinical-investigation|For further details contact Lissette Jimenez, MD Email: lissette.jimenez@childrens.harvard.edu
3179104|NCT04891679|PATIENT INFORMATION SHEET|Informed Consent Form|https://figshare.com/s/a6c10a2a4be65f30144b|
3179105|NCT04891679|STUDY PROTOCOL|Study Protocol|https://figshare.com/s/3f978a10eee4e90173bb|
3179106|NCT01267071|114136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179107|NCT01267071|114136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179108|NCT01267071|114136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179109|NCT01267071|114136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179110|NCT01267071|114136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179111|NCT01267071|114136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179112|NCT01267071|114136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174578|NCT00979641||Clinical Study Report|http://www.anticancerresearch.com|
3174579|NCT00533312||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3174580|NCT01295320|114825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174581|NCT01295320|114825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174582|NCT01295320|114825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174583|NCT01295320|114825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174584|NCT01295320|114825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174585|NCT01295320|114825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174586|NCT01295320|114825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174587|NCT00000591|TCD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/tcd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174588|NCT00000591||Study Forms|http://biolincc.nhlbi.nih.gov/studies/tcd/|
3174589|NCT00000474|PATHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/paths/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3174590|NCT00000474||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/paths/|
3174591|NCT00000474||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/paths/|
3174592|NCT06498882||Individual Participant Data Set|https://kdocs.cn/l/cftB6eP0xNOu|The authors have full control of all primary data and that they agree to allow other researchers to review their data if requested.
3174593|NCT01887171|10.15825/1995-1191-2015-3-24|Clinical Study Report|http://journal.transpl.ru/vtio/article/view/561/488|
3174594|NCT01887171|10.21614/jtmr-21-2-82|Clinical Study Report|http://www.jtmr.ro/article/portal-and-arterial-flushing-with-htk-and-tacrolimus-can-attenuate-the-incidence-of-early-liver-allograft-dysfunction|
3174595|NCT05244122||Individual Participant Data Set|https://osf.io/hck5n/|This is the Open Science Framework page for these data. The title is Levari Exp. 17: Feedback X Prevalence using dermatology stimuli
3174596|NCT00463697|B2C106996|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174597|NCT00463697|B2C106996|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174598|NCT00463697|B2C106996|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174599|NCT00463697|B2C106996|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174600|NCT00463697|B2C106996|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174601|NCT00463697|B2C106996|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179113|NCT06571357|NEU-2024-Protocol|Study Protocol|https://neu.edu.tr/research/scientific-research-ethics-board/?lang=en|The study protocol will be available through the Near East University research portal. For access, please contact the central research office at Near East University
3179114|NCT02143518||Clinical Study Report|https://gwvru.smhs.gwu.edu/clinical|
3179115|NCT00289796|210602-002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179116|NCT00289796|210602-002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179117|NCT00289796|210602-002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179118|NCT00289796|210602-002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179119|NCT00289796|210602-002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179120|NCT00289796|210602-002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179121|NCT00605241|DAN106593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179122|NCT00605241|DAN106593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179123|NCT00605241|DAN106593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179124|NCT00605241|DAN106593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179125|NCT00605241|DAN106593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179126|NCT00605241|DAN106593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179127|NCT00605241|DAN106593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179128|NCT00797667||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-049&kw=0974-049&tab=access|
3179129|NCT00420680||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179130|NCT00774995|110073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179131|NCT00774995|110073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179132|NCT00774995|110073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179133|NCT00774995|110073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179134|NCT00774995|110073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179135|NCT00774995|110073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179136|NCT00527566|PubMed ID: 20513524|Publication|http://www.ncbi.nlm.nih.gov/pubmed/20513524|"Mepolizumab as a steroid-sparing treatment option in patients with Churg-Strauss syndrome.~Kim S, Marigowda G, Oren E, Israel E, Wechsler ME. J Allergy Clin Immunol. 2010 Jun;125(6):1336-43. doi:10.1016/j.jaci.2010.03.028."
3179137|NCT00379613||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179138|NCT01059617|113483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179139|NCT01059617|113483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179140|NCT01059617|113483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179141|NCT01059617|113483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179142|NCT01059617|113483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179143|NCT01059617|113483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179144|NCT00996996|104517|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179145|NCT00996996|104517|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179146|NCT00996996|104517|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179147|NCT00996996|104517|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181483|NCT01016977|114566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181484|NCT01016977|114566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181485|NCT01016977|114566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179148|NCT00996996|104517|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179149|NCT00996996|104517|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179150|NCT00996996|104517|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179151|NCT00000463|CABG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/cabg/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3179152|NCT02207829|201316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179153|NCT02207829|201316|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179154|NCT02207829|201316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179155|NCT02207829|201316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179156|NCT02207829|201316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179157|NCT02207829|201316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179158|NCT02207829|201316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179159|NCT00560833||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06459&kw=P06459&tab=access|
3179160|NCT02701218|ENT-2558-03601|Study Protocol|http://ros.med.cmu.ac.th/Security/SignIn.aspx|Research administration section website
3179161|NCT00263666|444563/022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179162|NCT00263666|444563/022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179163|NCT00263666|444563/022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179164|NCT00263666|444563/022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179165|NCT00263666|444563/022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179166|NCT00263666|444563/022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179167|NCT06633263||Study Protocol|https://osf.io/dhmj8/|
3179168|NCT06633263||Individual Participant Data Set|https://osf.io/dhmj8/|
3179169|NCT03793101||Clinical Study Report|http://eyemed.pl|
3179170|NCT02019719|116099|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177182|NCT00348309|AVA102672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177183|NCT00348309|AVA102672|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177184|NCT00348309|AVA102672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177185|NCT00348309|AVA102672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177186|NCT00348309|AVA102672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177187|NCT00871338|111709|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177188|NCT00871338|111709|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177189|NCT00871338|111709|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177190|NCT00871338|111709|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177191|NCT00871338|111709|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177192|NCT00871338|111709|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177193|NCT00871338|111709|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177194|NCT01112787|114571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177195|NCT01112787|114571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177196|NCT01112787|114571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177197|NCT01112787|114571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177198|NCT01112787|114571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177199|NCT01112787|114571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177200|NCT01112787|114571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177201|NCT00532298|110620|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177202|NCT00532298|110620|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172626|NCT00748306|111834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172627|NCT00419237|FFA10013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172628|NCT00419237|FFA10013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172629|NCT00419237|FFA10013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172630|NCT00419237|FFA10013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172631|NCT00419237|FFA10013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181486|NCT00363870|108134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181487|NCT00363870|108134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172632|NCT00419237|FFA10013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172633|NCT00419237|FFA10013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172634|NCT01722903||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25807199|
3172635|NCT00345956|105722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172636|NCT00345956|105722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172637|NCT00345956|105722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172638|NCT00345956|105722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172639|NCT00345956|105722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172640|NCT00345956|105722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172641|NCT05859906||Clinical Study Report|http://doi.org/10.1093/bjaceaccp/mkh037|
3172642|NCT00732472|105211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172643|NCT00732472|105211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172644|NCT00732472|105211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172645|NCT00732472|105211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172646|NCT00732472|105211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172647|NCT00732472|105211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172648|NCT00732472|105211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172649|NCT00964249|112017|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172650|NCT00964249|112017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172651|NCT00964249|112017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172652|NCT00964249|112017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172653|NCT00964249|112017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172654|NCT00515099|START ITN028AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN028AIPUBLIC/Study%20Data/begin.view?|START ITN028AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
3172655|NCT00515099|START ITN028AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN028AIPUBLIC/Study%20Data/begin.view?pageId=study.PARTICIPANTS|START ITN028AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
3172656|NCT00515099|START ITN028AI|Study overview, -data and reports, -manuscripts and abstracts, -availability of biospecimens, et al|https://www.itntrialshare.org/project/Studies/ITN028AIPUBLIC/Study%20Data/begin.view?|START ITN028AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
3172657|NCT00772889|111738|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172658|NCT00772889|111738|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172659|NCT00772889|111738|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172660|NCT00772889|111738|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172661|NCT00772889|111738|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177203|NCT00532298|110620|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177204|NCT00532298|110620|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172662|NCT00772889|111738|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172663|NCT00772889|111738|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172664|NCT00985140||Peer reviewed article with pooled results.|https://www.ncbi.nlm.nih.gov/pubmed/25476993|This publication contains data from this study as well as two other clinical trials. Analysis was done on data pooled from the three trials.
3177205|NCT00532298|110620|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177206|NCT00532298|110620|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177207|NCT00532298|110620|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177208|NCT04153916|0266-19-TLV|Study Protocol|http://www.neurotrigger.info|Upon completion of the study, results will be published and the study data will be available from the PI
3177209|NCT00296140||Clinical Study Report|https://link.springer.com/article/10.1007/s13142-011-0070-y|Publication: Damush TM, Ofner S, Yu Z, Nicholas G, Williams LS. Implementation of a stroke self-management program. Translational Behavioral Medicine 2011;1:561-572
3177210|NCT02964767||Epidemiological report|http://www.who.int|
3177211|NCT02964767||Clinical Study Report|http://www.Wiley.com|
3177212|NCT00383162|TRX106571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177213|NCT00383162|TRX106571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177214|NCT00383162|TRX106571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177215|NCT00383162|TRX106571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181488|NCT00363870|108134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172665|NCT01808365|114991|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172666|NCT01808365|114991|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172667|NCT01808365|114991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172668|NCT01808365|114991|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172669|NCT01808365|114991|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172670|NCT01808365|114991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172671|NCT01808365|114991|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172672|NCT00034697||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172673|NCT02202161|201351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172674|NCT02202161|201351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172675|NCT02202161|201351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172676|NCT02202161|201351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172677|NCT02202161|201351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172678|NCT02202161|201351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172679|NCT02202161|201351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172680|NCT01086449|113819|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172681|NCT01086449|113819|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172682|NCT01086449|113819|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172683|NCT01086449|113819|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172684|NCT01086449|113819|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172685|NCT01086449|113819|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172686|NCT01086449|113819|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181489|NCT00363870|108134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181490|NCT00363870|108134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181491|NCT00363870|108134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181492|NCT00363870|108134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181493|NCT01323972|113398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181494|NCT01323972|113398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181495|NCT01323972|113398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181496|NCT01323972|113398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181497|NCT01323972|113398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181498|NCT01323972|113398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181499|NCT00353288|105908|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181500|NCT00353288|105908|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181501|NCT00353288|105908|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172687|NCT00290355|249553/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181502|NCT00353288|105908|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177216|NCT00383162|TRX106571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177217|NCT00383162|TRX106571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177218|NCT00383162|TRX106571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177219|NCT00500955|BRL-49653/137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177220|NCT00500955|BRL-49653/137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177221|NCT00500955|BRL-49653/137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177222|NCT00500955|BRL-49653/137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177223|NCT00500955|BRL-49653/137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177224|NCT00500955|BRL-49653/137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174602|NCT00463697|B2C106996|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175824|NCT01431976|115377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175825|NCT01431976|115377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175826|NCT01431976|115377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175827|NCT01431976|115377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175828|NCT01431976|115377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175829|NCT02035540||Study results|http://pubmed.ncbi.nlm.nih.gov/30879050/|
3175830|NCT01725672|116806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175831|NCT01725672|116806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175832|NCT01725672|116806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175833|NCT01725672|116806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175834|NCT01725672|116806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175835|NCT01725672|116806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175836|NCT01725672|116806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175837|NCT00687700|MAB110553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175838|NCT00687700|MAB110553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175839|NCT00687700|MAB110553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175840|NCT00687700|MAB110553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175841|NCT00687700|MAB110553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175842|NCT00687700|MAB110553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175843|NCT00687700|MAB110553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175844|NCT00090103|ARI40005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175845|NCT00090103|ARI40005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175846|NCT00090103|ARI40005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175847|NCT00090103|ARI40005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175848|NCT00090103|ARI40005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179171|NCT02019719|116099|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179172|NCT02019719|116099|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179173|NCT02019719|116099|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179174|NCT02019719|116099|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175849|NCT00090103|ARI40005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175850|NCT00090103|ARI40005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175851|NCT01134042|106829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175852|NCT01134042|106829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175853|NCT01134042|106829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175854|NCT01134042|106829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175855|NCT01134042|106829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175856|NCT01134042|106829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177225|NCT01053988|112206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177226|NCT01053988|112206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177227|NCT01053988|112206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177228|NCT01053988|112206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177229|NCT01053988|112206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177230|NCT01053988|112206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177231|NCT01053988|112206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177232|NCT00326248|NKT102553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177233|NCT00326248|NKT102553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177234|NCT00326248|NKT102553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177235|NCT00326248|NKT102553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177236|NCT00326248|NKT102553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177237|NCT00326248|NKT102553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177238|NCT00326248|NKT102553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177239|NCT00274677|SCA100223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177240|NCT00274677|SCA100223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177241|NCT00274677|SCA100223|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177242|NCT00274677|SCA100223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177243|NCT00274677|SCA100223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179175|NCT02019719|116099|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177244|NCT00274677|SCA100223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177245|NCT00274677|SCA100223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177246|NCT00240500|100448|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172688|NCT00290355|249553/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172689|NCT00290355|249553/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172690|NCT00290355|249553/004|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172691|NCT00290355|249553/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172692|NCT00290355|249553/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172693|NCT00290355|249553/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172694|NCT00686699||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04628&kw=P04628&tab=access|
3172695|NCT07317362||linical Data warehouse of Greater Paris University hospitals (Entrepôt de Données de Santé - EDS AP-HP )|https://eds.aphp.fr/|
3172696|NCT00067444|29060/874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172697|NCT00067444|29060/874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172698|NCT00067444|29060/874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172699|NCT00067444|29060/874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172700|NCT00067444|29060/874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172701|NCT00067444|29060/874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172702|NCT00518336|109616 (Y7)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172703|NCT00518336|109616 (Y7)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172704|NCT00518336|109616 (Y7)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 109624 are summarised with studies 109616 and 109625 on the GSK Clinical Study Register.
3172705|NCT00518336|109616 (Y7)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172706|NCT00518336|109616 (Y7)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172707|NCT00518336|109616 (Y7)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172708|NCT00829010|111634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172709|NCT00829010|111634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172710|NCT00829010|111634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172711|NCT00829010|111634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172712|NCT00829010|111634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172713|NCT00829010|111634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172714|NCT00829010|111634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172715|NCT01071369||Clinical Study Report|http://painphysicianjournal.com/current/pdf?article=MTk3Nw%3D%3D&journal=77|A Randomized, Double-Blind, Active Control Trial of Fluoroscopic Cervical Interlaminar Epidural Injections in Chronic Pain of Cervical Disc Herniation: Results of a 2-Year Follow-Up
3172716|NCT01021553|109059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172717|NCT01021553|109059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172718|NCT01021553|109059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172719|NCT01021553|109059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172720|NCT01021553|109059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172721|NCT01021553|109059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172722|NCT01021553|109059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172723|NCT02685839||Clinical Study Report|http://goo.gl/FilVtL|
3172724|NCT07100275|Supervisory authority|Study Protocol|https://bingolism.saglik.gov.tr/|The management that gives the necessary permission in the hospital where the study will be conducted
3172725|NCT07058831|British Sanatorium CIC|Study Protocol|https://www.cicbritanico.com.ar/|data will be at the website.You are reporting that the URL does not appear to link to a functioning web page. But the URL is wotking
3172726|NCT01619176|GSE59526|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/geo|
3172727|NCT05399836||Study Protocol|https://osf.io/hx75k/|Protocol on the Open Science Framework (OSF)
3172728|NCT05399836||Statistical Analysis Plan|https://osf.io/hx75k/|
3172729|NCT05399836||Individual Participant Data Set|https://osf.io/hx75k/|The study protocol and statistical analysis plan were pre-registered on the OSF prior to starting recruitment. Participant dataset (anonymised) will be made available when results are published.
3172730|NCT04746027||Study Protocol|https://www.stmarys.ac.uk/staff-directory/jonathan-nixon|
3172731|NCT00329459|TRX105850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172732|NCT00329459|TRX105850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172733|NCT00329459|TRX105850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174603|NCT00307021|105874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174604|NCT00307021|105874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174605|NCT00307021|105874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174606|NCT00307021|105874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174607|NCT00307021|105874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174608|NCT00307021|105874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181503|NCT00353288|105908|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181504|NCT00353288|105908|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181505|NCT06729515||Individual Participant Data Set|https://figshare.com/s/46ea85c406ec97afc17a|
3181506|NCT00071747|SCA30926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172734|NCT00329459|TRX105850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172735|NCT00329459|TRX105850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174609|NCT01332292|102942|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174610|NCT01332292|102942|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174611|NCT01332292|102942|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174612|NCT01332292|102942|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174613|NCT01332292|102942|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174614|NCT01332292|102942|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174615|NCT01332292|102942|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174616|NCT00306995|102499|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174617|NCT00306995|102499|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174618|NCT00306995|102499|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174619|NCT00306995|102499|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174620|NCT00306995|102499|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174621|NCT01744301|CSR Study Report Synopsis|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7112&studyid=674&filename=D9612N00017_Seizure_Study_report_synopsis_FINAL_redacted.pdf|D9612N00017\_Seizure\_Study\_report\_synopsis\_FINAL\_redacted
3174622|NCT00562848|MOT107043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174623|NCT00562848|MOT107043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174624|NCT00562848|MOT107043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174625|NCT00562848|MOT107043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174626|NCT00562848|MOT107043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174627|NCT00562848|MOT107043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174628|NCT00562848|MOT107043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174629|NCT00511823|NKV110483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174630|NCT00511823|NKV110483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181507|NCT00071747|SCA30926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181508|NCT00071747|SCA30926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172736|NCT00329459|TRX105850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172737|NCT00329459|TRX105850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174631|NCT00511823|NKV110483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174632|NCT00511823|NKV110483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174633|NCT00511823|NKV110483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174634|NCT00511823|NKV110483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174635|NCT00511823|NKV110483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174636|NCT01198769|114351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177247|NCT00240500|100448|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177248|NCT00240500|100448|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177249|NCT00240500|100448|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177250|NCT00240500|100448|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177251|NCT01140061||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-020&kw=0873-020&tab=access|
3177252|NCT02371603|200229|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177253|NCT02371603|200229|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177254|NCT02371603|200229|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177255|NCT02371603|200229|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177256|NCT02371603|200229|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177257|NCT02371603|200229|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177258|NCT03191227||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22984148|Cohort profile
3177259|NCT06040853|doi: 10.1371|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28282425/|
3172738|NCT05839236|10.5281/zenodo.7883407|Individual Participant Data Set|https://doi.org/10.5281/zenodo.7856000|The identifier is reserved and the repository team is helping solving the technical issues in updating the data with the renewed identifier.
3172739|NCT00998985||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-004&kw=5172-004&tab=access|
3172740|NCT01021293|112679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172741|NCT01021293|112679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174637|NCT01198769|114351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174638|NCT01198769|114351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174639|NCT01198769|114351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174640|NCT01198769|114351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181509|NCT00071747|SCA30926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181510|NCT00071747|SCA30926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181511|NCT00071747|SCA30926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181512|NCT01711723|115676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181513|NCT01711723|115676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181514|NCT01711723|115676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181515|NCT01711723|115676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181516|NCT01711723|115676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181517|NCT01711723|115676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181518|NCT01711723|115676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181519|NCT01602562|116100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172742|NCT01021293|112679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172743|NCT01021293|112679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172744|NCT01021293|112679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172745|NCT01021293|112679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172746|NCT02356770|PMID: 27310522|1. Publication|https://www.ncbi.nlm.nih.gov/pubmed/27310522|A first publication was published concerning the primary outcome of the transmucosal measurements.
3172747|NCT02356770|PMID: 28107560|2. publicaton|https://www.ncbi.nlm.nih.gov/pubmed/28107560|2\. publication concerning the volumetric changes of the soft tissue
3172748|NCT07100288||preprint|https://www.researchsquare.com/article/rs-283444/v1|
3172749|NCT00354991||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181520|NCT01602562|116100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181521|NCT01602562|116100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181522|NCT01602562|116100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172750|NCT00005128|LRC-PS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lrcps/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172751|NCT00005128||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrcps/|
3172752|NCT01760356|PMID: 25142246|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25142246|Tacrolimus pharmacodynamics and pharmacogenetics along the calcineurin pathway in human lymphocytes.
3172753|NCT01760356|PMID: 29054923|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/29054923|Activity of the Calcineurin Pathway in Patients on the Liver Transplantation Waiting List: Factors of Variability and Response to Tacrolimus Inhibition.
3172754|NCT03717727||Metadata|https://doi.org/10.17011/jyx/dataset/85350|Metadata published in the Jyväskylä University Digital Repository. Heinonen A, Janhunen M, Aartolahti E, et al. Metadata from: Gamification in Knee Replacement Rehabilitation (BEE-RCT)
3172755|NCT01371799|113746|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172756|NCT01371799|113746|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172757|NCT01371799|113746|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172758|NCT01371799|113746|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172759|NCT01371799|113746|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172760|NCT01371799|113746|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172761|NCT02896686||Study Protocol|https://cirurgiahj23.wordpress.com|
3172762|NCT00750360|218352/054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172763|NCT00750360|218352/054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172764|NCT00750360|218352/054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172765|NCT00750360|218352/054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172766|NCT00750360|218352/054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172767|NCT00750360|218352/054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172768|NCT01428479|115070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172769|NCT01428479|115070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172770|NCT01428479|115070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172771|NCT01428479|115070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172772|NCT01428479|115070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172773|NCT01428479|115070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172774|NCT05327309||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/22456397/|
3172775|NCT05386641|18192154|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3172776|NCT05386641|25977305|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3172777|NCT05386641|26079868|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3172778|NCT05386641|29332760|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3172779|NCT05386641|32031629|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3172780|NCT05386641|32767329|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3172781|NCT05386641||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3172782|NCT00989664|104504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172783|NCT00989664|104504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172784|NCT00989664|104504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172785|NCT00989664|104504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172786|NCT00989664|104504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172787|NCT00989664|104504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172788|NCT00989664|104504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172789|NCT02671786||Pilot Study Research Paper|http://www.worldwidejournals.com/ijar/file.php?val=April_2015_1427896145__152.pdf|
3172790|NCT01469299||Publication|https://www.ncbi.nlm.nih.gov/pubmed/24269069|6-Month Report: Guske et al. A New Method for Defining Balance: Promising Short-term outcomes of Sensor-Guided TKA. J Arthroplasty. 2014 May;29(5):955-60
3172791|NCT01469299||Publication|https://www.ncbi.nlm.nih.gov/pubmed/25210632|1-year Report: Gustke et al. Primary TKA patients with Quantifiably Balanced Soft-Tissue Achieve Significant Clinical Gains Sooner than Unbalanced Patients. Adv Orthop. 2014:628695
3172792|NCT01213849|102932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172793|NCT01213849|102932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172794|NCT01213849|102932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172795|NCT01213849|102932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174641|NCT01198769|114351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174642|NCT01198769|114351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174643|NCT03718832|doi:10.7910/DVN/LZUTU0|Individual Participant Data Set|https://doi.org/10.7910/DVN/LZUTU0|
3174644|NCT03718832|doi:10.7910/DVN/LZUTU0|Analytic Code|https://doi.org/10.7910/DVN/LZUTU0|
3174645|NCT02360215|NCT02360215|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3174646|NCT00696423|111535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174647|NCT00696423|111535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174648|NCT00696423|111535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172796|NCT01213849|102932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172797|NCT01213849|102932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172798|NCT01213849|102932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174649|NCT00696423|111535|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174650|NCT00696423|111535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174651|NCT00696423|111535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174652|NCT00696423|111535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174653|NCT06086106|70130623|Individual Participant Data Set|https://www.moh.gov.bh/Contact/SMC|This study was ethically approved by the Research and Research Ethics Committee Government Hospitals, Salmaniya Medical Complex (SMC), Kingdom of Bahrain, institution review board, (IRB) approval number: 70130623, which includes the use of patient data for research and educational purposes was obtained from all the patients/control's parents/guardians before the intervention. This study followed the guidelines laid down in the Declaration of Helsinki of 1975, and as revised in Edinburgh 2000.
3174654|NCT02836002||Individual Participant Data Set|https://datadryad.org//resource/doi:10.5061/dryad.60h41|
3174655|NCT07192640||Study Protocol|https://doi.org/10.1590/acb370702|https://doi.org/10.1590/acb370702
3174656|NCT00810667|2008-001441-26|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-001441-26/results|
3179176|NCT02019719|116099|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179177|NCT02824068||Clinical Study Report|https://link.springer.com/article/10.1007/s00415-021-10409-9|Open access of the full study report can be downloaded under above webpage of the Journal of Neurology
3179178|NCT01319006|114703|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179179|NCT01319006|114703|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179180|NCT01319006|114703|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179181|NCT01319006|114703|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179182|NCT01319006|114703|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179183|NCT01319006|114703|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179184|NCT01319006|114703|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179185|NCT00941603||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05675&kw=P05675&tab=access|
3179186|NCT01476046|110951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179187|NCT01476046|110951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179188|NCT01476046|110951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179189|NCT01476046|110951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179190|NCT01476046|110951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179191|NCT01476046|110951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174657|NCT03494712||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3174658|NCT03494712||Study Protocol|https://clinicaltrials.servier.com/|
3174659|NCT03494712||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3174660|NCT03494712||Informed Consent Form|https://clinicaltrials.servier.com/|
3174661|NCT03494712||Clinical Study Report|https://clinicaltrials.servier.com/|
3174662|NCT03494712||study-level clinical trial data|https://clinicaltrials.servier.com/|
3179192|NCT01476046|110951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179193|NCT00550225|MAB108115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179194|NCT00550225|MAB108115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179195|NCT00550225|MAB108115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174663|NCT01557504||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-296&kw=0431A-296&tab=access|
3174664|NCT01110018|112008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179196|NCT00550225|MAB108115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179197|NCT00550225|MAB108115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179198|NCT00550225|MAB108115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179199|NCT00550225|MAB108115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179200|NCT03331120|Neck pain,Ambulatory,Orthotic|Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-019-3337-0|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-019-3337-0
3179201|NCT06635343||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28990891|
3179202|NCT00345579|105987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172799|NCT00381472|101468/169|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172800|NCT00381472|101468/169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172801|NCT00381472|101468/169|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174665|NCT01110018|112008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172802|NCT00381472|101468/169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172803|NCT00381472|101468/169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172804|NCT00381472|101468/169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172805|NCT00381472|101468/169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172806|NCT04308668||Individual Participant Data Set|http://www.covidpep.umn.edu/data|
3172807|NCT02619942||Study Protocol|http://www.trialsjournal.com/content/17/1/582|
3172808|NCT01979250||Manuscript|http://www.ncbi.nlm.nih.gov/pubmed/27273977|To acces the results, please go to the above mentioned manuscript.
3172809|NCT02135848|114272|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172810|NCT02135848|114272|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174666|NCT01110018|112008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172811|NCT02135848|114272|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172812|NCT02135848|114272|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172813|NCT02135848|114272|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172814|NCT02135848|114272|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172815|NCT02135848|114272|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172816|NCT00115622|FFR30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172817|NCT00115622|FFR30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172818|NCT00115622|FFR30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172819|NCT00115622|FFR30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172820|NCT00115622|FFR30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172821|NCT00115622|FFR30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172822|NCT00115622|FFR30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172823|NCT00104299|SDY91|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY91|ImmPort study identifier is SDY91.
3172824|NCT00104299|SDY91|Study summary, -design, -adverse event(s), -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -mechanistic assays, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY91|ImmPort study identifier is SDY91.
3172825|NCT00104299|ITN021AI|Individual Participant Data Set|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
3172826|NCT00104299|ITN021AI|Study overview, -data and reports, -participant list, -manuscripts and abstracts, -availability of biospecimens.|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
3172827|NCT04340804||Study Protocol|https://osf.io/k369t/|
3172828|NCT04340804||Statistical Analysis Plan|https://osf.io/k369t/|
3179203|NCT00345579|105987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172829|NCT04340804||Informed Consent Form|https://osf.io/k369t/|
3172830|NCT04340804||Individual Participant Data Set|https://osf.io/k369t/|When results will be published
3172831|NCT00591786||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172832|NCT01733758|113121|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174667|NCT01110018|112008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174668|NCT01110018|112008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174669|NCT01110018|112008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174670|NCT01110018|112008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174671|NCT00070564||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3179204|NCT00345579|105987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179205|NCT00345579|105987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179206|NCT00345579|105987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174672|NCT01563042|114594|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174673|NCT01563042|114594|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174674|NCT01563042|114594|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174675|NCT01563042|114594|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179207|NCT00345579|105987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179208|NCT05166018|SUMO|Individual Participant Data Set|https://sumo.doc.cortexxmi.com/|
3179209|NCT02679690||Informed Consent Form|http://www.osiris.pitt.edu|
3179210|NCT00920192|111645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179211|NCT00920192|111645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179212|NCT00920192|111645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179213|NCT00920192|111645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179214|NCT00920192|111645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179215|NCT00920192|111645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179216|NCT06333444||Informed Consent Form|https://docs.google.com/forms/d/e/1FAIpQLScX9N2R8xP62390ly7vV8Ixyy_yfQsUUmUG3QCm_M-ZriXAnA/viewform|
3179217|NCT02322671|200107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174676|NCT01563042|114594|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174677|NCT01563042|114594|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179218|NCT02322671|200107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179219|NCT02322671|200107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179220|NCT02322671|200107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179221|NCT02322671|200107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179222|NCT02322671|200107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179223|NCT02322671|200107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179224|NCT02676479||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/4037016|
3179225|NCT01930773||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26365936|"Study design and rationale for Optimal aNtiplatelet pharmacotherapy guided by bedSIDE genetic or functional TESTing in elective percutaneous coronary intervention patients (ONSIDE TEST): a prospective, open-label, randomised parallel-group multicentre trial (NCT01930773).~Kołtowski Ł, Aradi D, Huczek Z, Tomaniak M, Sibbing D, Filipiak KJ, Kochman J, Balsam P, Opolski G.~Kardiol Pol. 2016;74(4):372-9. doi: 10.5603/KP.a2015.0172."
3179226|NCT01930773||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/28281736|"Optimal aNtiplatelet pharmacotherapy guided by bedSIDE genetic or functional TESTing in elective PCI patients: A pilot study: ONSIDE TEST pilot.~Koltowski L, Tomaniak M, Aradi D, Huczek Z, Filipiak KJ, Kochman J, Gajda S, Balsam P, Opolski G.~Cardiol J. 2017 Mar 10. doi: 10.5603/CJ.a2017.0026. \[Epub ahead of print\]"
3179227|NCT00345904|107507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179228|NCT00345904|107507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179229|NCT00345904|107507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179230|NCT00345904|107507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179231|NCT00345904|107507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179232|NCT01090453|113615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179233|NCT01090453|113615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179234|NCT01090453|113615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179235|NCT01090453|113615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174678|NCT01563042|114594|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174679|NCT01847404|116480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174680|NCT01847404|116480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174681|NCT01847404|116480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174682|NCT01847404|116480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174683|NCT01847404|116480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174684|NCT01847404|116480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174685|NCT01254643||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-008&kw=V503-008&tab=access|
3174686|NCT07034820||Study Protocol|https://kecioutdoor.com.tr/category/nimsai-academia/|Access is subject to ethical approval of the research proposal by the Nimsai Academia Ethics Committee and the execution of a Data Use Agreement. Researchers must agree to use the data solely for scientific research and to respect participant privacy.
3174687|NCT03173209|Calm Moments Cards program|intervention materials|http://www.everymomentcounts.org|Calm Moments Cards program
3174688|NCT06968286||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/39758269/|
3174689|NCT00695305|LP2105521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174690|NCT00695305|LP2105521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174691|NCT00695305|LP2105521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174692|NCT00695305|LP2105521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174693|NCT00695305|LP2105521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174694|NCT00695305|LP2105521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174695|NCT00695305|LP2105521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174696|NCT00197171|100386 (EXT Y5)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174697|NCT00197171|100386 (EXT Y5)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174698|NCT00197171|100386 (EXT Y5)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100386 are summarised with study 100387 on the GSK Clinical Study Register.
3174699|NCT00197171|100386 (EXT Y5)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174700|NCT00197171|100386 (EXT Y5)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174701|NCT00005235||NCBI website|http://www.ncbi.nlm.nih.gov/pubmed/8353919|
3174702|NCT00779935||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3174703|NCT07192172|No. 1611-124-811|Study Protocol|http://cris.snuh.org|http://cris.snuh.org
3174704|NCT01551771|115802|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174705|NCT01551771|115802|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174706|NCT01551771|115802|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174707|NCT01551771|115802|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174708|NCT01551771|115802|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174709|NCT01551771|115802|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174710|NCT01551771|115802|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179236|NCT01090453|113615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174711|NCT06676878||Study Protocol|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
3174712|NCT06676878||Informed Consent Form|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
3174713|NCT00485732|107291|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181523|NCT01055379|2009-011144-19|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2009-011144-19/results|
3181524|NCT00675090|H3B109689|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181525|NCT00675090|H3B109689|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181526|NCT00675090|H3B109689|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181527|NCT00675090|H3B109689|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181528|NCT00675090|H3B109689|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181529|NCT00675090|H3B109689|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181530|NCT00675090|H3B109689|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181531|NCT01395888|115247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181532|NCT01395888|115247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181533|NCT01395888|115247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181534|NCT01395888|115247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181535|NCT01395888|115247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181536|NCT01395888|115247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181537|NCT01395888|115247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181538|NCT02549014||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-001&kw=1064-001&tab=access|
3181539|NCT02437253||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=28119823|
3174714|NCT00485732|107291|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174715|NCT00485732|107291|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174716|NCT00485732|107291|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174717|NCT00485732|107291|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174718|NCT00485732|107291|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174719|NCT00485732|107291|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174720|NCT00471081|109375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174721|NCT00471081|109375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174722|NCT00471081|109375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174723|NCT00471081|109375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174724|NCT00471081|109375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174725|NCT00471081|109375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174726|NCT00471081|109375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172833|NCT01733758|113121|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172834|NCT01733758|113121|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172835|NCT01733758|113121|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172836|NCT01733758|113121|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172837|NCT01733758|113121|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172838|NCT01733758|113121|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172839|NCT00090246||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3172840|NCT00965458|SDY797|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797.
3172841|NCT00965458|SDY797|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797. The study protocol is located under the design tab.
3172842|NCT00965458|SDY797|Study summary, -design, -adverse event(s), -demographics, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797.ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public. Data shared through ImmPort has been provided by NIH-funded programs, other research organizations and individual scientists ensuring these discoveries will be the foundation of future research.
