id|nct_id|document_id|document_type|url|comment
2847447|NCT00397215|108251|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845260|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
2845261|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
2845262|NCT00134719|102370 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845263|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.
2845264|NCT00134719|102370 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847448|NCT00397215|108251|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847449|NCT00397215|108251|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847450|NCT00397215|108251|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847451|NCT00397215|108251|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847452|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.
2847453|NCT00318058|104540|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847454|NCT00318058|104540|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847455|NCT00318058|104540|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847456|NCT00318058|104540|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847457|NCT00318058|104540|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847458|NCT00318058|104540|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847459|NCT06652529||Study Protocol|https://www.aromics.es/en/|
2845265|NCT01996995||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/s13063-015-0622-4|
2845266|NCT02836769||Study Protocol|http://www.implementationscience.com/content/10/1/6|Publication of the initial project protocol
2847460|NCT01254032|114169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847461|NCT01254032|114169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849623|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
2849624|NCT03172468||Informed Consent Form|https://box.medunigraz.at/s/QuTYym3xsqXybWI|
2849625|NCT03172468||Study Protocol|https://box.medunigraz.at/s/YbufqAn3DBI1f4Q|
2849626|NCT00792636|110948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845267|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
2845268|NCT00127010|103388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845269|NCT00127010|103388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845270|NCT00127010|103388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845271|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.
2847462|NCT01254032|114169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849627|NCT00792636|110948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849628|NCT00792636|110948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849629|NCT00792636|110948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849630|NCT00792636|110948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849631|NCT00792636|110948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845272|NCT00127010|103388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845273|NCT00127010|103388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845274|NCT00729001|444563/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845275|NCT00729001|444563/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845276|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
2845277|NCT00729001|444563/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845278|NCT00729001|444563/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845279|NCT00729001|444563/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845280|NCT00496327||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845281|NCT07233525||Study Protocol|https://osf.io/ryq6k/overview?view_only=82691366adfe4dd3999bfba95ce6466d|The full study protocol
2845282|NCT00985790|113237|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845283|NCT00985790|113237|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845284|NCT00985790|113237|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845285|NCT00985790|113237|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845286|NCT00985790|113237|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847463|NCT01254032|114169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847464|NCT01254032|114169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847465|NCT00118690|SFA100316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849632|NCT00792636|110948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849633|NCT07048717||General information about the study plus information about application for data|https://www.umu.se/en/research/groups/the-mauritius-study/|
2851803|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.
2851804|NCT00196937|103514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851805|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.
2851806|NCT00196937|103514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851807|NCT00196937|103514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845287|NCT00985790|113237|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845288|NCT03496675||Individual Participant Data Set|https://osf.io/tpdhu/|
2845289|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.
2847466|NCT00118690|SFA100316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847467|NCT00118690|SFA100316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849634|NCT07065084|dilek.cecen@cbu.edu.tr|Clinical Study Report|https://cdn.clinicaltrials.gov/large-docs/02/NCT04069702/ICF_000.pdf|
2851808|NCT00196937|103514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851809|NCT00196937|103514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851810|NCT00196937|103514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845290|NCT00335075||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845291|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.
2845292|NCT04967703||Full Paper|http://www.europeanreview.org/article/32287|
2845293|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
2847468|NCT00118690|SFA100316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847469|NCT00118690|SFA100316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847470|NCT02714907||Study Protocol|http://cortrium.com|In Danish language
2847471|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
2845294|NCT04976725||Statistical Analysis Plan|https://doi.org/10.1016/J.JCM.2019.12.001|
2845295|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"
2845296|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."
2847472|NCT00851344|110163|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847473|NCT00851344|110163|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847474|NCT00851344|110163|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847475|NCT00851344|110163|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847476|NCT00851344|110163|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847477|NCT00851344|110163|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849635|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)
2849636|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)
2849637|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)
2851811|NCT00984659|112989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851812|NCT00984659|112989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851813|NCT00984659|112989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851814|NCT00984659|112989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851815|NCT00984659|112989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851816|NCT00984659|112989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851817|NCT00984659|112989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851818|NCT01516450|116119|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851819|NCT01516450|116119|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845297|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"
2847478|NCT00851344|110163|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845298|NCT00976391|108486|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849638|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
2849639|NCT00976105|111849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847479|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.
2849640|NCT00976105|111849|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849641|NCT00976105|111849|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849642|NCT00976105|111849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849643|NCT00976105|111849|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849644|NCT00976105|111849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849645|NCT07214896|De-identified biometric audit|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
2849646|NCT07214896|ESG compliance logs|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
2849647|NCT07214896|Wage token minting and transfe|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
2849648|NCT07214896|SHA-256 notarized study protoc|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
2849649|NCT07214896|Statistical analysis plan (SAP|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
2847480|NCT00000488||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|
2847481|NCT00968890|113525|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847482|NCT00968890|113525|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849650|NCT07214896|Informed consent form (ICF)|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
2849651|NCT07214896|Clinical study report (CSR)|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
2849652|NCT07214896|Analytic code for biometric sc|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
2849653|NCT07217600||Study Protocol|https://www.chictr.org.cn/showproj.html?proj=253510|
2847483|NCT00968890|113525|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847484|NCT00968890|113525|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849654|NCT04119284||Informed Consent Form|http://irbnet.org|The Informed consent form can be obtained while the patient is seen for scoliosis at Nemours-AIDHC.
2849655|NCT00611559|110478|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849656|NCT00611559|110478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849657|NCT00611559|110478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847485|NCT00968890|113525|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847486|NCT00968890|113525|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849658|NCT00611559|110478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849659|NCT00611559|110478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851820|NCT01516450|116119|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851821|NCT01516450|116119|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851822|NCT01516450|116119|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845299|NCT00976391|108486|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845300|NCT00976391|108486|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845301|NCT00976391|108486|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845302|NCT00976391|108486|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845303|NCT00976391|108486|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845304|NCT00976391|108486|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845305|NCT00120848|580299/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845306|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
2847487|NCT00968890|113525|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847488|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
2847489|NCT01622231|116365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847490|NCT01622231|116365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847491|NCT01622231|116365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849660|NCT00611559|110478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849661|NCT00611559|110478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849662|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
2849663|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
2849664|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
2847492|NCT01622231|116365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845307|NCT00120848|580299/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849665|NCT06795880||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/33062451/|
2845308|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
2847493|NCT01893203|25109244|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/|
2847494|NCT00347360|CFD105453|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849666|NCT06791993||Individual Participant Data Set|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op
2849667|NCT03423303||Statistical Analysis Plan|https://bmjopen.bmj.com/content/bmjopen/14/1/e075595.full.pdf|
2849668|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
2849669|NCT03739450|602d|Individual Participant Data Set|https://www.tbindsc.org/StaticFiles/SOP/602d%20-%20External%20Use%20TBIMS%20National%20Database%20Notification.pdf|
2849670|NCT03111290||Summary Data Set|http://dx.doi.org/10.5281/zenodo.45811|Dataset supporting Alagapan et al. 2016 PLoS Biology
2849671|NCT02073994||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2849672|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
2849673|NCT06447519||Study Protocol|https://ikee.lib.auth.gr|https://ikee.lib.auth.gr
2849674|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.
2849675|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
2849676|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
2851823|NCT01516450|116119|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851824|NCT01516450|116119|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851825|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.
2851826|NCT00000530||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rts/|
2851827|NCT00000530||Study Forms|http://biolincc.nhlbi.nih.gov/studies/rts/|
2851828|NCT02525224|DOI: 10.1111/jocd.12295|Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1111/jocd.12295/full|
2851829|NCT00440128|NKV100781|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851830|NCT00440128|NKV100781|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851831|NCT00440128|NKV100781|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851832|NCT00440128|NKV100781|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851833|NCT00440128|NKV100781|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851834|NCT00440128|NKV100781|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851835|NCT00440128|NKV100781|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851836|NCT05700344||Summary of Product Characteristics|https://www.ema.europa.eu/en/documents/product-information/bavencio-epar-product-information_en.pdf|Summary of Product Characteristics
2851837|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
2849677|NCT06830330||ethics committee approval|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
2849678|NCT02240472||Study Protocol|http://senomac.se/Home/study%20protocol.html|Study protocol and patient information (English)
2849679|NCT04522375||Study Protocol|http://clinicaltrials.gov|clinicaltrials.gov
2851838|NCT03136705|STU00089165|Study Protocol|https://irb.northwestern.edu/contact|
2851839|NCT03136705|STU00089165|Informed Consent Form|https://irb.northwestern.edu/contact|
2847495|NCT00347360|CFD105453|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847496|NCT00347360|CFD105453|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847497|NCT00347360|CFD105453|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847498|NCT00347360|CFD105453|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847499|NCT00347360|CFD105453|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847500|NCT00347360|CFD105453|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847501|NCT00354536|GLP106073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847502|NCT00354536|GLP106073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847503|NCT00354536|GLP106073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847504|NCT00354536|GLP106073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847505|NCT00354536|GLP106073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849680|NCT04522375||Statistical Analysis Plan|http://clinicaltrials.gov|clinicaltrials.gov
2849681|NCT06188754||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/38762486/|
2849682|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.
2847506|NCT00354536|GLP106073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849683|NCT06786429||Clinical Study Report|https://www.nust.ac.zw|
2849684|NCT06786429|tba|Clinical Study Report|https://www.nust.ac.zw|
2851840|NCT00945750||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0208-144&kw=0208-144&tab=access|
2845203|NCT00385840|108708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845204|NCT00385840|108708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845205|NCT07121348|END-7-25-3400|Study Protocol|http://www.tanta.edu.eg|
2845206|NCT05104346|COVID and acute appendicitis|Study Protocol|http://www.mans.edu.eg/|
2845207|NCT07080528||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2024-515545-41-00|
2845208|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
2845209|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.