3172843|NCT00965458|T1DAL ITN045AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
3172844|NCT00965458|T1DAL ITN045AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
3172845|NCT00965458|T1DAL ITN045AI|Study overview, -data and reports, -schedule of assessments, -study design, -original article & abstracts et al.|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3172846|NCT00635804||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3281-002&kw=3281-002&tab=access|
3174727|NCT01822639|116798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174728|NCT01822639|116798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174729|NCT01822639|116798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174730|NCT01822639|116798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172847|NCT02084316|CTN0056|Study Protocol|http://ctndisseminationlibrary.org/protocols/ctn0056.htm|
3172848|NCT00000565|IPPB|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/ippb/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172849|NCT00000565||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ippb/|
3172850|NCT00000565||Study Forms|http://biolincc.nhlbi.nih.gov/studies/ippb/|
3172851|NCT00000565||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/ippb/|
3172852|NCT00346775|FFR105693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172853|NCT00346775|FFR105693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172854|NCT00346775|FFR105693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172855|NCT00346775|FFR105693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172856|NCT00346775|FFR105693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172857|NCT00346775|FFR105693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172858|NCT00346775|FFR105693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172859|NCT00517634|HZA109912|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172860|NCT00517634|HZA109912|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172861|NCT00517634|HZA109912|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172862|NCT00517634|HZA109912|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172863|NCT00517634|HZA109912|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172864|NCT00517634|HZA109912|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172865|NCT00517634|HZA109912|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172866|NCT00539825|AC6108697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172867|NCT00539825|AC6108697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172868|NCT00539825|AC6108697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172869|NCT00539825|AC6108697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172870|NCT00539825|AC6108697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172871|NCT00539825|AC6108697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172872|NCT00539825|AC6108697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172873|NCT00422955|49653/376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172874|NCT00422955|49653/376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172875|NCT00422955|49653/376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172876|NCT00422955|49653/376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174731|NCT01822639|116798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174732|NCT01822639|116798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174733|NCT01822639|116798|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174734|NCT03411161||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3174735|NCT03411161||Study Protocol|https://clinicaltrials.servier.com/|
3177260|NCT01324362|SAM40065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177261|NCT01324362|SAM40065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177262|NCT01324362|SAM40065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177263|NCT01324362|SAM40065|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177264|NCT01324362|SAM40065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177265|NCT01324362|SAM40065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177266|NCT01324362|SAM40065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177267|NCT03214068||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282811/|
3177268|NCT03049917|Current FIT Protocol|Study Protocol|https://depts.washington.edu/globalwach/wordpress/wp-content/uploads/2020/12/2.18.18-FIT-Protocol_V4.0_clean_.pdf|
3177269|NCT05229185||Study Protocol|https://kuleuven-my.sharepoint.com/:b:/g/personal/marjan_coremans_kuleuven_be/EVK-M1j5Ax9GjNEFv1mk_NMB-YFjnBVTAR1V4FTJx5sc1w?e=3HuBGr|Find the document using the link above.
3177270|NCT05229185||Informed Consent Form|https://kuleuven-my.sharepoint.com/:b:/g/personal/marjan_coremans_kuleuven_be/EVB9pKxi-X5Mk5YjAqkTgoQByjOoqnPA8ccpmHqFrX-WMg?e=zGCWri|Find the document using the link above.
3177271|NCT04593108||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/m/pubmed/?term=Misoprostol+with+or+without+letrozole+in+treatment+of+missed+miscarriage+in+first+trimester+%5BJour%5D+AND+2018%5Bpdat%5D|"Albrecht ED, Aberdeen GW, Pepe GJ, (2000). The role of estrogen in the maintenance of primate pregnancy. Am J Obstet Gynecol. 182:432-8.~Albrecht ED, Robb VA, Pepe GJ, (2004). Regulation of placental vascular endothelial growth permeability factor expression and angiogenesis by estrogen during early baboon pregnancy. J Clin Endocrinol Metab. 89:"
3177272|NCT05347836||Study Protocol|https://www.degruyter.com/document/doi/10.1515/jpem-2015-0340/html|
3177273|NCT01870115||Publication|http://www.aging-us.com/article/101158|
3177274|NCT02636205|25014045|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25014045|
3177275|NCT02636205|21261965|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/?term=The+Armeo+Spring+as+training+tool+to+improve+upper+limb+functionality+in+multiple+sclerosis%3A+a+pilot+study|
3177276|NCT04119180||Study Protocol|https://bmcoralhealth.biomedcentral.com/articles/10.1186/s12903-021-01594-0|
3177277|NCT00799903|100601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174736|NCT03411161||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3174737|NCT03411161||Informed Consent Form|https://clinicaltrials.servier.com/|
3177278|NCT00799903|100601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177279|NCT00799903|100601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177280|NCT00799903|100601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177281|NCT00799903|100601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177282|NCT00799903|100601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177283|NCT00799903|100601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174738|NCT03411161||Clinical Study Report|https://clinicaltrials.servier.com/|
3174739|NCT03411161||study-level clinical trial data|https://clinicaltrials.servier.com/|
3174740|NCT00811967||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3174741|NCT00422604|AC2106956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174742|NCT00422604|AC2106956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174743|NCT00422604|AC2106956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174744|NCT00422604|AC2106956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174745|NCT00422604|AC2106956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174746|NCT00422604|AC2106956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174747|NCT00422604|AC2106956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174748|NCT04616612||Statistics|https://www.niddk.nih.gov/health-information/health-statistics/kidney-disease|US Department of Health \& Human Services. Kidney disease statistics for the United States. Bethesda, MD: National Kidney and Urologic Diseases Information Clearinghouse, National Institutes of Health. 2011.
3174749|NCT04616612||Clinical Study Report|https://kdigo.org/wp-content/uploads/2016/10/KDIGO-2012-Blood-Pressure-Guideline-English.pdf|KDIGO. Kidney Disease: Improving global outcomes blood pressure work group, KDIGO clinical practice guideline for the management of blood pressure in chronic kidney disease. Kidney International. 2012;Suppl. 2(5):337-414.
3174750|NCT04616612||Clinical Study Report|https://www.niddk.nih.gov/|National Institute of Diabetes and Digestive and Kidney Diseases. High Blood Pressure and Kidney Disease. In. NIH Publication No. 14-4572 ed. Bethesda, MD: National Kidney and Urologic Diseases Information Clearinghouse (NKUDIC); 2014:12.
3174751|NCT04616612||Pamphlet|https://www.nhlbi.nih.gov/resources/brief-your-guide-healthy-sleep-fact-sheet|U.S. Department of Health and Human Services. National Institutes of Health. In Brief: Your Guide to Healthy Sleep. In. Vol NIH Publication No. 11-5800. Bethesda, MA: NHLBI Health Information Center; 2011:1-4.
3174752|NCT04616612||Education|https://www.kidney.org/nutrition/Kidney-Disease-Stages-1-4|National Kidney Foundation. Nutrition and Chronic Kidney Disease (Stages 1-4). Are You Getting What You Need? In. Vol 11-10-1811\_HBE. 11-10-1811\_HBE ed. New York, NY: National Kidney Foundation; 2013-2014:1-28.
3174753|NCT04616612||Education|https://www.kidney.org/atoz/content/Diabetes-and-Kidney-Disease-Stages1-4|National Kidney Foundation. Hidden health risks: Kidney Disease, Diabetes, and High Blood Pressure. In. Vol 11-10-1811\_HBE. New York, NY: National Kidney Foundation 2014:1-20.
3174754|NCT07097649||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/33946001/|
3174755|NCT06881329|GSE290201|Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE290201|Gene Expression Omnibus repository
3174756|NCT04551690|helgaisabelv@gmail.com|Growth charts of newborns in Chile|https://scielo.conicyt.cl/pdf/rcp/v79n4/art03.pdf|helgaisabelv@gmail.com Rev Chil Pediatr 2008; 79 (4): 364-372
3174757|NCT00838903|112753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174758|NCT00838903|112753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174759|NCT00838903|112753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174760|NCT00838903|112753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174761|NCT00838903|112753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174762|NCT00838903|112753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174763|NCT00838903|112753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174764|NCT00235755|VRX-RET-E22-302|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174765|NCT00235755|VRX-RET-E22-302|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174766|NCT00235755|VRX-RET-E22-302|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174767|NCT00235755|VRX-RET-E22-302|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174768|NCT00235755|VRX-RET-E22-302|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174769|NCT00235755|VRX-RET-E22-302|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174770|NCT00235755|VRX-RET-E22-302|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177284|NCT01957202|200286|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177285|NCT01957202|200286|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177286|NCT01957202|200286|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174771|NCT00226499|100388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174772|NCT00226499|100388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174773|NCT00226499|100388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174774|NCT00226499|100388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174775|NCT00226499|100388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174776|NCT00226499|100388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174777|NCT07111143||Health-Damaging Climate Events Highlight the Need for Interdisciplinary, Engaged Research|https://pubmed.ncbi.nlm.nih.gov/38371354/|
3174778|NCT06941233||Study Protocol|https://hjpwd.ahs.uic.edu|study protocol may be accessed by contacting the research team
3174779|NCT00661557|107408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174780|NCT00661557|107408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174781|NCT00661557|107408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174782|NCT00661557|107408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174783|NCT00661557|107408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174784|NCT00661557|107408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174785|NCT00661557|107408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174786|NCT07089667||Study Protocol|https://drive.google.com/drive/folders/1QpzE6ACGieVNCGQ1nsLJHxUWtB-fUfLV?usp=sharing|
3174787|NCT06575504||Study Protocol|https://guides.lib.umich.edu/datamanagement/clinicaltrials|
3174788|NCT00133848|TOC103469|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174789|NCT00133848|TOC103469|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174790|NCT00133848|TOC103469|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174791|NCT00133848|TOC103469|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174792|NCT00133848|TOC103469|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174793|NCT00133848|TOC103469|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174794|NCT00133848|TOC103469|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174795|NCT01894386|200587|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174796|NCT01894386|200587|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174797|NCT01894386|200587|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174798|NCT01894386|200587|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174799|NCT01894386|200587|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174800|NCT01894386|200587|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174801|NCT01894386|200587|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174802|NCT07111780|example study protokol|Study Protocol|https://www.nature.com/articles/s41598-024-79811-3|
3174803|NCT01262872|114174|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174804|NCT01262872|114174|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174805|NCT01262872|114174|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174806|NCT01262872|114174|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174807|NCT01262872|114174|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177287|NCT01957202|200286|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177288|NCT01957202|200286|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177289|NCT01957202|200286|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177290|NCT01957202|200286|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177291|NCT07061483||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/JKAXZ|
3177292|NCT03110471||Publications|http://orcid.org/0000-0002-5691-2987|Prof Sue Jordan- publication list
3177293|NCT01196026|114451|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177294|NCT01196026|114451|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177295|NCT01196026|114451|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177296|NCT01196026|114451|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177297|NCT01196026|114451|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177298|NCT01196026|114451|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177299|NCT00398099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177300|NCT00000526|CAST|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/cast/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3177301|NCT00000526||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/cast/|
3177302|NCT00000526||Study Forms|http://biolincc.nhlbi.nih.gov/studies/cast/|
3177303|NCT06921174||Study Protocol|https://www.isemu.es|
3177304|NCT02744092|AFT-28|Study Protocol|https://www.allianceforclinicaltrialsinoncology.org/main/public/standard.xhtml?path=%2FPublic%2FAFT|Email the study team at CANVAS@AllianceFoundationTrials.org.
3177305|NCT00127023|104389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177306|NCT00127023|104389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177307|NCT00127023|104389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177308|NCT00127023|104389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177309|NCT00127023|104389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177310|NCT00127023|104389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177311|NCT02486016||AAPS presented poster|https://www.aaps.org/search?executeSearch=true&SearchTerm=published+posters&l=1|Shin SH, Yu M, Thomas S, Hammell DC, Ghosh, P, Raney SG, Hassan HH, Stinchcomb AL. Evaluation of level A in vitro/in vivo correlations (IVIVC) for nicotine and fentanyl transdermal delivery systems with transient heat exposure by using multiple approaches. Poster presentation at the 2017 AAPS Annual Meeting and Exposition; November 12-15, 2017; San Diego, CA
3177312|NCT04205721||Individual Participant Data Set|http://dataverse.unc.edu/dataverse/cpc|Search for South Africa Impact Evaluation
3177313|NCT00250276|104772|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177314|NCT00250276|104772|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177315|NCT00250276|104772|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177316|NCT00250276|104772|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177317|NCT00250276|104772|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177318|NCT00250276|104772|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177319|NCT00250276|104772|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174808|NCT01262872|114174|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174809|NCT00920439|112683|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174810|NCT00920439|112683|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174811|NCT00920439|112683|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174812|NCT00920439|112683|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174813|NCT00920439|112683|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174814|NCT00920439|112683|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174815|NCT00617890||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04720&kw=P04720&tab=access|
3174816|NCT07152041|CAMS-Ph+B-ALL|Individual Participant Data Set|https://login.imedidata.com|CAMS-Ph+ALL-2025 DATASET
3174817|NCT06456775||Individual Participant Data Set|https://bit.ly/49RBPuQ|
3174818|NCT00288626|SDY549|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY549|Deidentified participant ID mapping to manuscript ID. ImmPort study identifier is SDY549.
3174819|NCT00288626||Study summary, -design, -demographics, and -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY549|ImmPort study identifier is SDY549
3174820|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/22118062/|
3174821|NCT00095420||Clinical Study Report|http://www.researchgate.net/publication/10751612_General_Education_Teacher|
3174822|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/20673234/|
3174823|NCT00095420||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076578/|
3174824|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/27620949/|
3174825|NCT00566020|SCA106052|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174826|NCT00566020|SCA106052|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174827|NCT00566020|SCA106052|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174828|NCT00566020|SCA106052|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174829|NCT01154114|480848/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174830|NCT01154114|480848/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174831|NCT01154114|480848/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174832|NCT01154114|480848/028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174833|NCT01154114|480848/028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174834|NCT01154114|480848/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174835|NCT01154114|480848/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174836|NCT00996125|112022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174837|NCT00996125|112022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174838|NCT00996125|112022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174839|NCT00996125|112022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174840|NCT00996125|112022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174841|NCT00996125|112022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174842|NCT07184021|Protocol draft available|Study Protocol|https://www.aun.edu.eg/hospitals|Individual participant data and supporting documents will not be shared in order to protect patient confidentiality.
3174843|NCT02006589|200956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174844|NCT02006589|200956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174845|NCT02006589|200956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174846|NCT02006589|200956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174847|NCT02006589|200956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174848|NCT02006589|200956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174849|NCT02006589|200956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174850|NCT02637206|200920|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174851|NCT02637206|200920|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174852|NCT02637206|200920|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174853|NCT02637206|200920|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174854|NCT02637206|200920|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174855|NCT02637206|200920|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174856|NCT02637206|200920|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174857|NCT00812981|111954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174858|NCT00812981|111954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174859|NCT00812981|111954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174860|NCT00812981|111954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174861|NCT00812981|111954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174862|NCT00812981|111954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174863|NCT00812981|111954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174864|NCT01777282|116170|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174865|NCT01777282|116170|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174866|NCT01777282|116170|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174867|NCT01777282|116170|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174868|NCT01777282|116170|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174869|NCT01777282|116170|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174870|NCT07182617|Research Protocol|Study Protocol|https://drive.google.com/file/d/1Y8Ubu5Ie_BSDOER7_672YlAa5KttK5Wn/view?usp=sharing|https://drive.google.com/file/d/1Y8Ubu5Ie\_BSDOER7\_672YlAa5KttK5Wn/view?usp=sharing
3174871|NCT05189652||Individual Participant Data Set|https://doi.org/10.2478/hukin-2020-0043|Zhang, Q., Trama, R., Fouré, A., \& Hautier, C. A. (2020). The Immediate Effects of Self-Myofacial Release on Flexibility, Jump Performance and Dynamic Balance Ability. Journal of human kinetics, 75, 139-148.
3174872|NCT01521390|115487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174873|NCT01521390|115487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174874|NCT01521390|115487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174875|NCT01521390|115487|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174876|NCT01521390|115487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174877|NCT01521390|115487|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174878|NCT01521390|115487|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174879|NCT00116818|FFR20002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174880|NCT00116818|FFR20002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174881|NCT00116818|FFR20002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174882|NCT00116818|FFR20002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174883|NCT00116818|FFR20002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174884|NCT00116818|FFR20002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174885|NCT00116818|FFR20002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174886|NCT02476578||Study Protocol|https://goo.gl/B6j1oF|LIMIT HEBREW PROTOCOL Version 3 (Final)
3174887|NCT00291876|100571 (M138)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100571 are summarised with studies 100572, 100573, 100574, 100575, 110677, 110678, 110679, 110680, and 110681 on the GSK Clinical Study
3174888|NCT00291876|100571 (M138)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174889|NCT00291876|100571 (M138)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174890|NCT00291876|100571 (M138)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174891|NCT00291876|100571 (M138)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174892|NCT00291876|100571 (M138)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174893|NCT01863667||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3102-027&kw=3102-027&tab=access|
3174894|NCT00351702||published manuscript|http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0047400|the study has been published and has been provided in the citation. the paper conatins the required information regarding study results and conclusion
3174895|NCT00839527|112757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174896|NCT00839527|112757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174897|NCT00839527|112757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174898|NCT00839527|112757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174899|NCT00839527|112757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174900|NCT00839527|112757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174901|NCT00839527|112757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174902|NCT04132323||Study Protocol|https://www.venousregistry.org/index.php?f=1&id=97|
3174903|NCT06575127||Informed Consent Form|https://drive.google.com/file/d/1_CG_0wzCH_ZUxWXsfARsyWlcx37fOcRq/view?usp=drive_link|
3174904|NCT04068129||Individual Participant Data Set|http://www.abcd-vision.org/references/index.html|
3174905|NCT02064504|201010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174906|NCT02064504|201010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174907|NCT02064504|201010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174908|NCT02064504|201010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174909|NCT02064504|201010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174910|NCT02064504|201010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174911|NCT02064504|201010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174912|NCT06968169||Study Protocol|https://doi.org/10.17605/OSF.IO/AJDZS|
3174913|NCT05497518||Study Protocol|https://tuftsmedicalcenter.box.com/s/bplcm9clgjsnnq23zcwwwuze6up368q4|
3174914|NCT00347139|B2C106093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174915|NCT00347139|B2C106093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174916|NCT00347139|B2C106093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174917|NCT00347139|B2C106093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174918|NCT00347139|B2C106093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174919|NCT00347139|B2C106093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174920|NCT00347139|B2C106093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174921|NCT05664360||Individual Participant Data Set|https://www.doi.org/10.17605/OSF.IO/TRU4N|
3174922|NCT00381238|AVA104617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174923|NCT00381238|AVA104617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174924|NCT00381238|AVA104617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174925|NCT00381238|AVA104617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174926|NCT00381238|AVA104617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174927|NCT00381238|AVA104617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174928|NCT00381238|AVA104617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174929|NCT00115492|SCO100250|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174930|NCT00115492|SCO100250|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174931|NCT00115492|SCO100250|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174932|NCT00115492|SCO100250|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174933|NCT00115492|SCO100250|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174934|NCT00115492|SCO100250|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174935|NCT00115492|SCO100250|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174936|NCT01014988|113678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174937|NCT01014988|113678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174938|NCT01014988|113678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174939|NCT01014988|113678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174940|NCT01014988|113678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174941|NCT01014988|113678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174942|NCT01014988|113678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174943|NCT00256854|ROX104805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174944|NCT00256854|ROX104805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174945|NCT00256854|ROX104805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174946|NCT00256854|ROX104805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174947|NCT00256854|ROX104805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174948|NCT00256854|ROX104805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174949|NCT00256854|ROX104805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174950|NCT00784550|111114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174951|NCT00784550|111114|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174952|NCT00784550|111114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174953|NCT00784550|111114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174954|NCT00784550|111114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179237|NCT01090453|113615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179238|NCT02670629|Fx radio distal|Individual Participant Data Set|https://drive.google.com/open?id=0Bwd7ib0yn_zqMnBVZnY2NFFJTzA|Excel document with all the information regarding the patients included in this research protocol
3179239|NCT00493818|AKT106757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172877|NCT00422955|49653/376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172878|NCT00422955|49653/376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179240|NCT00493818|AKT106757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179241|NCT00493818|AKT106757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179242|NCT00493818|AKT106757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179243|NCT00493818|AKT106757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179244|NCT00493818|AKT106757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179245|NCT00493818|AKT106757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179246|NCT00833989|111539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179247|NCT00833989|111539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179248|NCT00833989|111539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179249|NCT00833989|111539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179250|NCT00833989|111539|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179251|NCT00833989|111539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179252|NCT00833989|111539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179253|NCT01827904||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
3179254|NCT02672631||Study Protocol|http://clinical-mri.com/mr-neurography-diagnostic-criteria-to-determine-lesions-of-peripheral-nerves/|
3179255|NCT03058211|PI16/00486|Study Protocol|http://www.iispv.cat|Protocol in Spanish language
3179256|NCT03058211|PI16/00486|Informed Consent Form|http://www.iispv.cat|Informed consent form in Spanish language
3179257|NCT00354874|B2C101762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179258|NCT00354874|B2C101762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179259|NCT00354874|B2C101762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179260|NCT00354874|B2C101762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172879|NCT00422955|49653/376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172880|NCT02250586|awtg7|Individual Participant Data Set|https://osf.io|The trial's outcome data and scripts are available for download: https://osf.io/awtg7/
3172881|NCT04743024|285489|Study Protocol|https://www.uib.no/en/rg/gmh/134660/treat-c-aud-project-page|IPD will be shared on reasonable request and the official DMP is archived with NFR
3172882|NCT00955682|112036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172883|NCT00955682|112036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172884|NCT00955682|112036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172885|NCT00955682|112036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172886|NCT00955682|112036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172887|NCT00955682|112036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172888|NCT01681004|INSITE|Individual Participant Data Set|http://yoda.yale.edu/|
3172889|NCT00950755|104505|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172890|NCT00950755|104505|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172891|NCT00950755|104505|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179261|NCT00354874|B2C101762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174955|NCT00784550|111114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174956|NCT00784550|111114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174957|NCT04304235|doi.org/10.5683/SP3/SIL|Individual Participant Data Set|https://borealisdata.ca/dataverse/smart_triage|Open access to all study materials and data
3177320|NCT00892775|108760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177321|NCT00892775|108760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177322|NCT00892775|108760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177323|NCT00892775|108760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177324|NCT00892775|108760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177325|NCT00892775|108760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177326|NCT00857857|110762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177327|NCT00857857|110762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177328|NCT00857857|110762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177329|NCT00857857|110762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177330|NCT00857857|110762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177331|NCT00857857|110762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177332|NCT00857857|110762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177333|NCT00985673|113536|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177334|NCT00985673|113536|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177335|NCT00985673|113536|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177336|NCT00985673|113536|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177337|NCT00985673|113536|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177338|NCT00985673|113536|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177339|NCT00985673|113536|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177340|NCT00481702||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177341|NCT01358825|115375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174958|NCT00976820|113482|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174959|NCT00976820|113482|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174960|NCT00976820|113482|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174961|NCT00976820|113482|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174962|NCT00976820|113482|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177342|NCT01358825|115375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177343|NCT01358825|115375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177344|NCT01358825|115375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177345|NCT01358825|115375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177346|NCT01358825|115375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181540|NCT00114413|SDY210|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY210|ImmPort study identifier is SDY210. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3181541|NCT00114413|SDY210|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY210|ImmPort study identifier is SDY210. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3181542|NCT00114413|SDY210|Study summary and schematic, -design, adverse event(s), -interventions,-medications, -demographics, and -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY210|ImmPort study identifier is SDY210. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
3181543|NCT06352476||Clinical Study Report|http://doi.org/10.1016/j.yebeh.2016.11.022|Bautista, R. E. D. Understanding the self-management skills of persons with epilepsy. Epilepsy \&amp;amp;amp; Behavior, 2017; 69, 7-11
3181544|NCT06352476||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/29505437/|Buelow, J., Miller, W., \&amp;amp;amp; Fishman, J. Development of an epilepsy nursing communication tool: improving the quality of interactions between nurses and patients with seizures. The Journal of Neuroscience Nursing, 2018; 50(2), 74
3181545|NCT01498653|113714|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181546|NCT01498653|113714|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181547|NCT01498653|113714|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181548|NCT01498653|113714|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181549|NCT01498653|113714|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181550|NCT01498653|113714|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181551|NCT01498653|113714|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181552|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Hand Shape Representation in Parietal Reach Region. The Journal of Neuroscience."
3181553|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Decoding motor imagery from the posterior parietal cortex of a tetraplegic human. Science"
3181554|NCT00704405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-009&kw=7009-009&tab=access|
3181555|NCT01362257|112014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181556|NCT01362257|112014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181557|NCT01362257|112014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181558|NCT01362257|112014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181559|NCT01362257|112014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181560|NCT01362257|112014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177347|NCT01358825|115375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177348|NCT00992758|104512|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177349|NCT00992758|104512|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177350|NCT00992758|104512|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177351|NCT00992758|104512|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177352|NCT00992758|104512|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177353|NCT00992758|104512|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177354|NCT00992758|104512|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177355|NCT06122506||Statistical Analysis Plan|https://drive.google.com/file/d/16iZkdhVtT_pnExSoUhJV5iprYyA1JYhx/view?usp=sharing|
3177356|NCT06122506||Study Protocol|https://drive.google.com/file/d/1Z_nDas-Emj7x3OnbkcmRl3Pujy0tjlmM/view?usp=sharing|
3177357|NCT00938184|112811|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177358|NCT00938184|112811|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177359|NCT00938184|112811|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177360|NCT00938184|112811|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177361|NCT00812773|112356|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177362|NCT00812773|112356|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177363|NCT00812773|112356|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177364|NCT00812773|112356|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177365|NCT00812773|112356|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177366|NCT00812773|112356|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177367|NCT00812773|112356|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177368|NCT06239740||Study Protocol|https://doi.org/10.5281/zenodo.10488186|
3177369|NCT00985465|113166|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177370|NCT00985465|113166|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177371|NCT00985465|113166|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177372|NCT00985465|113166|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177373|NCT00985465|113166|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177374|NCT00985465|113166|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177375|NCT00985465|113166|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177376|NCT01335139|ITN043AD|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN043ADJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3177377|NCT01335139|ITN043AD|Synopsis, Adverse Events, -Data and Reports, -Schedule of Assessments|https://www.itntrialshare.org/project/Studies/ITN043ADJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
3177378|NCT06342817||Study Protocol|https://drive.google.com/file/d/1YWyRsHac1y9eqsmQXVHCsmYArWwAdMoq/view?usp=sharing|
3177379|NCT06342817||Informed Consent Form|https://drive.google.com/file/d/1TfBgnmUMvF4tFJu-a1lGXlcawu0k5YeJ/view?usp=sharing|
3177380|NCT00387881|TXA107563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177381|NCT00387881|TXA107563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177382|NCT00387881|TXA107563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177383|NCT00387881|TXA107563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177384|NCT00387881|TXA107563|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177385|NCT00387881|TXA107563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177386|NCT00387881|TXA107563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177387|NCT00496015|107137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177388|NCT00496015|107137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177389|NCT00496015|107137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177390|NCT00496015|107137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177391|NCT00496015|107137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177392|NCT00496015|107137|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177393|NCT00496015|107137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177394|NCT00689390||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05063&kw=P05063&tab=access|
3174963|NCT00976820|113482|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174964|NCT00268177|SCO30005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174965|NCT00268177|SCO30005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174966|NCT00268177|SCO30005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174967|NCT00268177|SCO30005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174968|NCT00268177|SCO30005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174969|NCT00268177|SCO30005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174970|NCT00268177|SCO30005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174971|NCT01571999|114636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174972|NCT01571999|114636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174973|NCT01571999|114636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174974|NCT01571999|114636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174975|NCT01571999|114636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174976|NCT01571999|114636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174977|NCT01571999|114636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174978|NCT00370318|107017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174979|NCT00370318|107017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174980|NCT00370318|107017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174981|NCT00370318|107017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174982|NCT00370318|107017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174983|NCT00370318|107017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174984|NCT01154088|114248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174985|NCT01154088|114248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174986|NCT01154088|114248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174987|NCT01154088|114248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174988|NCT01154088|114248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174989|NCT01154088|114248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174990|NCT00325156|100917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174991|NCT00325156|100917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174992|NCT00325156|100917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174993|NCT00325156|100917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174994|NCT00325156|100917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174995|NCT00325156|100917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174996|NCT02004886||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0893-005&kw=0893-005&tab=access|
3174997|NCT02184585|117057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174998|NCT02184585|117057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3174999|NCT02184585|117057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175000|NCT02184585|117057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175001|NCT02184585|117057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175002|NCT02184585|117057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175003|NCT02184585|117057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175004|NCT03228316||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/27208713|
3175005|NCT00460707|NKV109990|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175006|NCT00460707|NKV109990|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175007|NCT00460707|NKV109990|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175008|NCT00460707|NKV109990|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175009|NCT00460707|NKV109990|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175010|NCT00460707|NKV109990|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175011|NCT00460707|NKV109990|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175012|NCT00197002|208109/220|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175013|NCT00197002|208109/220|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181561|NCT01362257|112014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175014|NCT00197002|208109/220|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181562|NCT01636960||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08556&kw=P08556&tab=access|
3181563|NCT00451100||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3181564|NCT01313637|113361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181565|NCT01313637|113361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181566|NCT01313637|113361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181567|NCT01313637|113361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181568|NCT01313637|113361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181569|NCT01313637|113361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177395|NCT00102765|SFA103153|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177396|NCT00102765|SFA103153|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177397|NCT00102765|SFA103153|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177398|NCT00102765|SFA103153|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177399|NCT00102765|SFA103153|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177400|NCT00102765|SFA103153|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177401|NCT00102765|SFA103153|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177402|NCT00539994|ALB110247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177403|NCT00539994|ALB110247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177404|NCT00539994|ALB110247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177405|NCT00539994|ALB110247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177406|NCT00539994|ALB110247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177407|NCT00539994|ALB110247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177408|NCT00539994|ALB110247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177409|NCT06697041|Lubaba Shahrin|Anonymous dataset upor request by scientific use. Data will be shared by the Institutional Review Board.|https://www.icddrb.org|https://www.icddrb.org
3177410|NCT07200050||Individual participant data and supporting information will not be shared.|https://notapplicable.org|Individual participant data and supporting information will not be shared due to privacy and confidentiality concerns.
3177411|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/22original18.pdf|
3177412|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/23original19.pdf|
3179262|NCT00354874|B2C101762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179263|NCT00354874|B2C101762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179264|NCT00951041|113574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179265|NCT00951041|113574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179266|NCT00951041|113574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179267|NCT00951041|113574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179268|NCT00951041|113574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179269|NCT00951041|113574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179270|NCT00951041|113574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179271|NCT06426537||Study Protocol|http://drive.google.com/drive/u/3/folders/15qW39gHRtgwIuP8rGm8ukhXtYnLRCFNO|
3179272|NCT00319098|107064|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179273|NCT00319098|107064|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179274|NCT00319098|107064|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179275|NCT00319098|107064|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179276|NCT00319098|107064|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 107064 are summarised with study 107217 on the GSK Clinical Study Register.
3179277|NCT00319098|107064|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179278|NCT01462344|115358|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179279|NCT01462344|115358|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179280|NCT01462344|115358|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179281|NCT01462344|115358|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175015|NCT00197002|208109/220|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175016|NCT00197002|208109/220|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175017|NCT00197002|208109/220|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175018|NCT01424514|114974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175019|NCT01424514|114974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177413|NCT05489341|10.5281/zenodo.6624726|Individual Participant Data Set|https://zenodo.org/record/6624726|Imaging for the PI-CAI: Public Training and Development Dataset, containing 1500 fully-anonymized prostate bpMRI scans from 1476 patients, acquired between 2012-2021, at three Dutch centers (Radboud University Medical Center, University Medical Center Groningen, Ziekenhuisgroep Twente).
3181570|NCT01313637|113361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181571|NCT01323647|114306|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181572|NCT01323647|114306|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181573|NCT01323647|114306|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181574|NCT01323647|114306|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181575|NCT01323647|114306|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181576|NCT01323647|114306|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181577|NCT01138007|113351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177414|NCT05489341|10.5281/zenodo.6667655|Study Protocol|https://zenodo.org/record/6667655|Preregistration of the PI-CAI challenge study design, in compliance with BIAS reporting guidelines (https://www.equator-network.org/reporting-guidelines/bias-transparent-reporting-of-biomedical-image-analysis-challenges/).
3181578|NCT01138007|113351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181579|NCT01138007|113351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181580|NCT01138007|113351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181581|NCT01138007|113351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181582|NCT01287065|114624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181583|NCT01287065|114624|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181584|NCT01287065|114624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181585|NCT01287065|114624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181586|NCT01287065|114624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181587|NCT01287065|114624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181588|NCT01287065|114624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181589|NCT01751074|115677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181590|NCT01751074|115677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181591|NCT01751074|115677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181592|NCT01751074|115677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181593|NCT01751074|115677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181594|NCT01751074|115677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181595|NCT01751074|115677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181596|NCT00839657|COAG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/coag/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175020|NCT01424514|114974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175021|NCT01424514|114974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177415|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_prep/|Source code for preprocessing prostate MRI data archives.
3177416|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_baseline|Source code for training baseline diagnostic AI models.
3172892|NCT00950755|104505|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172893|NCT00950755|104505|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177417|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_eval/|Source code for evaluating csPCa detection and diagnosis performance, and performing all statistical tests with respect to the same.
3181597|NCT00839657||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coag/|
3172894|NCT00950755|104505|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181598|NCT00839657||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coag/|
3181599|NCT00839657||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coag/|
3181600|NCT04817761||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3181601|NCT04817761||Study Protocol|https://clinicaltrials.servier.com/|
3181602|NCT04817761||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3181603|NCT04817761||Informed Consent Form|https://clinicaltrials.servier.com/|
3181604|NCT04817761||Clinical Study Report|https://clinicaltrials.servier.com/|
3181605|NCT04817761||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3181606|NCT05905003||Individual Participant Data Set|https://nda.nih.gov/ampscz/|
3181607|NCT04140383||Clinical Study Report|http://rdcu.be/bUabz|
3181608|NCT01808482|116702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181609|NCT01808482|116702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181610|NCT01808482|116702|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181611|NCT01808482|116702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181612|NCT01808482|116702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181613|NCT01808482|116702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181614|NCT01808482|116702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181615|NCT01128894|114179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181616|NCT01128894|114179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181617|NCT01128894|114179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181618|NCT01128894|114179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181619|NCT01128894|114179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181620|NCT01128894|114179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181621|NCT01128894|114179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181622|NCT02917278||Meeting abstract|https://www.asn-online.org/api/download/?file=/education/kidneyweek/archives/KW16Abstracts.pdf|Abstract presented as a poster at the ASN Kidney Week 2016 (TH-PO762)
3181623|NCT05981599||Actuality report|https://www.santepubliquefrance.fr/content/download/504135/3759948?version=2|French Report on the epidemic situation of meningococcal disease in december 2022
3181624|NCT05981599||Clinical Study Report|https://doi.org/10.1371/journal.pone.0281544|
3181625|NCT06727760|Survey in efficacy of probioti|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
3181626|NCT06727760|Effectiveness of massage|article|https://scholar.google.com.tr/scholar?q=Effectiveness+of+massage+therapy+for+treatment+of+infantile+colic.&hl=tr&as_sdt=0&as_vis=1&oi=scholart|
3181627|NCT06727760|The effect of massage|article|https://tumj.tums.ac.ir/browse.php?a_id=11133&slc_lang=en&sid=1&printcase=1&hbnr=1&hmb=1|
3181628|NCT06727760|0-1 Yaş Arası Bebekler|rewiev|https://dergipark.org.tr/tr/pub/firattip/issue/6338/84544|
3181629|NCT06727760|kangroo care guide|Guide|https://www.who.int/publications/i/item/9241590351|
3181630|NCT06727760|The Effects of Kangaroo Mother|article|https://ijn.mums.ac.ir/article_4152.html|
3181631|NCT06727760|efficacy of probiotic|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
3181632|NCT06727760|Effect of massage|article|https://scholar.google.com.tr/scholar?q=Effectiveness+of+massage+therapy+for+treatment+of+infantile+colic.&hl=tr&as_sdt=0&as_vis=1&oi=scholart|
3181633|NCT06727760|The Effect of Aromatherapy|doctora thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
3181634|NCT00402363|OM8 Afib|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181635|NCT00402363|OM8 Afib|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181636|NCT00402363|OM8 Afib|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177418|NCT05489341||Individual Participant Data Set|https://github.com/DIAGNijmegen/picai_labels|Annotations for the PI-CAI: Public Training and Development Dataset, containing basic clinical and acquisition variables, csPCa annotations and outcomes for 1500 fully-anonymized prostate bpMRI exams from 1476 patients, acquired between 2012-2021, at three Dutch centers (Radboud University Medical Center, University Medical Center Groningen, Ziekenhuisgroep Twente).
3177419|NCT00861705||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov|
3177420|NCT03847766|31484523|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31484523/|Data can be accessed by request from the corresponding author
3177421|NCT01387217|114070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177422|NCT01387217|114070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177423|NCT01387217|114070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177424|NCT01387217|114070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177425|NCT01387217|114070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177426|NCT01387217|114070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177427|NCT01387217|114070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177428|NCT01928927||Grading table|https://rsc.tech-res.com/clinical-research-sites/safety-reporting/daids-grading-tables|
3177429|NCT01009060|113147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177430|NCT01009060|113147|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177431|NCT01009060|113147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177432|NCT01009060|113147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177433|NCT01009060|113147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177434|NCT01009060|113147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177435|NCT01009060|113147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177436|NCT06938126|TE-KEB/22/2023|Individual Participant Data Set|https://tf.hu/en/|For more information please email to: petridis.leonidas@tf.hu
3177437|NCT01342913|113107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177438|NCT01342913|113107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177439|NCT01342913|113107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177440|NCT01342913|113107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177441|NCT01342913|113107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177442|NCT01342913|113107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177443|NCT01342913|113107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177444|NCT00938158|108370|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177445|NCT00938158|108370|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177446|NCT00938158|108370|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177447|NCT00938158|108370|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177448|NCT00938158|108370|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177449|NCT00938158|108370|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177450|NCT00938158|108370|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177451|NCT00605852|HH3110161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177452|NCT00605852|HH3110161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177453|NCT00605852|HH3110161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177454|NCT00605852|HH3110161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172895|NCT00950755|104505|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181637|NCT00402363|OM8 Afib|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181638|NCT00402363|OM8 Afib|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181639|NCT00402363|OM8 Afib|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181640|NCT00402363|OM8 Afib|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181641|NCT00710021|SDY474|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474.
3181642|NCT00710021|SDY474|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474. The study protocol is located in the Design tab content.
3181643|NCT00710021|SDY474|Study summary, -design, -adverse event(s), -meds,-demographics, -lab tests, -mechanistic assays, - files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474.
3181644|NCT01457547|217744/094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181645|NCT01457547|217744/094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175022|NCT01424514|114974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175023|NCT01424514|114974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175024|NCT01424514|114974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175025|NCT00035295||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175026|NCT00005276|ACCESS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/access|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175027|NCT00005276||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/access|
3175028|NCT00005276||Study Forms|http://biolincc.nhlbi.nih.gov/studies/access|
3175029|NCT00005276||Procedures Manual|http://biolincc.nhlbi.nih.gov/studies/access|
3175030|NCT01899742|116960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175031|NCT01899742|116960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175032|NCT01899742|116960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175033|NCT01899742|116960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175034|NCT01899742|116960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175035|NCT01899742|116960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175036|NCT01899742|116960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175037|NCT00036491|SDY625|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|Participant level data and additional relevant materials are available to the public in the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts.
3175038|NCT00036491|SDY625|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|ImmPort study identifier is SDY625.
3175039|NCT00036491|SDY625|Study summary, -design, -adverse event(s), -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -study files, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|ImmPort study identifier is SDY625.
3175040|NCT01446237|115576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175041|NCT01446237|115576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175042|NCT01446237|115576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175043|NCT01446237|115576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175044|NCT01446237|115576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175045|NCT01446237|115576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175046|NCT01446237|115576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175047|NCT05376241||Individual Participant Data Set|https://osf.io/y8stc/|
3181646|NCT01457547|217744/094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181647|NCT01457547|217744/094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175048|NCT03347734||Clinical Study Report|https://en.wikipedia.org/wiki/Bates_method|
3181648|NCT01457547|217744/094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179282|NCT01462344|115358|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179283|NCT01462344|115358|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179284|NCT01462344|115358|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179285|NCT01217073||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-006&kw=3102-006&tab=access|
3179286|NCT04411290||Principal investigator data|https://scholar.google.com.tr/citations?user=6bFlCZwAAAAJ&hl=tr|
3179287|NCT01196975|112963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179288|NCT01196975|112963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175049|NCT01357070|DOI:10.4172/2472-1921.100060|Clinical Study Report|https://clinical-nutrition.imedpub.com/consumption-of-broccoli-sprouts-attenuatesintracellular-p38-map-kinase-and-reactiveoxygen-species-proinflammatory-activationin-hum.php?aid=21325|RESULTS REPORT
3175050|NCT05442606||Full Paper|https://www.e-arm.org/journal/view.php?doi=10.5535/arm.23058|
3175051|NCT02920541||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3175052|NCT02920541||Study Protocol|https://clinicaltrials.servier.com/|
3175053|NCT02920541||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3175054|NCT02920541||Informed Consent Form|https://clinicaltrials.servier.com/|
3175055|NCT02920541||study-level clinical trial data|https://clinicaltrials.servier.com/|
3175056|NCT02920541||Clinical Study Report|https://clinicaltrials.servier.com/|
3175057|NCT00345878|105926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175058|NCT00345878|105926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175059|NCT00345878|105926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175060|NCT00345878|105926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175061|NCT00345878|105926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175062|NCT00345878|105926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175063|NCT01453478|115550|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175064|NCT01453478|115550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175065|NCT01453478|115550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175066|NCT01453478|115550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175067|NCT01453478|115550|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175068|NCT01453478|115550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175069|NCT01453478|115550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175070|NCT00092339||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179289|NCT01196975|112963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179290|NCT01196975|112963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175071|NCT06623838|HNYZ6|Study Protocol|https://doi.org/10.17605/OSF.IO/HNYZ6|
3175072|NCT05336292||Individual Participant Data Set|https://drive.google.com/drive/folders/1Z6K71rEcfJHXIzsurwREdgHRweFwgFW3|Data will be made available upon reasonable request
3175073|NCT05544773||Study Protocol|https://drive.google.com/file/d/1gKwThkhpbD7eQxFYL4CkTEhzWtcLS1jZ/view?usp=sharing|
3175074|NCT00831545||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175075|NCT00984139|112682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175076|NCT00984139|112682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175077|NCT00984139|112682|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177455|NCT00605852|HH3110161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177456|NCT00605852|HH3110161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177457|NCT00605852|HH3110161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177458|NCT01527123|115959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177459|NCT01527123|115959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177460|NCT01527123|115959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177461|NCT01527123|115959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177462|NCT01527123|115959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177463|NCT01527123|115959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177464|NCT00988884||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-005&kw=V503-005&tab=access|
3177465|NCT00960063||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05883&kw=P05883&tab=access|
3177466|NCT06357481|doi: 10.1111/iej.13304|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32266988/|
3177467|NCT00550407|SCA104779|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177468|NCT00550407|SCA104779|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177469|NCT00550407|SCA104779|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177470|NCT00550407|SCA104779|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177471|NCT02481154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3177472|NCT02481154||Study Protocol|https://clinicaltrials.servier.com/|
3177473|NCT02481154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3177474|NCT02481154||Informed Consent Form|https://clinicaltrials.servier.com/|
3177475|NCT02481154||Clinical Study Report|https://clinicaltrials.servier.com/|
3177476|NCT02481154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3177477|NCT04701814||Book|http://www.elsevier.com.|Neumann, D. D. (2010). kinesology of musculoskeletal system. In Mosby, Inc., an affiliate of Elsevier Inc. The book described normal biomechanics of the shoulder during the elevation.
3177478|NCT04701814||Book|https://doi.org/10.1017/CBO9781107415324.004|the posterior glid and inferior glid of GH joint is increasing the range of motion and decreasing the pain
3177479|NCT06555185|10.17632/2cwcz2vx4v.1|Individual Participant Data Set|https://data.mendeley.com/datasets/2cwcz2vx4v/1|
3177480|NCT00405080|NKV105091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177481|NCT00405080|NKV105091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177482|NCT00405080|NKV105091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177483|NCT00405080|NKV105091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177484|NCT00405080|NKV105091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177485|NCT00405080|NKV105091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177486|NCT00390143|108595 Mth18|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177487|NCT00390143|108595 Mth18|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177488|NCT00390143|108595 Mth18|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177489|NCT00390143|108595 Mth18|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177490|NCT00390143|108595 Mth18|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177491|NCT00390143|108595 Mth18|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177492|NCT00382772|107876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177493|NCT00382772|107876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177494|NCT00382772|107876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177495|NCT00382772|107876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177496|NCT00382772|107876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175078|NCT00984139|112682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175079|NCT00984139|112682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175080|NCT00984139|112682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175081|NCT00984139|112682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175082|NCT01573767|106853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175083|NCT01573767|106853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175084|NCT01573767|106853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175085|NCT01573767|106853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175086|NCT01573767|106853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175087|NCT01573767|106853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175088|NCT01573767|106853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175089|NCT00742508|CRV110734|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175090|NCT00742508|CRV110734|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175091|NCT00742508|CRV110734|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175092|NCT00742508|CRV110734|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175093|NCT00742508|CRV110734|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175094|NCT00514904|109495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175095|NCT00514904|109495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175096|NCT00514904|109495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175097|NCT00514904|109495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175098|NCT00514904|109495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175099|NCT00514904|109495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175100|NCT00514904|109495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175101|NCT00322361||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175102|NCT03030274|NCT03030274|Publications|http://pubmed.ncbi.nlm.nih.gov/31130524/|Christina Paitazoglou 1, Ramazan Özdemir, Roman Pfister, Martin W Bergmann, Jozef Bartunek, Teoman Kilic, Alexander Lauten, Alexander Schmeisser, Mehdi Zoghi, Stefan Anker, Horst Sievert, Felix Mahfoud\_The AFR-PRELIEVE trial: a prospective, non-randomised, pilot study to assess the Atrial Flow Regulator (AFR) in heart failure patients with either preserved or reduced ejection fraction
3175103|NCT03030274|NCT03030274|Publications|http://pubmed.ncbi.nlm.nih.gov/33555114/|Christina Paitazoglou 1, Martin W Bergmann 1, Ramazan Özdemir 2, Roman Pfister 3, Jozef Bartunek 4, Teoman Kilic 5, Alexander Lauten 6, Alexander Schmeisser 7, Mehdi Zoghi 8, Stefan D Anker 6, Horst Sievert 9, Felix Mahfoud 10, AFR-PRELIEVE Investigators\_One-year results of the first-in-man study investigating the Atrial Flow Regulator for left atrial shunting in symptomatic heart failure patients: the PRELIEVE study
3175104|NCT03030274|NCT03030274|Publiactions|http://pubmed.ncbi.nlm.nih.gov/34763641/|Nijad Bakhshaliyev 1, Ramazan Ozdemir 1\_The impact of atrial flow regulator implantation on hemodynamic parameters in patients with heart failure
3175105|NCT01639066|25800784|pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25800784|Publication for the primary study results
3175106|NCT04852770||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35055641/|Duran, É. P., Hemanny, C., Vieira, R., Nascimento, O., Machado, L., de Oliveira, I. R., \& Demarzo, M. (2022). A Randomized Clinical Trial to Assess the Efficacy of Online-Treatment with Trial-Based Cognitive Therapy, Mindfulness-Based Health Promotion and Positive Psychotherapy for Post-Traumatic Stress Disorder during the COVID-19 Pandemic: A Study Protocol. International Journal of Environmental Research and Public Health, 19(2), 819.
3175107|NCT02262689|201402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175108|NCT02262689|201402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175109|NCT02262689|201402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175110|NCT02262689|201402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175111|NCT02262689|201402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181649|NCT01457547|217744/094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181650|NCT07330089||literature review|https://www.dental-research.com/idr/article/view/403|esearchgate.net/publication/377562421\_Pit\_and\_Fissure\_Sealants\_as\_a\_Viable\_Preventive\_Tool\_for\_Dental\_Caries
3172896|NCT01711736|116926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172897|NCT01711736|116926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172898|NCT01711736|116926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172899|NCT01711736|116926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172900|NCT01711736|116926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172901|NCT01711736|116926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172902|NCT01270139|doi: 10.13140/2.1.3109.5847|Study Protocol|https://www.researchgate.net/publication/273623828_Protocol_v31_of_NANOM-FIM_trial|The protocol of the trial (v. 3.1.) was released in ResearchGate in March 2015.
3172903|NCT01270139|doi: 10.17632/rkz98ttjrd.1|Study Protocol|https://data.mendeley.com/datasets/rkz98ttjrd/1|This is a protocol of NANOM-FIM trial released in Mendeley Datasets.
3172904|NCT01270139|doi: 10.17632/5hzb3249hn.1|Individual Participant Data Set|https://data.mendeley.com/datasets/5hzb3249hn/1|There is Atomic Force Microscopy data from random patients.
3172905|NCT01270139|doi: 10.13140/RG.2.1.4913|Protocol and Proposal of the Research Project|https://www.researchgate.net/publication/286927115_Development_of_bioresorbable_scaffolds_and_nanotechnologies_for_reversal_of_atherosclerosis_DREAM|This is a set of documents of the related DREAM project funded by the FP7/ European Commission. The DREAM study was a collaborative project at the loop between Erasmus MC (Rotterdam, The Netherlands) and Ural Institute of Cardiology (Yekaterinburg, Russia) including NANOM-FIM trial.
3172906|NCT00407979|SDY5|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY5|ImmPort study identifier is SDY5
3172907|NCT00407979|SDY5|Study design, -schedule of events, -demographics, -adverse events, -interventions, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY5|ImmPort study identifier is SDY5
3172908|NCT01852565|115679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172909|NCT01852565|115679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172910|NCT01852565|115679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172911|NCT01852565|115679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172912|NCT01852565|115679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172913|NCT01852565|115679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172914|NCT01852565|115679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172915|NCT06047886||Prodigy technical sheet|https://www.miltenyibiotec.com/US-en/products/clinimacs-prodigy.html|
3172916|NCT00455572|107240|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181651|NCT07334951|enaswagdydaib@gmail.com|Study Protocol|https://doing.org/10.1016/j.neulet.2021.136393.|No comments
3172917|NCT00455572|107240|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172918|NCT00455572|107240|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172919|NCT00455572|107240|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172920|NCT00455572|107240|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172921|NCT00455572|107240|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172922|NCT00455572|107240|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172923|NCT00000610|MAGIC|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/magic/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3172924|NCT00000610||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/magic/|
3172925|NCT00000610||Study Forms|http://biolincc.nhlbi.nih.gov/studies/magic/|
3172926|NCT01587716|115658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172927|NCT01587716|115658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172928|NCT01587716|115658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172929|NCT01587716|115658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3181652|NCT07340905||original article|https://pmc.ncbi.nlm.nih.gov/articles/PMC11370812/|
3181653|NCT07343401|statistics|Statistical Analysis Plan|https://pubmed.ncbi.nlm.nih.gov/20594135/|pending
3181654|NCT03910075||Study Protocol|http://www.nihstrokenet.org/i-acquire/resources|
3175112|NCT02262689|201402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175113|NCT02262689|201402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175114|NCT04909372||Study Protocol|https://osf.io/du58k/|
3175115|NCT04909372||Statistical Analysis Plan|https://osf.io/du58k/|
3175116|NCT04909372||Individual Participant Data Set|https://osf.io/du58k/|
3175117|NCT04928469||Statistical Analysis Plan|https://docs.google.com/document/d/11uN0slg6N6K_10vm4BuXVtB7_QcZOAf5M6P0I-okGkU/edit#|
3175118|NCT05546216||REFERENCE|https://doi.org/10.1016/j.ctcp.2019.101068|
3175119|NCT05546216||REFERENCE|http://dx.doi.org/10.1016/j.ijcard.2016.11.043|
3175120|NCT05546216||REFERENCE|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540812/|
3175121|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30367542/|
3175122|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/18065335/|
3175123|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/35307131/|
3175124|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/17056770/|
3175125|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/27252099/|
3175126|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/33632127/|
3175127|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/26171374/|
3175128|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/29476940/|
3175129|NCT00954512||CSR Synospsi Links|http://www.merck.com/clinical-trials/study.html?id=P04722&kw=P04722&tab=access|
3175130|NCT01120249||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3175131|NCT01009255|110651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175132|NCT01009255|110651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175133|NCT01009255|110651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175134|NCT01009255|110651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175135|NCT01009255|110651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175136|NCT01009255|110651|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175137|NCT01009255|110651|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175138|NCT00483704||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-031&kw=0974-031&tab=access|
3175139|NCT03273465||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
3175140|NCT03707366||Individual Participant Data Set|https://osf.io/673eu/|
3175141|NCT05416645|post LSG GERD|Study Protocol|http://www.mans.edu.eg/|Postlaparoscopic sleeve gastrectomy
3175142|NCT00849134|111383|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175143|NCT00849134|111383|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175144|NCT00849134|111383|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175145|NCT00849134|111383|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175146|NCT00849134|111383|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175147|NCT00849134|111383|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177497|NCT00382772|107876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177498|NCT00551317|LPL110077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177499|NCT00551317|LPL110077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177500|NCT00551317|LPL110077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177501|NCT00551317|LPL110077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175148|NCT00849134|111383|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175149|NCT00005300|CSSCD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/csscd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175150|NCT00005300||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/csscd/|
3175151|NCT00005300||Study Forms|http://biolincc.nhlbi.nih.gov/studies/csscd/|
3175152|NCT00553397|SDY293|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
3175153|NCT00553397|SDY293|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293. The study protocol is available in the Design tab section.
3175154|NCT00553397|SDY293|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
3175155|NCT04214405||Clinical Study Report|https://www.ncbi.nlm.nih.gov|Birgfeld CB, Mundinger GS, Gruss JS. Evidence-based medicine: Evaluation and treatment of zygoma fractures. Plast Reconstr Surg 2017;139(1): 168e-80e.\[http://dx.doi.org/10.1097/PRS.0000000000002852\] \[PMID: 28027253\]
3175156|NCT00005159|NLMS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nlms/|Public-use IPD through BioLINCC. Registration is required for access.
3175157|NCT00282386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175857|NCT01134042|106829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175858|NCT00544271|263855/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175859|NCT00544271|263855/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175860|NCT00544271|263855/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175861|NCT00544271|263855/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175862|NCT00544271|263855/035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175863|NCT00544271|263855/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175864|NCT07178119|JNL-BridgingNL-2025|Study Protocol|https://ascenciaa.com/docs/study-protocol-version-1-0-jnl-bridgingnl-2025/|"The study protocol (Version 1.0, 27 August 2025, REC approved) is publicly available on the sponsor's website, Ascencia Aesthetics Academy. It can be accessed directly via the link above or by navigating to the About page under the Vision section of the website."
3175865|NCT00453687|AC2108380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175866|NCT00453687|AC2108380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175867|NCT00453687|AC2108380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175868|NCT00453687|AC2108380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175869|NCT00453687|AC2108380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177502|NCT00551317|LPL110077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177503|NCT00551317|LPL110077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177504|NCT00551317|LPL110077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177505|NCT01969708|PB2016-103333|Study Protocol|https://ntrl.ntis.gov/NTRL/|SCORE2 Protocol Version 3.0 (the Identifier for the appendices is PB2016-103334)
3177506|NCT00506350|109817|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177507|NCT00506350|109817|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177508|NCT00506350|109817|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177509|NCT00506350|109817|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177510|NCT00506350|109817|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177511|NCT00506350|109817|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177512|NCT00506350|109817|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177513|NCT01673529|115246|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177514|NCT01673529|115246|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177515|NCT01673529|115246|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177516|NCT01673529|115246|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177517|NCT01673529|115246|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177518|NCT01673529|115246|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177519|NCT01673529|115246|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177520|NCT06644573|PSHW Statistical Analysis Plan|Statistical Analysis Plan|https://drive.google.com/file/d/1iSQ5KoBNJtChtg1vSJDVFlar7D8ntaxI/view?usp=sharing|Study Protocol and Statistical Analysis Plan (SAP)
3177521|NCT06644573|Virtual Consultation SOAP Note|Individual Participant Data Set|https://drive.google.com/file/d/1uAAbC0gRFOthwnUiWz3O2sDyLgkGkiKf/view?usp=sharing|Virtual Consultation SOAP Note
3177522|NCT06644573|PSHW Informed Consent|Informed Consent Form|https://docs.google.com/document/d/1Otiwf8P6Rozk_MyA5qDgCnx-J7lXfJsfm0He5j5U9_I/edit?usp=sharing|PSHW Informed Consent For Research
3177523|NCT06644573|PROSOMNIA Sleep Quiz|Individual Participant Data Set|https://drive.google.com/file/d/1XWzVYL0L2OR8FzFUGtd0vggjwBflBAFa/view?usp=sharing|PROSOMNIA Sleep Quiz
3177524|NCT06644573|Sleep Quiz Evaluation|Clinical Study Report|https://drive.google.com/file/d/1Hzw1OvpbAn44nCbvqbtPwC25clwCbclW/view?usp=sharing|PSHES Sleep Quiz Scoring System
3177525|NCT06644573|Mood/Emotion Quality Scale|Individual Participant Data Set|https://drive.google.com/file/d/1-UzkVbn7UG57aZMg9d1LRB9yoLkjUlWS/view?usp=sharing|Mood/Emotion Quality Scale
3177526|NCT02257398|115775|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177527|NCT02257398|115775|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177528|NCT02257398|115775|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177529|NCT02257398|115775|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177530|NCT02257398|115775|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177531|NCT02257398|115775|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177532|NCT02257398|115775|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177533|NCT00674817|MAB110123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177534|NCT00674817|MAB110123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177535|NCT00674817|MAB110123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177536|NCT00674817|MAB110123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177537|NCT00674817|MAB110123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177538|NCT00674817|MAB110123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177539|NCT00674817|MAB110123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177540|NCT01424384|105012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177541|NCT01424384|105012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177542|NCT01424384|105012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177543|NCT01424384|105012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177544|NCT01424384|105012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177545|NCT01424384|105012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177546|NCT01424384|105012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177547|NCT03435250||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3177548|NCT03435250||Lay summary|https://clinicaltrials.servier.com/trial/a-phase-1-study-of-ag-270-in-the-treatment-of-subjects-with-advanced-solid-tumors-or-lymphoma-with-homozygous-deletion-of-mtap/|Study summary in lay language
3177549|NCT00379964||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177550|NCT01054885|112207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177551|NCT01054885|112207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177552|NCT01054885|112207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177553|NCT01054885|112207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177554|NCT01054885|112207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177555|NCT01054885|112207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177556|NCT01054885|112207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179291|NCT01196975|112963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179292|NCT01196975|112963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179293|NCT01196975|112963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179294|NCT00989287|113866|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179295|NCT00989287|113866|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179296|NCT00989287|113866|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179297|NCT00989287|113866|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179298|NCT00989287|113866|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179299|NCT00989287|113866|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177557|NCT00837434|SDY824|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|The Immunology Database and Analysis Portal (ImmPort) is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. The portal includes available analysis tools for researchers.
3177558|NCT00837434|SDY824|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|ImmPort study identifier is SDY824.
3177559|NCT00837434|SDY824|Study summary, -design, -adverse event(s), -summary of participant assessments, -medications, -demographics, -lab tests, -mechanistic assays, -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|ImmPort study identifier is SDY824.
3177560|NCT00951353|SDY951|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study identifier is SDY951.
3177561|NCT00951353|SDY951|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/studySearch|"ImmPort study identifier is SDY951.~ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public."
3177562|NCT00269217||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177563|NCT03941470|IRB17200056|Study Protocol|http://Email:ethics_committee12@yahoo.com|
3177564|NCT06602661||Study Protocol|https://docs.google.com/document/d/1-NMx1lP-_x1KHA0t49yEG7tNsFgepmyWPkbdFfWMPMc/edit?usp=sharing|
3177565|NCT06602661||Informed Consent Form|https://drive.google.com/file/d/1rON8VADRvws1J_I_rmqAAy2sNgL0I9c5/view?usp=sharing|
3177566|NCT00360230|106367|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177567|NCT00360230|106367|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177568|NCT00360230|106367|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177569|NCT00360230|106367|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177570|NCT00360230|106367|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177571|NCT00360230|106367|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177572|NCT05711810|10.5281/zenodo.7534361|Clinical Study Report|https://doi.org/10.5281/zenodo.7534361|The local hospital and medicare information are deidentified for their protection.
3177573|NCT02711891|Loperamide|Study Protocol|http://www.rush.edu/clinical-trials-rush-university-medical-center|Contact the Rush Office of Research Affairs for all materials 312 942-5498
3177574|NCT02711891|Loperamide|Informed Consent Form|http://www.rush.edu/clinical-trials-rush-university-medical-center|Contact the Rush Office of Research Affairs for all materials 312 942-5498
3177575|NCT06471972||Study Protocol|http://stepcare.org/biomarkers|Lab manuals and sample collection form
3177576|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/18426039|
3177577|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/19952380|
3177578|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/20922783|
3177579|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/?term=In+vitro+effects+of+detergent+sclerosants+on+coagulation%2C+platelets+and+microparticles.|
3177580|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/21725957|
3177581|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/16226898|
3177582|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/11231246|
3177583|NCT06999954||Informed Consent Form|https://www.sdsalliance.org/sds-gps|Available from the SDS-GPS program team at gps@sdsalliance.org
3177584|NCT01357850|112670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177585|NCT01357850|112670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177586|NCT01357850|112670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177587|NCT01357850|112670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177588|NCT01357850|112670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175158|NCT01440387|115418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175159|NCT01440387|115418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175160|NCT01440387|115418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175161|NCT01440387|115418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175162|NCT01440387|115418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175163|NCT01440387|115418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175164|NCT01485445|115440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175165|NCT01485445|115440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175166|NCT01485445|115440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175167|NCT01485445|115440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175168|NCT01485445|115440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175169|NCT01485445|115440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175170|NCT01485445|115440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175171|NCT00000589|TRAP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/trap/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175172|NCT00000589||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/trap/|
3175173|NCT00000589||Study Forms|http://biolincc.nhlbi.nih.gov/studies/trap/|
3175174|NCT01716520|116133|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175175|NCT01716520|116133|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175176|NCT01716520|116133|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175177|NCT01716520|116133|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175178|NCT01716520|116133|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175179|NCT01716520|116133|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175180|NCT01716520|116133|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175181|NCT00232596|VRX-RET-E22-301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175182|NCT00232596|VRX-RET-E22-301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175183|NCT00232596|VRX-RET-E22-301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175184|NCT00232596|VRX-RET-E22-301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175185|NCT00232596|VRX-RET-E22-301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175186|NCT00232596|VRX-RET-E22-301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175187|NCT00232596|VRX-RET-E22-301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175188|NCT00568334|109705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175189|NCT00568334|109705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175190|NCT00568334|109705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175191|NCT00568334|109705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175192|NCT00568334|109705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175193|NCT00568334|109705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175194|NCT03816618||Individual Participant Data Set|https://www.nice.org.uk/guidance/CG10|National Institute for Health and Clinical Excellence. Type 2 diabetes; prevention and management of foot problems
3175195|NCT02839564||Study Protocol|http://gmail.com|Study data can be requested by mailing to mjmolegraaf@gmail.com
3177589|NCT01357850|112670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177590|NCT01357850|112670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177591|NCT06054490|10.17605/OSF.IO/EFBC2|Study Protocol|https://osf.io/efbc2/|Supporting information for this study is available in the open science framework (OSF): the data set of individual participants, study protocol, statistical analysis plan, and informed consent form
3177592|NCT03038061||Informed Consent Form|http://ventilation.fbmi.cvut.cz/wp-content/uploads/2017/01/Informed-Consent-Form.pdf|Informed Consent
3177593|NCT06604390||Analytic Code|https://docs.google.com/spreadsheets/d/1jEVgkxVaewBnQVrAg7jR44Au-PHpsxi-/edit?usp=sharing&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;ouid=109214101212266635448&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;rtpof=true&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;sd=true|
3177594|NCT01353898||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1972-003&kw=1972-003&tab=access|
3177595|NCT03825406||Study Protocol|http://va.gov|Type Study Protocol To request an electronic copy send email to Anthony.bavry@va.gov or debra.robertson1@va.gov
3177596|NCT03825406||Individual Participant Data Set|http://va.gov|De-identified data set for primary and secondary outcomes measures To request an electronic copy send email to Anthony.bavry@va.gov or Debra.robertson1@va.gov
3177597|NCT01929317|116991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177598|NCT01929317|116991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177599|NCT06700473|10.1097/JNR.0000000000000129.|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/28277391/|https://pubmed.ncbi.nlm.nih.gov/28277391/
3177600|NCT06473740||Individual Participant Data Set|https://patientdatabase.ishemii.net/login|
3177601|NCT06591234||Study Protocol|https://www.ausl.bologna.it/|To send a request by mail
3177602|NCT06081816|10.4314/ahs.v19i1.55|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
3177603|NCT06081816|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
3177604|NCT04498598||Journal Abstracts|https://doi.org/10.1093/bja/aex194|A. Varvinskiy, T. Hinde, 21st Annual Scientific Meeting of the Difficult Airway Society: lessons learned and glimpses of the future , BJA: British Journal of Anaesthesia, Volume 119, Issue 3, September 2017, Pages e31-e47,
3177605|NCT04498598||Journal Abstacts|https://doi.org/10.1016/j.bja.2018.02.037|J. Law, I. Morris, Historical cohort study of 10 288 tracheal intubations facilitated by video laryngoscopy, British Journal of Anaesthesia, Volume 121, Issue 1, 2018, Pages e1-e2, ISSN 0007-0912, https://doi.org/10.1016/j.bja.2018.02.037. (https://www.sciencedirect.com/science/article/pii/S0007091218301831)
3177606|NCT00090207||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177607|NCT00614731|SDY3|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
3177608|NCT00614731|SDY3|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
3177609|NCT00614731|SDY3|Study design, -schedule of events, -demographics, -adverse events, -interventions, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
3177610|NCT01656408||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-002&kw=8150-002&tab=access|
3177611|NCT03584789||Study Protocol|https://www.researchprotocols.org/2021/4/e24342|
3177612|NCT01416324|114985|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177613|NCT01416324|114985|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177614|NCT01416324|114985|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177615|NCT01416324|114985|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177616|NCT01416324|114985|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177617|NCT01416324|114985|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177618|NCT01416324|114985|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177619|NCT04666220||This will be the repository containing Individual Participant Data, Study Protocol, Statistical Analysis Plan, Informed Consent Form, Clinical Study Report, Analytic Code of the VETC predictive Study|https://github.com/slrenne/VETC_Predictive_RCC-AC|
3177620|NCT00742261|MET111516|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177621|NCT00742261|MET111516|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177622|NCT00742261|MET111516|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177623|NCT00742261|MET111516|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177624|NCT00742261|MET111516|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177625|NCT00742261|MET111516|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177626|NCT00742261|MET111516|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177627|NCT05345652||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31571625/|
3177628|NCT06096961||thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|Kara, A. (2022). Bebekleri yenidoğan yoğun bakım ünitesi'nde yatan annelerde bebek kokusunun anksiyete ve süt miktarına etkisi \[Yüksek Lisans Tezi, Marmara Üniversitesi Sağlık Bilimleri Enstitüsü\]. YÖK Ulusal Tez Merkezi.
3177629|NCT06096961||thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|Turhan İ. (2020). Bebeği yenidoğan ünitesinde yatan annelere bebeğinin video görüntüsünün izletilmesinin anne sütü ve maternal bağlanmaya etkisi \[Yüksek Lisans Tezi, Erciyes Üniversitesi Sağlık Bilimleri Enstitüsü\]. YÖK Ulusal Tez Merkezi.
3177630|NCT06096961||thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|Varişoğlu, Y. (2019). Yenidoğan yoğun bakım ünitesinde prematüre bebeği olan annelere dinletilen müziğin anne sütü üretimine etkisi. \[Doktora Tezi, İstanbul Üniversitesi Cerrahpaşa Lisansüstü Eğitim Enstitüsü\]. YÖK Ulusal Tez Merkezi.
3177631|NCT00345358|107058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177632|NCT00345358|107058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177633|NCT00345358|107058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177634|NCT00345358|107058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177635|NCT00345358|107058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177636|NCT00345358|107058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177637|NCT01128634|113950|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177638|NCT01128634|113950|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177639|NCT01128634|113950|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177640|NCT01128634|113950|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177641|NCT01128634|113950|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177642|NCT01128634|113950|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177643|NCT01128634|113950|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177644|NCT02094924|200957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177645|NCT02094924|200957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177646|NCT02094924|200957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177647|NCT02094924|200957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172930|NCT01587716|115658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177648|NCT02094924|200957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177649|NCT02094924|200957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177650|NCT02094924|200957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177651|NCT05350397|REFERENCE|REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30982782/|
3177652|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_35_70_76_127.pdf|
3177653|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/30982782/|
3177654|NCT05350397|REFERENCE|REFERENCE|http://dergipark.org.tr/tr/pub/ikcusbfd/issue/60165/705219|
3177655|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_37_60_1_10.pdf|
3177656|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/18992625/|
3177657|NCT05350397|REFERENCE|REFERENCE|http://www.ncbi.nlm.nih.gov/books/NBK72567/|
3177658|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1016/j.ctcp.2021.101304|
3177659|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1097/HNP.0000000000000384|
3177660|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/23981400/|
3177661|NCT01745822||Individual Participant Data Set|https://dash.nichd.nih.gov/study/17511|
3177662|NCT01587924|116582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177663|NCT01587924|116582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177664|NCT01587924|116582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177665|NCT01587924|116582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177666|NCT01587924|116582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177667|NCT01587924|116582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177668|NCT01587924|116582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177669|NCT06595771||Study Protocol|https://haydarpasanumuneah.saglik.gov.tr/|
3177670|NCT02581410|201198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177671|NCT02581410|201198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177672|NCT02581410|201198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177673|NCT02581410|201198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177674|NCT02581410|201198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177675|NCT02581410|201198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177676|NCT02581410|201198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177677|NCT04591808||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3172931|NCT01587716|115658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172932|NCT01587716|115658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172933|NCT02173470||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26857421|Ultra low-dose chest ct with iterative reconstructions as an alternative to conventional chest x-ray prior to heart surgery (CRICKET study): Rationale and design of a multicenter randomized trial.