2845210|NCT00536835|PLK107427|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845211|NCT00536835|PLK107427|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845212|NCT00536835|PLK107427|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845213|NCT00536835|PLK107427|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845214|NCT00536835|PLK107427|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845215|NCT00536835|PLK107427|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845216|NCT00536835|PLK107427|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845309|NCT00120848|580299/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849685|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.
2849686|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.
2845310|NCT00120848|580299/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845311|NCT00120848|580299/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849687|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.
2849688|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.
2845312|NCT00676052|AC2110664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845313|NCT00676052|AC2110664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847507|NCT00354536|GLP106073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847508|NCT06462885||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
2847509|NCT00043901|LAM40097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847510|NCT00043901|LAM40097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847511|NCT00043901|LAM40097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847512|NCT00043901|LAM40097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847513|NCT00043901|LAM40097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845314|NCT00676052|AC2110664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845315|NCT00676052|AC2110664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845316|NCT00676052|AC2110664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845317|NCT00676052|AC2110664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845318|NCT00676052|AC2110664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845319|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.
2845320|NCT00000544||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dash/|
2845321|NCT00000544||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/dash/|
2845322|NCT05872945||Individual Participant Data Set|https://github.com/dradolfomunoz/PF12RED|
2847514|NCT00043901|LAM40097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851841|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.
2851842|NCT00283712|SDY655|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|ImmPort study identifier is SDY655
2845323|NCT07055932||Study Protocol|https://theses.gla.ac.uk/1017/|
2845324|NCT01313676|113782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847515|NCT00043901|LAM40097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847516|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.
2847517|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
2847518|NCT00094172|ITN020AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN020AI
2847519|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.
2847520|NCT01254071|114694|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847521|NCT01254071|114694|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847522|NCT01254071|114694|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847523|NCT01254071|114694|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847524|NCT01254071|114694|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851843|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
2851844|NCT01097616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-028&kw=4305-028&tab=access|
2851845|NCT01367743||Statistical Analysis Plan|http://cic-p-nancy.fr/wp-content/uploads/2019/01/revUS_SAP_OPTIMA_CC_KD_NG.pdf|
2851846|NCT00404768||Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851847|NCT00404768||Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845325|NCT01313676|113782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845326|NCT01313676|113782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845327|NCT01313676|113782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845328|NCT01313676|113782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845329|NCT01313676|113782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845330|NCT01313676|113782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845331|NCT01894360|117100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845332|NCT01894360|117100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845333|NCT01894360|117100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845334|NCT01894360|117100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845335|NCT01894360|117100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847525|NCT01254071|114694|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847526|NCT01254071|114694|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847527|NCT01471678|115707|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847528|NCT01471678|115707|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847529|NCT01471678|115707|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851848|NCT00404768||Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851849|NCT00404768||Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851850|NCT00404768||Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851851|NCT00404768||Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851852|NCT00404768||Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845336|NCT01894360|117100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845337|NCT01894360|117100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845338|NCT01379937|115115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849689|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.
2845339|NCT01379937|115115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845340|NCT01379937|115115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845341|NCT01379937|115115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845342|NCT01379937|115115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845343|NCT01379937|115115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845344|NCT00705965||treatment manual and supplemental content|http://links.lww.com/PSYMED/A275|
2845345|NCT00552279|109179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845346|NCT00552279|109179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845347|NCT00552279|109179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849690|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.
2849691|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.
2849692|NCT03060421||Study Protocol|http://www.parkerinst.dk|
2849693|NCT02132936||Clinical Study Report|https://www.leopharmatrials.com/en|Clinical Trials at LEO Pharma
2851853|NCT01101568|113506|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851854|NCT01101568|113506|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851855|NCT01101568|113506|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845348|NCT00552279|109179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845349|NCT00552279|109179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847530|NCT01471678|115707|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849694|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
2849695|NCT05459688||Trial Results Summary|https://www.trialsummaries.com/Study/StudyDetails?id=25790&tenant=MT_MED_9011|Trial Results Summary
2845350|NCT00552279|109179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845351|NCT00552279|109179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849696|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
2849697|NCT06852430|042025201171|Study Protocol|https://docs.google.com/document/d/18-WWwL8l_EB2nHv4wr1-Q1cslJ1VUYUf/edit?usp=drivesdk&ouid=111849282554145262325&rtpof=true&sd=true|
2849698|NCT06272903|MBRU IRB-2023-228|Study Protocol|http://www.mbru.ac.ae|
2849699|NCT04979351||Review|https://dergipark.org.tr/tr/download/article-file/117117|
2847531|NCT01471678|115707|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849700|NCT04979351||Clinical Study Report|https://dergipark.org.tr/tr/download/article-file/29524|
2849701|NCT02733159||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/PePS2/index.aspx|
2849702|NCT07063940||Study Protocol|http://www.birmingham.ac.uk/ExaLT|
2849703|NCT07063940||Informed Consent Form|http://www.birmingham.ac.uk/ExaLT|
2849704|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
2849705|NCT06836102|drmostafanasr1988@gmail.com|Study Protocol|https://doi.org/10.1016/j.hermed.2021.100468|
2845352|NCT01064284|NEJM2016;374:2054-206|Article|http://www.nejm.org/doi/full/10.1056/NEJMoa1516437?af=R&rss=currentIssue&|
2849706|NCT05989685||Statistical Analysis Plan|https://osf.io/dmyuq/files/osfstorage/67cb0a2098ee14b2b7fd7157|Statistical Analysis Plan available in OSF.
2849707|NCT06821919|2022-09-22_012059|Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
2849708|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"
2851856|NCT01101568|113506|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849709|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"
2851857|NCT01101568|113506|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851858|NCT01101568|113506|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851859|NCT01101568|113506|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851860|NCT00126451||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851861|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
2847532|NCT01471678|115707|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849710|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"
2849711|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"
2849712|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"
2849713|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"
2849714|NCT01385189||Clinical Study Report|http://smhs.gwu.edu/mitm-crg/clinical-trials|
2849715|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).
2849716|NCT06814223||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
2849717|NCT06817746||Study Protocol|https://www.fsm.unipi.it|
2849718|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)
2851862|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/22607780/|Dysfunctional movement patterns are directly related to the mechanism of injury
2849719|NCT06805448|2024-516715-25-00|Study Protocol|https://euclinicaltrials.eu/|
2849720|NCT05591924||C3RP Laboratory Website|https://c3rp.org/leligdowiczlab|
2847533|NCT01471678|115707|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847534|NCT00289783|103813|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851863|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
2851864|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.
2851865|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
2851866|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
2851867|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
2851868|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
2851869|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
2851870|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
2851871|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.
2845353|NCT01691482|114956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845354|NCT01691482|114956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847535|NCT00289783|103813|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847536|NCT00289783|103813|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851872|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
2851873|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
2851874|NCT00866294|112810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843216|NCT01573819|115719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849721|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"
2849722|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
2851875|NCT00866294|112810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851876|NCT00866294|112810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851877|NCT00866294|112810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851878|NCT00866294|112810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851879|NCT04552236||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
2851880|NCT02345161|116853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851881|NCT02345161|116853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851882|NCT02345161|116853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843217|NCT01573819|115719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843218|NCT01573819|115719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843219|NCT01573819|115719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843220|NCT01573819|115719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843221|NCT01573819|115719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845355|NCT01691482|114956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845356|NCT01691482|114956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843222|NCT01573819|115719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843228|NCT01989884||Clinical Study Report|https://doi.org/10.1007/s11060-019-03116-z|
2843229|NCT07138755||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/39489090/|
2843230|NCT05341453||Study Protocol|https://www.chmirakl.cz/aktuality/study-protokol|
2843231|NCT05341453||Statistical Analysis Plan|https://www.chmirakl.cz/aktuality/statistical-analysis-plan|
2847537|NCT00289783|103813|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847538|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.
2847539|NCT01148472|2004-005069-39|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2004-005069-39/results|
2847540|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.
2847541|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.
2851883|NCT02345161|116853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851884|NCT02345161|116853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851885|NCT02345161|116853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843232|NCT05341453||Informed Consent Form|https://www.chmirakl.cz/aktuality/type-informed-consent-form|
2843233|NCT03045458||Clinical Study Report|http://mc.manuscriptcentral.com/jperio|
2843234|NCT05895435||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/12841881/|
2843235|NCT00279045|49653/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843236|NCT00279045|49653/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843237|NCT00279045|49653/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843238|NCT00279045|49653/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845357|NCT01691482|114956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845358|NCT01691482|114956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845359|NCT01691482|114956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845360|NCT03142451||Study Protocol|http://foamix.co.il/|
2847542|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.
2845361|NCT00132912||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845362|NCT01362530||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-208&kw=0869-208&tab=access|
2847543|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.
2849723|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
2849724|NCT06824922|Protocolo_ECA_piloto|Study Protocol|https://drive.google.com/file/d/1PhNe1G9PVs2FkOmKeyXazMLW3l-sxRR7/view?usp=sharing|
2849725|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
2851886|NCT02345161|116853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851887|NCT02124798|200339|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851888|NCT02124798|200339|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851889|NCT02124798|200339|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851890|NCT02124798|200339|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851891|NCT02124798|200339|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851892|NCT02124798|200339|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851893|NCT02124798|200339|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851894|NCT01614769||CSR Snyposis Link|http://www.merck.com/clinical-trials/study.html?id=0000-253&kw=0000-253&tab=access|
2843239|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
2843240|NCT00279045|49653/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843241|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
2845363|NCT01370642||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-043&kw=7009-043&tab=access|
2845364|NCT03755154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2845365|NCT03755154||Study Protocol|https://clinicaltrials.servier.com/|
2845366|NCT03755154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2845367|NCT03755154||Informed Consent Form|https://clinicaltrials.servier.com/|
2845368|NCT03755154||Clinical Study Report|https://clinicaltrials.servier.com/|
2845369|NCT03755154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2847544|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.