3172934|NCT01231620|114373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177678|NCT04591808||Study Protocol|https://clinicaltrials.servier.com/|
3177679|NCT04591808||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3177680|NCT04591808||Informed Consent Form|https://clinicaltrials.servier.com/|
3177681|NCT04591808||Clinical Study Report|https://clinicaltrials.servier.com/|
3177682|NCT04591808||[study-level clinical trial data]|https://clinicaltrials.servier.com/|
3177683|NCT00555061|TOC106489|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177684|NCT00555061|TOC106489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177685|NCT00555061|TOC106489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175196|NCT02064465|200697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175197|NCT02064465|200697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175198|NCT02064465|200697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175199|NCT02064465|200697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175200|NCT02064465|200697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175201|NCT02064465|200697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175202|NCT02064465|200697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175203|NCT00359177|NKT102785|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175204|NCT00359177|NKT102785|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175205|NCT00359177|NKT102785|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175206|NCT00359177|NKT102785|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175207|NCT00359177|NKT102785|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175208|NCT00359177|NKT102785|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175209|NCT00359177|NKT102785|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175210|NCT01636947||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-225&kw=0869-225&tab=access|
3175211|NCT00103922|CIL103657|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175212|NCT00103922|CIL103657|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175213|NCT00103922|CIL103657|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175214|NCT00103922|CIL103657|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175215|NCT00103922|CIL103657|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175216|NCT00103922|CIL103657|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175217|NCT00005131|ARIC|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/aric/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175218|NCT00005131||Study Forms|http://www2.cscc.unc.edu/aric/cohort-forms|
3175219|NCT00005131||Study Manuals|http://www2.cscc.unc.edu/aric/cohort-forms|
3175220|NCT03532815||Study Protocol|https://sites.google.com/view/lifestyle-intervention-/home|
3177686|NCT00555061|TOC106489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177687|NCT00555061|TOC106489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175221|NCT02713438||Study Protocol|https://drive.google.com/file/d/1bosgzFmvKglMyMjhELiSg-fqzw1pn1nf/view?usp=sharing|The handbook with the protocol for experimenters (in English)
3177688|NCT00555061|TOC106489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177689|NCT00555061|TOC106489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177690|NCT01175083|114056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177691|NCT01175083|114056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177692|NCT01175083|114056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177693|NCT01175083|114056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177694|NCT01175083|114056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177695|NCT01175083|114056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177696|NCT01175083|114056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177697|NCT00976560|113009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177698|NCT00976560|113009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177699|NCT00976560|113009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177700|NCT00976560|113009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177701|NCT00976560|113009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177702|NCT00976560|113009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177703|NCT00976560|113009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177704|NCT00951977|SDY290|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
3177705|NCT00951977|SDY290|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
3177706|NCT00951977|SDY290|Study summary, -design, -demographics, -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
3177707|NCT03286517||Any information required can be provided|http://www.qau.edu.pk/profile.php?id=802001|Prof. Muhammad Shahab will provide the information upon request.
3177708|NCT00760617|111737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177709|NCT00760617|111737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177710|NCT00760617|111737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177711|NCT00760617|111737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177712|NCT00760617|111737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177713|NCT00760617|111737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177714|NCT00760617|111737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177715|NCT01192191|114156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177716|NCT01192191|114156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177717|NCT01192191|114156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177718|NCT01192191|114156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177719|NCT01192191|114156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177720|NCT01192191|114156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177721|NCT01192191|114156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177722|NCT06947681|Not available at moment|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|Most of the informations available at This site and Google Scholar
3177723|NCT02914301|FWA00005945|Informed Consent Form|https://files.acrobat.com/a/preview/c262292c-6de1-4f73-bae3-689555b8c77f|
3177724|NCT02914301|Post-Partum Survey|Individual Participant Data Set|https://files.acrobat.com/a/preview/5ec925dd-52ad-4b07-b6fc-2084d2f751d5|
3177725|NCT02914301|Prenatal Participant Data -22|Individual Participant Data Set|https://files.acrobat.com/a/preview/984213bb-ccef-419b-8f56-87336004ec5a|
3177726|NCT03189238||Informed Consent Form|http://cvvd.org/research|"Link for the informed consent is in the section titled PLATELET RICH PLASMA (PRP) INJECTIONS FOR THE TREATMENT OF FEMALE ORGASMIC DISORDER."
3177727|NCT01485172|111662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177728|NCT01485172|111662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175222|NCT01362244|111782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175223|NCT01362244|111782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175224|NCT01362244|111782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175225|NCT01362244|111782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175226|NCT01362244|111782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175227|NCT01362244|111782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175228|NCT01362244|111782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175229|NCT01370616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0826-061&kw=0826-061&tab=access|
3175230|NCT00411073|SB 480848/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175231|NCT00411073|SB 480848/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175232|NCT00411073|SB 480848/035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175233|NCT00411073|SB 480848/035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175234|NCT00411073|SB 480848/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175235|NCT00411073|SB 480848/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175236|NCT00411073|SB 480848/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175237|NCT02638051|10.3892/mco.2017.1221|Clinical Study Report|https://www.spandidos-publications.com/mco/6/5/723?articleTypes=ARTICLE&articleTypes=REVIEW&fileTypes=LETTER_TO_THE_EDITOR&fileTypes=MANUSCRIPT&fileTypes=TABLE&fileTypes=IMAGE&fileTypes=LANG_EDIT|Pang CLK, Zhang X, Wang Z, Ou J, Lu Y, Chen P, Zhao C, Wang X, Zhang H, Roussakow SV. Local modulated electro-hyperthermia in combination with traditional Chinese medicine vs. intraperitoneal chemoinfusion for the treatment of peritoneal carcinomatosis with malignant ascites: A phase II randomized trial. Mol Clin Oncol. 2017;6:723-32,
3175238|NCT02983916||Clinical Study Report|https://doi.org/10.1038/s41395-018-0158-9|
3175239|NCT02095405||Published article|http://onlinelibrary.wiley.com/doi/10.1111/jce.12504/full|DOI: 10.1111/jce.12504
3175240|NCT03449992||Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.5873190.v1|
3175241|NCT06908941|CCUREC111122101|Informed Consent Form|https://rec.ccu.edu.tw/p/412-1152-3134.php?Lang=zh-tw|National Chung Cheng University Human Research Ethics Center
3175242|NCT00530790|107846|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175243|NCT00530790|107846|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175244|NCT00530790|107846|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175245|NCT00530790|107846|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175246|NCT01648192|116681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175247|NCT01648192|116681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175248|NCT01648192|116681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175249|NCT01648192|116681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175250|NCT01648192|116681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175251|NCT01648192|116681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175252|NCT01648192|116681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175253|NCT01119846|111598|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177729|NCT01485172|111662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175254|NCT01119846|111598|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175255|NCT01119846|111598|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175256|NCT01119846|111598|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175257|NCT01119846|111598|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175258|NCT01119846|111598|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175259|NCT01119846|111598|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175260|NCT01148459|112745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175261|NCT01148459|112745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175262|NCT01148459|112745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175263|NCT01148459|112745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175264|NCT01148459|112745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175265|NCT01148459|112745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175266|NCT02785562||Study Protocol|http://www.g-f-p-c.org|The login can be obtained directly on gfpc site.
3175267|NCT00034944||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175268|NCT00482599||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175269|NCT03075332|plataforma brasil|Ethics committee project|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|all project
3175270|NCT01088711||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-004&kw=3102-004&tab=access|
3175271|NCT00603382|FFA109687|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175272|NCT00603382|FFA109687|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175273|NCT00603382|FFA109687|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175274|NCT00603382|FFA109687|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175275|NCT00603382|FFA109687|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175276|NCT00603382|FFA109687|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175277|NCT00603382|FFA109687|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175278|NCT00329745|107070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175279|NCT00329745|107070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175280|NCT00329745|107070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175281|NCT00329745|107070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 107070 are summarised with studies 444563/028, 444563/029, 444563/030, 107072, and 107076 on the GSK Clinical Study Register.
3175282|NCT00329745|107070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177730|NCT01485172|111662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177731|NCT01485172|111662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177732|NCT01485172|111662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177733|NCT00535288||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06472&kw=P06472&tab=access|
3177734|NCT00389987||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177735|NCT00329355|TRX105852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177736|NCT00329355|TRX105852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177737|NCT00329355|TRX105852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177738|NCT00329355|TRX105852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177739|NCT00329355|TRX105852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177740|NCT00329355|TRX105852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177741|NCT00329355|TRX105852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177742|NCT01818011|116266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175283|NCT00329745|107070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177743|NCT01818011|116266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172935|NCT01231620|114373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172936|NCT01231620|114373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172937|NCT01231620|114373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172938|NCT01231620|114373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172939|NCT01231620|114373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172940|NCT01231620|114373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172941|NCT01366846|LEAP-On (ITN049AD)|Individual Participant Data Set|https://www.itntrialshare.org/|
3172942|NCT01366846|LEAP-On (ITN049AD)|Study protocol synopsis; datasets and figures from published NEJM 2016 article|https://www.itntrialshare.org/|
3172943|NCT01590810||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-001&kw=8150-001&tab=access|
3172944|NCT00540228|110794|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172945|NCT00540228|110794|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172946|NCT00540228|110794|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172947|NCT00540228|110794|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172948|NCT00540228|110794|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172949|NCT00540228|110794|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172950|NCT05814744||Individual Participant Data Set|https://drive.google.com/file/d/12gNVWYJj8dyy6Bh-6G59rFn2AQzjHycS/view?usp=share_link|
3172951|NCT05814744||Informed Consent Form|https://drive.google.com/file/d/1qPpYheG63CcWJqwWAD3ma3jFmmqCPWgm/view?usp=share_link|
3172952|NCT05814744||Study Protocol|https://drive.google.com/file/d/16x_dHL6GsO6V-K3p13T9EluZi20l4WtN/view?usp=share_link|
3172953|NCT00570492|FFR101782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175284|NCT02696174||Study Protocol|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Total protocol FILE named protocol.pdf
3175285|NCT02696174||Informed Consent Form|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Patient Information Sheet and Consent forms in English and Bahasa Malaysia
3175286|NCT02696174||Questionnaires|https://www.flipdrive.com/site/login|Username: HMI Password: insurance All questionnaires (English) uploaded
3175287|NCT01039805|112571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175288|NCT01039805|112571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175289|NCT01039805|112571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175290|NCT01039805|112571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175291|NCT01039805|112571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175292|NCT01039805|112571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175293|NCT01039805|112571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175294|NCT03249168||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/26705527|
3175295|NCT02922075||Individual Participant Data Set|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|"Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets.~All data can be downloaded from the website, if there are any questions please feel free to contact us."
3175296|NCT02922075||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
3175297|NCT02922075||Statistical Analysis Plan|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
3175298|NCT02922075||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
3175299|NCT02922075||Clinical Study Report|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
3175300|NCT02922075||Analytic Code|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
3175301|NCT00519467|714703/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175302|NCT00519467|714703/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175303|NCT00519467|714703/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175304|NCT00519467|714703/003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175305|NCT00519467|714703/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175306|NCT00519467|714703/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175307|NCT00519467|714703/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175308|NCT00370591|SAM40104|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175309|NCT00370591|SAM40104|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175310|NCT00370591|SAM40104|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175311|NCT00370591|SAM40104|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175312|NCT00370591|SAM40104|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175313|NCT00370591|SAM40104|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175314|NCT00370591|SAM40104|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175315|NCT01400906|114748|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175316|NCT01400906|114748|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175317|NCT01400906|114748|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177744|NCT01818011|116266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177745|NCT01818011|116266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177746|NCT01818011|116266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177747|NCT01818011|116266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177748|NCT01818011|116266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177749|NCT01049009|26285691|Publication|https://www.ncbi.nlm.nih.gov/pubmed/26285691|
3177750|NCT01318980|114604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177751|NCT01318980|114604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177752|NCT01318980|114604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177753|NCT01318980|114604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177754|NCT01318980|114604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177755|NCT01318980|114604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177756|NCT01318980|114604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177757|NCT00265148|BRL-49653/461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177758|NCT00265148|BRL-49653/461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177759|NCT00265148|BRL-49653/461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177760|NCT00265148|BRL-49653/461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177761|NCT00265148|BRL-49653/461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177762|NCT00265148|BRL-49653/461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177763|NCT00265148|BRL-49653/461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177764|NCT01015638|114546|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177765|NCT01015638|114546|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177766|NCT01015638|114546|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177767|NCT01015638|114546|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177768|NCT01015638|114546|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177769|NCT03105713|2016/1102|Study Protocol|https://prosjektbanken.forskningsradet.no/en/project/FORISS/320475|Study protocol version 2.1 is up-loaded in ClinicalTrials.gov along with the SAP. English version of the trial and other relevant information on this study can be accessed by e-mail to arvid.steinar.haugen@helse-bergen.no
3177770|NCT07157371|PMID: 28811774|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28811774/|Intervention is being used on other metabolic disorder. And the main principal investigator is the co-supervisor of the current research and i have taken the permission.
3177771|NCT01696604|116715|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177772|NCT01696604|116715|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177773|NCT01696604|116715|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177774|NCT01696604|116715|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177775|NCT01696604|116715|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177776|NCT01696604|116715|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177777|NCT01696604|116715|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177778|NCT00368199||Individual Participant Data Set|https://peerj.com/articles/2037/|
3177779|NCT01702493|117041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177780|NCT01702493|117041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177781|NCT01702493|117041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177782|NCT01702493|117041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177783|NCT01702493|117041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177784|NCT01702493|117041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177785|NCT01702493|117041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177786|NCT01209104|113722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177787|NCT01209104|113722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177788|NCT01209104|113722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177789|NCT01209104|113722|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177790|NCT01209104|113722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177791|NCT01209104|113722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177792|NCT01209104|113722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177793|NCT01449799|113423|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177794|NCT01449799|113423|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177795|NCT01449799|113423|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177796|NCT01449799|113423|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177797|NCT01449799|113423|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177798|NCT01449799|113423|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177799|NCT01449799|113423|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177800|NCT06757920|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3177801|NCT07156396|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
3177802|NCT03139591||Textbook|https://books.google.co.id/books/about/Laryngeal_Mask_Anesthesia.html?id=XBJsAAAAMAAJ&redir_esc=y|Problems. In: Brimacombe JR. Laryngeal Mask Anesthesia principles and practice. London: Saunders Ltd, 2004;551-71.
3177803|NCT00435045|OM9L|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177804|NCT00435045|OM9L|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177805|NCT00435045|OM9L|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177806|NCT00435045|OM9L|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177807|NCT00435045|OM9L|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177808|NCT00435045|OM9L|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177809|NCT00435045|OM9L|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177810|NCT06940778|blenti|Study Protocol|https://hcor.com.br|blenti
3177811|NCT03673397||Individual Participant Data Set|https://doi.org/10.7910/DVN/WASN36|
3177812|NCT00776919|114677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177813|NCT00776919|114677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177814|NCT00776919|114677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177815|NCT00776919|114677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177816|NCT00776919|114677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177817|NCT00776919|114677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177818|NCT00776919|114677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177819|NCT00376714|AC2105333|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177820|NCT00376714|AC2105333|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177821|NCT00376714|AC2105333|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177822|NCT00376714|AC2105333|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177823|NCT00376714|AC2105333|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177824|NCT00376714|AC2105333|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177825|NCT00376714|AC2105333|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177826|NCT01128621|113132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177827|NCT01128621|113132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177828|NCT01128621|113132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177829|NCT01128621|113132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177830|NCT01128621|113132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177831|NCT01128621|113132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177832|NCT01128621|113132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177833|NCT00533676||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177834|NCT02758483|63683417.1.0000.5257|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
3177835|NCT07144891||article|https://pmc.ncbi.nlm.nih.gov/articles/PMC7488296/|
3177836|NCT01115322|114573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177837|NCT01115322|114573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177838|NCT01115322|114573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177839|NCT01115322|114573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177840|NCT01115322|114573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179300|NCT00989287|113866|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179301|NCT00695669|111626|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179302|NCT00695669|111626|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179303|NCT00695669|111626|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179304|NCT00695669|111626|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179305|NCT00695669|111626|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179306|NCT00695669|111626|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179307|NCT00695669|111626|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179308|NCT00374842|108656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179309|NCT00374842|108656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172954|NCT00570492|FFR101782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172955|NCT00570492|FFR101782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175318|NCT01400906|114748|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175319|NCT01400906|114748|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175320|NCT01400906|114748|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175321|NCT01400906|114748|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175322|NCT00435461|FFU109045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175323|NCT00435461|FFU109045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175324|NCT00435461|FFU109045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175325|NCT00435461|FFU109045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175326|NCT00435461|FFU109045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175327|NCT00435461|FFU109045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175328|NCT00657657|110071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175329|NCT00657657|110071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177841|NCT01115322|114573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177842|NCT01115322|114573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177843|NCT00363545|107077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177844|NCT00363545|107077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175330|NCT00657657|110071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175331|NCT00657657|110071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177845|NCT00363545|107077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177846|NCT00363545|107077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177847|NCT00363545|107077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177848|NCT00363545|107077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177849|NCT07145281||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/TCRUW|
3177850|NCT06947330||Study Protocol|https://www.ilovepdf.com/download/6bhl069fp1wzcttl2h9kympvwcw0z348Az4p933p7tx6gm77hss9dbx3gbxjvm9ypjzwt97hdptj659jxht28ybgh1m4lyj34sth4k980tx1wzvm0A2pjghl7rs70r7pk67kblvbcfl9fn68lp5c06pjtdd07x9jqh7grqdl8b1kkp3b6271/88w|
3177851|NCT01106092|113264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177852|NCT01106092|113264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177853|NCT01106092|113264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177854|NCT01106092|113264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177855|NCT01106092|113264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177856|NCT01106092|113264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177857|NCT01106092|113264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177858|NCT01144299|114292|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177859|NCT01144299|114292|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177860|NCT01144299|114292|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177861|NCT01144299|114292|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177862|NCT01144299|114292|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177863|NCT01144299|114292|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177864|NCT01144299|114292|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177865|NCT07131241||Individual Participant Data Set|https://www.fjmu.edu.cn|For more information, please contact: dajunchai@126.com
3177866|NCT02853799||Study Protocol|http://journals.lww.com/annalsofsurgery/pages/articleviewer.aspx?year=2016&issue=03000&article=00007&type=abstract|"2\. Chowdhury, Abeed H., et al. Effects of Bolus and Continuous Nasogastric Feeding on Gastric Emptying, Small Bowel Water Content, Superior Mesenteric Artery Blood Flow, and Plasma Hormone Concentrations in Healthy Adults: A Randomized Crossover Study. Annals of Surgery (2014)."
3177867|NCT00386542||Interim results presentation|https://web.archive.org/web/20210528232541/https://siamlotus.com/ppt-2013-meetingpresentations/Palomeque&Weniger_History-Cutaneous-Influenza+Trial-Results_CDC-Atlanta_2013-09-24_Color-handouts.pdf|Palomeque FS, Weniger BG, Jet-Injected Cutaneous Influenza Vaccination Study Group. History and Technologies for Cutaneous Influenza Vaccination; and Preliminary Results from a CDC Trial of Jet-Injected, Needle-free Influenza Vaccine in ≥6 to \<24-month-old Children in the Dominican Republic. CDC Vaccine Technology Seminar Series \& CDC Influenza Division Seminar Series (Centers for Disease Control and Prevention), Atlanta, GA, 24 September 2013
3177868|NCT00794898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175332|NCT00657657|110071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175333|NCT00657657|110071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175334|NCT05880095||Study Protocol|https://ensati.wixsite.com/ensati/qu%C3%A9-es-ensati|
3175335|NCT03602833||Summary of Product Characteristics|https://www.medicines.org.uk/emc/product/8453|
3175336|NCT05543031||Study Protocol|http://dc.etsu.edu/etd/772|
3175337|NCT05543031||Study Protocol|http://encompass.eku.edu/honors_theses|
3175338|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Baothman+OA%2C+Zamzami+MA%2C+Taher+I%2C+ABugaker+J%2C+Abu-Farhca+MA.+The+role+of+Gut+Microbiota+in+the+development+of+obesity+and+diabetes|
3175339|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Barengolts+E.+Vitamin+D+and+prebiotics+may+benefit+the+intestinal+microbacteria+and+improve+glucose+homeostasis+in+prediabetes+and+type+2+diabetes.|
3175340|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Capdor+J%2C+Foster+M%2C+Petocz+P%2C+Samman+S.+Zinc+and+glycemic+control%3A+a+meta-analysis+of+randomised+placebo+controlled+supplementation+trials+in+humans.|
3175341|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Fruit+and+vegetable+intake+and+the+association+with+glucose+parameters%3A+a+cross-sectional+analysis+of+the+Let%27s+Prevent+Diabetes+Study|
3175342|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/15008827|
3175343|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Foster+M%2C+Petocz+P%2C+Samman+S.+Inflammation+markers+predict+zinc+transporter+gene+expression+in+women+with+type+2+diabetes+mellitus|
3175344|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Gokhale+NH%2C+Acharya+AB%2C+Patil+VS%2C+Trivedi+DJ%2C+Thakur+SL.+(2013)+A+short-term+evaluation+of+the+relationship+between+plasma+ascorbic+acid+levels+and+periodontal+disease+in+systemically+healthy+and+type+2+diabetes+mellitus+subjects|
3179310|NCT00374842|108656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179311|NCT00374842|108656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179312|NCT00374842|108656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175345|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Jansen+J%2C+Rosenkranz+E%2C+Overbeck+S%2C+Warmuth+S%2C+Mocchegiani+E%2C+Giacconi+R%2C+Weiskirchen+R%2C+Karges+W%2C+Rink+L.+Disturbed+zinc+homeostasis+in+diabetic+patients+by+in+vitro+and+in+vivo+analysis+of+insulinomimetic+activity+of+zinc|
3175346|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/20606205|
3175347|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22699609|
3175348|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Kayaniyil+S%2C+Vieth+R%2C+Retnakaran+R%2C+Knight+JA%2C+Qi+Y%2C+Gerstein+HC%2C+et+al.+Association+of+vitamin+D+with+insulin+resistance+and+beta-cell+dysfunction+in+subjects+at+risk+for+type+2+diabetes.+Diabetes+care|
3175349|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Ley%2C+R.+E.%2C+Lozupone%2C+C.+A.%2C+Hamady%2C+M.%2C+Knight%2C+R.+%26+Gordon%2C+J.+I.+Worlds+within+worlds%3A+evolution+of+the+vertebrate+gut+microbiota|
3175350|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Mandl+J%2C+Szarka+A%2C+Bángheyl.+(2009)+Vitamin+C%3A+update+on+physiology+and+pharmacology.+B+J+Pharmacol|
3175351|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Efficacy+of+supplementary+vitamins+C+and+E+on+anxiety%2C+depression+and+stress+in+type+2+diabetic+patients%3A+a+randomized%2C+single-blind%2C+placebo-controlled+trial|
3179313|NCT00137930|104480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179314|NCT00137930|104480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179315|NCT00137930|104480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179316|NCT00137930|104480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179317|NCT00137930|104480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175352|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Effect+of+vitamin+C+supplementation+on+postprandial+oxidative+stress+and+lipid+profile+in+type+2+diabetic+patients.|
3179318|NCT00137930|104480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179319|NCT00355082|LAM30055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179320|NCT00355082|LAM30055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179321|NCT00355082|LAM30055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179322|NCT00355082|LAM30055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179323|NCT00355082|LAM30055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179324|NCT00355082|LAM30055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179325|NCT00355082|LAM30055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179326|NCT00464815|109069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179327|NCT00464815|109069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179328|NCT00464815|109069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179329|NCT00464815|109069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179330|NCT00464815|109069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179331|NCT00464815|109069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175353|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/9794114|
3175354|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Rafighi%2C+Z.%2C+Shiva+A.%2C+Arab%2C+S.+and+Mohd+Yousof%2C+R.+(2013)+Association+of+dietary+vitamin+C+and+E+intake+and+antioxidant+enzymes+in+type+2+diabetes+mellitus+patients|
3175355|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Zinc+as+a+potential+coadjuvant+in+therapy+for+type+2+diabetes.|
3175356|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Sarmento+RA%2C+Silva+FM%2C+Sbruzzi+G%2C+Schaan+BD%2C+Almeida+JC.+Antioxidant+micronutrients+and+cardiovascular+risk+in+patients+with+diabetes%3A+a+systematic+review|
3179332|NCT00464815|109069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179333|NCT06485817||Analytic Code|https://osf.io/3jvw8/|Project directory where study relevant documentation can be found and data will be uploaded.
3179334|NCT00515502|AC4108123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179335|NCT00515502|AC4108123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179336|NCT00515502|AC4108123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179337|NCT00515502|AC4108123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179338|NCT00515502|AC4108123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179339|NCT00515502|AC4108123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179340|NCT00515502|AC4108123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179341|NCT06520111|sice|Study Protocol|https://siceitalia.com/|SICE- Team di ricerca Endocrino-metabolica- crisal
3179342|NCT00679939|AVD111179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179343|NCT00679939|AVD111179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179344|NCT00679939|AVD111179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179345|NCT00679939|AVD111179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179346|NCT00679939|AVD111179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179347|NCT00679939|AVD111179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179348|NCT00679939|AVD111179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179349|NCT01258608|200149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179350|NCT01258608|200149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179351|NCT01258608|200149|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179352|NCT01258608|200149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175357|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/25284151|
3175358|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/27915988|
3175359|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Insulino-mimetic+and+anti-diabetic+effects+of+zinc|
3175360|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/28615382|
3175361|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/12502486|
3175362|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22375253|
3179353|NCT01258608|200149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179354|NCT01258608|200149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179355|NCT06182306||Study Protocol|https://www.pearbio.com/pearmet|Company website with background and information and links to protocol, etc.
3179356|NCT04605978||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3179357|NCT04605978||Study Protocol|https://clinicaltrials.servier.com/|
3179358|NCT04605978||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3179359|NCT04605978||Informed Consent Form|https://clinicaltrials.servier.com/|
3179360|NCT04605978||Clinical Study Report|https://clinicaltrials.servier.com/|
3179361|NCT04605978||study-level clinical trial data|https://clinicaltrials.servier.com/|
3175363|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Iman+M+Ibrahim%2C+and+Manal+M+Alkady.+Role+of+Vitamin+D+on+glycemic+control+and+oxidative+stress+in+type+2+diabetes+mellitus|
3179362|NCT05154279||Study Protocol|https://www.ijrcog.org/index.php/ijrcog/article/view/3925|
3179363|NCT05154279||Study Protocol|https://ebwhj.journals.ekb.eg/article_125772.html|
3175364|NCT01147718|111680|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179364|NCT01627327|115805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175365|NCT01147718|111680|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179365|NCT01627327|115805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179366|NCT01627327|115805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179367|NCT01627327|115805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179368|NCT01627327|115805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179369|NCT01627327|115805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179370|NCT01627327|115805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179371|NCT00746122||Study Protocol|http://www.imperial.ac.uk/department-surgery-cancer/research/surgery/clinical-trials/improve/documents/|Final protocol version 6.0 dated 28th August 2013
3179372|NCT06038760||Study Protocol|https://www.pearbio.com/pearglio|
3179373|NCT01377480||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05267&kw=P05267&tab=access|
3179374|NCT00428090|105640|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179375|NCT00428090|105640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179376|NCT00428090|105640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179377|NCT00428090|105640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179378|NCT00428090|105640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179379|NCT00428090|105640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179380|NCT00428090|105640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179381|NCT00306982|106622|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179382|NCT00306982|106622|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179383|NCT00306982|106622|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179384|NCT00306982|106622|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179385|NCT00306982|106622|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179386|NCT00306982|106622|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179387|NCT00518115|GLP110125|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179388|NCT00518115|GLP110125|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179389|NCT00518115|GLP110125|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179390|NCT00518115|GLP110125|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179391|NCT00518115|GLP110125|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179392|NCT00518115|GLP110125|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179393|NCT00518115|GLP110125|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179394|NCT00697749|208129/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179395|NCT00697749|208129/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179396|NCT00697749|208129/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179397|NCT00697749|208129/034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179398|NCT00697749|208129/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179399|NCT00697749|208129/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179400|NCT01825213|PMID: 25181365|Peer reviewed article|http://ieeexplore.ieee.org/document/6887313/?arnumber=6887313|
3179401|NCT06313762|(IRRID): PRR1-10.2196/35910|Study Protocol|https://www.researchprotocols.org/2022/4/e35910|Protocol: Use of Virtual Reality in the Reduction of Pain After the Administration of Vaccines Among Children in Primary Care Centers: Protocol for a Randomized Clinical Trial
3175366|NCT01147718|111680|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179402|NCT00708916|PMID: 23134988|Clinical Study Report|http://jddonline.com/articles/dermatology/S1545961612P1224X|"Apremilast for discoid lupus erythematosus: results of a phase 2, open-label, single-arm, pilot study. De Souza A, Strober BE, Merola JF, Oliver S, Franks AG Jr.~J Drugs Dermatol. 2012 Oct;11(10):1224-6. PMID: 23134988"
3179403|NCT06264479||Study Protocol|https://www.pearbio.com/peartree2|
3175367|NCT01147718|111680|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175368|NCT01147718|111680|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175369|NCT01147718|111680|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175370|NCT01147718|111680|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175371|NCT00547248|109509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175372|NCT00547248|109509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175373|NCT00547248|109509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175374|NCT00547248|109509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175375|NCT00547248|109509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175376|NCT00547248|109509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175377|NCT00547248|109509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175378|NCT00406081|SDY2|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
3175379|NCT00406081|SDY2|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
3175380|NCT00406081|SDY2|Study design, -schedule of events, -demographics, -adverse events, -interventions, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
3175381|NCT01934127|115415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175382|NCT01934127|115415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175383|NCT01934127|115415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175384|NCT01934127|115415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175385|NCT01934127|115415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175386|NCT01934127|115415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175387|NCT00610168|110806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175388|NCT00610168|110806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175389|NCT00610168|110806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175390|NCT00610168|110806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175391|NCT00610168|110806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175392|NCT00610168|110806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175393|NCT00610168|110806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175394|NCT03126253||Report of the survey along with sampling plan|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|
3175395|NCT04842552||Informed Consent Form|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3175396|NCT04842552||Clinical Study Report|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3175397|NCT04842552||Study Protocol|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3175398|NCT04842552||Statistical Analysis Plan|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3175399|NCT00346749|ADC105931|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175400|NCT00346749|ADC105931|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175401|NCT00346749|ADC105931|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179404|NCT01337674||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4618-010&kw=4618-010&tab=access|
3179405|NCT04322123||Study Protocol|https://www.medrxiv.org/content/10.1101/2020.05.19.20106997v1|Preprint of the Protocol
3179406|NCT01777321|116760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179407|NCT01777321|116760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179408|NCT01777321|116760|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179409|NCT01777321|116760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179410|NCT01777321|116760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179411|NCT01777321|116760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179412|NCT01777321|116760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179413|NCT01477853||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431E-211&kw=0431E-211&tab=access|
3179414|NCT01506895|115403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179415|NCT01506895|115403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179416|NCT01506895|115403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179417|NCT01506895|115403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179418|NCT01506895|115403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179419|NCT01506895|115403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179420|NCT01506895|115403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179421|NCT01879423|115207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179422|NCT01879423|115207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179423|NCT01879423|115207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179424|NCT01879423|115207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179425|NCT01879423|115207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179426|NCT01879423|115207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179427|NCT01879423|115207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179428|NCT00361959|SCO40036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179429|NCT00361959|SCO40036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179430|NCT00361959|SCO40036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179431|NCT00361959|SCO40036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179432|NCT00361959|SCO40036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179433|NCT00361959|SCO40036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179434|NCT00361959|SCO40036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179435|NCT02920697||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3179436|NCT02920697||Study Protocol|https://clinicaltrials.servier.com/|
3179437|NCT02920697||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3179438|NCT02920697||Informed Consent Form|https://clinicaltrials.servier.com/|
3179439|NCT02920697||study-level clinical trial data|https://clinicaltrials.servier.com/|
3179440|NCT02920697||Clinical Study Report|https://clinicaltrials.servier.com/|
3179441|NCT02254447|201713|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179442|NCT02254447|201713|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179443|NCT02254447|201713|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179444|NCT02254447|201713|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179445|NCT02254447|201713|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172956|NCT00570492|FFR101782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175402|NCT00346749|ADC105931|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175403|NCT00346749|ADC105931|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179446|NCT02254447|201713|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179447|NCT02254447|201713|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179448|NCT01218126|113006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179449|NCT01218126|113006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179450|NCT01218126|113006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179451|NCT01218126|113006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179452|NCT01218126|113006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179453|NCT01218126|113006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179454|NCT01218126|113006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179455|NCT03117725|31098|Study Protocol|https://ezdrug.mfds.go.kr|
3179456|NCT00508261|109835|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179457|NCT00508261|109835|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172957|NCT00570492|FFR101782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179458|NCT00508261|109835|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179459|NCT00508261|109835|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179460|NCT00508261|109835|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179461|NCT00508261|109835|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179462|NCT00508261|109835|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179463|NCT04792125|31270846|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31270846/|External electrical stimulation compared with intravaginal electrical stimulation for the treatment of stress urinary incontinence in women: A randomized controlled noninferiority trial
3179464|NCT03077464||preliminary results|http://hdl.handle.net/2097/19148|Rodicheva master's thesis document with preliminary analyses
3179465|NCT02614443|10.1186/s40814-016-0068-9|Study Protocol|https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-016-0068-9|
3179466|NCT03681574|study protocol|Study Protocol|https://www.justbeamit.com/k7ciq|study protocol
3179467|NCT03681574|data set|Individual Participant Data Set|https://www.justbeamit.com/nwxjr|individual participant data set
3179468|NCT03681574|informed consent form|Informed Consent Form|https://www.justbeamit.com/n2c2d|consert form
3179469|NCT03681574|statistical plan|Statistical Analysis Plan|https://www.justbeamit.com/43kxq|statistical plan
3179470|NCT00453986|109067|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179471|NCT00453986|109067|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179472|NCT00453986|109067|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179473|NCT00453986|109067|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179474|NCT00453986|109067|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179475|NCT00453986|109067|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179476|NCT00453986|109067|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179477|NCT00796250||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179478|NCT01376323|114728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172958|NCT00570492|FFR101782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179479|NCT01376323|114728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179480|NCT01376323|114728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179481|NCT01376323|114728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179482|NCT01376323|114728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179483|NCT01376323|114728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179484|NCT01376323|114728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179485|NCT00118716|SFA100314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179486|NCT00118716|SFA100314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179487|NCT00118716|SFA100314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179488|NCT00118716|SFA100314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179489|NCT00118716|SFA100314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179490|NCT00118716|SFA100314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179491|NCT05435352||Study Protocol|https://www.pearbio.com/peartnbc|
3179492|NCT06599567|sample size|Individual Participant Data Set|https://bmjopen.bmj.com/content/10/11/e039976|reference article to see sample size with g power
3179493|NCT06599567|Nintendo Wii protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28330586/|
3179494|NCT06599567|Graded motor imagery protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32003812/|
3179495|NCT06670183||Individual Participant Data Set|https://www.ukbiobank.ac.uk/enable-your-research/apply-for-access|Apply for access to UK Biobank
3179496|NCT06733311|ICF-UPDLC-2023|Informed Consent Form|https://www.jianguoyun.com/p/DY7P7M4Qw5SJDRiJ4d8FIAA|"This identifier is specific to the informed consent form for the study titled Urine Proteomic Diagnostic Model for Early-Stage Lung Cancer. It can be used to search the designated data repository or request the document from the study administrators."
3179497|NCT06733311|SP-UPDLC-2023|Study Protocol|https://www.jianguoyun.com/p/DSL9Sy4Qw5SJDRio4d8FIAA|"This link provides access to the official project task document for the study titled Urine Proteomic Diagnostic Model for Early-Stage Lung Cancer. The document includes detailed descriptions of the research objectives, tasks, timelines, and expected outcomes, serving as a comprehensive guide for the study implementation."
3179498|NCT06733311|EA-UPDLC-2023|Ethics Approval Document|https://www.jianguoyun.com/p/DVp7UdEQw5SJDRi14d8FIAA|"This document provides the ethics approval for the study Urine Proteomic Diagnostic Model for Early-Stage Lung Cancer. It confirms compliance with ethical standards for the protection of participant rights and safety throughout the research process."
3179499|NCT06901193||Study Protocol|https://orapps.osu.edu/buck-irb/index/view/study/64513|
3179500|NCT01678131||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-048&kw=7009-048&tab=access|
3179501|NCT04699955||Individual Participant Data Set|https://osf.io/akef9/|
3179502|NCT06453655||Study Protocol|https://doi.org/10.1097/MEG.0b013e328333fca6|
3179503|NCT00441701||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04592&kw=7123-012&tab=access|
3179504|NCT00452686|108638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179505|NCT00452686|108638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179506|NCT00452686|108638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179507|NCT00452686|108638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179508|NCT00452686|108638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179509|NCT00452686|108638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179510|NCT00452686|108638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179511|NCT06579820||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|pubmed
3179512|NCT07088770||Study Informational Website|https://sig.columbia.edu/research-projects/techmpower|The Social Intervention Group (SIG), Columbia School of Social Work organizational website announcing the TechMPower study.
3179513|NCT06320626|37369395|Study Protocol|http://bmjopen.bmj.com/content/13/6/e072363.long|Published study protocol
3179514|NCT01691521|115588|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179515|NCT01691521|115588|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179516|NCT01691521|115588|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179517|NCT01691521|115588|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179518|NCT01691521|115588|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179519|NCT01691521|115588|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179520|NCT01691521|115588|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179521|NCT02786264||Statistical Analysis Plan|https://docs.google.com/document/d/1SUzYG_9aKT5sSkPXEmhvRTqvhXRflQLBiXJe59inDh4/edit?usp=sharing|
3179522|NCT03408275||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data available to researchers on application through the website
3179523|NCT07165288|different example|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/23473911/|Our study found that the support provided had a significant impact on primiparous mothers.
3179524|NCT02948881|BON103593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179525|NCT02948881|BON103593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179526|NCT02948881|BON103593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179527|NCT02948881|BON103593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179528|NCT02948881|BON103593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179529|NCT02948881|BON103593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179530|NCT02948881|BON103593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179531|NCT00979602|113480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179532|NCT00979602|113480|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179533|NCT00979602|113480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179534|NCT00979602|113480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179535|NCT00979602|113480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179536|NCT00979602|113480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179537|NCT00979602|113480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179538|NCT05525936|University of Sydney|Individual Participant Data Set|https://redcap.sydney.edu.au/|
3179539|NCT07165613||thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp
3179540|NCT01590771||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-253&kw=0431-253&tab=access|
3179541|NCT04599686|NCT04599686|Study Protocol|http://clinicaltrials.gov/ct2/results?cond=&term=NCT04599686&cntry=&state=&city=&dist=|Please see the clinical trials NCT04599686
3179542|NCT00082537||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175404|NCT00346749|ADC105931|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179543|NCT00652938|111507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179544|NCT00652938|111507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179545|NCT00652938|111507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179546|NCT00652938|111507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179547|NCT00652938|111507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179548|NCT00652938|111507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179549|NCT00652938|111507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179550|NCT07165366||Informed Consent Form|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EalUzspTf7VClbHYAyBlJg4BVp2wl1gK8uHn7MzUbZ4tbA?e=1vfYnE|
3179551|NCT07165366||Statistical Analysis Plan|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EbDir0nT8JNAlpv4-vfnOxMBCBxsvrV2UjY2_ua4APTs2g?e=zJdPmF|
3179552|NCT00327184|106388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179553|NCT00327184|106388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179554|NCT00327184|106388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179555|NCT00327184|106388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179556|NCT00327184|106388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179557|NCT00327184|106388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 106388 are summarised with study 106390 on the GSK Clinical Study Register.
3179558|NCT00980005|112999|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179559|NCT00980005|112999|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179560|NCT00980005|112999|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179561|NCT00980005|112999|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179562|NCT00980005|112999|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179563|NCT00980005|112999|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179564|NCT00980005|112999|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179565|NCT00344006|CDA 714703/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175405|NCT02588664||Full Data Package|https://www.pcori.org/about-us/governance/policy-data-management-and-data-sharing|
3177869|NCT00470834|AVO108943|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177870|NCT00470834|AVO108943|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177871|NCT00470834|AVO108943|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177872|NCT00470834|AVO108943|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177873|NCT00470834|AVO108943|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177874|NCT00470834|AVO108943|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177875|NCT00470834|AVO108943|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177876|NCT00000590|PACTG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/pactg/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3177877|NCT00000590||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pactg/|
3177878|NCT00000590||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/pactg/|
3177879|NCT03111186|HS-15-00706|Study Protocol|http://istar.usc.edu|
3177880|NCT03111186|HS-15-00706|Informed Consent Form|http://istar.usc.edu|
3177881|NCT00456807|109801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177882|NCT00456807|109801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177883|NCT00456807|109801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177884|NCT00456807|109801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177885|NCT00456807|109801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177886|NCT00456807|109801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177887|NCT04570059|Booklet of recommendation|intervention material|https://hal.archives-ouvertes.fr/|Booklet of recommendation provided to the intervention group (in French)
3177888|NCT00406562|107924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177889|NCT00406562|107924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177890|NCT00406562|107924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177891|NCT00406562|107924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177892|NCT00406562|107924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177893|NCT00406562|107924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177894|NCT00406562|107924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177895|NCT00400608|SAS105519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177896|NCT00400608|SAS105519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177897|NCT00400608|SAS105519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179566|NCT00344006|CDA 714703/005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179567|NCT00344006|CDA 714703/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179568|NCT00344006|CDA 714703/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179569|NCT00344006|CDA 714703/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179570|NCT00344006|CDA 714703/005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179571|NCT00344006|CDA 714703/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179572|NCT00674635|104972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179573|NCT00674635|104972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179574|NCT00674635|104972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179575|NCT00674635|104972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179576|NCT00674635|104972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179577|NCT00674635|104972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179578|NCT00674635|104972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179579|NCT02726776||Study Protocol|https://cloud.scientificnet.org/index.php/s/7vKbCJ1vs0UOYNN|Unfortunately available only in German
3179580|NCT02726776||Informed Consent Form|https://cloud.scientificnet.org/index.php/s/9RXyWhRxEgUgbTd|Unfortunately available only in German or Italian
3179581|NCT00144872|LAM100118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179582|NCT00144872|LAM100118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179583|NCT00144872|LAM100118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179584|NCT00144872|LAM100118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179585|NCT00144872|LAM100118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179586|NCT00144872|LAM100118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179587|NCT00144872|LAM100118|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179588|NCT04599738||Study Protocol|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
3179589|NCT04599738||Informed Consent Form|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
3179590|NCT00682643|FFR110537|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179591|NCT00682643|FFR110537|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179592|NCT00682643|FFR110537|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179593|NCT00682643|FFR110537|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179594|NCT00682643|FFR110537|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179595|NCT00682643|FFR110537|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179596|NCT00682643|FFR110537|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172959|NCT00570492|FFR101782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172960|NCT03626337||Statistical Analysis Plan|https://osf.io/jfke3/|
3179597|NCT00116844|VLX103596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179598|NCT00116844|VLX103596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179599|NCT00116844|VLX103596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179600|NCT00116844|VLX103596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179601|NCT00116844|VLX103596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172961|NCT00403962|NKP103401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179602|NCT00116844|VLX103596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179603|NCT00116844|VLX103596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179604|NCT05051332|NCT03545269|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Efficacy and Safety of Treatment of Articular Cartilage Lesions With CartiLife®
3179605|NCT05051332|NCT03517046|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Safety of Treatment of Articular Cartilage Lesions With CartiLife®
3179606|NCT00289770|100551 (EXT Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179607|NCT00289770|100551 (EXT Y11)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100551 are summarised with studies 100552, 100553, 100554, and 100555 on the GSK Clinical Study Register.
3179608|NCT00289770|100551 (EXT Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179609|NCT00289770|100551 (EXT Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179610|NCT00289770|100551 (EXT Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179611|NCT02916992|NL50605.091.14|Study Protocol|https://www.toetsingonline.nl/to/ccmo_search.nsf/Searchform?OpenForm|ABR form (Algemeen Beoordelings en Registratie formulier; document of dutch board of human research (Centrale Commissie Mensgebonden Onderzoek)
3179612|NCT02777996||Study Protocol|http://www.ispo.it|In Italian, available under request
3179613|NCT00196989|ADG20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179614|NCT00196989|ADG20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179615|NCT00196989|ADG20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179616|NCT00196989|ADG20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179617|NCT00196989|ADG20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179618|NCT00196989|ADG20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179619|NCT00196989|ADG20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179620|NCT04020003|mengxinke|Individual Participant Data Set|http://www.chictr.org.cn|
3179621|NCT00352898|105909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179622|NCT00352898|105909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179623|NCT00352898|105909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179624|NCT00352898|105909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179625|NCT00352898|105909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179626|NCT00352898|105909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179627|NCT01598298||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3179628|NCT00197028|103967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179629|NCT00197028|103967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179630|NCT00197028|103967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179631|NCT00197028|103967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179632|NCT00197028|103967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179633|NCT00197028|103967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179634|NCT01036022|111407|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179635|NCT01036022|111407|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179636|NCT01036022|111407|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179637|NCT01036022|111407|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179638|NCT01036022|111407|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179639|NCT01036022|111407|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177898|NCT00400608|SAS105519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177899|NCT00400608|SAS105519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177900|NCT00400608|SAS105519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177901|NCT00400608|SAS105519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177902|NCT01328444|114417|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177903|NCT01328444|114417|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177904|NCT01328444|114417|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177905|NCT01328444|114417|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177906|NCT01328444|114417|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177907|NCT01328444|114417|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177908|NCT01328444|114417|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177909|NCT03009370||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26806685|
3177910|NCT00920803|113221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177911|NCT00920803|113221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177912|NCT00920803|113221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177913|NCT00920803|113221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177914|NCT00920803|113221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179640|NCT01036022|111407|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179641|NCT06900699|Not available at moment|papers|https://pubmed.ncbi.nlm.nih.gov/|Most of thé informations available at This site and Google Scholar
3175406|NCT06785090|inas.abd2206m@comed.uobaghdad.|Individual Participant Data Set|https://doi.org/10.5281/zenodo.14318557|This link provides access to the de-identified raw data from the clinical trial investigating the effects of bromfenac on macular thickness in cataract patients following phacoemulsification surgery.
3175407|NCT02527629||Study results|https://pubmed.ncbi.nlm.nih.gov/32386409/|
3175408|NCT01808261|104615|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175409|NCT01808261|104615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175410|NCT01808261|104615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175411|NCT01808261|104615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175412|NCT01808261|104615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175413|NCT01808261|104615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175414|NCT01808261|104615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175415|NCT00693615|580299/004|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175416|NCT00693615|580299/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175417|NCT00693615|580299/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175418|NCT00693615|580299/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175419|NCT00693615|580299/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175420|NCT00693615|580299/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175421|NCT00693615|580299/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175422|NCT00481767|106069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175423|NCT00481767|106069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175424|NCT00481767|106069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175425|NCT00481767|106069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175426|NCT00481767|106069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175427|NCT00481767|106069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175428|NCT00481767|106069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175429|NCT03783117||Clinical Study Report|https://www.facebook.com/Cardiovasculartherapy/?modal=admin_todo_tour|After the clinical trials are completed, the clinical study report will be provided upon request via rtao@temple.edu.
3175430|NCT00230243||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175431|NCT00107757|FFR100010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175432|NCT00107757|FFR100010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175433|NCT00107757|FFR100010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175434|NCT00107757|FFR100010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175435|NCT00107757|FFR100010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175436|NCT00107757|FFR100010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175437|NCT00107757|FFR100010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175438|NCT01158742|SDY291|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
3175439|NCT01158742|SDY291|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291. The study protocol is available through the Design tab on the site.
3175440|NCT01158742|SDY291|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
3175441|NCT00534638|106636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175442|NCT00534638|106636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177915|NCT00920803|113221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177916|NCT00400478||Clinical Study Report|https://www.clinicaltrialsregister.eu/ctr-search/search;jsessionid=cJHnlkSBP30JjfQV2K-KXCK3mdjOE64o0FAsUcmzHmslzlaX5yhQ!675812678|
3177917|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/34004390/|This article is from the National Library of Medicine.
3177918|NCT06078150||Systematic Review|https://pubmed.ncbi.nlm.nih.gov/32375184/|This article is from the National Library of Medicine.
3177919|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/24905451/|This article is from the National Library of Medicine.
3177920|NCT02003274||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov|
3177921|NCT02184624|200301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177922|NCT02184624|200301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177923|NCT02184624|200301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177924|NCT02184624|200301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177925|NCT02184624|200301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177926|NCT02184624|200301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177927|NCT02184624|200301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177928|NCT05386628|26079868|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3177929|NCT05386628|16225693|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3177930|NCT05386628|12924842|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3177931|NCT05386628|31864435|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3177932|NCT05386628|22018755|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3177933|NCT05386628|18192154|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3177934|NCT05386628|25977305|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3177935|NCT05386628|20068255|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3177936|NCT05053373||Individual Participant Data Set|http://www.medresman.org.cn/pub/en/proj/projectshow.aspx?proj=1282|
3177937|NCT01587898|116581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177938|NCT01587898|116581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177939|NCT01587898|116581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177940|NCT01587898|116581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177941|NCT01587898|116581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177942|NCT01587898|116581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177943|NCT01587898|116581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177944|NCT02045953|201092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177945|NCT02045953|201092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177946|NCT02045953|201092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177947|NCT02045953|201092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177948|NCT02045953|201092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177949|NCT02045953|201092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177950|NCT02045953|201092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177951|NCT00169442|104065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177952|NCT00169442|104065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175443|NCT00534638|106636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175444|NCT00534638|106636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175445|NCT00534638|106636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175446|NCT00534638|106636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175447|NCT00534638|106636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175448|NCT00370097|FAS106533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175449|NCT00370097|FAS106533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175450|NCT00370097|FAS106533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175451|NCT00370097|FAS106533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175452|NCT00370097|FAS106533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175453|NCT00370097|FAS106533|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175454|NCT00370097|FAS106533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175455|NCT01046331|H1N1|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/h1n1/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175456|NCT01046331||Study Forms|http://biolincc.nhlbi.nih.gov/studies/h1n1/|
3175457|NCT00268983|393229/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175458|NCT00268983|393229/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175459|NCT00268983|393229/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175460|NCT00268983|393229/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175461|NCT00268983|393229/028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175462|NCT00268983|393229/028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175463|NCT00268983|393229/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175464|NCT01630135|116364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175465|NCT01630135|116364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175466|NCT01630135|116364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175467|NCT01630135|116364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175468|NCT01236040|114371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175469|NCT01236040|114371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175470|NCT01236040|114371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175471|NCT01236040|114371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175472|NCT01236040|114371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175473|NCT01236040|114371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175474|NCT00354965|AUG102821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175475|NCT00354965|AUG102821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175476|NCT00354965|AUG102821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175477|NCT00354965|AUG102821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175478|NCT00354965|AUG102821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175479|NCT00354965|AUG102821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175480|NCT01061541|208108/091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179642|NCT00451217||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179643|NCT01929330|117342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179644|NCT01929330|117342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179645|NCT01929330|117342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179646|NCT01929330|117342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179647|NCT01929330|117342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179648|NCT01929330|117342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179649|NCT01929330|117342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179650|NCT01812382|117151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179651|NCT01812382|117151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179652|NCT01812382|117151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179653|NCT01812382|117151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179654|NCT01812382|117151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179655|NCT01812382|117151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179656|NCT01812382|117151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179657|NCT00453479|AC2108378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179658|NCT00453479|AC2108378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179659|NCT00453479|AC2108378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179660|NCT00453479|AC2108378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179661|NCT00453479|AC2108378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179662|NCT00453479|AC2108378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179663|NCT00453479|AC2108378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179664|NCT01190215|114452|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179665|NCT01190215|114452|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179666|NCT01190215|114452|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179667|NCT01190215|114452|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179668|NCT01190215|114452|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179669|NCT01190215|114452|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179670|NCT01678820||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-266&kw=0431D-266&tab=access|
3179671|NCT06925763||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/?term=nitroglycerin+in+bone+regeneration|
3179672|NCT01235975|113807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179673|NCT01235975|113807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172962|NCT00403962|NKP103401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179674|NCT01235975|113807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179675|NCT01235975|113807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179676|NCT01235975|113807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179677|NCT01235975|113807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179678|NCT00044460|49653/326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179679|NCT00044460|49653/326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179680|NCT00044460|49653/326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179681|NCT00044460|49653/326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179682|NCT00044460|49653/326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179683|NCT00044460|49653/326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179684|NCT00044460|49653/326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179685|NCT02378402|ClinicalTrials.gov/NCT02378402|Clinical Study Report|http://jcmr-online.biomedcentral.com/articles/10.1186/s12968-016-0228-3|
3179686|NCT01017120|114576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179687|NCT01017120|114576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179688|NCT01017120|114576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179689|NCT01017120|114576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179690|NCT01017120|114576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179691|NCT01017120|114576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179692|NCT01017120|114576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179693|NCT00047983|SDY352|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
3179694|NCT00047983|SDY352|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
3175481|NCT01061541|208108/091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 208108/091 are summarised with study 208108/092 on the GSK Clinical Study Register.
3179695|NCT00047983|SDY352|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
3179696|NCT03176446|1.941.369|Approval of the ethics committee|http://plataformabrasil.saude.gov.br|
3179697|NCT03047122|P110006|U.S. Food and Drug Administration. somo-v Automated Breast Ultrasound System|http://www.accessdata.fda.gov/cdrh_docs/pdf11/P110006b.pdf|
3179698|NCT00535743||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179699|NCT06480682|RED-D|Individual Participant Data Set|https://figshare.com/account/home|All anonymised data will be published on figshare
3179700|NCT06480682|RED-D|Study Protocol|https://figshare.com/account/home|Study protocol will be published on figshare
3179701|NCT01147692|108366|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179702|NCT01147692|108366|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179703|NCT01147692|108366|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179704|NCT01147692|108366|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179705|NCT01147692|108366|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179706|NCT01147692|108366|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179707|NCT01147692|108366|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179708|NCT01868035|393229/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179709|NCT01868035|393229/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179710|NCT01868035|393229/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179711|NCT01868035|393229/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179712|NCT01868035|393229/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179713|NCT01868035|393229/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179714|NCT01868035|393229/007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179715|NCT00579982|LBI108884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179716|NCT00579982|LBI108884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179717|NCT00579982|LBI108884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179718|NCT00579982|LBI108884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179719|NCT00579982|LBI108884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179720|NCT00579982|LBI108884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179721|NCT00579982|LBI108884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179722|NCT00240526|100450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179723|NCT00240526|100450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179724|NCT00240526|100450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179725|NCT00240526|100450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179726|NCT00240526|100450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179727|NCT00240526|100450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179728|NCT00092170||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179729|NCT06233123||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/32021311/|
3179730|NCT00034645||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179731|NCT01607385|116511|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179732|NCT01607385|116511|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179733|NCT01607385|116511|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179734|NCT01607385|116511|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179735|NCT01607385|116511|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179736|NCT01607385|116511|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179737|NCT01607385|116511|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179738|NCT01424436|113043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179739|NCT01424436|113043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179740|NCT01424436|113043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179741|NCT01424436|113043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179742|NCT01424436|113043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179743|NCT01424436|113043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179744|NCT01424436|113043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179745|NCT00460148|ROP109087|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179746|NCT00460148|ROP109087|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179747|NCT00460148|ROP109087|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179748|NCT00460148|ROP109087|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179749|NCT00460148|ROP109087|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179750|NCT00460148|ROP109087|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179751|NCT00460148|ROP109087|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179752|NCT00517309||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179753|NCT01751113|116572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179754|NCT01751113|116572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179755|NCT01751113|116572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179756|NCT01751113|116572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179757|NCT01751113|116572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179758|NCT01648179|116595|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179759|NCT01648179|116595|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179760|NCT01648179|116595|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179761|NCT01648179|116595|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179762|NCT01648179|116595|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179763|NCT01648179|116595|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179764|NCT01648179|116595|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179765|NCT03990714|Proyect|Study Protocol|https://drive.google.com/file/d/1EEFxi3XpaRW12IAzVctIrrOSo6EKi70_/view?usp=sharing|A project that compares both surgical techniques in the treatment of right colon cancer and assess which is associated with a lower postoperative morbidity
3179766|NCT00742885|111756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179767|NCT00742885|111756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179768|NCT00742885|111756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179769|NCT00742885|111756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179770|NCT00742885|111756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179771|NCT00742885|111756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179772|NCT00742885|111756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179773|NCT00432679|AVD105248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179774|NCT00432679|AVD105248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179775|NCT00432679|AVD105248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179776|NCT00432679|AVD105248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179777|NCT00432679|AVD105248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179778|NCT00432679|AVD105248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179779|NCT00432679|AVD105248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179780|NCT00551213||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04721&kw=P04721&tab=access|
3179781|NCT03877705|Pubmed|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/m/pubmed/30455769/?i=6&from=xylitol%20review|
3179782|NCT01340911|115444|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179783|NCT01340911|115444|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179784|NCT01340911|115444|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179785|NCT01340911|115444|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179786|NCT01340911|115444|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179787|NCT01340911|115444|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179788|NCT00318149|104886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179789|NCT00318149|104886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179790|NCT00318149|104886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179791|NCT00318149|104886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179792|NCT00318149|104886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179793|NCT00318149|104886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179794|NCT00224523|FFR104503|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179795|NCT00224523|FFR104503|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179796|NCT00224523|FFR104503|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179797|NCT00224523|FFR104503|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179798|NCT00224523|FFR104503|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179799|NCT00224523|FFR104503|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179800|NCT00224523|FFR104503|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179801|NCT00000556|AFFIRM|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/affirm/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3179802|NCT00000556||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/affirm/|
3179803|NCT00000556||Study Forms|http://biolincc.nhlbi.nih.gov/studies/affirm/|
3179804|NCT00317174|759346/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179805|NCT00317174|759346/002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179806|NCT00317174|759346/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179807|NCT00317174|759346/002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179808|NCT00317174|759346/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179809|NCT00317174|759346/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179810|NCT07257237|10.5281/zenodo.16529837|Individual Participant Data Set|https://doi.org/10.5281/zenodo.16529837|Deidentified individual participant data set including sociodemographic variables, baseline and 8-week PSQI scores, and systolic and diastolic blood pressure measurements for all randomized participants. Data are shared together with a data dictionary under the license specified on the Zenodo record.
3179811|NCT06138236||Study Protocol|https://www.sanita.puglia.it/web/policlinico-di-bari-ospedale-giovanni-xxiii/comitato-etico|
3179812|NCT00605371|LEP111102|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179813|NCT00605371|LEP111102|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179814|NCT00605371|LEP111102|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179815|NCT00605371|LEP111102|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179816|NCT00605371|LEP111102|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179817|NCT00605371|LEP111102|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179818|NCT00605371|LEP111102|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179819|NCT04731714|mtbzf|Individual Participant Data Set|https://osf.io/mtbzf/|IPD, study protocol, SAP, and ICF will all be posted at this location.
3179820|NCT00992160|111364|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179821|NCT00992160|111364|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179822|NCT00992160|111364|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179823|NCT00992160|111364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179824|NCT00992160|111364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179825|NCT00992160|111364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179826|NCT00992160|111364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179827|NCT00000568|LHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/LHS/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3179828|NCT00090272||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3179829|NCT00920374|113018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179830|NCT00920374|113018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179831|NCT00920374|113018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179832|NCT00920374|113018|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179833|NCT00920374|113018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179834|NCT00920374|113018|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179835|NCT00920374|113018|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179836|NCT05776030||Statistical Analysis Plan|https://osf.io/87wfq/files/osfstorage|
3179837|NCT03904082||Clinical Study Report|http://doi.org/10.1016/j.jclinane.2018.06.033|
3179838|NCT02693626|15OCCSULiaoYanhui|Study Protocol|http://pan.baidu.com/disk/home#list/path=%2F|Please send me email: tangliaoyanhui@163.com if you cannot open it.
3179839|NCT00519636|FFU105927|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179840|NCT00519636|FFU105927|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179841|NCT00519636|FFU105927|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179842|NCT00519636|FFU105927|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179843|NCT00519636|FFU105927|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179844|NCT00519636|FFU105927|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179845|NCT00519636|FFU105927|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179846|NCT01161160|114495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179847|NCT01161160|114495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179848|NCT01161160|114495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179849|NCT01161160|114495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179850|NCT01161160|114495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179851|NCT01161160|114495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179852|NCT01161160|114495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179853|NCT04610203||Study Protocol|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3179854|NCT04610203||Informed Consent Form|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3179855|NCT04610203||Clinical Study Report|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3179856|NCT04610203||Individual Participant Data Set|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3177953|NCT00169442|104065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177954|NCT00169442|104065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177955|NCT00169442|104065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177956|NCT00169442|104065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177957|NCT00627575|LEP108937|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177958|NCT00627575|LEP108937|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177959|NCT00627575|LEP108937|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177960|NCT00627575|LEP108937|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177961|NCT00627575|LEP108937|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177962|NCT00627575|LEP108937|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177963|NCT00627575|LEP108937|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177964|NCT02700087|Consent form cycle 3|Informed Consent Form|https://eprotocol.stanford.edu/irb/ControlServlet?updateFlag=Y|
3177965|NCT01451437||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=P07649&kw=P07649&tab=access|
3179857|NCT04610203||Statistical Analysis Plan|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|Included in the Study Protocol and Clinical Study report
3179858|NCT01323660|114418|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179859|NCT01323660|114418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179860|NCT01323660|114418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177966|NCT02691585||Study Protocol|http://rguhs.ac.in/|
3179861|NCT01323660|114418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179862|NCT01323660|114418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179863|NCT01323660|114418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179864|NCT01323660|114418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179865|NCT00933062|113140|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179866|NCT00933062|113140|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179867|NCT00933062|113140|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179868|NCT00933062|113140|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177967|NCT00197158|104387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177968|NCT00197158|104387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177969|NCT00197158|104387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177970|NCT00197158|104387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177971|NCT00197158|104387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177972|NCT00197158|104387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177973|NCT00955383|112359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177974|NCT00955383|112359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177975|NCT00955383|112359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177976|NCT00955383|112359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177977|NCT00955383|112359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177978|NCT00955383|112359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177979|NCT00955383|112359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177980|NCT00541463||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3177981|NCT00005132|NGHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nghs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3177982|NCT00005132||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nghs/|
3177983|NCT00005132||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nghs/|
3177984|NCT01155479||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05664&kw=P05664&tab=access|
3177985|NCT00000485|HDFP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hdfp/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3177986|NCT00000485||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hdfp/|
3177987|NCT07239076|AssitU|Informed Consent Form|https://pmc.ncbi.nlm.nih.gov/articles/PMC10049812/|For treatment
3177988|NCT03016676||Study Protocol|http://www.ijpbs.net/abstract.php?article=5240|
3177989|NCT00067938|SCA40917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177990|NCT00067938|SCA40917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177991|NCT00067938|SCA40917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177992|NCT00067938|SCA40917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177993|NCT00067938|SCA40917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177994|NCT00067938|SCA40917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3177995|NCT02748603||Report on National Journal|http://www.giornaledicardiologia.it/r.php?v=1015&a=11055&l=15130&f=allegati/01015_2012_01/fulltext/06.De%20Servi%20(47-49).pdf|De Servi S, Klugmann S: Qualità e appropriatezza dell'angioplastica coronarica in Lombardia: qualche riflessione sui dati di attivita' del registro della Società Italiana di Cardiologia Invasiva SICI-GISE) . G. Ital Cardiol 2012; 13: 47-9
3177996|NCT01338779|ImmPort Study ID: SDY546|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
3177997|NCT01338779|ImmPort Study ID: SDY546|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
3177998|NCT01338779|ImmPort Study ID: SDY546|Study summary,-design, demographics,mechanistic assays,-study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
3177999|NCT01338779|Study ID: FACTOR/ITN507ST|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN507STAJT/Study%20Data/begin.view|FACTOR/ITN507ST is the Study Identifier in the ITN TrialShare Clinical Trials Research Portal.
3178000|NCT01338779|Study ID: FACTOR/ITN507ST|Original articles w/data and reports; abstracts et al.|http://www.itntrialshare.org/project/Studies/ITN507STAJT/Study%20Data/begin.view|FACTOR/ITN507ST is the Study Identifier in the ITN TrialShare Clinical Trials Research Portal.
3178001|NCT06995794||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/|
3178002|NCT06995794||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
3178003|NCT02393586||Link to Pubmed (Final publication)|https://www.ncbi.nlm.nih.gov/pubmed/28333342|
3178004|NCT06449963||Data not yet available|https://atauni.edu.tr/tr/index|Data and supporting information will be made available 6 months after the study completion. For access, researchers need to submit a methodologically sound proposal and sign a data access agreement.
3178005|NCT04224545||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/HPCZW|"The datasets analyzed during the current study are publicly available. The data is available in the general repository Open Science Framework at the link"
3178006|NCT00829985|SDY223|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
3178007|NCT00829985|SDY223|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
3178008|NCT00829985|SDY223|Study summary, -design, -adverse event(s), -interventions, -medications, -demographics, -study files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
3178009|NCT02848443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3178010|NCT02848443||Study Protocol|https://clinicaltrials.servier.com/|
3178011|NCT02848443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3178012|NCT02848443||Informed Consent Form|https://clinicaltrials.servier.com/|
3178013|NCT02848443||Clinical Study Report|https://clinicaltrials.servier.com/|
3178014|NCT02848443||study-level clinical trial data|https://clinicaltrials.servier.com/|
3178015|NCT04488107|ICH topic S9|ICH topic S9 - nonclinical evaluation for anticancer pharmaceuticals. 2009|https://database.ich.org/sites/default/files/S9_Guideline.pdf|
3178016|NCT04488107|IBRANCE® (palbociclib) capsule|label for IBRANCE® (palbociclib) capsules|https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/207103s000lbl.pdf|
3178017|NCT04488107|IBRANCE® (palbociclib) tablets|label for IBRANCE® (palbociclib) tablets,|https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf|
3178018|NCT04488107|KISQALI® (ribociclib) tablets|Label for KISQALI® (ribociclib) tablets|https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209092s005lbl.pdf|
3178019|NCT04488107|ICH Topic E6 (R1)|ICH Topic E6 (R1) Guideline for Good Clinical Practice|https://www.ema.europa.eu/en/documents/scientific-guideline/ich-e6-r1-guideline-good-clinical-practice_en.pdf|
3178020|NCT04488107|ICH Topic E9|ICH Topic E9 Statistical Principles for Clinical Trials|https://www.ema.europa.eu/en/documents/scientific-guideline/ich-e-9-statistical-principles-clinical-trials-step-5_en.pdf|
3178021|NCT07304921||Individual Participant Data Set|https://zenodo.org/records/16900133|
3178022|NCT07164989|MI_Education_Link|"Educational resource supporting the study's behavioral intervention strategy using motivational interviewing in dental settings."|https://motivationalinterviewing.org/motivate-your-dental-patients-workbook|Publicly available educational resource supporting the behavioral component of the study.
3178023|NCT04335422||references|https://www.ncbi.nlm.nih.gov/pubmed/28540536|
3178024|NCT01277042|114590|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178025|NCT01277042|114590|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178026|NCT01277042|114590|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178027|NCT01277042|114590|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179869|NCT00933062|113140|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179870|NCT00933062|113140|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179871|NCT00933062|113140|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179872|NCT01627340|115918|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179873|NCT01627340|115918|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179874|NCT01627340|115918|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179875|NCT01627340|115918|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179876|NCT01627340|115918|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179877|NCT01627340|115918|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179878|NCT03173248||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3179879|NCT03173248||Study Protocol|https://clinicaltrials.servier.com/|
3179880|NCT03173248||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3179881|NCT03173248||Informed Consent Form|https://clinicaltrials.servier.com/|
3179882|NCT03173248||Clinical Study Report|https://clinicaltrials.servier.com/|
3179883|NCT03173248||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3178028|NCT01277042|114590|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178029|NCT01277042|114590|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178030|NCT02777736||Study Protocol|http://www.lymphoma.cz/docs/studies/dlbcl/CLSG-CNS-01_en.pdf|
3179884|NCT06919211||Study Protocol|https://eyewiki.org/Retinal_Detachment|
3179885|NCT02985697|DEXProtocol|Study Protocol|https://drive.google.com/open?id=0BwBFaEmsvS0PYnlzVDUyMGREWFk|Protocol for the study; includes introduction, design, and references/citations.