2847545|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
2847546|NCT00369824|107682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847547|NCT00369824|107682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847548|NCT00369824|107682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847549|NCT00369824|107682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847550|NCT00369824|107682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847551|NCT00369824|107682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849726|NCT06824558|Fear of Childbirth Scale|Individual Participant Data Set|https://gcris.pau.edu.tr/bitstream/11499/6124/1/7ba3f584-23f9-4af0-9a4a-56f72570f94d.pdf|
2849727|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.
2851895|NCT00875784|103629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851896|NCT00875784|103629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851897|NCT00875784|103629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843242|NCT04748991||Product monograph - Vernakalant|https://pdf.hres.ca/dpd_pm/00038441.PDF|
2845370|NCT00871000|111815|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845371|NCT00871000|111815|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851898|NCT00875784|103629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845372|NCT00871000|111815|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845373|NCT00871000|111815|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847552|NCT00109122||CSR Synopsiis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847553|NCT02809612||Study Protocol|http://www.kbh.uu.se|
2847554|NCT03733470|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
2849728|NCT06863207||Individual Participant Data Set|https://vivli.org/|
2849729|NCT06883916|Ethics Committee Approval|Informed Consent Form|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
2849730|NCT02415933||Study Protocol|https://knowledge.uchicago.edu/handle/11417/69|
2849731|NCT06744946|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2849732|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
2849733|NCT04098276|10.1186/s12889-021-11930-2|Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-021-11930-2|
2851899|NCT00875784|103629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851900|NCT00875784|103629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851901|NCT00875784|103629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847555|NCT05695209|VIV00009027|Individual Participant Data Set|https://vivli.org|https://doi.org/10.25934/PR00009027
2849734|NCT06997874|COMBAT trial|Study Protocol|https://nictu.hscni.net/service/combat/|
2849735|NCT06886594||Study Protocol|https://bap.ksu.edu.tr/|
2843243|NCT04748991||Product monograph - Amiodarone|https://pdf.hres.ca/dpd_pm/00035425.PDF|
2845374|NCT00871000|111815|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845375|NCT00871000|111815|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845376|NCT00871000|111815|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845377|NCT00202852||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845378|NCT01101555|113299|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847556|NCT00043914|LAM40013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847557|NCT00043914|LAM40013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849736|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
2849737|NCT06881381||Study Protocol|https://docs.google.com/document/d/19ZwAv6y0UUaSa_Hjb3jlzuhMfTro0Y6p/edit?usp=drive_link&ouid=101334879348395838064&rtpof=true&sd=true|STUDY PROTOKOL DIAGRAM
2847558|NCT00043914|LAM40013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847559|NCT00043914|LAM40013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847560|NCT00043914|LAM40013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847561|NCT00043914|LAM40013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849738|NCT06692621|Yöktez|Individual Participant Data Set|https://tez.yok.gov.tr/UlusalTezMerkezi/tezlerim.jsp?sira=0|You can reach us at harunzengin71@gmail.com
2851902|NCT03246035|CODIM-MBM-17-052|Study Protocol|http://www.ladydavis.ca/en/jonathanafilalo|Pilot study protocol
2851903|NCT03246035|CODIM-MBM-17-052|Informed Consent Form|http://www.ladydavis.ca/en/jonathanafilalo|Patient consent Caregiver consent French and English available
2849739|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.
2851904|NCT00169494|580299/012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851905|NCT00169494|580299/012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851906|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
2851907|NCT00169494|580299/012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851908|NCT00169494|580299/012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851909|NCT00169494|580299/012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851910|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.
2851911|NCT01254604||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=2452-002&kw=2452-002&tab=access|
2851912|NCT06253286||Study Protocol|https://drive.google.com/file/d/1edivKccFOAyt3_A6aNnNROe7JQnRmp4C/view?usp=sharing|
2843244|NCT00533507|109861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843245|NCT00533507|109861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845379|NCT01101555|113299|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845380|NCT01101555|113299|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845381|NCT01101555|113299|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845382|NCT01101555|113299|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845383|NCT01101555|113299|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845384|NCT01101555|113299|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849740|NCT06762756||Analytic Code|https://osf.io/v5deq/?view_only=d5dd1f5903a0480d94402c7c6528c6a4|Scripts are available on Open Science Framework
2849741|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
2851913|NCT06253286||Informed Consent Form|https://drive.google.com/file/d/1gA2nThyz6di3bSZKJQ7aQ_Usy1_wpOrR/view?usp=sharing|
2851914|NCT03102775||final report (Norwegian)|https://skriftserien.hioa.no/index.php/skriftserien/article/view/649|
2851915|NCT00828867|111341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851916|NCT00828867|111341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845385|NCT01934231|117150|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845386|NCT01934231|117150|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847562|NCT00043914|LAM40013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847563|NCT00508365|CFD109701|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847564|NCT00508365|CFD109701|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847565|NCT00508365|CFD109701|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847566|NCT00508365|CFD109701|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847567|NCT00508365|CFD109701|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847568|NCT00508365|CFD109701|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851917|NCT00828867|111341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851918|NCT00828867|111341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843246|NCT00533507|109861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843247|NCT00533507|109861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851919|NCT00828867|111341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851920|NCT00828867|111341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851921|NCT00828867|111341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851922|NCT01147731|111681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851923|NCT01147731|111681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851924|NCT01147731|111681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851925|NCT01147731|111681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851926|NCT01147731|111681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851927|NCT01147731|111681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851928|NCT01147731|111681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851929|NCT01323673|115054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851930|NCT01323673|115054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851931|NCT01323673|115054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851932|NCT01323673|115054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851933|NCT01323673|115054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851934|NCT01323673|115054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851935|NCT01323673|115054|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851936|NCT01702363|115361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851937|NCT01702363|115361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851938|NCT01702363|115361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851939|NCT01702363|115361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851940|NCT01702363|115361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845387|NCT01934231|117150|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851941|NCT01702363|115361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851942|NCT01702363|115361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845388|NCT01934231|117150|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849742|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.
2849743|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.
2845389|NCT01934231|117150|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845390|NCT01934231|117150|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851943|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.
2851944|NCT00000567||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/hifi/|
2851945|NCT00000567||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hifi/|
2843248|NCT00533507|109861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843249|NCT00533507|109861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843250|NCT00533507|109861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849744|NCT03869892||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2847569|NCT00508365|CFD109701|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847570|NCT01323959|113060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847571|NCT01323959|113060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847572|NCT01323959|113060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849745|NCT03869892||Study Protocol|https://clinicaltrials.servier.com/|
2849746|NCT03869892||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2849747|NCT03869892||Informed Consent Form|https://clinicaltrials.servier.com/|
2851946|NCT00000567||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hifi/|
2847573|NCT01323959|113060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851947|NCT03731416||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27283920|
2851948|NCT00933335|393229/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851949|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
2847574|NCT01323959|113060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847575|NCT01323959|113060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847576|NCT00758836||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-046&kw=0974-046&tab=access|
2849748|NCT03869892||Clinical Study Report|https://clinicaltrials.servier.com/|
2849749|NCT03869892||study-level clinical trial data|https://clinicaltrials.servier.com/|
2849750|NCT06764238|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
2851950|NCT00933335|393229/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849751|NCT06776536||institutional review board|https://camsakurasehir.saglik.gov.tr/|
2849752|NCT06667661||NIH Reporter Information|https://reporter.nih.gov/search/w2y2LWuI50aTEgDfuqR7lg/project-details/11017278|Final Data set will be deposited into NICHD DASH database.
2849753|NCT06828367|not necessary|Study Protocol|https://docs.google.com/document/d/1hvjyp_RfCDDpHWkrTv_s7qhztM4Pqw9T/edit|is a public document
2849754|NCT07038772|EAT-40|Study Protocol|https://www.eat-26.com/|
2851951|NCT00933335|393229/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851952|NCT00933335|393229/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843251|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
2851953|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
2851954|NCT00933335|393229/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851955|NCT01165203|112673|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851956|NCT01165203|112673|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847577|NCT05930912||Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
2847578|NCT05930912|zenodo.7382529|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7382529|
2847579|NCT05930912|zenodo.6942208|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6942208|
2847580|NCT05930912|zenodo.7188211|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7188211|
2847581|NCT05930912|zenodo.6941906|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6941906|
2847582|NCT05930912|zenodo.6952516|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6952516|
2847583|NCT05930912|zenodo.7022873|Analytic Code|http://doi.org/10.5281/zenodo.7022873|The technological-psychoanalytic mass psychological observation and analysis schemes.
2851957|NCT01165203|112673|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851958|NCT01165203|112673|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851959|NCT01165203|112673|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851960|NCT01165203|112673|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847584|NCT00169546|SAM40100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847585|NCT00169546|SAM40100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851961|NCT01165203|112673|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847586|NCT00169546|SAM40100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847587|NCT00169546|SAM40100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847588|NCT00169546|SAM40100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847589|NCT00169546|SAM40100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847590|NCT00169546|SAM40100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847591|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/auad/issue/60075/826745|
2847592|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/411491|
2847593|NCT06253572||Review|http://journalofomepturkey.org/index.php/eccd/article/view/78|
2847594|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.
2847595|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/199140|
2847596|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/rep/issue/63330/827844|
2847597|NCT01606800||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8908B-059&kw=8908B-059&tab=access|
2847598|NCT01648101|114855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849755|NCT05018143|GUID|Individual Participant Data Set|https://nda.nih.gov/|
2849756|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.