3179886|NCT03205020||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25118503|
3179887|NCT04553302||Clinical Study Report|http://ard.bmj.com/content/79/Suppl_1/555.2|
3179888|NCT00410384|HGS1006-C1056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179889|NCT00410384|HGS1006-C1056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179890|NCT00410384|HGS1006-C1056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179891|NCT00410384|HGS1006-C1056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179892|NCT00410384|HGS1006-C1056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179893|NCT00410384|HGS1006-C1056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179894|NCT00410384|HGS1006-C1056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179895|NCT00359619|108052 (FU month 18)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179896|NCT00359619|108052 (FU month 18)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179897|NCT00359619|108052 (FU month 18)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179898|NCT00359619|108052 (FU month 18)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179899|NCT00359619|108052 (FU month 18)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179900|NCT00119743|347414/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179901|NCT00119743|347414/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179902|NCT00119743|347414/010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179903|NCT00119743|347414/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179904|NCT00119743|347414/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179905|NCT00119743|347414/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179906|NCT01648283||Publication|https://www.ncbi.nlm.nih.gov/pubmed?term=%22Anesthesiology%22[Jour]%20AND%202015[pdat]%20AND%20Kharasch[author]%20AND%20methadone%20cyp2b6&cmd=correctspelling|Study results published Anesthesiology. 2015 Nov;123(5):1142-53. doi: 10.1097/ALN.0000000000000867
3179907|NCT00578227|110886|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179908|NCT00578227|110886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179909|NCT00578227|110886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179910|NCT00578227|110886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179911|NCT00578227|110886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179912|NCT00578227|110886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179913|NCT00578227|110886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179914|NCT03668067||Individual Participant Data Set|http://www.abcd-vision.org/references/2WIN%20Bus%20de-identified%209-6-18.pdf|Public de-identified ongoing
3179915|NCT01577732|115389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179916|NCT01577732|115389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179917|NCT01577732|115389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179918|NCT01577732|115389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179919|NCT01577732|115389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179920|NCT01577732|115389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179921|NCT01125774||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-065&kw=0974-065&tab=access|
3179922|NCT00364442|SAS10019|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179923|NCT00364442|SAS10019|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179924|NCT00364442|SAS10019|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179925|NCT00364442|SAS10019|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179926|NCT00364442|SAS10019|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179927|NCT00364442|SAS10019|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179928|NCT00364442|SAS10019|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179929|NCT00097370|100901|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179930|NCT00097370|100901|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179931|NCT00097370|100901|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179932|NCT00097370|100901|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179933|NCT00097370|100901|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179934|NCT00097370|100901|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179935|NCT00097370|100901|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179936|NCT00697554|208129/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179937|NCT00697554|208129/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179938|NCT00697554|208129/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179939|NCT00697554|208129/036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179940|NCT00697554|208129/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179941|NCT00263679|100406/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179942|NCT00263679|100406/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179943|NCT00263679|100406/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179944|NCT00263679|100406/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179945|NCT00263679|100406/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179946|NCT00263679|100406/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179947|NCT01096056|114182|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179948|NCT01096056|114182|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179949|NCT01096056|114182|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179950|NCT01096056|114182|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179951|NCT01096056|114182|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179952|NCT01096056|114182|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179953|NCT01114620|114270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179954|NCT01114620|114270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179955|NCT01114620|114270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179956|NCT01114620|114270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179957|NCT01114620|114270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179958|NCT01114620|114270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179959|NCT01114620|114270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179960|NCT01244984|113989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179961|NCT01244984|113989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179962|NCT01244984|113989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179963|NCT01244984|113989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179964|NCT01244984|113989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179965|NCT01244984|113989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179966|NCT01244984|113989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179967|NCT00140673|444563/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179968|NCT00140673|444563/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179969|NCT00140673|444563/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179970|NCT00140673|444563/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179971|NCT00140673|444563/023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179972|NCT00140673|444563/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179973|NCT00140673|444563/023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179974|NCT01738867|116753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179975|NCT01738867|116753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179976|NCT01738867|116753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179977|NCT01738867|116753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179978|NCT01738867|116753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179979|NCT01738867|116753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179980|NCT01738867|116753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179981|NCT00197236|208109/232|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179982|NCT00197236|208109/232|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179983|NCT00197236|208109/232|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179984|NCT00197236|208109/232|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179985|NCT00197236|208109/232|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179986|NCT00197236|208109/232|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179987|NCT06103422||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/26935213/|
3179988|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/26935213/|
3179989|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/11078134/|
3179990|NCT06918288|Arnaud W Thille et al|Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/21765357/|Extubation failure is associated with a poor prognosis, but the respective roles for reintubation per se and underlying disease severity remain unclear. Our objectives were to evaluate the impact of failed extubation, whether planned or unplanned, on patient outcomes and to identify a patient subset at risk for extubation failure.
3179991|NCT04401722|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|through elnakeebayman@yahoo.com
3179992|NCT00538213|110263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179993|NCT00538213|110263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179994|NCT00538213|110263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179995|NCT00538213|110263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179996|NCT00538213|110263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179997|NCT00538213|110263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179998|NCT00538213|110263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3179999|NCT01457560|217744/060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180000|NCT01457560|217744/060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180001|NCT01457560|217744/060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180002|NCT01457560|217744/060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172963|NCT00403962|NKP103401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180003|NCT01457560|217744/060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180004|NCT01984086|200921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180005|NCT01984086|200921|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180006|NCT01984086|200921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180007|NCT01984086|200921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180008|NCT01984086|200921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180009|NCT01984086|200921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180010|NCT01984086|200921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180011|NCT00004560|PAD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/pad/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180012|NCT00004560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pad/|
3180013|NCT04405713|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
3180014|NCT01078233||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-058&kw=0518-058&tab=access|
3180015|NCT01196988|113275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180016|NCT01196988|113275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180017|NCT01196988|113275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180018|NCT01196988|113275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180019|NCT01196988|113275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180020|NCT01196988|113275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180021|NCT01196988|113275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180022|NCT02281318|200862|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180023|NCT02281318|200862|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180024|NCT02281318|200862|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180025|NCT02281318|200862|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180026|NCT02281318|200862|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180027|NCT02281318|200862|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180028|NCT02281318|200862|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180029|NCT00502593|107066|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180030|NCT00502593|107066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study are summarised with studies 108498 (second cohort study) and 108500 (third cohort study) on the GSK Clinical Study Register.
3180031|NCT00502593|107066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180032|NCT00502593|107066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180033|NCT00502593|107066|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180034|NCT00502593|107066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180035|NCT00502593|107066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180036|NCT00586339|107863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180037|NCT00586339|107863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180038|NCT00586339|107863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180039|NCT00586339|107863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178031|NCT02812888||Individual Participant Data Set|https://www.opendrive.com/|"Using network platform: https://www.opendrive.com/ username: 18361811955@163.com password: woaini1314 The repository and management of the data can be obtained via Public Folder."
3178032|NCT00510874|110028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178033|NCT00510874|110028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178034|NCT00510874|110028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178035|NCT00510874|110028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178036|NCT00510874|110028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178037|NCT00510874|110028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178038|NCT00510874|110028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178039|NCT01067443||Study Protocol|http://journals.plos.org/plosntds/article/file?type=supplementary&id=info:doi/10.1371/journal.pntd.0004880.s002|Final Study Protocol
3178040|NCT03333733||Childrens Food Trust Report 2012|http://media.childrensfoodtrust.org.uk/2015/06/CFT_Early_Years_Guide_Interactive_Sept-12.pdf|Reference 4 in citations \[there-on other citations are referenced 1 citation later\]
3178041|NCT00042029||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3178042|NCT01286831|106181|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178043|NCT01286831|106181|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178044|NCT01286831|106181|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178045|NCT01286831|106181|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178046|NCT01286831|106181|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178047|NCT01286831|106181|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178048|NCT01286831|106181|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178049|NCT03121027||Individual Participant Data Set|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|Detail about sampling and BDHS 2011 report
3178050|NCT00688207|AVA109941|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178051|NCT00688207|AVA109941|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178052|NCT00688207|AVA109941|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178053|NCT00688207|AVA109941|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178054|NCT00688207|AVA109941|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178055|NCT00688207|AVA109941|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178056|NCT00688207|AVA109941|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178057|NCT01266941|111789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178058|NCT01266941|111789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178059|NCT01266941|111789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178060|NCT01266941|111789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178061|NCT01266941|111789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178062|NCT01266941|111789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3178063|NCT01266941|111789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180040|NCT00586339|107863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180041|NCT00586339|107863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180042|NCT04727489||Study Protocol|http://www.inserm.fr|
3180043|NCT04727489||Informed Consent Form|http://www.inserm.fr|
3180044|NCT07299383|AYÇA ÇALBAY|Study Protocol|https://atauni.edu.tr/|online access is not available, accessible via e-mail
3180045|NCT02808442||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3180046|NCT02808442||Study Protocol|https://clinicaltrials.servier.com/|
3180047|NCT02808442||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3180048|NCT02808442||Informed Consent Form|https://clinicaltrials.servier.com/|
3180049|NCT02808442||Clinical Study Report|https://clinicaltrials.servier.com/|
3180050|NCT02808442||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3180051|NCT00420316|109810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180052|NCT00420316|109810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180053|NCT00420316|109810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180054|NCT00420316|109810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180055|NCT00420316|109810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180056|NCT00420316|109810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180057|NCT00420316|109810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180058|NCT00501020|49653/284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180059|NCT00501020|49653/284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180060|NCT00501020|49653/284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180061|NCT00501020|49653/284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180062|NCT00501020|49653/284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180063|NCT00501020|49653/284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180064|NCT00501020|49653/284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180065|NCT00843193|106870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180066|NCT00843193|106870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180067|NCT00843193|106870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180068|NCT00843193|106870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180069|NCT00843193|106870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180070|NCT00843193|106870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180071|NCT00843193|106870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180072|NCT02683811||Study Protocol|http://www.diariodellasalute.it|Study protocol (Italian version) can be requested by contacting the project manager (lmarinaro@aslcn2.it)
3180073|NCT02683811||program materials and tools|http://www.diariodellasalute.it|The Italian version of program materials and tools (teachers' manual, students' booklet and parents' booklet) can be freely accessed and downloaded from project web site.
3180074|NCT04415333||De-identified data set|https://library.unc.edu/scholarly-communications/open-access/carolina-digital-repository-cdr/|Data will be accessible at the above Carolina Data Repository for the UNC library system.
3180075|NCT01025843||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5478-001&kw=5478-001&tab=access|
3180076|NCT01651949||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-003&kw=V503-003&tab=access|
3180077|NCT00197015|208109/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180078|NCT00197015|208109/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180079|NCT00197015|208109/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180080|NCT00197015|208109/231|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180081|NCT00197015|208109/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180082|NCT00197015|208109/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180083|NCT01013974|113377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180084|NCT01013974|113377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180085|NCT01013974|113377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180086|NCT01013974|113377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180087|NCT01013974|113377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180088|NCT01013974|113377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180089|NCT01013974|113377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180090|NCT00961142||Results|https://www.clinicaltrialsregister.eu/ctr-search/search?query=2007-006016-33|
3180091|NCT06615128||Study Protocol|https://doi.org/10.4049/jimmunol.182.3.1541|
3180092|NCT06615128||Study Protocol|https://doi.org/10.1371/journal.pone.0047748|
3180093|NCT06706882||INFORMATION SHEET|https://drive.google.com/file/d/1Y90Fr8O30tFqNL_OjAjMfrayrK8-KKxt/view?usp=sharing|
3180094|NCT06706882|Informed Consent Form|Informed Consent Form|https://drive.google.com/file/d/1eQLHRV80sIPlZNoHR5HFS4uauF8RWoDI/view?usp=sharing|
3180095|NCT00937846|110771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180096|NCT00937846|110771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180097|NCT00937846|110771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180098|NCT00937846|110771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180099|NCT00937846|110771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180100|NCT00937846|110771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180101|NCT00937846|110771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180102|NCT01224678||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3180103|NCT00972504|112864|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180104|NCT00972504|112864|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180105|NCT00972504|112864|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180106|NCT00972504|112864|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180107|NCT00972504|112864|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180108|NCT00972504|112864|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180109|NCT00972504|112864|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180110|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25939657|Report of vascular function testing
3180111|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/24548114|Report of platelet function and physiology
3180112|NCT00970307|112157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180113|NCT00970307|112157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180114|NCT00970307|112157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180115|NCT00970307|112157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180116|NCT00970307|112157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172964|NCT00403962|NKP103401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180117|NCT00970307|112157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180118|NCT00970307|112157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180119|NCT00241644|102248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 102248 are summarised with study 111274 on the GSK Clinical Study Register.
3180120|NCT00241644|102248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180121|NCT00241644|102248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180122|NCT00241644|102248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180123|NCT00241644|102248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180124|NCT00241644|102248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180125|NCT00241644|102248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180126|NCT01235949|112921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180127|NCT01235949|112921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180128|NCT01235949|112921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180129|NCT01235949|112921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180130|NCT01235949|112921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180131|NCT01235949|112921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180132|NCT06210334||Clinical Study Report|https://www.researchdata.org.cn/|
3180133|NCT01930045||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-295&kw=0518-295&tab=access|
3180134|NCT01370694||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=8808-001&kw=8808-001&tab=access|
3180135|NCT03912948||Web site for patient information on studies bases on patients data (RGPD)|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|
3180136|NCT00004124||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
3180137|NCT00711126|B2C106180|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180138|NCT00711126|B2C106180|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180139|NCT00711126|B2C106180|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180140|NCT00711126|B2C106180|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180141|NCT00711126|B2C106180|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180142|NCT00711126|B2C106180|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180143|NCT00711126|B2C106180|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180144|NCT05888155|01095697530|Clinical Study Report|http://Shaimaa4796@gmail.com|
3180145|NCT02289560||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
3180146|NCT00622830|LPL110736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180147|NCT00622830|LPL110736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180148|NCT00622830|LPL110736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180149|NCT00622830|LPL110736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180150|NCT00622830|LPL110736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180151|NCT00622830|LPL110736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180152|NCT00622830|LPL110736|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180153|NCT01405924||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-030&kw=0517-030&tab=access|
3180154|NCT02918916||Tables. Training program, Phototherapy parameters, Time point of outcomes|https://pt.scribd.com/document/325401697/Documents-ClinicalTrials-ID-2015-25219-0|
3180155|NCT01648140|115879|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180156|NCT01648140|115879|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180157|NCT01648140|115879|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180158|NCT01648140|115879|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180159|NCT01648140|115879|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180160|NCT01648140|115879|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180161|NCT01406262|107085|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180162|NCT01406262|107085|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180163|NCT01406262|107085|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180164|NCT01406262|107085|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180165|NCT01406262|107085|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180166|NCT01406262|107085|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180167|NCT01406262|107085|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180168|NCT05171218||Individual Participant Data Set|https://osf.io/efya2/|
3180169|NCT05171218||Study Protocol|https://doi.org/10.17605/OSF.IO/VHCA5|
3180170|NCT05171218||Statistical Analysis Plan|https://doi.org/10.17605/OSF.IO/VHCA5|
3180171|NCT05171218||Informed Consent Form|https://osf.io/efya2/|
3180172|NCT00688519|114741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180173|NCT00688519|114741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180174|NCT00688519|114741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180175|NCT00688519|114741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180176|NCT00688519|114741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180177|NCT00688519|114741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180178|NCT00688519|114741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180179|NCT01123083|115494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180180|NCT01123083|115494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180181|NCT01123083|115494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180182|NCT01123083|115494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180183|NCT01123083|115494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180184|NCT01123083|115494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180185|NCT01123083|115494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180186|NCT00723450|SCA102833|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180187|NCT00723450|SCA102833|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180188|NCT00723450|SCA102833|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180189|NCT00723450|SCA102833|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180190|NCT00723450|SCA102833|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180191|NCT00723450|SCA102833|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180192|NCT00723450|SCA102833|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180193|NCT04893213||Study Protocol|https://osf.io/yku5q/|Protocol on the Open Science Framework (OSF)
3180194|NCT04893213||Statistical Analysis Plan|https://osf.io/yku5q/|
3180195|NCT04893213||Individual Participant Data Set|https://osf.io/yku5q/|The study protocol and statistical analysis plan were pre-registered on the OSF prior to starting recruitment. IPD will be made available when results are published.
3180196|NCT07293052||Study Protocol|https://pdf.ac/0wrnmMTIc3|
3180197|NCT07236905||Individual Participant Data Set|https://nda.nih.gov/nda/access-data-info|data is not yet available but will be added to respository once acquired.
3180198|NCT06729164|Open Science Framework|The study's relevant instructional context measures. Supporting materials include the assessment instrument, protocols, etc.|https://osf.io/eq5s8/overview|
3180199|NCT00465816|109063|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180200|NCT00465816|109063|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180201|NCT00465816|109063|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180202|NCT00465816|109063|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180203|NCT00465816|109063|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180204|NCT00465816|109063|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180205|NCT00465816|109063|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175482|NCT01061541|208108/091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175483|NCT01061541|208108/091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175484|NCT01061541|208108/091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175485|NCT01061541|208108/091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175486|NCT03271593||Clinical Study Report|https://www.gsk-clinicalstudyregister.com/study/205369?search=study&search_terms=205369#csr|Results disclosed in the Clinical Study Report.
3180206|NCT01831791|114264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175487|NCT00461097|SDY218|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY218|ImmPort study identifier is SDY218
3180207|NCT01831791|114264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180208|NCT01831791|114264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180209|NCT01831791|114264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180210|NCT01831791|114264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180211|NCT01831791|114264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180212|NCT01831791|114264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180213|NCT02744521|Study protocol|Study Protocol|https://sites.google.com/site/relevantdocuments2016|I shared this protocol on Google Plus.
3170953|NCT06078579||Study Protocol|https://www.ijhsr.org/IJHSR_Vol.5_Issue.10_Oct2015/20.pdf|www.researchgate.net/publication/344178013\_Serum\_Leptin\_and\_Lipid\_Profile\_in\_Lichen\_Planus\_A\_case\_control\_study
3170954|NCT01177787||Individual Participant Data Set|http://dx.doi.org/10.4172/2165-7904.1000203|
3170955|NCT02885298||Study Protocol|https://drive.google.com/drive/folders/0B5w-TjIZHObhSWxqbElCUmxINnc|Study protocol can be provided via email if requested. Please email turnjose@iu.edu
3170956|NCT01294683||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-118&kw=0524B-118&tab=access|
3170957|NCT00398645|FFA106783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170958|NCT00398645|FFA106783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170959|NCT00398645|FFA106783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170960|NCT00398645|FFA106783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170961|NCT00398645|FFA106783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170962|NCT00398645|FFA106783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170963|NCT00398645|FFA106783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170964|NCT00530868||Clinical Study Report|https://doi.org/10.1186/s13058-020-01258-x|Bevacizumab and Letrozole
3170965|NCT03761511|NICOFA|Study Protocol|https://ukaachen.sharepoint.com/:b:/s/NICOFA/ESUAT8h1fTBHlTcsdu48LrQBbvvAABdsy81bvQ4Egq696g?e=8Xliis|
3170966|NCT01323634|113109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170967|NCT01323634|113109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170968|NCT01323634|113109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170969|NCT01323634|113109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170970|NCT01323634|113109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170971|NCT01323634|113109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170972|NCT01323634|113109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170973|NCT01545570|114403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170974|NCT01545570|114403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170975|NCT01545570|114403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170976|NCT01545570|114403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170977|NCT01545570|114403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170978|NCT01545570|114403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170979|NCT01545570|114403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170980|NCT00407069|SDY10|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
3170981|NCT00407069|SDY10|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
3170982|NCT00407069|SDY10|Study design, -summary, -files; participant demographics, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
3170983|NCT00753272|106372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170984|NCT00753272|106372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170985|NCT00753272|106372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170986|NCT00753272|106372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170987|NCT00753272|106372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170988|NCT00753272|106372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170989|NCT00753272|106372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170990|NCT01323621|112352|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170991|NCT01323621|112352|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170992|NCT01323621|112352|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170993|NCT01323621|112352|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170994|NCT01323621|112352|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170995|NCT01323621|112352|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170996|NCT01323621|112352|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170997|NCT03992469||Individual Participant Data Set|https://vivli.org/|
3170998|NCT00992511|113809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172965|NCT00403962|NKP103401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172966|NCT00403962|NKP103401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172967|NCT00403962|NKP103401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172968|NCT00329225|49653/347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175488|NCT00461097|SDY218|Study summary, -design, -adverse events, -demographics,-lab tests,-mechanistic assays, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY218|ImmPort study identifier is SDY218
3175489|NCT01212094||Paper describing the results of interim analysis|http://onlinelibrary.wiley.com/doi/10.1002/acn3.293/full|
3175490|NCT03180203|Study Intensive Care|Study Protocol|https://www.catharinaziekenhuis.nl/contact.html|Contact can be made to request the study protocol (Dutch)
3175491|NCT00933595|LUNG-HIV|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3180214|NCT00891176|112830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180215|NCT00891176|112830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180216|NCT00891176|112830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180217|NCT00891176|112830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180218|NCT00891176|112830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180219|NCT00891176|112830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175492|NCT00933595||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
3175493|NCT00933595||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
3175494|NCT00933595||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
3175495|NCT00920959|SAS30021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180220|NCT00346151|SDY674|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674
3180221|NCT00346151|SDY674|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674. The study protocol is available in the Design tab section.
3180222|NCT00346151|SDY674|Study summary, -design, -synopsis,- medications, -demographics, -lab tests, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674
3180223|NCT00346151|ITN023ST|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN023STPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
3180224|NCT00346151|ITN023ST|Protocol synopsis, -data and reports, -specimens availability|http://www.itntrialshare.org/project/Studies/ITN023STPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
3180225|NCT00478738|MAB104958|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180226|NCT00478738|MAB104958|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180227|NCT00478738|MAB104958|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180228|NCT00478738|MAB104958|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180229|NCT00478738|MAB104958|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180230|NCT00478738|MAB104958|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180231|NCT00478738|MAB104958|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180232|NCT00202865||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3180233|NCT06783530||Study Protocol|https://dentfac.mans.edu.eg|Faculty of Dentistry, Mansoura University - Ethical Committee Information.
3180234|NCT02916758||Individual Participant Data Set|http://grad.kean.edu/ot/faculty|Please contact cmulry@kean.edu to request the data set
3180235|NCT00880477|217744/069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180236|NCT00880477|217744/069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180237|NCT00880477|217744/069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180238|NCT00880477|217744/069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175496|NCT00920959|SAS30021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3170999|NCT00992511|113809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171000|NCT00992511|113809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171001|NCT00992511|113809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171002|NCT00992511|113809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171003|NCT00992511|113809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171004|NCT00992511|113809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171005|NCT03434782|60622416.1.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
3171006|NCT01387230|115408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171007|NCT01387230|115408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171008|NCT01387230|115408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171009|NCT01387230|115408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171010|NCT01387230|115408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171011|NCT01387230|115408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171012|NCT01387230|115408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171013|NCT00437671||FDA approved labeling information|http://www.talecris-pi.info/inserts/hypertet.pdf|
3171014|NCT05512637||Study Protocol|https://bmjopen.bmj.com/content/14/11/e084110|
3171015|NCT00000491|AMIS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/amis/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3171016|NCT01372410|115321|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171017|NCT01372410|115321|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171018|NCT01372410|115321|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171019|NCT01372410|115321|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171020|NCT01372410|115321|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171021|NCT01372410|115321|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171022|NCT01372410|115321|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171023|NCT01405937||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-044&kw=7009-044&tab=access|
3171024|NCT00390910|107737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171025|NCT00390910|107737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171026|NCT00390910|107737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171027|NCT00390910|107737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171028|NCT00390910|107737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171029|NCT00390910|107737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171030|NCT00390910|107737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171031|NCT01436071|115283|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171032|NCT01436071|115283|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171033|NCT01436071|115283|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171034|NCT01436071|115283|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171035|NCT01436071|115283|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171036|NCT01436071|115283|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171037|NCT01436071|115283|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180239|NCT00880477|217744/069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180240|NCT00327665|106068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180241|NCT00327665|106068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180242|NCT00327665|106068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180243|NCT00327665|106068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180244|NCT00327665|106068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180245|NCT00327665|106068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180246|NCT01780298||Individual Participant Data Set|https://doi.org/10.12688/f1000research.11698.2|
3180247|NCT01424397|111924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180248|NCT01424397|111924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180249|NCT01424397|111924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180250|NCT01424397|111924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180251|NCT01424397|111924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180252|NCT01424397|111924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3180253|NCT01424397|111924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171038|NCT00863109||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05278&kw=P05278&tab=access|
3171039|NCT04024644|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
3171040|NCT04024644|10.1016/j.joms.2011.09.034|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
3171041|NCT02294084||Clinical Study Report|https://www.health-holland.com/project/2015/effect-of-antidiabetic-drug-on-brown-adipose-tissue-bat-in-overweight-men|A simplified summary of the main results of the study can be found when following the link. In addition, the results are described in a paper that will be published by Diabetologia later this year.
3171042|NCT04561804||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/MOH_2017-06-07_000470.aspx|Israel Ministry of Health registration number
3171043|NCT01313650|113373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171044|NCT01313650|113373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171045|NCT01313650|113373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171046|NCT01313650|113373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171047|NCT01313650|113373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171048|NCT01313650|113373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171049|NCT01313650|113373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171050|NCT05452096|TRLS-D-21-00760R2|Study Protocol|https://trialsjournal.biomedcentral.com/|Study protocol has been accepted for publication on https://trialsjournal.biomedcentral.com/ . However, BMC requires registration of all clinical trials reported in manuscripts submitted to its journals in a registry listed on the ICMJE website or in any of the primary registries that participate in the WHO International Clinical Trials Registry Platform.
3171051|NCT04100629||Study Protocol|https://drive.google.com/open?id=1vNjwT5j9Y32e7vdayZAMBp-3PvJWCiSK|
3171052|NCT01829360||Treatment & Testing Scripts|http://doi.org/10.23641/asha.9745181|See item S4 and S7.
3171053|NCT01829360||Published report of findings|http://doi.org/10.1044/2019_LSHSS-VOIA-18-0131|This article is open access
3171054|NCT05833087||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08079-9|
3171055|NCT05833087||Statistical Analysis Plan|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
3171056|NCT05833087||Informed Consent Form|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08079-9|Informed Consent Forms will be provided at reasonable request from the project investigator, Stine Bjerrum Moeller, email: stinebm@health.sdu.dk
3171057|NCT05833087||Analytic Code|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
3171058|NCT00525889|SDY565|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY565|ImmPort study identifier is SDY565. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts available to the Public.
3171059|NCT00525889|SDY565|Study protocol summary and -schematic, -design, -demographics, -lab tests, -mechanistic assays, and -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY565|ImmPort study identifier is SDY565. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts available to the Public.
3171060|NCT03068000||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/21874720|The study by Bala and Drid (2010) was used for the sample calculation of the participants.
3171061|NCT07060235|fascial tarining|statics|https://www.anatomytrains.com/fascialfitness/fascial_fitness1.pdf|fascia and mobile app
3171062|NCT01153802|112773|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171063|NCT01153802|112773|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171064|NCT01153802|112773|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171065|NCT01153802|112773|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171066|NCT01153802|112773|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171067|NCT01153802|112773|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171068|NCT01153802|112773|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171069|NCT00378833||CSR synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171070|NCT00139347|444563/024|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171071|NCT00139347|444563/024|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171072|NCT00139347|444563/024|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171073|NCT00139347|444563/024|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171074|NCT00139347|444563/024|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171075|NCT00139347|444563/024|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171076|NCT00139347|444563/024|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171077|NCT01013766|111823|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171078|NCT01013766|111823|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171079|NCT01013766|111823|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171080|NCT01013766|111823|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171081|NCT01013766|111823|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171082|NCT01013766|111823|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171083|NCT01013766|111823|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171084|NCT01667107||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5592-105&kw=5592-105&tab=access|
3171085|NCT01086410|106851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171086|NCT01086410|106851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171087|NCT01086410|106851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171088|NCT01086410|106851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171089|NCT01086410|106851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171090|NCT01086410|106851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172969|NCT00329225|49653/347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172970|NCT00329225|49653/347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172971|NCT00329225|49653/347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172972|NCT00329225|49653/347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172973|NCT00329225|49653/347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172974|NCT00938392|112662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172975|NCT00938392|112662|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172976|NCT00938392|112662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172977|NCT00938392|112662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172978|NCT00938392|112662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172979|NCT00938392|112662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172980|NCT00938392|112662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172981|NCT03350880||Clinical Study Report|https://periodicos.unicesumar.edu.br/index.php/saudpesq/article/view/9938|
3172982|NCT06724874||Individual Participant Data Set|https://www.stat.ubc.ca/~rollin/stats/ssize/n2.html|
3172983|NCT04631432||Statistical Analysis Plan|https://docs.google.com/document/d/16IlMPOgJMoh8tLIhB4JK5yeHI-0MfJVvRnQ8PdNp8-o/edit?usp=sharing|
3172984|NCT04631432||Study Protocol|https://drive.google.com/file/d/1YoXgB4ifoeu2Z8OnG6_hVWP4sBLRp9wP/view?usp=sharing|
3172985|NCT04631432||Informed Consent Form|https://drive.google.com/file/d/1WHJz01_y_b-gO4ZpZNAQsnqNf_SwdwNX/view?usp=sharing|
3172986|NCT01453296|112776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172987|NCT01453296|112776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172988|NCT01453296|112776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172989|NCT01453296|112776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172990|NCT01453296|112776|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172991|NCT01453296|112776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172992|NCT01453296|112776|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172993|NCT01439308|111925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171091|NCT01086410|106851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171092|NCT01177384||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-130&kw=0431-130&tab=access|
3171093|NCT07129356|m.a.fathi@uomosul.edu.iq|Individual Participant Data Set|https://osf.io/9u2vx/?view_only=daea272a2161482b8dde69fe29d406f0|De-identified individual participant data is available through the provided OSF link
3171094|NCT02689531|VIV00008648|Individual Participant Data Set|https://doi.org/10.25934/PR00008648|
3171095|NCT05689970|PubMed ID: 34763217|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/34763217/|
3171096|NCT00108914|FFR30008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171097|NCT00108914|FFR30008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171098|NCT00108914|FFR30008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171099|NCT00108914|FFR30008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171100|NCT00108914|FFR30008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171101|NCT00108914|FFR30008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171102|NCT00108914|FFR30008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171103|NCT02509104|201897|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171104|NCT02509104|201897|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171105|NCT02509104|201897|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171106|NCT02509104|201897|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171107|NCT02509104|201897|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171108|NCT02509104|201897|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171109|NCT02509104|201897|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171110|NCT04160169|doi:10.15139/S3/XEXQXO|Individual Participant Data Set|https://dataverse.unc.edu/dataset.xhtml?persistentId=doi:10.15139/S3/XEXQXO|
3171111|NCT01159912|112059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171112|NCT01159912|112059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171113|NCT01159912|112059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171114|NCT01159912|112059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171115|NCT01159912|112059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171116|NCT01159912|112059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171117|NCT01159912|112059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171118|NCT00067951|712753/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171119|NCT00067951|712753/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171120|NCT00067951|712753/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171121|NCT00067951|712753/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171122|NCT00067951|712753/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171123|NCT00067951|712753/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171124|NCT00067951|712753/004|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171125|NCT00330395||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171126|NCT00370227|107706|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171127|NCT00370227|107706|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171128|NCT00370227|107706|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171129|NCT00370227|107706|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171130|NCT00370227|107706|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171131|NCT00370227|107706|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171132|NCT00766090|112202|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171133|NCT00766090|112202|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171134|NCT00766090|112202|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171135|NCT00766090|112202|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171136|NCT00766090|112202|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171137|NCT00766090|112202|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171138|NCT00766090|112202|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171139|NCT01717287||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-248&kw=0518-248&tab=access|
3171140|NCT01086462|114041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171141|NCT01086462|114041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171142|NCT01086462|114041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171143|NCT01086462|114041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171144|NCT01086462|114041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171145|NCT01086462|114041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171146|NCT01086462|114041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171147|NCT00169455|103477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171148|NCT00169455|103477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171149|NCT00169455|103477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171150|NCT00169455|103477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171151|NCT00169455|103477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171152|NCT00169455|103477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171153|NCT05060705||thesis of online seminar|http://infectiousdiseases.heraldmeetings.com/0|Gulnara A Yuldasheva and A I Ilin Inhibition of the catalytic fragment of the ExoN domain of the exoribonuclease of SARS-CoV-2-betacoronavirus B virus by FS-1 drug containing molecular iodine and lithium and magnesium halides International conference on infectious diseases, Infectious Diseases Prevention, Control and Cure, August 27 - 28, 2020 online seminar
3171154|NCT00279019|AC2103473|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171155|NCT00279019|AC2103473|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171156|NCT00279019|AC2103473|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171157|NCT00279019|AC2103473|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171158|NCT00279019|AC2103473|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171159|NCT00279019|AC2103473|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171160|NCT00279019|AC2103473|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171161|NCT00376584||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171162|NCT06725225||Individual Participant Data Set|https://vivli.org|
3171163|NCT00309634|106750|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171164|NCT00309634|106750|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171165|NCT00309634|106750|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171166|NCT00309634|106750|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171167|NCT00309634|106750|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171168|NCT00309634|106750|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171169|NCT03662165||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/UULS6T|
3171170|NCT00861250||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25303369|First study article: http://www.ncbi.nlm.nih.gov/pubmed/23206270
3171171|NCT01973777||Clinical Study Report|http://www.contraceptionjournal.org/article/S0010-7824%2815%2930125-6/abstract|
3171172|NCT00346073|106316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171173|NCT00346073|106316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171174|NCT00346073|106316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171175|NCT00346073|106316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171176|NCT00346073|106316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171177|NCT00346073|106316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171178|NCT00980200|113310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171179|NCT00980200|113310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171180|NCT00980200|113310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172994|NCT01439308|111925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172995|NCT01439308|111925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172996|NCT01439308|111925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172997|NCT01439308|111925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172998|NCT01439308|111925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3172999|NCT01439308|111925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173000|NCT03473821||Statistical Analysis Plan|https://lucris.lub.lu.se/admin/files/138815992/MOTIFS_Data_Management_Protocol_1.6_2023_02_24.pdf|
3173001|NCT06934421||Study Protocol|https://osf.io/8ywq6/|
3173002|NCT06934421||Statistical Analysis Plan|https://osf.io/8ywq6/|
3173003|NCT06934421||Informed Consent Form|https://osf.io/8ywq6/|
3173004|NCT06934421||Analytic Code|https://osf.io/8ywq6/|
3173005|NCT06934421||Individual Participant Data Set|https://osf.io/8ywq6/|
3173006|NCT01867996|116073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173007|NCT01867996|116073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173008|NCT01867996|116073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173009|NCT01867996|116073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173010|NCT01867996|116073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173011|NCT01867996|116073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173012|NCT01867996|116073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173013|NCT00968539|113456|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173014|NCT00968539|113456|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173015|NCT00968539|113456|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173016|NCT00968539|113456|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173017|NCT00968539|113456|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173018|NCT00968539|113456|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173019|NCT00968539|113456|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173020|NCT00326118|106445|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173021|NCT00326118|106445|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173022|NCT00326118|106445|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173023|NCT00326118|106445|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171181|NCT00980200|113310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171182|NCT00980200|113310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171183|NCT00980200|113310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171184|NCT00980200|113310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171185|NCT00082524||CSRSynopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171186|NCT00714285|111295|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171187|NCT00714285|111295|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171188|NCT00714285|111295|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173024|NCT00326118|106445|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173025|NCT00326118|106445|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173026|NCT00109278||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3173027|NCT00005009|SDY357|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357.
3171189|NCT00714285|111295|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171190|NCT00714285|111295|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171191|NCT00714285|111295|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171192|NCT00714285|111295|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171193|NCT00000551|ACT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/act/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3171194|NCT00000551||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/act/|
3171195|NCT00000551||Study Forms|http://biolincc.nhlbi.nih.gov/studies/act/|
3171196|NCT00000551||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/act/|
3171197|NCT00282295|105753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171198|NCT00282295|105753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171199|NCT00282295|105753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171200|NCT00282295|105753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171201|NCT00282295|105753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171202|NCT00282295|105753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173028|NCT00005009|SDY357|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357
3173029|NCT00005009|SDY357|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357
3173030|NCT00471237|CR9108963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173031|NCT00471237|CR9108963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173032|NCT00471237|CR9108963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173033|NCT00471237|CR9108963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173034|NCT00471237|CR9108963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173035|NCT00471237|CR9108963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173036|NCT00471237|CR9108963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173037|NCT01016366|2008-003662-25|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-003662-25/results|
3173038|NCT00297063|AVD104742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173039|NCT00297063|AVD104742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173040|NCT00297063|AVD104742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173041|NCT00297063|AVD104742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173042|NCT00297063|AVD104742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173043|NCT00297063|AVD104742|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173044|NCT00297063|AVD104742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173045|NCT02437175||Methodology paper|https://www.dovepress.com/articles.php?article_id=25534|
3173046|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/106014|
3173047|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/143046|
3173048|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889771|
3173049|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889781|
3173050|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889773|
3173051|NCT00538473|110223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173052|NCT00538473|110223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173053|NCT00538473|110223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173054|NCT00538473|110223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173055|NCT00538473|110223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173056|NCT00538473|110223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173057|NCT06107348|10.17605/OSF.IO/2MGJK|Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
3173058|NCT03196960||Scoring Sheet|https://docs.google.com/document/d/1pqYbMe4S-W-vgYRHzd1d4Is7s6ZbMt_MGDlWtndRRdM/edit?usp=sharing|Mobilization Quantification Score
3173059|NCT03011385||Study Protocol|https://drive.google.com/file/d/1xGrVkCeXwUZbih7NuOujjlNJcWvQ4j6H/view?usp=sharing|The file includes the protocol for data collection and intervention sessions
3173060|NCT00539006|FFU105924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173061|NCT00539006|FFU105924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173062|NCT00539006|FFU105924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175497|NCT00920959|SAS30021|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175498|NCT00920959|SAS30021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175499|NCT00920959|SAS30021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175500|NCT00920959|SAS30021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175501|NCT00920959|SAS30021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175502|NCT00371735|CDA 714703/006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175503|NCT00371735|CDA 714703/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175504|NCT00371735|CDA 714703/006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175505|NCT00371735|CDA 714703/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175506|NCT00371735|CDA 714703/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175507|NCT00371735|CDA 714703/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175508|NCT00371735|CDA 714703/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175509|NCT05002504||Clinical Study Report|http://dx.doi.org/10.1016/S0482-5985(05)74383-2|Shapiro F, Forriol F. El cartílago de crecimiento: biología y biomecánica del desarrollo. Rev Ortop y Traumatol \[Internet\]. 2005;49(1):55-67.
3175510|NCT05002504||Clinical Study Report|http://dx.doi.org/10.1016/j.ft.2012.01.003|Vázquez M, Rodríguez A, Arroyo A, Benjumea A. Desalineaciones de los miembros inferiores en niños con síndrome de Down. Fisioterapia \[Internet\]. 2012;34(4):140-5.
3175511|NCT05002504||Clinical Study Report|http://doi.org/10.1016/j.ft.2018.10.003|Gatti C, Montero S. Effectiveness of treadmill training on gait development in children with Down syndrome: A systematic review. Fisioterapia \[Internet\]. 2019;41(1):37-47
3175512|NCT05002504||Clinical Study Report|http://scielo.sld.cu/scielo.php?script=sci%7B%5C_%7Darttext%7B%5C&%7Dpid=S0864-03002019000200086%7B%5C&%7Dlang=es%7B%5C%25%7D0Ahttp://scielo.sld.cu/pdf/ibi/v38n2/1561-3011-ibi-38-02-86.pdf|Taboada J, Díaz L, Hernández M. Restauración del patrón biomecánico de la marcha en niños cubanos. Rev Cuba Investig Biomédicas \[Internet\]. 2019;38(2):86-103
3175513|NCT05002504||Clinical Study Report|http://doi.org/10.1016/j.ft.2018.10.001|Millar P, Navarro J, Martella D, Gallardo C. Prevalencia de alteraciones del neurodesarrollo motriz en niños prematuros sin diagnóstico de parálisis cerebral. Fisioterapia \[Internet\]. 2018;40(6):305-11.
3175514|NCT05002504||Clinical Study Report|http://dx.doi.org/10.1016/S1762-827X(14)68508-4|Darmana R, Cahuzac J. Trastornos estáticos de los miembros inferiores y sus consecuencias sobre la marcha del niño. Trastornos rotacionales. EMC - Podol \[Internet\]. 2014;16(3):1-10.
3175515|NCT00903201|110399|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175516|NCT00903201|110399|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175517|NCT00903201|110399|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175518|NCT00903201|110399|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175519|NCT00903201|110399|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175520|NCT00903201|110399|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175521|NCT00903201|110399|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175522|NCT01299558|102934|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175523|NCT01299558|102934|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175524|NCT01299558|102934|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171203|NCT00768326|2006-003739-57|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2006-003739-57/results|
3171204|NCT00674583|111414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171205|NCT00674583|111414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171206|NCT00674583|111414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171207|NCT00674583|111414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171208|NCT00674583|111414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171209|NCT00674583|111414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171210|NCT00674583|111414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171211|NCT00111800|100925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171212|NCT00111800|100925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171213|NCT00111800|100925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171214|NCT00111800|100925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171215|NCT00111800|100925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171216|NCT00111800|100925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171217|NCT00111800|100925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171218|NCT03743311||the SF36 scale questioner|https://clinmedjournals.org/articles/jmdt/jmdt-2-023-figure-1.pdf|The scale the SF36 scale questioner can be sent by email.
3171219|NCT00449670|109630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171220|NCT00449670|109630|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171221|NCT00449670|109630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171222|NCT00449670|109630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171223|NCT00449670|109630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171224|NCT00449670|109630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171225|NCT00449670|109630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171226|NCT07257666|Ethics Committee approval No.|Informed Consent Form|http://www.kcs.ac.rs/index.php/eticki-odbor|
3171227|NCT00789880|SDY14|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
3171228|NCT00789880|SDY14|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
3171229|NCT00789880|SDY14|Study summary, -design, -assessments, -adverse events, -intervention(s), -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
3171230|NCT07280962||Study Protocol|https://heyzine.com/flip-book/0d5ec370d6.html|https://heyzine.com/flip-book/0d5ec370d6.html
3171231|NCT05820633||Study Protocol|https://www.sealedenvelope.com/simple-randomiser/v1/lists|
3171232|NCT07171515||Study Protocol|https://data.doi.or.kr/10.22694/CANCERDATA032018070101|1\. 1. Guidelines for the Pancreatic Cancer Registry, National Cancer Center Big Data
3171233|NCT07171515||Study Protocol|https://cancerportal.kr/ncc/clinicalLibraryInfo.do|2\. CONNECT Cancer Big Data Library: Pancreatic Cancer Section
3171234|NCT07171515||Study Protocol|https://www.kahbps.or.kr/bbs/index.kin?bbs_mode=view&f_wbcode=board_request&f_master_idx=770&f_template_type=list|Korean clinical practice guideline for pancreatic cancer 2021
3171235|NCT00315744|102318|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171236|NCT00315744|102318|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171237|NCT00315744|102318|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171238|NCT00315744|102318|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171239|NCT00315744|102318|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171240|NCT00315744|102318|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171241|NCT06089148|Cairo unversity|Study Protocol|https://medicine.cu.edu.eg/index.php/en/postgraduate/32-research/161-research-ethics-committee|upon requirement
3171242|NCT02257372|201314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171243|NCT02257372|201314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171244|NCT02257372|201314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171245|NCT02257372|201314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171246|NCT02257372|201314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173063|NCT00539006|FFU105924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173064|NCT00539006|FFU105924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173065|NCT00539006|FFU105924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173066|NCT00539006|FFU105924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173067|NCT01817764|114930|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173068|NCT01817764|114930|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173069|NCT01817764|114930|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173070|NCT01817764|114930|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173071|NCT01817764|114930|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173072|NCT01817764|114930|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173073|NCT01817764|114930|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173074|NCT00005274|P2C2|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/p2c2/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3173075|NCT00005274||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
3173076|NCT00005274||Study Forms|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
3173077|NCT00005274||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
3173078|NCT06942169||Informed Consent Form|https://www.inonu.edu.tr/sagbilgiretik/menu/12561/bilgilendirici-onam-formu|"Informed consent is the process by which a patient freely and consciously gives consent after receiving sufficient information about the medical procedure, treatment or intervention to be applied to him/her.~The written form of this process is the Informed Consent Form."
3173079|NCT00479739|SAM40056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173080|NCT00479739|SAM40056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173081|NCT00479739|SAM40056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173082|NCT00479739|SAM40056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173083|NCT00479739|SAM40056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173084|NCT00479739|SAM40056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173085|NCT00479739|SAM40056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173086|NCT01563029|106855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173087|NCT01563029|106855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173088|NCT01563029|106855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173089|NCT01563029|106855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173090|NCT01563029|106855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173091|NCT01563029|106855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173092|NCT01563029|106855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173093|NCT03052374||Informed Consent Form|http://childstudies.ca/contact|
3173094|NCT03052374||Study Protocol|http://childstudies.ca/contact|
3173095|NCT03052374||Statistical Analysis Plan|http://childstudies.ca/contact|
3173096|NCT00197184|208127/132 (EXT Y2)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173097|NCT00197184|208127/132 (EXT Y2)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171247|NCT02257372|201314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175525|NCT01299558|102934|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175526|NCT01299558|102934|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175527|NCT01299558|102934|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175528|NCT01299558|102934|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175529|NCT02787499||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/SKUUOP|Publicly available, de-identified datasets are available on the Harvard Dataverse Platform.
3175530|NCT00792909|111736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175531|NCT00792909|111736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175532|NCT00792909|111736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175533|NCT00792909|111736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175534|NCT00792909|111736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175535|NCT00792909|111736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175536|NCT00731822|HZC111348|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175537|NCT00731822|HZC111348|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175538|NCT00731822|HZC111348|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175539|NCT00731822|HZC111348|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175540|NCT00731822|HZC111348|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175541|NCT00731822|HZC111348|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175542|NCT00731822|HZC111348|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175543|NCT02689804||Publication|http://dx.doi.org/10.1016/j.contraception.2017.01.004|Results Reference: Yes
3175544|NCT03074695|Pro00079368|Informed Consent Form|https://eirb.mc.duke.edu/|
3175545|NCT00612820|IPR110723|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175546|NCT00612820|IPR110723|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175547|NCT00612820|IPR110723|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175548|NCT00612820|IPR110723|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175549|NCT00612820|IPR110723|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175550|NCT00612820|IPR110723|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171248|NCT02257372|201314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171249|NCT02938884||Study Protocol|https://oncore.umn.edu/login/|
3171250|NCT01669070|115441|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171251|NCT01669070|115441|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171252|NCT01669070|115441|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171253|NCT01669070|115441|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171254|NCT01669070|115441|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171255|NCT01669070|115441|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171256|NCT01669070|115441|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171257|NCT01147744|112186|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171258|NCT01147744|112186|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171259|NCT01147744|112186|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173098|NCT00197184|208127/132 (EXT Y2)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173099|NCT00197184|208127/132 (EXT Y2)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173100|NCT00197184|208127/132 (EXT Y2)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173101|NCT00197184|208127/132 (EXT Y2)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 208127/132 are summarised with studies 208122/133, 208127/134 and 208127/137 on the GSK Clinical Study Register.
3173102|NCT00364273|B2F104300|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173103|NCT00364273|B2F104300|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173104|NCT00364273|B2F104300|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173105|NCT00364273|B2F104300|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173106|NCT00364273|B2F104300|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173107|NCT00364273|B2F104300|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173108|NCT00364273|B2F104300|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173109|NCT00903409|111818|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173110|NCT00903409|111818|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173111|NCT00903409|111818|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173112|NCT00903409|111818|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173113|NCT00903409|111818|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173114|NCT00903409|111818|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173115|NCT00549120|MAB104954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173116|NCT00549120|MAB104954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173117|NCT00549120|MAB104954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173118|NCT00549120|MAB104954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173119|NCT00549120|MAB104954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173120|NCT00549120|MAB104954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173121|NCT00549120|MAB104954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173122|NCT01153685|110628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173123|NCT01153685|110628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173124|NCT01153685|110628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173125|NCT01153685|110628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173126|NCT01153685|110628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173127|NCT01153685|110628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173128|NCT00938275|113261|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173129|NCT00938275|113261|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173130|NCT00938275|113261|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173131|NCT00938275|113261|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173132|NCT00938275|113261|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173133|NCT00938275|113261|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173134|NCT00938275|113261|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175551|NCT00612820|IPR110723|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175552|NCT00358358|SCO104925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175553|NCT00358358|SCO104925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175554|NCT00358358|SCO104925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175555|NCT00358358|SCO104925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171260|NCT01147744|112186|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171261|NCT01147744|112186|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171262|NCT01147744|112186|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171263|NCT01147744|112186|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171264|NCT00695448|PIK111051|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171265|NCT00695448|PIK111051|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171266|NCT00695448|PIK111051|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171267|NCT00695448|PIK111051|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171268|NCT00695448|PIK111051|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171269|NCT00695448|PIK111051|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171270|NCT00695448|PIK111051|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171271|NCT00290342|104871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171272|NCT00290342|104871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171273|NCT00290342|104871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171274|NCT00290342|104871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171275|NCT00290342|104871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171276|NCT00290342|104871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171277|NCT02134483||Article|https://www.ncbi.nlm.nih.gov/pubmed/26375142|
3171278|NCT05705609|Kim H, Kim S, Choe K, Kim JS|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/29579508/|web site is provided
3171279|NCT00316680|104489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171280|NCT00316680|104489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171281|NCT00316680|104489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171282|NCT00316680|104489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171283|NCT00316680|104489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171284|NCT00316680|104489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171285|NCT03686436||Study Protocol|https://www.clinicaltrials.gov|
3171286|NCT03070470|ECGCIPA|Individual Participant Data Set|https://physionet.org/physiobank/database/ecgcipa/|ECG effects of ranolazine, verapamil, lopinavir+ritonavir, chloroquine, dofetilide, diltiazem, and dofetilide+diltiazem in a small sample size clinical study. The ECGCIPA database contains multi-channel ECG recordings, pharmacokinetic, and clinical data of 60 subjects participating in the CiPA ECG validation study.
3171287|NCT00490568|AVA102675|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171288|NCT00490568|AVA102675|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171289|NCT00490568|AVA102675|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171290|NCT00490568|AVA102675|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171291|NCT00490568|AVA102675|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171292|NCT00490568|AVA102675|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171293|NCT00490568|AVA102675|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171294|NCT03715153||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3171295|NCT03715153||Study Protocol|https://clinicaltrials.servier.com/|
3171296|NCT03715153||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3171297|NCT03715153||Informed Consent Form|https://clinicaltrials.servier.com/|
3171298|NCT03715153||Clinical Study Report|https://clinicaltrials.servier.com/|
3171299|NCT03715153||study-level clinical trial data]|https://clinicaltrials.servier.com/|
3171300|NCT04630587||Study Protocol|http://www.oulu.fi/medicine/node/52771|
3171301|NCT00122681|580299/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171302|NCT00122681|580299/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171303|NCT00122681|580299/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171304|NCT00122681|580299/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171305|NCT00122681|580299/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171306|NCT00122681|580299/008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171307|NCT00122681|580299/008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171308|NCT03177772|dtp38|Study Protocol|https://osf.io/dtp38/|Open Science Framework. we are registered
3171309|NCT00996944|113079|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171310|NCT00996944|113079|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171311|NCT00996944|113079|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171312|NCT00996944|113079|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171313|NCT02699957|Data Collection Form|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|
3171314|NCT02699957|Data Dictionary|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|Element definitions and coding instructions.
3171315|NCT00996268|113412|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171316|NCT00996268|113412|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171317|NCT00996268|113412|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171318|NCT00996268|113412|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171319|NCT00996268|113412|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171320|NCT00996268|113412|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171321|NCT00996268|113412|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171322|NCT02467933|449|Study Protocol|https://www.socialscienceregistry.org/trials/729|Study protocol archived on American Economic Association Social Science Registry page.
3171323|NCT02467933|448|Statistical Analysis Plan|https://www.socialscienceregistry.org/trials/729|"Pre-specified analysis plan archived on American Economic Association Social Science Registry page.~Final version prior to unblinding: Version 2.0 (March 5, 2016)"
3171324|NCT00382993|TRX106573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171325|NCT00382993|TRX106573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171326|NCT00382993|TRX106573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171327|NCT00382993|TRX106573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171328|NCT00382993|TRX106573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171329|NCT00382993|TRX106573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171330|NCT00382993|TRX106573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171331|NCT00034658||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171332|NCT04411355|10128359|National Thesis Center|https://tez.yok.gov.tr/UlusalTezMerkezi|thesis Number: 494582
3171333|NCT00385255|106323|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173135|NCT00381667|B2C104604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173136|NCT00381667|B2C104604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173137|NCT00381667|B2C104604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173138|NCT00381667|B2C104604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173139|NCT00381667|B2C104604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173140|NCT00381667|B2C104604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175556|NCT00358358|SCO104925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175557|NCT00358358|SCO104925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175558|NCT00358358|SCO104925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175559|NCT00097006|REDS II-CORE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/core/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175560|NCT00097006|REDS II-CORE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/core/|
3175561|NCT00097006|REDS II-LAPS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/laps/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175562|NCT00097006|REDS II-LAPS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/laps/|
3175563|NCT00097006|REDS II-LAPS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/laps/|
3175564|NCT00097006|REDS II-LAPS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/laps/|
3175565|NCT00097006|REDS II-MS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/redsms/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175566|NCT00097006|REDS II-MS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/redsms/|
3175567|NCT00097006|REDS II-MS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/redsms/|
3175568|NCT00097006|REDS II-RISE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/rise/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3175569|NCT00097006|REDS II-RISE|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rise/|
3175570|NCT00097006|REDS II-RISE|Study Forms|http://biolincc.nhlbi.nih.gov/studies/rise/|
3175571|NCT00097006|REDS II-RISE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/rise/|
3175572|NCT00427908|108658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175573|NCT00427908|108658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175574|NCT00427908|108658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173141|NCT00381667|B2C104604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175575|NCT00427908|108658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175576|NCT00427908|108658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175577|NCT00427908|108658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175578|NCT00427908|108658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study is summarised with long term immunogenicity studies 108660 (year 1), 108661 (year 2), 108663 (year 3) and 108665 (year 4) on the GSK Cli
3175579|NCT00239720|ITN011AI/NPA01 is Study ID|Study overview, - synopsis, -navigator, -schedule of events, -available biospecimen(s) et al.|https://www.itntrialshare.org/project/Studies/ITN011AIPUBLIC/Study%20Data/begin.view?|TrialShare is the ITN clinical research portal that provides public access to study data.
3175580|NCT01405560||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-045&kw=7009-045&tab=access|
3175581|NCT00969228|112269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175582|NCT00969228|112269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175583|NCT00969228|112269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175584|NCT00969228|112269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175585|NCT00969228|112269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175586|NCT00969228|112269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173142|NCT02751086||Study Protocol, study information, news|http://www.imigastric.com|"The study is open to other interested Institutions.~Correspondance to:~Jacopo Desiderio, MD djdesi85@hotmail.it"
3173143|NCT01294709||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-014&kw=0974-014&tab=access|
3173144|NCT02446496|201529|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173145|NCT02446496|201529|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173146|NCT02446496|201529|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173147|NCT02446496|201529|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173148|NCT02446496|201529|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173149|NCT02446496|201529|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173150|NCT02677675||Study Protocol|http://www.nmrr.gov.my|
3173151|NCT01480271|114450|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173152|NCT01480271|114450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173153|NCT01480271|114450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173154|NCT01480271|114450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173155|NCT01480271|114450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175587|NCT00969228|112269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175588|NCT02855476||Study Protocol|http://hdclarity.net/study-information/|
3175589|NCT02855476||Informed Consent Form|http://hdclarity.net/study-information/|Draft informed consent form, not yet approved by an Institutional Review Board for clinical use
3175590|NCT04579848||Study Protocol|https://drive.google.com/file/d/1AKuis2zJlqhUqY4OEPyVhQPpIiuPnnhr/view?usp=sharing|
3175591|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1mB2pEgRmuMhaVM_eNnnyXdqsyev4wev5/view?usp=sharing|
3175592|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1oE_9J-5uwLpboVWEsUJL6tHn4st1ea9r/view?usp=sharing|
3171334|NCT00385255|106323|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171335|NCT00385255|106323|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171336|NCT00385255|106323|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171337|NCT00385255|106323|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171338|NCT00385255|106323|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171339|NCT00835237|111413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171340|NCT00835237|111413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171341|NCT00835237|111413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173156|NCT01480271|114450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173157|NCT01480271|114450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173158|NCT02691312||FDA 501(k)|https://www.accessdata.fda.gov/cdrh_docs/pdf10/K101935.pdf|
3173159|NCT00981409|106206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173160|NCT00981409|106206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173161|NCT00981409|106206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173162|NCT00607906|AXO110461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173163|NCT00607906|AXO110461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175593|NCT01573000|104515|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175594|NCT01573000|104515|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171342|NCT00835237|111413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171343|NCT00835237|111413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171344|NCT00835237|111413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171345|NCT00835237|111413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171346|NCT00092846||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171347|NCT02692495|10.17632/8bk6h6bmkr.1|Individual Participant Data Set|https://data.mendeley.com/datasets/8bk6h6bmkr/1|
3171348|NCT02692495||Clinical Study Report|http://www.aurametrix.com/nct02692495|
3171349|NCT02692495|10.1101/139014|Preprint|http://biorxiv.org/content/early/2017/05/19/139014|Study results
3171350|NCT01225731||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05495&kw=P05495&tab=access|
3171351|NCT01018628|114011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171352|NCT01018628|114011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171353|NCT01018628|114011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171354|NCT01018628|114011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171355|NCT01018628|114011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171356|NCT01018628|114011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171357|NCT01018628|114011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171358|NCT01857869|117014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171359|NCT01857869|117014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171360|NCT01857869|117014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171361|NCT01857869|117014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171362|NCT01857869|117014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171363|NCT01857869|117014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171364|NCT01857869|117014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171365|NCT00790907|108888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171366|NCT00790907|108888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171367|NCT00790907|108888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171368|NCT00790907|108888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171369|NCT00790907|108888|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171370|NCT00790907|108888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171371|NCT00790907|108888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171372|NCT00452699|ADA109055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171373|NCT00452699|ADA109055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171374|NCT00452699|ADA109055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171375|NCT00452699|ADA109055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171376|NCT00452699|ADA109055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171377|NCT00452699|ADA109055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171378|NCT00452699|ADA109055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171379|NCT04329728||Published Abstract|https://www.alliedacademies.org/proceedings/a-novel-lymphoablation-preconditioning-agent-avm0703-via-receptor-mediated-induction-of-apoptosis-to-reduce-patient-toxi-4764.html|https://www.alliedacademies.org/proceedings/a-novel-lymphoablation-preconditioning-agent-avm0703-via-receptor-mediated-induction-of-apoptosis-to-reduce-patient-toxi-4764.html
3171380|NCT00092430||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3171381|NCT00513409|110031|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171382|NCT00513409|110031|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171383|NCT00513409|110031|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175595|NCT01573000|104515|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175596|NCT01573000|104515|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175597|NCT01573000|104515|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175598|NCT01573000|104515|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175599|NCT01573000|104515|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175600|NCT00092196||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175601|NCT01702467|116698|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175602|NCT01702467|116698|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175603|NCT01702467|116698|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175604|NCT01702467|116698|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175605|NCT01702467|116698|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175606|NCT01702467|116698|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175607|NCT01702467|116698|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173164|NCT00607906|AXO110461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173165|NCT00607906|AXO110461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173166|NCT00607906|AXO110461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173167|NCT00607906|AXO110461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173168|NCT00607906|AXO110461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173169|NCT00633217|111117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173170|NCT00633217|111117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173171|NCT00633217|111117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173172|NCT00633217|111117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173173|NCT00633217|111117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173174|NCT00633217|111117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173175|NCT00633217|111117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173176|NCT00443131|107731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173177|NCT00443131|107731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173178|NCT00443131|107731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173179|NCT00443131|107731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173180|NCT00443131|107731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173181|NCT00443131|107731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173182|NCT00000478|ACIP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/acip|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3173183|NCT01336608|113108|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173184|NCT01336608|113108|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175608|NCT00896064|112993|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175609|NCT00896064|112993|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175610|NCT00896064|112993|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175611|NCT00896064|112993|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175612|NCT00896064|112993|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175613|NCT00103454|FFR30002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175614|NCT00103454|FFR30002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175615|NCT00103454|FFR30002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175616|NCT00103454|FFR30002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175617|NCT00103454|FFR30002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171384|NCT00513409|110031|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171385|NCT00513409|110031|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171386|NCT00513409|110031|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171387|NCT02931058||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2366-9|
3171388|NCT02931058||Clinical Study Report|https://www.clinicalkey.com/#!/content/journal/1-s2.0-S1063458422007154|
3171389|NCT02700490|10.17863/CAM.43399|Complete Data Set|https://doi.org/10.17863/CAM.43399|
3175618|NCT00103454|FFR30002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171390|NCT01627587|115893|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171391|NCT01627587|115893|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171392|NCT01627587|115893|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171393|NCT01627587|115893|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171394|NCT01627587|115893|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171395|NCT01627587|115893|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171396|NCT01627587|115893|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171397|NCT01425203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08160&kw=P08160&tab=access|
3171398|NCT00731250|111611|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171399|NCT00731250|111611|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171400|NCT00731250|111611|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171401|NCT00731250|111611|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171402|NCT00731250|111611|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171403|NCT00731250|111611|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171404|NCT00731250|111611|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171405|NCT00548496|CR9108914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171406|NCT00548496|CR9108914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171407|NCT00548496|CR9108914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171408|NCT00548496|CR9108914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171409|NCT00548496|CR9108914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171410|NCT00548496|CR9108914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171411|NCT00548496|CR9108914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171412|NCT00090194|SDY356|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
3171413|NCT00090194|SDY356|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
3171414|NCT00090194|SDY356|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
3171415|NCT00317109|104756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173185|NCT01336608|113108|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173186|NCT01336608|113108|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173187|NCT01336608|113108|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173188|NCT01336608|113108|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173189|NCT01336608|113108|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173190|NCT00627458|111344|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173191|NCT00627458|111344|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173192|NCT00627458|111344|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173193|NCT00627458|111344|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175619|NCT00103454|FFR30002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175620|NCT00523913|AVD105720|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175621|NCT00523913|AVD105720|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175622|NCT00523913|AVD105720|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175623|NCT00523913|AVD105720|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175624|NCT00523913|AVD105720|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175625|NCT00523913|AVD105720|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175626|NCT00523913|AVD105720|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175627|NCT06810570||Individual Participant Data Set|https://netscc-webapps.soton.ac.uk/damps/damps-document.phtml?id=NIHR159040|This is the Data Management And Access Plan for the project, posted on the funders webpage (NIHR)
3171416|NCT00317109|104756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171417|NCT00317109|104756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171418|NCT00317109|104756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171419|NCT00317109|104756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171420|NCT00317109|104756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171421|NCT00976066|111848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171422|NCT00976066|111848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171423|NCT00976066|111848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171424|NCT00976066|111848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175628|NCT00526474||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04737&kw=P04737&tab=access|
3175629|NCT02944292||Study Protocol|https://drive.google.com/open?id=0B-XpW352z4ZJMFdseHNwTWI2clU|
3175630|NCT01545388||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-136&kw=0431A-136&tab=access|
3175631|NCT03160040|MINOCIN® (minocycline)|Package Insert|http://www.minociniv.com/pdfs/minocin-us-prescribing-information.pdf|MINOCIN® (minocycline) for Injection 100 mg/vial. United States Prescribing Information.
3175632|NCT04087239||Individual Participant Data Set|http://www.redcap.uzchs.ac.zw/redcap|Data being entered, now verification of enrolment case report forms
3175633|NCT01218308|114541|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175634|NCT01218308|114541|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175635|NCT01218308|114541|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175636|NCT01218308|114541|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175637|NCT01218308|114541|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175638|NCT01218308|114541|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175639|NCT01218308|114541|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175640|NCT01204671|114269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175641|NCT01204671|114269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175642|NCT01204671|114269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175643|NCT01204671|114269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175644|NCT01204671|114269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175645|NCT01204671|114269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171425|NCT00976066|111848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171426|NCT00976066|111848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171427|NCT00976066|111848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171428|NCT04106648||Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/|
3171429|NCT00972673|112018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171430|NCT00972673|112018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171431|NCT00972673|112018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171432|NCT00972673|112018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171433|NCT01110200|113874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171434|NCT01110200|113874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171435|NCT01110200|113874|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171436|NCT01110200|113874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171437|NCT01110200|113874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171438|NCT01110200|113874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171439|NCT01110200|113874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171440|NCT00505453|110502|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171441|NCT00505453|110502|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171442|NCT00505453|110502|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171443|NCT00505453|110502|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171444|NCT00505453|110502|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171445|NCT00505453|110502|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171446|NCT00505453|110502|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171447|NCT02256514|PMCID: PMC4649454|Abstract of 75-patient Phase II study|http://doi.org/10.1186/2051-1426-3-S2-P200|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649454/pdf/2051-1426-3-S2-P200.pdf
3171448|NCT07273786|merve özkul/author|Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/|
3171449|NCT00861744|111870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171450|NCT00861744|111870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171451|NCT00861744|111870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171452|NCT00861744|111870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171453|NCT00861744|111870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171454|NCT00861744|111870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171455|NCT00861744|111870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171456|NCT01014117|114009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175646|NCT01204671|114269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173194|NCT00627458|111344|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173195|NCT00627458|111344|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173196|NCT00627458|111344|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173197|NCT04230785||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=Differential+long+noncoding+RNA+expressions+in+peripheral+blood+mononuclear+cells+for+detection+of+acute+ischemic+stroke|
3173198|NCT05016765|2y7fs|Study Protocol|https://osf.io/2y7fs/|
3173199|NCT00803673|110106|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173200|NCT00803673|110106|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173201|NCT00803673|110106|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173202|NCT00803673|110106|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173203|NCT00803673|110106|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173204|NCT00803673|110106|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173205|NCT00803673|110106|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173206|NCT00552617||CSr Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3173207|NCT04688814||Study Protocol|http://www.med.alexu.edu.eg|
3173208|NCT02149537|PR00007593|Individual Participant Data Set|http://doi.org/10.25934/PR00007593|De-identified and anonymized IPD can be requested at http://doi.org/10.25934/PR00007593
3173209|NCT05187663||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/29652462/|Rakašević D, Lazić Z, Rakonjac B, Soldatović I, Janković S, Magić M, Aleksić Z. Efficiency of photodynamic therapy in the treatment of peri-implantitis - A three-month randomized controlled clinical trial. Srp Arh Celok Lek. 2016 Sep-Oct;144(9-10):478-84. PMID: 29652462.
3173210|NCT01440595||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-012&kw=5172-012&tab=access|
3173211|NCT02524665|114553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173212|NCT02524665|114553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173213|NCT02524665|114553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173214|NCT02524665|114553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173215|NCT02524665|114553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173216|NCT02524665|114553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173217|NCT04845451|Cluster Headaches-Neuroma|Clinical Study Report|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
3173218|NCT04845451|Cluster Headaches-Neuroma|Statistical Analysis Plan|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
3173219|NCT02647554||Study Protocol|http://pan.baidu.com/s/1eQJUJDK|
3173220|NCT00975884|113630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173221|NCT00975884|113630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173222|NCT00975884|113630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175647|NCT00887484|114544|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173223|NCT00975884|113630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173224|NCT00975884|113630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173225|NCT00975884|113630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175648|NCT00887484|114544|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175649|NCT00887484|114544|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175650|NCT00887484|114544|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175651|NCT00887484|114544|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175652|NCT02577536||Individual Participant Data Set|https://dash.nichd.nih.gov/study/424642|Deidentified data from this study are not available in the NICHD Data and Specimen Repository.
3175653|NCT05512117||Study Protocol|https://www.uv.es/uvweb/servei-investigacio/ca/grups-investigacio/grup-1285949714098.html?p2=GIUV2019-456|All study information can be requested via email.
3173226|NCT04537585|guyguytshimakabundi@gmail.com|Clinical Study Report|http://cancovid.slack.com|"It is a case of a baby from a COVID-9 positive mother who had a urogenital infection in the last two weeks of pregnancy.~After the usual inflammatory assessment, investigators concluded that he had NEONATAL INFECTION, and put him on a triple combination of antibiotics (cefotaxime-clamoxyl-Gentamicin).~On Day 3, the evolution was marked by a slight abdominal bloating, with a suspicion of a BEGINNING ULCERONECROSAN ENTEROCOLITIS and motivate the addition of Flagyl.~On Day 4, the mother's anti-COVID serology came back positive and the father was also positive that motivated testing baby.~Maybe the Covid-19 test was positive, investigators continued the same therapeutic regimen until Day 10; without the gentamicin that investigators had given for 5 days.~On Day 10, the baby was asymptomatic. The baby was born by cesarean section indicated for scarring uterus. Free access data on demand. Review Board approval was required by the investigators by the time patient recruitment begins."