2849757|NCT06744270|Inonu University Clinical Rese|Clinical Study Report|https://www.inonu.edu.tr/klinik.etik|https://www.inonu.edu.tr/klinik.etik
2849758|NCT00857766|112355|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851962|NCT06011005|MBRU IRB-2022-174|Study Protocol|http://www.mbru.ac.ae|
2851963|NCT06527274||Study Protocol|https://nagano.umontreal.ca/login|Protocol and other documentation available upon request to the principal investigator email
2845217|NCT06855810|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
2845218|NCT01610388|113376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845219|NCT01610388|113376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847599|NCT01648101|114855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847600|NCT01648101|114855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849759|NCT00857766|112355|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851964|NCT01299597|109652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851965|NCT01299597|109652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851966|NCT01299597|109652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851967|NCT01299597|109652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851968|NCT01299597|109652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851969|NCT01299597|109652|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851970|NCT01299597|109652|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851971|NCT00861484|111155|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851972|NCT00861484|111155|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851973|NCT00861484|111155|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851974|NCT00861484|111155|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845391|NCT01934231|117150|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845392|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.
2845393|NCT00000603||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coblt/|
2845394|NCT00000603||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coblt/|
2845395|NCT00000603||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coblt/|
2845396|NCT02100644|200776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845397|NCT02100644|200776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845398|NCT02100644|200776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845399|NCT02100644|200776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845400|NCT02100644|200776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845401|NCT01266980|113970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851975|NCT00861484|111155|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851976|NCT00861484|111155|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851977|NCT00861484|111155|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851978|NCT01425190||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07614&kw=P07614&tab=access|
2845402|NCT01266980|113970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845403|NCT01266980|113970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847601|NCT01648101|114855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847602|NCT01648101|114855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847603|NCT01648101|114855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847604|NCT01648101|114855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847605|NCT00963937|111035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847606|NCT00963937|111035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847607|NCT00963937|111035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849760|NCT00857766|112355|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849761|NCT00857766|112355|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849762|NCT00857766|112355|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849763|NCT00857766|112355|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849764|NCT00857766|112355|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845404|NCT01266980|113970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845405|NCT01266980|113970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845406|NCT01266980|113970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845407|NCT01266980|113970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845408|NCT02477046||Statistical Analysis Plan|https://idmod.sharepoint.com/projects/_layouts/15/guestaccess.aspx?guestaccesstoken=3%2bxJO%2bcBwXx6PfMuzCQmu8ESB0X7mhLPtowTTLaYTmY%3d&docid=02ab39752ccb14c10bdfd61c0a731e6ff&rev=1|
2845409|NCT00289900||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-024&kw=0524B-024&tab=access|
2845410|NCT01703221||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-020&kw=3102-020&tab=access|
2845411|NCT02842671||Study Protocol|http://irb.psu.edu|
2845412|NCT02842671||Informed Consent Form|http://irb.psu.edu|for participants
2845413|NCT02842671||Accommodation Survey|http://irb.psu.edu|
2845414|NCT02842671||Patient Satisfaction Survey|http://irb.psu.edu|
2845415|NCT02842671||Medical Student Survey|http://irb.psu.edu|
2845416|NCT02842671||Summary Explanation of Research|http://irb.psu.edu|for medical students
2845417|NCT02592655||Primary Outcome Ultrasound Images|https://doi.org/10.5281/zenodo.236263|NCT02592655 Primary Outcome Tourniquet Study
2845418|NCT02592655||Individual Participant Data Set|https://doi.org/10.5281/zenodo.237773|NCT02592655 Individual level data set
2845419|NCT02592655||Informed Consent Form|https://doi.org/10.5281/zenodo.245150|Informed consent form containing description of study and procedures.
2845420|NCT00911157|111436|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851979|NCT00139334|103992|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851980|NCT00139334|103992|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845421|NCT00911157|111436|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851981|NCT00139334|103992|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851982|NCT00139334|103992|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851983|NCT00139334|103992|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851984|NCT00139334|103992|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851985|NCT00726323|MET111644|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851986|NCT00726323|MET111644|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851987|NCT00726323|MET111644|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845422|NCT00911157|111436|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845423|NCT00298155||Paper with attached protocol and outcomes|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887479/|
2845424|NCT01316900|113360|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845425|NCT01316900|113360|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845426|NCT01316900|113360|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851988|NCT00726323|MET111644|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851989|NCT00726323|MET111644|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851990|NCT00726323|MET111644|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851991|NCT03167580||Study Protocol|https://sites.google.com/view/relaxtrial/study-details-and-documents/protocol|
2845427|NCT01316900|113360|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845428|NCT01316900|113360|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845429|NCT01316900|113360|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845430|NCT01316900|113360|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845431|NCT00480025|109493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845432|NCT00480025|109493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845433|NCT00480025|109493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851992|NCT00606697|NKI110334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851993|NCT00606697|NKI110334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851994|NCT00606697|NKI110334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847608|NCT00963937|111035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847609|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.
2847610|NCT00000557||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
2847611|NCT00000557||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
2847612|NCT01762878|116617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847613|NCT01762878|116617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847614|NCT01762878|116617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847615|NCT01762878|116617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847616|NCT01762878|116617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849765|NCT06762743||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|registered clinical trial about Brivaracetam oral solution on Chinese website
2849766|NCT06950970|tetinstitute.rn@gmail.com|Informed Consent Form|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
2849767|NCT06950970|tetinstitute.rn@gmail.com|Statistical Analysis Plan|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
2849768|NCT01128595|113126|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849769|NCT01128595|113126|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849770|NCT01128595|113126|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851995|NCT00606697|NKI110334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851996|NCT00606697|NKI110334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851997|NCT00606697|NKI110334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843252|NCT00139815|103420|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845434|NCT00480025|109493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845435|NCT00480025|109493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845436|NCT00480025|109493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845437|NCT00480025|109493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845438|NCT06694064||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/36464977/|
2849771|NCT01128595|113126|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849772|NCT01128595|113126|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851998|NCT00606697|NKI110334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851999|NCT00441441|SFA106484|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843253|NCT00139815|103420|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843254|NCT00139815|103420|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845439|NCT02074839||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2852000|NCT00441441|SFA106484|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845440|NCT02074839||Study Protocol|https://clinicaltrials.servier.com/|
2845441|NCT02074839||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2845442|NCT02074839||Informed Consent Form|https://clinicaltrials.servier.com/|
2845443|NCT02074839||Clinical Study Report|https://clinicaltrials.servier.com/|
2845444|NCT02074839||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2847617|NCT01762878|116617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849773|NCT01128595|113126|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849774|NCT01128595|113126|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852001|NCT00441441|SFA106484|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852002|NCT00441441|SFA106484|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852003|NCT00441441|SFA106484|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852004|NCT00441441|SFA106484|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845445|NCT00078195|SDY1|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
2845446|NCT00078195|SDY1|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
2845447|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
2845448|NCT00078195|CASALE ITN019AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
2845449|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
2845450|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."
2845451|NCT04292496||Study Protocol|https://doi.org/10.1007/s00464-023-10025-w|
2845452|NCT02233088|PMC6589338|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/30234352|A manuscript summarizing the development of the intervention.
2847618|NCT01762878|116617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847619|NCT01262911|115083|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847620|NCT01262911|115083|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847621|NCT01262911|115083|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849775|NCT01119651|114574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849776|NCT01119651|114574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849777|NCT01119651|114574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849778|NCT01119651|114574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849779|NCT01119651|114574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849780|NCT01119651|114574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852005|NCT00441441|SFA106484|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849781|NCT01119651|114574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849782|NCT01702376|113789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849783|NCT01702376|113789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849784|NCT01702376|113789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852006|NCT01640990|115387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849785|NCT01702376|113789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843255|NCT00139815|103420|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843256|NCT00139815|103420|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847622|NCT01262911|115083|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847623|NCT01262911|115083|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847624|NCT01262911|115083|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847625|NCT01262911|115083|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852007|NCT01640990|115387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852008|NCT01640990|115387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852009|NCT01640990|115387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852010|NCT01640990|115387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852011|NCT01640990|115387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852012|NCT01640990|115387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843257|NCT00139815|103420|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843258|NCT00139815|103420|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843259|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)"
2843260|NCT06793592||More information on IPD sharing|https://osf.io/preprints/osf/6pwxe|
2843261|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"
2843262|NCT01119625|113266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845453|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.
2845454|NCT06791044||Study Protocol|https://eka-hosp.gr/|
2845455|NCT00434811|SDY1178|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study ID is SDY1178.
2845456|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.
2847626|NCT04329871||Individual Participant Data Set|http://Metabolic-institute.com|
2847627|NCT01168167|01168167|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT01168167|
2847628|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.
2847629|NCT00684593||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04481&kw=7123-009&tab=access|
2847630|NCT04213079||Study Protocol|http://mdds.nyc/|
2849786|NCT01702376|113789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849787|NCT01702376|113789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849788|NCT01702376|113789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849789|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.
2849790|NCT00979121||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/sails/|
2849791|NCT00979121||Study Forms|http://biolincc.nhlbi.nih.gov/studies/sails/|
2849792|NCT06662136||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2849793|NCT06861205||Study Protocol|https://doi.org/10.3389/fnut.2024.1438740|
2852013|NCT00256867|AVS101946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852014|NCT00256867|AVS101946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852015|NCT00256867|AVS101946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852016|NCT00256867|AVS101946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852017|NCT00256867|AVS101946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852018|NCT00256867|AVS101946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843263|NCT01119625|113266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843264|NCT01119625|113266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843265|NCT01119625|113266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843266|NCT01119625|113266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843267|NCT01119625|113266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843268|NCT01119625|113266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843269|NCT05583097||Study Protocol|https://www.gu.se/forskning/tyreoideacancer|
2843270|NCT00346892|444563/014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843271|NCT00346892|444563/014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843272|NCT00346892|444563/014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843273|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
2843274|NCT00346892|444563/014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843275|NCT00346892|444563/014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843276|NCT00633022|PM1111138|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843277|NCT00633022|PM1111138|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845457|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.