3173227|NCT01294605|263855/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173228|NCT01294605|263855/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175654|NCT03057886|56202616.9.0000.0083|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|There you may find the project and all step to get the approval
3175655|NCT01350219|PMC5689778|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=stem+cell+educator+type+1+diabetes%2C+platelets|Yong Zhao\*, Zhaoshun Jiang, Elias Delgado, Heng Li, Huimin Zhou, Wei Hu, Marcos Perez-Basterrechea, Anna Janostakova, Qidong Tan, Jing Wang, Mao Mao, Zhaohui Yin, Ye Zhang, Ying Li, Quanhai Li, Jing Zhou, Yunxiang Li, Eva Martinez Revuelta, Jose Maria García-Gala, Honglan Wang, Silvia Perez-López, Maria Alvarez-Viejo, Edelmiro Menendez, Thomas Moss, Edward Guindi, Jesus Otero. Platelets-derived mitochondria display embryonic stem cell markers and improve pancreatic islet β-cell function in humans. STEM CELLS Translational Medicine. July 7, 2017. DOI: 10.1002/sctm.17-0078.
3175656|NCT01035749|113883|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175657|NCT01035749|113883|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175658|NCT01035749|113883|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175659|NCT01035749|113883|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175660|NCT01035749|113883|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175661|NCT01035749|113883|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175662|NCT04602286|10.17605/OSF.IO|Statistical Analysis Plan|https://osf.io/qxtrv|The Statistical Analysis Plan for this trial was prospectively registered on the Open Science Framework on October 8, 2020
3175663|NCT00423046|108933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175664|NCT00423046|108933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175665|NCT00423046|108933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175666|NCT00423046|108933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175667|NCT00423046|108933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175668|NCT00423046|108933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175669|NCT00423046|108933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175670|NCT01494636|115419|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175671|NCT01494636|115419|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175672|NCT01494636|115419|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175673|NCT01494636|115419|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175674|NCT01494636|115419|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175675|NCT01494636|115419|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175676|NCT01494636|115419|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175677|NCT01725685|116524|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175678|NCT01725685|116524|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175679|NCT01725685|116524|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175680|NCT01725685|116524|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175681|NCT01725685|116524|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173229|NCT01294605|263855/034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173230|NCT01294605|263855/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173231|NCT01294605|263855/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173232|NCT01294605|263855/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173233|NCT01332513|114552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173234|NCT01332513|114552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173235|NCT01332513|114552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173236|NCT01332513|114552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173237|NCT01332513|114552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173238|NCT01332513|114552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173239|NCT01332513|114552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173240|NCT03284073|NCT01844362|Study Protocol|http://clinicaltrials.gov|
3173241|NCT00289731|100382|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173242|NCT00289731|100382|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173243|NCT00289731|100382|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100382 are summarised with studies 100383, 100384, and 100385 on the GSK Clinical Study Register.
3173244|NCT00289731|100382|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173245|NCT00289731|100382|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173246|NCT00289731|100382|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173247|NCT01077531|111601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173248|NCT01077531|111601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173249|NCT01077531|111601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173250|NCT01077531|111601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173251|NCT01077531|111601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173252|NCT01077531|111601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173253|NCT01077531|111601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173254|NCT00370396|107046|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173255|NCT00370396|107046|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173256|NCT00370396|107046|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173257|NCT00370396|107046|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173258|NCT00370396|107046|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173259|NCT00370396|107046|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173260|NCT00879970|111960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173261|NCT00879970|111960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173262|NCT00879970|111960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173263|NCT00879970|111960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173264|NCT00879970|111960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173265|NCT00879970|111960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173266|NCT00879970|111960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173267|NCT03567330||Study Protocol|https://link-springer-com.udel.idm.oclc.org/article/10.1186/s12885-018-5052-8|
3173268|NCT06565754||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563562/|
3173269|NCT04355767||Individual Participant Data Set|https://biodatacatalyst.nhlbi.nih.gov/|
3173270|NCT00140738|100633|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173271|NCT00140738|100633|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173272|NCT00140738|100633|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173273|NCT00140738|100633|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173274|NCT00140738|100633|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173275|NCT00140738|100633|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173276|NCT00969059|112967|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173277|NCT00969059|112967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173278|NCT00969059|112967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173279|NCT00969059|112967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173280|NCT00969059|112967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173281|NCT00969059|112967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173282|NCT00969059|112967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173283|NCT00550420|AVA102677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173284|NCT00550420|AVA102677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173285|NCT00550420|AVA102677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173286|NCT00550420|AVA102677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173287|NCT00550420|AVA102677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173288|NCT00550420|AVA102677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173289|NCT00550420|AVA102677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173290|NCT03189797||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed|
3173291|NCT00386100|AVT105913|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173292|NCT00386100|AVT105913|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173293|NCT00386100|AVT105913|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173294|NCT00386100|AVT105913|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173295|NCT00386100|AVT105913|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173296|NCT00386100|AVT105913|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173297|NCT00386100|AVT105913|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173298|NCT00411697|106789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173299|NCT00411697|106789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173300|NCT00411697|106789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173301|NCT00411697|106789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173302|NCT00411697|106789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173303|NCT00411697|106789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173304|NCT00524576|108988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173305|NCT00524576|108988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173306|NCT00524576|108988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173307|NCT00524576|108988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173308|NCT00524576|108988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173309|NCT02879747||Study Protocol|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
3173310|NCT02879747||Statistical Analysis Plan|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
3173311|NCT01416376|115830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173312|NCT01416376|115830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173313|NCT01416376|115830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173314|NCT01416376|115830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173315|NCT01416376|115830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173316|NCT01416376|115830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175682|NCT01725685|116524|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175683|NCT01725685|116524|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175684|NCT00413023|NKF100096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175685|NCT00413023|NKF100096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175686|NCT00413023|NKF100096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175687|NCT00413023|NKF100096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175688|NCT00413023|NKF100096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175689|NCT00413023|NKF100096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175690|NCT00413023|NKF100096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175691|NCT00023231|SDY131|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
3175692|NCT00023231|SDY131|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
3175693|NCT00023231|SDY131|Study summary, -design,-demographics, -mechanistic assays, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
3175694|NCT05198141||Study Protocol|http://www.staffdata.zu.edu.eg/ar/ShowData/23528|you can send a Data request e-mail to Dr Mohamed at drno99@yahoo.com
3175695|NCT05198141|drno99@yahoo.com|Statistical Analysis Plan|http://www.staffdata.zu.edu.eg/ar/ShowData/23528|you can send a Data request e-mail to Dr Mohamed at drno99@yahoo.com
3175696|NCT05198141||Informed Consent Form|http://www.staffdata.zu.edu.eg/ar/ShowData/23528|you can send a Data request e-mail to Dr Mohamed at drno99@yahoo.com
3175697|NCT05198141||Individual Participant Data Set|http://www.staffdata.zu.edu.eg/ar/ShowData/23528|you can send a Data request e-mail to Dr Mohamed at drno99@yahoo.com
3175698|NCT04801251|Sarah bakry|Study Protocol|https://www.outlook.com/aun.edu.eg|All data or information will be uploaded on the website
3175699|NCT06523712||Informed Consent Form|https://schoolsplus.pk/schools/sharif-education-complex/|
3175700|NCT06523712||Informed Consent Form|https://apseducation123.wixsite.com/website|
3175701|NCT06523712||Informed Consent Form|https://apsaskarixi.pk/|
3175702|NCT00478621|109836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175703|NCT00478621|109836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175704|NCT00478621|109836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175705|NCT00478621|109836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175706|NCT00478621|109836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175707|NCT00478621|109836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175708|NCT00355641|101468/206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175709|NCT00355641|101468/206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173317|NCT05163379||Study Protocol|https://khgmekodemedb.saglik.gov.tr/Eklenti/23273/0/fizik-tedavi-ve-rehabilitasyon-islemleri-degerlendirme-olcekleripdf.pdf|
3173318|NCT00297206|HS210914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175710|NCT00355641|101468/206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175711|NCT00355641|101468/206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175712|NCT00355641|101468/206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175713|NCT00355641|101468/206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175714|NCT00355641|101468/206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175715|NCT06955000||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35015445/|"Döner A, Taşci S, Bilgin A. The Effect of Massage, Acupressure and Reflexology on Restless Legs Syndrome Severity and Sleep Quality in Patients Receiving Haemodialysis Treatment: A Systematic Review and Meta-Analysis. Nursing Open. 2025 Feb;12(2):e70135.~26-Mitchell UH, Johnson AW, Myrer B. Comparison of two infrared devices in their effectiveness in reducing symptoms associated with RLS. Physiotherapy theory and practice. 2011 Jun 1;27(5):352-9.~27-Tang L, Zhao N, Gao X, Li J, Yu X, Liang R, Xie C, Li L, Wang Q, Yang W. Acupuncture treatment of restless legs syndrome: a randomized clinical controlled study protocol based on PET-CT and fMRI. Frontiers in Psychiatry. 2024 Dec 24; 15:1481167."
3175870|NCT00453687|AC2108380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175871|NCT00453687|AC2108380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175872|NCT06108921||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
3171457|NCT01014117|114009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171458|NCT01014117|114009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171459|NCT01014117|114009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171460|NCT01014117|114009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171461|NCT01014117|114009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171462|NCT01961479||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/1745-6215-15-472|Kues, J. N., Janda, C., Kleinstaeuber, M., \& Weise, C. (2014). Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial. Trials, 15(1), 472. doi:10.1186/1745-6215-15-472
3171463|NCT00808444|111654|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171464|NCT00808444|111654|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171465|NCT00808444|111654|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171466|NCT00808444|111654|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171467|NCT00808444|111654|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171468|NCT00808444|111654|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171469|NCT00808444|111654|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171470|NCT01471665|115134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171471|NCT01471665|115134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171472|NCT01471665|115134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171473|NCT01471665|115134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171474|NCT01471665|115134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171475|NCT01471665|115134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171476|NCT01471665|115134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171477|NCT00039988|Study identifier is SDY471|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
3171478|NCT00039988|Study identifier is SDY471|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
3171479|NCT00039988|Study identifier is SDY471|Study summary, -design, -adverse events, -medications, -demographics, -lab tests, -mechanistic assays, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
3171480|NCT02889458|BrCA.risk.001|Study Protocol|http://www.hkuctr.com/Study/Show/b122235f3995420a97d570a85d03b542|
3171481|NCT01353703|111157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173319|NCT00297206|HS210914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173320|NCT00297206|HS210914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173321|NCT00297206|HS210914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173322|NCT00297206|HS210914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173323|NCT00297206|HS210914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173324|NCT00297206|HS210914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173325|NCT02094937|201135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173326|NCT02094937|201135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173327|NCT02094937|201135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173328|NCT02094937|201135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173329|NCT02094937|201135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173330|NCT01663714|104514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173331|NCT01663714|104514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173332|NCT01663714|104514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173333|NCT01663714|104514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173334|NCT01663714|104514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173335|NCT01663714|104514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173336|NCT01663714|104514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173337|NCT00950833|112801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173338|NCT00950833|112801|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173339|NCT00950833|112801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173340|NCT00950833|112801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173341|NCT00950833|112801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171482|NCT01353703|111157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171483|NCT01353703|111157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171484|NCT01353703|111157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171485|NCT01353703|111157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171486|NCT01353703|111157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171487|NCT02480933|https://doi.org/10.3892/mco.20|Study Protocol|http://www.spandidos-publications.com/mco|feasibility of the protocol paper
3171488|NCT00814957|110269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171489|NCT00814957|110269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171490|NCT00814957|110269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171491|NCT00814957|110269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171492|NCT00814957|110269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171493|NCT00814957|110269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171494|NCT00814957|110269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3171495|NCT00132730||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-005&kw=0873-005&tab=access|
3171496|NCT00288080|NCT00288080|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
3173342|NCT00950833|112801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173343|NCT00950833|112801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173344|NCT00964223|114547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173345|NCT00964223|114547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173346|NCT00964223|114547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173347|NCT00964223|114547|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173348|NCT00964223|114547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173349|NCT00964223|114547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173350|NCT00964223|114547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173351|NCT00000531|AVID|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/avid/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3173352|NCT00000531||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/avid/|
3173353|NCT00000531||Study Forms|http://biolincc.nhlbi.nih.gov/studies/avid/|
3175716|NCT00113165|LAM100034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175717|NCT00113165|LAM100034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175718|NCT00113165|LAM100034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175719|NCT00113165|LAM100034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175720|NCT00113165|LAM100034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175721|NCT00113165|LAM100034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175722|NCT00113165|LAM100034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175723|NCT00481663||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175724|NCT01027845|112640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175725|NCT01027845|112640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175726|NCT01027845|112640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175727|NCT01027845|112640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175728|NCT01027845|112640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175729|NCT01027845|112640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175730|NCT00545025|110674|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175731|NCT00545025|110674|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173354|NCT00000531||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/avid/|
3173355|NCT05709054||Clinical Study Report|https://doi.org/10.1016/j.ijosm.2018.07.006|
3173356|NCT02496221|201834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173357|NCT02496221|201834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173358|NCT02496221|201834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173359|NCT02496221|201834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173360|NCT02496221|201834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173361|NCT02496221|201834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173362|NCT02496221|201834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175732|NCT00545025|110674|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173363|NCT01165242|114249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175733|NCT00545025|110674|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173364|NCT01165242|114249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173365|NCT01165242|114249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173366|NCT01165242|114249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173367|NCT01165242|114249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173368|NCT01165242|114249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173369|NCT00606684|B2C111045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173370|NCT00606684|B2C111045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173371|NCT00606684|B2C111045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173372|NCT00606684|B2C111045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173373|NCT00606684|B2C111045|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173374|NCT00606684|B2C111045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173375|NCT00606684|B2C111045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173376|NCT06538168||Informed Consent Form|https://www.facebook.com/gghgmabadfsd/?paipv=0&eav=AfbwgEmoehvAkH8F8E-KZ9WClHEgcLyNQwBOij0PYLNHpvrJZ1KZbTJdZYuWB21J8rA&_rdr|
3173377|NCT01162590|113545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173378|NCT01162590|113545|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173379|NCT01162590|113545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173380|NCT01162590|113545|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173381|NCT01162590|113545|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173382|NCT01162590|113545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173383|NCT02169583|201022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173384|NCT02169583|201022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173385|NCT02169583|201022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173386|NCT02169583|201022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173387|NCT02169583|201022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173388|NCT02169583|201022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173389|NCT02169583|201022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173390|NCT00345683|105988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173391|NCT00345683|105988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173392|NCT00345683|105988|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173393|NCT00345683|105988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173394|NCT00345683|105988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173395|NCT00345683|105988|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173396|NCT00345683|105988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173397|NCT02224521|112071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173398|NCT02224521|112071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173399|NCT02224521|112071|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173400|NCT02224521|112071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173401|NCT02224521|112071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173402|NCT02224521|112071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173403|NCT02224521|112071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173404|NCT00000606|NETT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nett/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3173405|NCT00000606||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nett/|
3173406|NCT00000606||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nett/|
3173407|NCT00551564|DIX110434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173408|NCT00551564|DIX110434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173409|NCT00551564|DIX110434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173410|NCT00551564|DIX110434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173411|NCT00551564|DIX110434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173412|NCT00551564|DIX110434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173413|NCT00551564|DIX110434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173414|NCT04716673||Individual Participant Data Set|https://info.swissubase.ch|
3173415|NCT01001169|113847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173416|NCT01001169|113847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173417|NCT01001169|113847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173418|NCT01001169|113847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173419|NCT01001169|113847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173420|NCT01001169|113847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173421|NCT01001169|113847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173422|NCT02058628|200398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173423|NCT02058628|200398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173424|NCT02058628|200398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173425|NCT02058628|200398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173426|NCT02058628|200398|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173427|NCT02058628|200398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173428|NCT02058628|200398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173429|NCT05216614|10.7599/hmr.2014.34.3.107|Clinical Study Report|http://www.researchgate.net/publication/271283284_Clinical_Diagnosis_and_Treatment_of_Olfactory_Dysfunction|Research article published in Hanyang Medical Reviews discussing diagnosis and treatment of olfactory dysfunction
3173430|NCT01626820|116664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173431|NCT01626820|116664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173432|NCT01626820|116664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173433|NCT01626820|116664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173434|NCT01626820|116664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173435|NCT01626820|116664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173436|NCT01626820|116664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173437|NCT00229112||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3173438|NCT00274703|MEE103226|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173439|NCT00274703|MEE103226|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173440|NCT00274703|MEE103226|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173441|NCT00274703|MEE103226|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173442|NCT00274703|MEE103226|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173443|NCT00616928|110464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173444|NCT00616928|110464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173445|NCT00616928|110464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173446|NCT00616928|110464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173447|NCT00616928|110464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173448|NCT00616928|110464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173449|NCT00616928|110464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173450|NCT01209052|112483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173451|NCT01209052|112483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173452|NCT01209052|112483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173453|NCT01209052|112483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173454|NCT01209052|112483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173455|NCT01209052|112483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173456|NCT01209052|112483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173457|NCT00197275|104733|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173458|NCT00197275|104733|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173459|NCT00197275|104733|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173460|NCT00197275|104733|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173461|NCT00197275|104733|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173462|NCT00197275|104733|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173463|NCT00946257|112438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173464|NCT00946257|112438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173465|NCT00946257|112438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173466|NCT00946257|112438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173467|NCT00946257|112438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173468|NCT00946257|112438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173469|NCT00946257|112438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173470|NCT00743067|MET111648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173471|NCT00743067|MET111648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173472|NCT00743067|MET111648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173473|NCT00743067|MET111648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173474|NCT00743067|MET111648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173475|NCT00743067|MET111648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173476|NCT00743067|MET111648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175734|NCT00545025|110674|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175735|NCT00545025|110674|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173477|NCT01000857|112812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173478|NCT01000857|112812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173479|NCT01000857|112812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173480|NCT01000857|112812|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173481|NCT04413747|guest_1|Study Protocol|http://giardinostlucia.it|
3173482|NCT04413747|guest_2|Informed Consent Form|http://giardinostlucia.it|
3173483|NCT04413747|guest_3|Individual Participant Data Set|http://giardinostlucia.it|
3173484|NCT04517006||Individual Participant Data Set|https://osf.io/63yg9/|Not yet available, but will be posted once study is complete.
3173485|NCT04517006||Statistical Analysis Plan|https://osf.io/63yg9/|The investigators intend to publish this study as a registered report. The analysis plan is current as of this registration, but will likely change during the review process.
3173486|NCT04517006||Informed Consent Form|https://osf.io/63yg9/|
3173487|NCT04517006||Analytic Code|https://osf.io/63yg9/|Will be posted after study is complete.
3173488|NCT04956666||Individual Participant Data Set|https://clinicaltrials.servier.com|
3173489|NCT04956666||Study Protocol|https://clinicaltrials.servier.com|
3173490|NCT04956666||Statistical Analysis Plan|https://clinicaltrials.servier.com|
3173491|NCT04956666||Informed Consent Form|https://clinicaltrials.servier.com|
3173492|NCT04956666||Clinical Study Report|https://clinicaltrials.servier.com|
3173493|NCT04956666||Study-level clinical trial data|https://clinicaltrials.servier.com|
3173494|NCT00684671|111572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173495|NCT00684671|111572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173496|NCT00684671|111572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173497|NCT00684671|111572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173498|NCT00684671|111572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173499|NCT00684671|111572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173500|NCT00996671|113581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173501|NCT00996671|113581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173502|NCT00996671|113581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173503|NCT00996671|113581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173504|NCT00996671|113581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173505|NCT00996671|113581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173506|NCT00996671|113581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173507|NCT06098755|014/BR/612|Individual Participant Data Set|https://virtualtribunalmonastery.vhx.tv/|Regarding an individual means test, the Holistic Healthcare needs exceed the costs associated with the service. As a licensed referral, ordering, and nonclinical prescribing Holistic Medicine provider only, cost-effective pastoral counseling serve its purpose.
3173508|NCT06098755||Study Protocol|https://www.ncbi.nlm.nih.gov/myncbi/goddess%20zena.jones.1/bibliography/public/|
3173509|NCT07314671|10.1136/bjsports-2012-091746|Protocol background|https://pubmed.ncbi.nlm.nih.gov/23511698/|
3173510|NCT07314671|10.1136/bmjsem-2019-000570|Protocol background|https://pubmed.ncbi.nlm.nih.gov/31673404/|
3173511|NCT07314671|10.1080/24733938.2024.2419659|Protocol background|https://pubmed.ncbi.nlm.nih.gov/39444266/|
3173512|NCT07314671|10.1177/0363546517720194|Protocol background|https://pubmed.ncbi.nlm.nih.gov/28806100/|
3173513|NCT01691508|115575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173514|NCT01691508|115575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173515|NCT01691508|115575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173516|NCT01691508|115575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173517|NCT01691508|115575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173518|NCT01691508|115575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173519|NCT01691508|115575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173520|NCT00317161|100480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173521|NCT00317161|100480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173522|NCT00317161|100480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173523|NCT00317161|100480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173524|NCT00317161|100480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173525|NCT00317161|100480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173526|NCT03974633||Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1dEjSUmhIkqAOvh30WaJ0svs6jrdEGDyU5FXHeBuTOF8/edit?usp=sharing|
3173527|NCT00035009||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3173528|NCT00425737|444563/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173529|NCT00425737|444563/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173530|NCT00425737|444563/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173531|NCT00425737|444563/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173532|NCT00425737|444563/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173533|NCT00425737|444563/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173534|NCT07296640|BPIT-GFFI-2024-001|Individual Participant Data Set|https://mmsxauthority.com/BPIT-2024doc.html|"De-identified individual participant data (strength, HRV, knee valgus, injury logs) available upon reasonable request to Principal Investigator: Dr. Neeraj Mehta, PhD (info@mmsxauthority.com). All supporting documents (Protocol, Ethics, Consent, Observation Logs, AE Forms, Final Report) uploaded under Study Documents tab."
3173535|NCT06705400||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/40866846/|
3173536|NCT06705400||Statistical Analysis Plan|https://findresearcher.sdu.dk/ws/portalfiles/portal/298847036/Statistical_Analysis_Plan_for_the_Bloom_Study_14112025_FINAL.pdf|
3173537|NCT03869892||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3173538|NCT03869892||Study Protocol|https://clinicaltrials.servier.com/|
3173539|NCT03869892||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3173540|NCT03869892||Informed Consent Form|https://clinicaltrials.servier.com/|
3173541|NCT03869892||Clinical Study Report|https://clinicaltrials.servier.com/|
3173542|NCT03869892||study-level clinical trial data|https://clinicaltrials.servier.com/|
3173543|NCT00376779|106786|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173544|NCT00376779|106786|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173545|NCT00376779|106786|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173546|NCT00376779|106786|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173547|NCT00376779|106786|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173548|NCT00376779|106786|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173549|NCT06935656|DOI 10.17605/OSF.IO/Y4SGJ|All of the information regarding the Consent forms, IRB certificate as well as the analytic code and data can be found here.|https://osf.io/y4sgj/files/osfstorage/67d6ddfb6a60610ab9a72a9b|The analytic code and data will be uploaded once the data is collected (est. December, 2025) and analyzed (est. June, 2026)
3173550|NCT06935656||Study Protocol|https://osf.io/9mp83|
3173551|NCT01928914|114582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173552|NCT01928914|114582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173553|NCT01928914|114582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173554|NCT01928914|114582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173555|NCT01928914|114582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173556|NCT01928914|114582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173557|NCT01928914|114582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173558|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/33036555/|
3173559|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/32247709/|
3173560|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/34252034/|
3173561|NCT00502775|FFU109047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173562|NCT00502775|FFU109047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173563|NCT00502775|FFU109047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173564|NCT00502775|FFU109047|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173565|NCT00502775|FFU109047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173566|NCT00502775|FFU109047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173567|NCT00502775|FFU109047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173568|NCT01974895|200806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173569|NCT01974895|200806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173570|NCT01974895|200806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173571|NCT01974895|200806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173572|NCT01974895|200806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173573|NCT01974895|200806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173574|NCT01974895|200806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173575|NCT00109109||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3173576|NCT00000619|ESCAPE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/escape/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3173577|NCT00000619||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/escape/|
3173578|NCT00000619||Study Forms|http://biolincc.nhlbi.nih.gov/studies/escape/|
3173579|NCT00861809|111809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173580|NCT00861809|111809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173581|NCT00861809|111809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173582|NCT00861809|111809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173583|NCT00861809|111809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173584|NCT00861809|111809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173585|NCT00861809|111809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173586|NCT00404274|NKV105097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173587|NCT00404274|NKV105097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173588|NCT00404274|NKV105097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173589|NCT00404274|NKV105097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173590|NCT00404274|NKV105097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173591|NCT00404274|NKV105097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173592|NCT00404274|NKV105097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173593|NCT00436007|106369|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173594|NCT00436007|106369|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173595|NCT00436007|106369|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173596|NCT00436007|106369|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173597|NCT00436007|106369|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173598|NCT00436007|106369|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173599|NCT00329602|ROR104836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173600|NCT00329602|ROR104836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173601|NCT00329602|ROR104836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173602|NCT00329602|ROR104836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173603|NCT00329602|ROR104836|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173604|NCT00329602|ROR104836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173605|NCT00329602|ROR104836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173606|NCT06000280|Repositorio|Informed Consent Form|http://repositorio.bc.ufg.br|Repositorio da Biblioteca Central da Universidade Federal de Goias
3173607|NCT00269048|LPL104884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173608|NCT00269048|LPL104884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173609|NCT00269048|LPL104884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173610|NCT00269048|LPL104884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173611|NCT00269048|LPL104884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173612|NCT00269048|LPL104884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173613|NCT00269048|LPL104884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173614|NCT01385033||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3328-002&kw=3328-002&tab=access|
3173615|NCT00569062|PKI108574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173616|NCT00569062|PKI108574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173617|NCT00569062|PKI108574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173618|NCT00569062|PKI108574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173619|NCT00569062|PKI108574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173620|NCT01047345||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-006&kw=V503-006&tab=access|
3173621|NCT00950807|113073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173622|NCT00950807|113073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173623|NCT00950807|113073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173624|NCT00950807|113073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173625|NCT00950807|113073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173626|NCT00950807|113073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173627|NCT00950807|113073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173628|NCT04025034||Informed Consent Form|http://microsoftwindows.com|Navigator
3173629|NCT00394056|NKP106254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173630|NCT00394056|NKP106254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173631|NCT00394056|NKP106254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173632|NCT00394056|NKP106254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173633|NCT00394056|NKP106254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173634|NCT00394056|NKP106254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173635|NCT01019603|114565|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173636|NCT01019603|114565|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173637|NCT01019603|114565|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173638|NCT01019603|114565|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173639|NCT01019603|114565|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173640|NCT01019603|114565|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173641|NCT01019603|114565|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173642|NCT02197468||Clinical Study Report|https://www.frontiersin.org/articles/10.3389/fped.2018.00347/full|Publication from this study
3173643|NCT00442936||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-011&kw=0974-011&tab=access|
3173644|NCT02746952||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3173645|NCT02746952||Study Protocol|https://clinicaltrials.servier.com/|
3173646|NCT02746952||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3173647|NCT02746952||Informed Consent Form|https://clinicaltrials.servier.com/|
3173648|NCT02746952||Clinical Study Report|https://clinicaltrials.servier.com/|
3173649|NCT02746952||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3173650|NCT00000566|PIOPED|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/pioped/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
3173651|NCT00000566||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pioped/|
3173652|NCT00000566||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pioped/|
3173653|NCT04786080||Statistical Analysis Plan|https://www.kcl.ac.uk/research/supporting-parents-and-kids-through-lockdown-experiences-sparkle-trial|The SAP can be accessed on this website.
3173654|NCT00062790|ARI40014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173655|NCT00062790|ARI40014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173656|NCT00062790|ARI40014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173657|NCT00062790|ARI40014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173658|NCT00062790|ARI40014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173659|NCT00062790|ARI40014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173660|NCT00062790|ARI40014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173661|NCT00622609|MAG103114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173662|NCT00622609|MAG103114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173663|NCT00622609|MAG103114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173664|NCT00622609|MAG103114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173665|NCT00622609|MAG103114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173666|NCT00622609|MAG103114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3173667|NCT01974999|SDY1094|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|Participant level data and additional relevant materials are available to the public in the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. Data analysis tools are also available to researchers.
3173668|NCT01974999|SDY1094|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|ImmPort study identifier is SDY1094.
3173669|NCT01974999|SDY1094|Study summary, -design, -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|ImmPort study identifier is SDY1094.
3173670|NCT00056134||Publication|https://www.ncbi.nlm.nih.gov/pubmed/23958949|"Denileukin diftitox (ONTAK) induces a tolerogenic phenotype in dendritic cells and stimulates survival of resting Treg.~Baur AS1, Lutz MB, Schierer S, Beltrame L, Theiner G, Zinser E, Ostalecki C, Heidkamp G, Haendle I, Erdmann M, Wiesinger M, Leisgang W, Gross S, Pommer AJ, Kämpgen E, Dudziak D, Steinkasserer A, Cavalieri D, Schuler-Thurner B, Schuler G."
3173671|NCT00056134|DOI:10.1182/blood-2012-09-4569|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/23958949|Denileukin diftitox (ONTAK) induces... Baur AS et al
3173672|NCT01295372|2010-022181-28|EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2010-022181-28/result|
3173673|NCT04247308|Mendeley Data|Individual Participant Data Set|http://data.mendeley.com/datasets/k4j689jfwj/2|Contains 56 Preterm Infants data which includes, gestational age, chronological age, corrected gestational age, sex, birth weight, birth length, birth occipitofrontal circumference (OFC), APGAR at 1-min, and APGAR at 5-min, pre-post intervention (5 days) changes of weight, length, OFC, INFANIB (Infant Neurological International Battery) and NIPS (Neonatal Infant Pain Scale).
3173674|NCT04437693||Clinical Study Report|https://www.worldometers.info/coronavirus/|https://www.worldometers.info/coronavirus/
3173675|NCT04437693||Clinical Study Report|https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf|https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf
3173676|NCT03167671|ISBN-10: 1886039224|Book|https://www.amazon.com/Prescription-Drug-Abuse-Epidemic-Understanding/dp/1886039224|
3173677|NCT06294080||Individual Participant Data Set|http://figshare.com|Study data will be submitted to Figshare for open science access - all identifying codes will be removed
3173678|NCT03222765||Study Protocol|http://www.epredice.eu|Study Protocol Version 5.0
3173679|NCT05240222|DOI 10.17605/OSF.IO/D5T4M|Individual Participant Data Set|http://osf.io/d5t4m/|The de-identified datasets generated and analyzed during the current study are made available in the Open Science Framework repository, \[osf.io/d5t4m/\].
3173680|NCT07217353|IRB 2025-158|Study Protocol|https://www.axiommentor.com/pages/irb/sectionsOfProtocol.cfm?id=977&b=MP|
3173681|NCT01866319||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3475-006&kw=3475-006&tab=access|
3175736|NCT01663389|112167|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175737|NCT01663389|112167|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175738|NCT01663389|112167|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175739|NCT01663389|112167|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175740|NCT01663389|112167|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175741|NCT01663389|112167|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175742|NCT01663389|112167|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175743|NCT04434508|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
3175744|NCT02256865||Statistical Analysis Plan|https://research.labiomed.org/redcap/redcap_v7.2.2/FileRepository/file_download.php?pid=174&id=19887|Data Analysis Plan available by request to PI
3175745|NCT00325169|104962|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175746|NCT00325169|104962|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175747|NCT00325169|104962|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175748|NCT00325169|104962|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175749|NCT00325169|104962|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175750|NCT00325169|104962|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175751|NCT00325169|104962|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175752|NCT00420745|106481|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175753|NCT00420745|106481|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175754|NCT00420745|106481|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175755|NCT00420745|106481|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175756|NCT00420745|106481|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175757|NCT00420745|106481|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175758|NCT00420745|106481|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175759|NCT00126945|104702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175760|NCT00126945|104702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175761|NCT00126945|104702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175762|NCT00126945|104702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175763|NCT00126945|104702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175764|NCT00126945|104702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175765|NCT03512652||scientific Article|https://ijmbs.info/index.php/ijmbs/article/view/971|
3175766|NCT03045172||Informed Consent Form|http://www.cvvd.org/research|"Click the link titled NEW STUDY FOR LICHEN SCLEROSUS- PLATELET RICH PLASMA (PRP)- Open to new participants to open the informed consent."
3175767|NCT01704261||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-022&kw=3102-022&tab=access|
3175768|NCT00764790|111751|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175769|NCT00764790|111751|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175770|NCT00764790|111751|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175771|NCT00764790|111751|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175772|NCT00764790|111751|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175773|NCT00764790|111751|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175774|NCT00764790|111751|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175775|NCT00849056|112755|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175776|NCT00849056|112755|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175777|NCT00849056|112755|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175778|NCT00849056|112755|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175779|NCT00849056|112755|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175780|NCT00849056|112755|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175781|NCT00849056|112755|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175782|NCT04109963|Not yet available|Individual Participant Data Set|https://dataverse.scholarsportal.info/dataverse/calgary|The dataset with individual de-identified participant data will be hosted on the University of Calgary PRISM dataverse once the main results results are published. The identifier will be assigned when the dataset is uploaded.
3175783|NCT00358488|B2E106359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175784|NCT00358488|B2E106359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175785|NCT00358488|B2E106359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175786|NCT00358488|B2E106359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175787|NCT00358488|B2E106359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175788|NCT00358488|B2E106359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175789|NCT00358488|B2E106359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175790|NCT00034632||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3175791|NCT03641729||Study Protocol|http://aline.priori.fioritto@gmail.com|More information contact the principal investigator
3175792|NCT03602001||Study Protocol|https://osf.io/btzhw/|The study protocol was pre-registered prior to starting recruitment on the Open Science Framework and is available via this link. IPD underlying publications will also be available here.
3175793|NCT00321763|107192|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175794|NCT00321763|107192|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175795|NCT00321763|107192|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175796|NCT00321763|107192|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175797|NCT00321763|107192|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175798|NCT06113978|orcid.org/0000-0002-6328-6419|Study Protocol|http://orcid.org/0000-0002-6328-6419|the corresponding author (sponsor/principal investigator) of this work can be contacted for help anytime by colleagues who concern
3175799|NCT01416571|112691|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175800|NCT01416571|112691|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175801|NCT01416571|112691|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175802|NCT01416571|112691|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175803|NCT01416571|112691|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175804|NCT01416571|112691|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175805|NCT00706563|111631|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175806|NCT00706563|111631|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175807|NCT00706563|111631|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175808|NCT00706563|111631|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3175873|NCT06493253|NCT01030484|Clinical Study Report|https://repository.niddk.nih.gov/studies/nafld-adult-database-2/|The NAFLD Adult Database 2 continued the longitudinal follow-up of participants enrolled in earlier NASH CRN studies and recruited new participants with recent liver biopsies. Comprehensive data, including demographics, medical history, symptoms, medication use, alcohol use and routine laboratory studies were collected on all participants at entry and at annual visits for up to 10 years after enrollment. A liver biopsy was collected at baseline if not collected in a prior NASH CRN study.