2845458|NCT00459550|106006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845459|NCT00459550|106006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845460|NCT00459550|106006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847631|NCT00783003|112146|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847632|NCT00783003|112146|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849794|NCT00449774|LBI108617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849795|NCT00449774|LBI108617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849796|NCT00449774|LBI108617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849797|NCT00449774|LBI108617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843278|NCT00633022|PM1111138|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845461|NCT00459550|106006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845462|NCT00459550|106006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845463|NCT00459550|106006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845464|NCT05600517|10.1016/j.ebiom.2017.11.019|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832611/|
2845465|NCT02988076|CNSR012 Protocol|Study Protocol|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of the protocol
2845466|NCT02988076|CNSR012 ICD|Informed Consent Form|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of ICD
2845467|NCT03495635|osf.io/8ukfv|Individual Participant Data Set|https://osf.io/|
2845468|NCT00970710||Study Protocol|http://bmcpediatr.biomedcentral.com/articles/10.1186/1471-2431-12-93|
2847633|NCT00783003|112146|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843279|NCT00633022|PM1111138|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843280|NCT00633022|PM1111138|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847634|NCT00783003|112146|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847635|NCT00783003|112146|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843281|NCT00633022|PM1111138|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843282|NCT00633022|PM1111138|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843283|NCT03221972||Study Protocol|http://www.chinanutri.cn/gzrw_132/zgjmyyyjkzkjcxm/201412/t20141229_108493.html|
2843284|NCT00377572|SDY211|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
2847636|NCT00783003|112146|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847637|NCT00783003|112146|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847638|NCT01577680|114637|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849798|NCT00449774|LBI108617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843285|NCT00377572|SDY211|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
2845469|NCT00970710||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=mustila+taina+vacopp|
2847639|NCT01577680|114637|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847640|NCT01577680|114637|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847641|NCT01577680|114637|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849799|NCT00449774|LBI108617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849800|NCT00449774|LBI108617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849801|NCT05201599|zxt4|Study Protocol|https://pan.baidu.com/s/1PNKfPWrpeJtodX1RwH8k-w|
2847642|NCT01577680|114637|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847643|NCT01577680|114637|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847644|NCT01577680|114637|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849802|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.
2847645|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
2849803|NCT00756067|111652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849804|NCT00756067|111652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849805|NCT00756067|111652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849806|NCT00756067|111652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849807|NCT00756067|111652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849808|NCT00309166|580299/011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849809|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
2849810|NCT00309166|580299/011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852019|NCT00256867|AVS101946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852020|NCT01245426|114749|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852021|NCT01245426|114749|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852022|NCT01245426|114749|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852023|NCT01245426|114749|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847646|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
2849811|NCT00309166|580299/011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843286|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.
2843287|NCT00452348|ADA109057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843288|NCT00452348|ADA109057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847647|NCT05792709||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788277/|
2847648|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.
2847649|NCT00907777|112807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847650|NCT00907777|112807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847651|NCT00907777|112807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847652|NCT00907777|112807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852024|NCT01245426|114749|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852025|NCT01245426|114749|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852026|NCT01245426|114749|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852027|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.
2852028|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
2852029|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Forms|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
2852030|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.
2852031|NCT00000579|ARDSNet-LASRS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
2852032|NCT00000579|ARDSNet-LASRS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
2852033|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.
2852034|NCT00000579|ARDSNet-ALVEOLI|Study Forms|http://biolincc.nhlbi.nih.gov/studies/alveoli/|
2852035|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.
2852036|NCT00000579|ARDSNet-FACTT|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/factt/|
2852037|NCT00000579|ARDSNet-FACTT|Study Forms|http://biolincc.nhlbi.nih.gov/studies/factt/|
2852038|NCT01842620|117219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852039|NCT01842620|117219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852040|NCT01842620|117219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852041|NCT01842620|117219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852042|NCT01842620|117219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852043|NCT01842620|117219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852044|NCT01842620|117219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852045|NCT00048594||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852046|NCT00444509|HZA108799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852047|NCT00444509|HZA108799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843289|NCT00452348|ADA109057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843290|NCT00452348|ADA109057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843291|NCT00452348|ADA109057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843292|NCT00452348|ADA109057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843293|NCT00452348|ADA109057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843294|NCT00307541|105554|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843295|NCT00307541|105554|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845470|NCT00979407|113535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845471|NCT00979407|113535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845472|NCT00979407|113535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845473|NCT00979407|113535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845474|NCT00979407|113535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845475|NCT00979407|113535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845476|NCT04164186|NSCLC Radiomics Interobserver|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics-Interobserver1|
2845477|NCT04164186|NSCLC Radiomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics|
2847653|NCT00907777|112807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847654|NCT00907777|112807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847655|NCT02446483|201527|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847656|NCT02446483|201527|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847657|NCT02446483|201527|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847658|NCT02446483|201527|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847659|NCT02446483|201527|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847660|NCT01916720|480848/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847661|NCT01916720|480848/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847662|NCT01916720|480848/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847663|NCT01916720|480848/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847664|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
2847665|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
2847666|NCT01916720|480848/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847667|NCT00617123||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05183&kw=P05183&tab=access|
2847668|NCT00318630|104385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847669|NCT00318630|104385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847670|NCT00318630|104385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847671|NCT00318630|104385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847672|NCT00318630|104385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847673|NCT00318630|104385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843296|NCT00307541|105554|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843297|NCT00307541|105554|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843298|NCT00307541|105554|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843299|NCT00307541|105554|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847674|NCT00318630|104385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847675|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.
2847676|NCT01802931|117016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843300|NCT00296530|ADA103578|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843301|NCT00296530|ADA103578|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845478|NCT04164186|NSCLC Radiogenomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC+Radiogenomics|
2849812|NCT00309166|580299/011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845479|NCT01353729|114346|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845480|NCT01353729|114346|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845481|NCT01353729|114346|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845482|NCT01353729|114346|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845483|NCT01353729|114346|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845484|NCT01353729|114346|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845485|NCT01353729|114346|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845486|NCT01817777|116086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845487|NCT01817777|116086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849813|NCT00309166|580299/011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849814|NCT06753526|ahmed-mahmoud@sohag.med.edu.eg|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/9008325/|
2849815|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"
2849816|NCT03019835||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/7880668|
2852048|NCT00444509|HZA108799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852049|NCT00444509|HZA108799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852050|NCT00444509|HZA108799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847677|NCT01802931|117016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847678|NCT01802931|117016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852051|NCT00444509|HZA108799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852052|NCT00444509|HZA108799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847679|NCT01802931|117016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847680|NCT01802931|117016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847681|NCT01802931|117016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847682|NCT01802931|117016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847683|NCT00843024|107979|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847684|NCT00843024|107979|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845488|NCT01817777|116086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845489|NCT01817777|116086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845490|NCT01817777|116086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845491|NCT01817777|116086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845492|NCT01817777|116086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845493|NCT00492544|110168|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845494|NCT00492544|110168|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845495|NCT00492544|110168|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845496|NCT00492544|110168|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845497|NCT00492544|110168|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845498|NCT00492544|110168|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845499|NCT00492544|110168|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845500|NCT00332566|106602|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845501|NCT00332566|106602|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845502|NCT00332566|106602|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845503|NCT00332566|106602|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845504|NCT00332566|106602|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845505|NCT00332566|106602|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845506|NCT01051661|114000|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845507|NCT01051661|114000|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845508|NCT01051661|114000|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849817|NCT06750744|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2849818|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
2849819|NCT06952582|doi.org/10.17605/OSF.IO/SE8M7|Individual Participant Data Set|https://osf.io/puxgw/|
2849820|NCT01491815||Study Protocol|http://www.biomedcentral.com/search?query=glinatsi&searchType=publisherSearch|Publication of the protocol. Glinatsi et al. Trials (2017) 18:161
2849821|NCT01332552|115040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852053|NCT01258530|115096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843302|NCT00296530|ADA103578|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843303|NCT00296530|ADA103578|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843304|NCT00296530|ADA103578|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845509|NCT01051661|114000|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845510|NCT01051661|114000|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845511|NCT01051661|114000|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845512|NCT01916226|200165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845513|NCT01916226|200165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845514|NCT01916226|200165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847685|NCT00843024|107979|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843305|NCT00296530|ADA103578|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845515|NCT01916226|200165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845516|NCT01916226|200165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849822|NCT01332552|115040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849823|NCT01332552|115040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849824|NCT01332552|115040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849825|NCT01332552|115040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849826|NCT01332552|115040|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849827|NCT01332552|115040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849828|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|
2849829|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|
2849830|NCT02224469|k9f10|Individual Participant Data Set|http://datadryad.org/resource/doi:10.5061/dryad.k9f10|
2849831|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.
2849832|NCT00985088|113440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849833|NCT00985088|113440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849834|NCT00985088|113440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849835|NCT00985088|113440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852054|NCT01258530|115096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852055|NCT01258530|115096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852056|NCT01258530|115096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852057|NCT01258530|115096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852058|NCT01258530|115096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852059|NCT01258530|115096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852060|NCT01000727|480848/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852061|NCT01000727|480848/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852062|NCT01000727|480848/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852063|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
2852064|NCT01000727|480848/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852065|NCT01000727|480848/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852066|NCT06459622||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29337030/|
2852067|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.
2852068|NCT00120289|AIM-HIGH|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
2852069|NCT00120289|AIM-HIGH|Study forms|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
2843306|NCT00296530|ADA103578|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843307|NCT01873339|115678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843308|NCT01873339|115678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847686|NCT00843024|107979|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847687|NCT00843024|107979|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847688|NCT00843024|107979|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843309|NCT01873339|115678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843310|NCT01873339|115678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852070|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
2845517|NCT01916226|200165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845518|NCT01916226|200165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845519|NCT00680914|110808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845520|NCT00680914|110808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845521|NCT00680914|110808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845522|NCT00680914|110808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845523|NCT00680914|110808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845524|NCT00680914|110808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845525|NCT00680914|110808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845526|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
2845527|NCT00005479||NCBI website|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724776/|
2845528|NCT06250257||Individual Participant Data Set|https://kf.kobotoolbox.org/#/forms/aSWyWhEb2TmCqshx54qTW7|
2845529|NCT03044899||Study Protocol|http://www.asos.org.za/|ASOS Protocol version 1.0
2845530|NCT00140920||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845531|NCT00323622|104297|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845532|NCT00323622|104297|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845533|NCT00323622|104297|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845534|NCT00323622|104297|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845535|NCT00323622|104297|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845536|NCT00323622|104297|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845537|NCT00734032|LPL110118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847689|NCT00843024|107979|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847690|NCT00694993|HHI110157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847691|NCT00694993|HHI110157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852071|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
2845538|NCT00734032|LPL110118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847692|NCT00694993|HHI110157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845539|NCT00734032|LPL110118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852072|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
2852073|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
2852074|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
2852075|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
2852076|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
2852077|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
2852078|NCT00718666|112021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852079|NCT00718666|112021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852080|NCT00718666|112021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847693|NCT00694993|HHI110157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847694|NCT00694993|HHI110157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847695|NCT00694993|HHI110157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847696|NCT00694993|HHI110157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847697|NCT00530309|GLP107865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847698|NCT00530309|GLP107865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847699|NCT00530309|GLP107865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847700|NCT00530309|GLP107865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847701|NCT00530309|GLP107865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847702|NCT00530309|GLP107865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847703|NCT00530309|GLP107865|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847704|NCT01372137|doi: 10.1111/bph.13433|Manuscript|http://onlinelibrary.wiley.com/doi/10.1111/bph.13433/abstract;jsessionid=E657A6C9667BB70DE92E5B69B86B1D3F.f01t01|
2843311|NCT01873339|115678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843312|NCT01873339|115678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843313|NCT01873339|115678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843314|NCT03211039|37114|Individual Participant Data Set|http://view.ncbi.nlm.nih.gov/dbgap-controlled|
2843315|NCT03211039|37114|Summary level phenotype data|http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs002094.v1.p1|
2843316|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|
2843317|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.
2847705|NCT00197132|49653/375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847706|NCT00197132|49653/375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847707|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
2847708|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
2847709|NCT00197132|49653/375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849836|NCT00985088|113440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849837|NCT00985088|113440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849838|NCT00985088|113440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849839|NCT01767688||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-031&kw=3102-031&tab=access|
2849840|NCT01827839|116796|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849841|NCT01827839|116796|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843318|NCT00000516||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/solvd/|
2849842|NCT01827839|116796|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849843|NCT01827839|116796|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843319|NCT00000516||Study Forms|http://biolincc.nhlbi.nih.gov/studies/solvd/|
2849844|NCT01827839|116796|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849845|NCT01827839|116796|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849846|NCT01827839|116796|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849847|NCT00614614|110870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849848|NCT00614614|110870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849849|NCT00614614|110870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849850|NCT00614614|110870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849851|NCT00614614|110870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849852|NCT00614614|110870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849853|NCT00614614|110870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843320|NCT00000516||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/solvd/|
2843321|NCT01706263|114551|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843322|NCT01706263|114551|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843323|NCT01706263|114551|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843324|NCT01706263|114551|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847710|NCT00197132|49653/375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847711|NCT00197132|49653/375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847712|NCT07001969||Individual Participant Data Set|https://t.me/drmassoud77/24301|Book of author about technique
2847713|NCT02877615||Study Protocol|https://clinicaltrials.servier.com/|
2847714|NCT02877615||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2843325|NCT01706263|114551|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843326|NCT01706263|114551|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843327|NCT00333450|106623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843328|NCT00333450|106623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843329|NCT00333450|106623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843330|NCT00333450|106623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843331|NCT00333450|106623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843332|NCT00333450|106623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847715|NCT02877615||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2847716|NCT02877615||Informed Consent Form|https://clinicaltrials.servier.com/|
2849854|NCT00057499|SDY568|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY568|ImmPort study identifier is SDY568.
2849855|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.
2849856|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.
2849857|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.
2849858|NCT00910962|111810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849859|NCT00910962|111810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849860|NCT00910962|111810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843333|NCT00224484|208141/040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843334|NCT00224484|208141/040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843335|NCT00224484|208141/040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843336|NCT00224484|208141/040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843337|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
2843338|NCT00224484|208141/040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843339|NCT02416180|201909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843340|NCT02416180|201909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843341|NCT02416180|201909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843342|NCT02416180|201909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843343|NCT02416180|201909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843344|NCT02416180|201909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843345|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.
2843346|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.
2843347|NCT00000555||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/wave/|
2843348|NCT00000555||Study Forms|http://biolincc.nhlbi.nih.gov/studies/wave/|
2843349|NCT00000555||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/wave/|
2843350|NCT00139932||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2843351|NCT00396630|106260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843352|NCT00396630|106260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843353|NCT00396630|106260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843354|NCT00396630|106260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843355|NCT00396630|106260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843356|NCT00396630|106260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843357|NCT00396630|106260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843358|NCT00108082|COR100216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843359|NCT00108082|COR100216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843360|NCT00108082|COR100216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843361|NCT00108082|COR100216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849861|NCT00910962|111810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849862|NCT00910962|111810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849863|NCT00910962|111810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849864|NCT00910962|111810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849865|NCT01074242||CSR Synopsis|http://www.merck.com/clinical-trials/search.html?kw=V260-037|
2849866|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
2849867|NCT00489554|109661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849868|NCT00489554|109661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849869|NCT00489554|109661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849870|NCT00489554|109661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849871|NCT00489554|109661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849872|NCT00489554|109661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849873|NCT01772199|116477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849874|NCT01772199|116477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849875|NCT01772199|116477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845540|NCT00734032|LPL110118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845541|NCT00734032|LPL110118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845542|NCT00734032|LPL110118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845543|NCT01706315|116778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845544|NCT01706315|116778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847717|NCT02877615||Clinical Study Report|https://clinicaltrials.servier.com/|
2849876|NCT01772199|116477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849877|NCT01772199|116477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849878|NCT01772199|116477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849879|NCT01772199|116477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852081|NCT00718666|112021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852082|NCT00718666|112021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852083|NCT00718666|112021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852084|NCT01098461|110932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852085|NCT01098461|110932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852086|NCT01098461|110932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852087|NCT01098461|110932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852088|NCT01098461|110932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852089|NCT01098461|110932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852090|NCT01098461|110932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852091|NCT01062074||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-059&kw=V501-059&tab=access|
2852092|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
2852093|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
2852094|NCT00380211|IDB-200-001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852095|NCT00380211|IDB-200-001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852096|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
2852097|NCT00377611|107564|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852098|NCT00377611|107564|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852099|NCT00377611|107564|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852100|NCT00377611|107564|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852101|NCT00377611|107564|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852102|NCT00377611|107564|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852103|NCT01954251|117036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843362|NCT00108082|COR100216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843363|NCT00108082|COR100216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852104|NCT01954251|117036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852105|NCT01954251|117036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852106|NCT01954251|117036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852107|NCT01954251|117036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852108|NCT01954251|117036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852109|NCT01954251|117036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852110|NCT04987853|BR10965164|Study Protocol|https://is.ncste.kz/login|
2852111|NCT04987853|BR10965164|Informed Consent Form|https://is.ncste.kz/login|
2852112|NCT04987853|BR10965164|Clinical Study Report|https://is.ncste.kz/login|
2852113|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.
2852114|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
2852115|NCT00757770|444563/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852116|NCT00757770|444563/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852117|NCT00757770|444563/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852118|NCT00757770|444563/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852119|NCT00757770|444563/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852120|NCT00043875|LAM20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852121|NCT00043875|LAM20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843364|NCT00108082|COR100216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843365|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
2843366|NCT00363857|101468/249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843367|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
2845545|NCT01706315|116778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843368|NCT00363857|101468/249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843369|NCT00363857|101468/249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843370|NCT00363857|101468/249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843371|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
2843372|NCT00363857|101468/249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843373|NCT00743860|LPL112498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843374|NCT00743860|LPL112498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843375|NCT00743860|LPL112498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843376|NCT00743860|LPL112498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843377|NCT00743860|LPL112498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843378|NCT00743860|LPL112498|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843379|NCT00743860|LPL112498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843380|NCT00129116|792014/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843381|NCT00129116|792014/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843382|NCT00129116|792014/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843383|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
2843384|NCT00129116|792014/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843385|NCT00476307|110221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845546|NCT01706315|116778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843386|NCT00476307|110221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843387|NCT00476307|110221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843388|NCT00476307|110221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843389|NCT00476307|110221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843390|NCT00476307|110221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843391|NCT00476307|110221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845547|NCT01706315|116778|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845548|NCT01706315|116778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845549|NCT01706315|116778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845550|NCT02743221||Individual Participant Data Set|http://clinicaltrials.servier.com/|
2845551|NCT02743221||Study Protocol|https://clinicaltrials.servier.com/|
2845552|NCT02743221||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2845553|NCT02743221||Informed Consent Form|https://clinicaltrials.servier.com/|
2845554|NCT02743221||Clinical Study Report|https://clinicaltrials.servier.com/|
2845555|NCT02743221||study-level clinical trial data|https://clinicaltrials.servier.com/|
2845556|NCT00157872||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845557|NCT02989857||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2845558|NCT02989857||Study Protocol|https://clinicaltrials.servier.com/|
2843392|NCT01098539|114130|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847718|NCT02877615||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2847719|NCT00811798|111712|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847720|NCT00811798|111712|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847721|NCT00811798|111712|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847722|NCT00811798|111712|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847723|NCT00811798|111712|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847724|NCT00811798|111712|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847725|NCT00811798|111712|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847726|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)."
2847727|NCT01366521|114092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847728|NCT01366521|114092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847729|NCT01366521|114092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843393|NCT01098539|114130|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843394|NCT01098539|114130|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843395|NCT01098539|114130|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843396|NCT01098539|114130|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843397|NCT01098539|114130|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843398|NCT01098539|114130|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843399|NCT02724826||Clinical Study Report|http://resolver.ebscohost.com/openurl?sid=Entrez%3aPubMed&id=pmid%3a18090079&site=ftf-live|
2843400|NCT04056663|CONNECARE|Framework|http://www.connecare.eu|The ambition of the CONNECARE consortium is to co-design, develop, deploy, and evaluate a novel smart, adaptive integrated care system for chronic care management
2843401|NCT01039454|109710|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843402|NCT01039454|109710|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843403|NCT01039454|109710|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843404|NCT01039454|109710|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843405|NCT01039454|109710|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843406|NCT01039454|109710|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843407|NCT01077505|107032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843408|NCT01077505|107032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843409|NCT01077505|107032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843410|NCT01077505|107032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843411|NCT01077505|107032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843412|NCT01077505|107032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843413|NCT01077505|107032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843414|NCT00197080|101468/205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843415|NCT00197080|101468/205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843416|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
2843417|NCT00197080|101468/205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847730|NCT01366521|114092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847731|NCT01366521|114092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847732|NCT01366521|114092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847733|NCT01366521|114092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847734|NCT01366560|114639|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847735|NCT01366560|114639|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847736|NCT01366560|114639|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847737|NCT01366560|114639|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847738|NCT01366560|114639|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847739|NCT01366560|114639|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847740|NCT01366560|114639|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852122|NCT00043875|LAM20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852123|NCT00043875|LAM20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852124|NCT00043875|LAM20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852125|NCT00043875|LAM20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852126|NCT00043875|LAM20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852127|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.
2852128|NCT00377585|104888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852129|NCT00377585|104888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852130|NCT00377585|104888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852131|NCT00377585|104888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852132|NCT00377585|104888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852133|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."
2852134|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."
2852135|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."
2852136|NCT00430521|107495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852137|NCT00430521|107495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852138|NCT00430521|107495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852139|NCT00430521|107495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847741|NCT00372112|B2C108562|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847742|NCT00372112|B2C108562|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847743|NCT00372112|B2C108562|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847744|NCT00372112|B2C108562|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847745|NCT00372112|B2C108562|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847746|NCT00372112|B2C108562|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845559|NCT02989857||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2849880|NCT01957163|200109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849881|NCT01957163|200109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849882|NCT01957163|200109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849883|NCT01957163|200109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849884|NCT01957163|200109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849885|NCT01957163|200109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849886|NCT01957163|200109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849887|NCT00273052|COR103561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849888|NCT00273052|COR103561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849889|NCT00273052|COR103561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849890|NCT00273052|COR103561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849891|NCT00273052|COR103561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849892|NCT00273052|COR103561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849893|NCT00273052|COR103561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849894|NCT00240994|SDY134|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
2849895|NCT00240994|SDY134|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
2849896|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
2849897|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
2849898|NCT00907933|111610|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849899|NCT00907933|111610|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849900|NCT00907933|111610|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849901|NCT00907933|111610|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849902|NCT00907933|111610|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849903|NCT00907933|111610|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849904|NCT00907933|111610|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849905|NCT02236611|201315|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849906|NCT02236611|201315|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849907|NCT02236611|201315|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849908|NCT02236611|201315|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849909|NCT02236611|201315|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849910|NCT02236611|201315|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849911|NCT02236611|201315|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849912|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32532623/|Study scientific background
2849913|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.
2849914|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32727835/|Study scientific background.
2849915|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32769063/|Study scientific background.
2849916|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/25636714/|Study scientific background.
2849917|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/24444048/|Alemtuzumab medication
2849918|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/27766281/|Alemtuzumab medication
2852140|NCT00430521|107495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852141|NCT00430521|107495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852142|NCT00430521|107495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852143|NCT00992784|113094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852144|NCT00992784|113094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852145|NCT00992784|113094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852146|NCT00992784|113094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852147|NCT00992784|113094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852148|NCT00992784|113094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852149|NCT00992784|113094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852150|NCT00289185|104298|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852151|NCT00289185|104298|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852152|NCT00289185|104298|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852153|NCT00289185|104298|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843418|NCT00197080|101468/205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852154|NCT00289185|104298|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852155|NCT00289185|104298|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852156|NCT01021852||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6096-011&kw=6096-011&tab=access|
2852157|NCT05532995||Informed Consent Form|https://drive.google.com/file/d/1qiU0UgEzvPBntfA0lLWFe_AzOGngacl9/view?usp=sharing|
2852158|NCT00135486|711202/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852159|NCT00135486|711202/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852160|NCT00135486|711202/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852161|NCT00135486|711202/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852162|NCT00135486|711202/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852163|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
2852164|NCT00838916|112754|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852165|NCT00838916|112754|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852166|NCT00838916|112754|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852167|NCT00838916|112754|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852168|NCT00838916|112754|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852169|NCT00838916|112754|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852170|NCT00838916|112754|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852171|NCT01842607|115661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852172|NCT01842607|115661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852173|NCT01842607|115661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852174|NCT01842607|115661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852175|NCT01842607|115661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852176|NCT01842607|115661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852177|NCT01842607|115661|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852178|NCT01153893|113199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852179|NCT01153893|113199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852180|NCT01153893|113199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852181|NCT01153893|113199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852182|NCT01153893|113199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852183|NCT01153893|113199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852184|NCT01551758|115151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852185|NCT01551758|115151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852186|NCT01551758|115151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852187|NCT01551758|115151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852188|NCT01551758|115151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852189|NCT01551758|115151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852190|NCT01551758|115151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852191|NCT01615796|115198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845560|NCT02989857||Informed Consent Form|https://clinicaltrials.servier.com/|
2852192|NCT01615796|115198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852193|NCT01615796|115198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852194|NCT01615796|115198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852195|NCT01615796|115198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852196|NCT01615796|115198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852197|NCT01615796|115198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852198|NCT01245764||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-046&kw=V501-046&tab=access|
2852199|NCT00731393|100351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852200|NCT00731393|100351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852201|NCT00731393|100351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852202|NCT00731393|100351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852203|NCT00731393|100351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852204|NCT00731393|100351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852205|NCT00731393|100351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852206|NCT00989404|113625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852207|NCT00989404|113625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852208|NCT00989404|113625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852209|NCT00989404|113625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852210|NCT00989404|113625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852211|NCT00989404|113625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852212|NCT00989404|113625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852213|NCT01231607|114263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852214|NCT01231607|114263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852215|NCT01231607|114263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852216|NCT01231607|114263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852217|NCT01231607|114263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852218|NCT01231607|114263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852219|NCT01231607|114263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852220|NCT01299610|113434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852221|NCT01299610|113434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852222|NCT01299610|113434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852223|NCT01299610|113434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852224|NCT01299610|113434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852225|NCT01299610|113434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852226|NCT01299610|113434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852227|NCT00671216|DB1111509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852228|NCT00671216|DB1111509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852229|NCT00671216|DB1111509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852230|NCT00671216|DB1111509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852231|NCT00671216|DB1111509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852232|NCT00671216|DB1111509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852233|NCT00671216|DB1111509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852234|NCT00880763||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-016&kw=7009-016&tab=access|
2852235|NCT00989612|113519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852236|NCT00989612|113519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852237|NCT00989612|113519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852238|NCT00989612|113519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852239|NCT00989612|113519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852240|NCT00989612|113519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852241|NCT00989612|113519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852242|NCT01293006||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-032&kw=4305-032&tab=access|
2852243|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)
2852244|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)
2852245|NCT00083343||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852246|NCT00823940|111497|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852247|NCT00823940|111497|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852248|NCT00823940|111497|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852249|NCT00823940|111497|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852250|NCT00823940|111497|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852251|NCT00823940|111497|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852252|NCT00823940|111497|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852253|NCT04744636||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2852254|NCT04744636||Study Protocol|https://clinicaltrials.servier.com/|
2845561|NCT02989857||Clinical Study Report|https://clinicaltrials.servier.com/|
2852255|NCT04744636||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2843419|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
2843420|NCT00197080|101468/205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843421|NCT00489099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2843422|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.
2843423|NCT06899438||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/tezDetay.jsp?id=ojJkM_gxQRaH4Sn9fMdQWw&no=8WIZbpBlZOGWvkUUwksxFg|
2843424|NCT00725764|MET111646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843425|NCT00725764|MET111646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843426|NCT00725764|MET111646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843427|NCT00725764|MET111646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843428|NCT00725764|MET111646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843429|NCT00725764|MET111646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843430|NCT00725764|MET111646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843431|NCT02940678|10.6084/m9.figshare.4042572.v1|Study Protocol|https://dx.doi.org/10.6084/m9.figshare.4042572.v1|
2843432|NCT02369120||Study Protocol|http://www.biomedcentral.com/1472-6947/15/97|
2843433|NCT01956487|116371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843434|NCT01956487|116371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843435|NCT01956487|116371|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843436|NCT01956487|116371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843437|NCT01956487|116371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843438|NCT01956487|116371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843439|NCT01956487|116371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843440|NCT00480324|107625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843441|NCT00480324|107625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843442|NCT00480324|107625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843443|NCT00480324|107625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843444|NCT00480324|107625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843445|NCT00480324|107625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843446|NCT00480324|107625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843447|NCT00784134|Data repository-VISTA|Data repository-VISTA|http://vista.gla.ac.uk|when available
2843448|NCT00784134||Study Protocol|http://vista.gla.ac.uk|when available
2843449|NCT00784134||Statistical Analysis Plan|http://vista.gla.ac.uk|when available
2843450|NCT00749411|DB1111581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843451|NCT00749411|DB1111581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843452|NCT00749411|DB1111581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843453|NCT00749411|DB1111581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843454|NCT00749411|DB1111581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843455|NCT00749411|DB1111581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843456|NCT00749411|DB1111581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843457|NCT00792623|208133/178|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852256|NCT04744636||Informed Consent Form|https://clinicaltrials.servier.com/|
2845562|NCT02989857||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2852257|NCT04744636||Clinical Study Report|https://clinicaltrials.servier.com/|
2843458|NCT00792623|208133/178|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843459|NCT00792623|208133/178|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843460|NCT00792623|208133/178|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843461|NCT00792623|208133/178|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843462|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
2843463|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
2843464|NCT00240617|TRX103635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843465|NCT00240617|TRX103635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843466|NCT00240617|TRX103635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843467|NCT00240617|TRX103635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843468|NCT00240617|TRX103635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843469|NCT00240617|TRX103635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843470|NCT00240617|TRX103635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843471|NCT00109486|FFR101747|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843472|NCT00109486|FFR101747|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843473|NCT00109486|FFR101747|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843474|NCT00109486|FFR101747|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843475|NCT00109486|FFR101747|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843476|NCT00109486|FFR101747|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843477|NCT00109486|FFR101747|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843478|NCT02502734|107112|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843479|NCT02502734|107112|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843480|NCT02502734|107112|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843481|NCT02502734|107112|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843482|NCT02502734|107112|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843483|NCT02502734|107112|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843484|NCT02502734|107112|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843485|NCT01043926||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-017&kw=4305-017&tab=access|
2843486|NCT02682147|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
2843487|NCT04828434||International Cognitive Stimulation Therapy Centre Website|http://www.ucl.ac.uk/international-cognitive-stimulation-therapy|
2843488|NCT06290219||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
2843489|NCT01294566|114422|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843490|NCT01294566|114422|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843491|NCT01294566|114422|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843492|NCT01294566|114422|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843493|NCT01294566|114422|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843494|NCT01294566|114422|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843495|NCT01294566|114422|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843496|NCT01797926|116799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843497|NCT01797926|116799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843498|NCT01797926|116799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843499|NCT01797926|116799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843500|NCT01797926|116799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843501|NCT01797926|116799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843502|NCT01797926|116799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843503|NCT00964106|112684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843504|NCT00964106|112684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843505|NCT00964106|112684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843506|NCT00964106|112684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843507|NCT00964106|112684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843508|NCT00964106|112684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843509|NCT00964106|112684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843510|NCT01466322|114919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843511|NCT01466322|114919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843512|NCT01466322|114919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843513|NCT01466322|114919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843514|NCT01466322|114919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843515|NCT01466322|114919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843516|NCT01466322|114919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843517|NCT01577693|115148|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843518|NCT01577693|115148|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843519|NCT01577693|115148|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843520|NCT01577693|115148|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843521|NCT01577693|115148|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843522|NCT01577693|115148|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843523|NCT01577693|115148|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843524|NCT01267006|114922|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843525|NCT01267006|114922|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843526|NCT01267006|114922|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843527|NCT01267006|114922|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843528|NCT01267006|114922|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843529|NCT01267006|114922|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843530|NCT01267006|114922|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843531|NCT02662231||Study Protocol|http://globalsurg.org/globalsurg-2-protocol/|GlobalSurg-II Study Protocol: available in multiple languages
2843532|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
2843533|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
2843534|NCT00333723|49653/143|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843535|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
2843536|NCT00333723|49653/143|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843537|NCT00333723|49653/143|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843538|NCT00333723|49653/143|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843539|NCT00333723|49653/143|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843540|NCT02119286|200110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843541|NCT02119286|200110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843542|NCT02119286|200110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843543|NCT02119286|200110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843544|NCT02119286|200110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843545|NCT02119286|200110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843546|NCT02119286|200110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843547|NCT00296491|ADA103575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843548|NCT00296491|ADA103575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843549|NCT00296491|ADA103575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843550|NCT00296491|ADA103575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843551|NCT00296491|ADA103575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843552|NCT00296491|ADA103575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843553|NCT00296491|ADA103575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843554|NCT05917691||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
2843555|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
2843556|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|
2843557|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
2843558|NCT00158756|104021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843559|NCT00158756|104021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843560|NCT00158756|104021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843561|NCT00158756|104021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843562|NCT00158756|104021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843563|NCT00158756|104021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843564|NCT00144911|SCO40043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843565|NCT00144911|SCO40043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843566|NCT00144911|SCO40043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843567|NCT00144911|SCO40043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843568|NCT00144911|SCO40043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843569|NCT00144911|SCO40043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843570|NCT00144911|SCO40043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843571|NCT01849016|Version 7.0 - 5/31/2016|Statistical Analysis Plan|http://www2.hematologie-amc.nl/nac_studie|
2843572|NCT00289757|100576 (Y11)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843573|NCT00289757|100576 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843574|NCT00289757|100576 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843575|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
2843576|NCT00289757|100576 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843577|NCT00289757|100576 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843578|NCT00048204|NKD20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843579|NCT00048204|NKD20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843580|NCT00048204|NKD20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843581|NCT00048204|NKD20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843582|NCT00048204|NKD20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843583|NCT00048204|NKD20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843584|NCT00048204|NKD20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845563|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.
2845564|NCT04831229|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
2845565|NCT00086515||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845566|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
2845567|NCT00140686|102247/036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845568|NCT00140686|102247/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845569|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
2845570|NCT00140686|102247/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845571|NCT00140686|102247/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845572|NCT00140686|102247/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845573|NCT02738463||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/pubmed|
2845574|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
2845575|NCT01999530||Publication|https://www.ncbi.nlm.nih.gov/pubmed/28233334|
2845576|NCT07004348|PROM link|Statistical Analysis Plan|https://livenorthumbriaac-my.sharepoint.com/:w:/g/personal/frank_lai_northumbria_ac_uk/EbKJJ3cbnk5Ikr-NpppTxHoBmGuJLYpePT6qQ1ZnXA4P-w?e=ZZuX7U|
2845577|NCT06835959|Informed consent form|Informed Consent Form|https://drive.google.com/file/d/1q09u34SVFOO2TXC7vXuDAE0MAjJfgVyA/view?usp=drive_link|
2845578|NCT01702298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-312&kw=0431D-312&tab=access|
2845579|NCT05162755||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2845580|NCT05162755||Study Protocol|https://clinicaltrials.servier.com/|
2845581|NCT05162755||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2845582|NCT05162755||Informed Consent Form|https://clinicaltrials.servier.com/|
2845583|NCT05162755||Clinical Study Report|https://clinicaltrials.servier.com/|
2845584|NCT05162755||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2845585|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
2845586|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.
2845587|NCT00005121|FHS-Cohort|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
2845588|NCT00005121|FHS-Cohort|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
2845589|NCT00005121|FHS-Cohort|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
2845590|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.
2845591|NCT00005121|FHS-OS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
2845592|NCT00005121|FHS-OS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
2845593|NCT00005121|FHS-OS|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
2843585|NCT03182582||Study Protocol|https://eprotocol.stanford.edu/|
2843586|NCT00316147|104005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843587|NCT00316147|104005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843588|NCT00316147|104005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843589|NCT00316147|104005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843590|NCT00316147|104005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843591|NCT00316147|104005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843592|NCT02006537|117023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843593|NCT02006537|117023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843594|NCT02006537|117023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843595|NCT02006537|117023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843596|NCT02006537|117023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843597|NCT02006537|117023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843598|NCT02006537|117023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843599|NCT00306943|104745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843600|NCT00306943|104745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843601|NCT00306943|104745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843602|NCT00306943|104745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843603|NCT00306943|104745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843604|NCT00929331|110586|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843605|NCT00929331|110586|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843606|NCT00929331|110586|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843607|NCT00929331|110586|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843608|NCT00929331|110586|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843609|NCT00929331|110586|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843610|NCT00929331|110586|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843611|NCT01195792|111850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843612|NCT01195792|111850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843613|NCT01195792|111850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843614|NCT01195792|111850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845594|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.
2845595|NCT00005121|FHS-Gen III|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/gen3/|
2845596|NCT00005121|FHS-Gen III|Study Forms|http://biolincc.nhlbi.nih.gov/studies/gen3/|
2845597|NCT00005121|FHS-Gen III|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/gen3/|
2845598|NCT00317122|759346/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845599|NCT00317122|759346/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845600|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
2843615|NCT01195792|111850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845601|NCT00317122|759346/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849919|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31898276/|Alemtuzumab medication
2845602|NCT00317122|759346/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845603|NCT00317122|759346/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845604|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
2845605|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).
2845606|NCT01110057|113049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845607|NCT01110057|113049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845608|NCT01110057|113049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845609|NCT01110057|113049|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845610|NCT01110057|113049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845611|NCT01110057|113049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845612|NCT01110057|113049|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845613|NCT00373542|RRL103660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845614|NCT00373542|RRL103660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845615|NCT00373542|RRL103660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845616|NCT00373542|RRL103660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845617|NCT00373542|RRL103660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845618|NCT00373542|RRL103660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845619|NCT00373542|RRL103660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845620|NCT07150442||Study Protocol|https://bit.ly/45NuVGB|https://bit.ly/45NuVGB
2845621|NCT07003204|msabry776@yahoo.com|Clinical Study Report|https://pmc.ncbi.nlm.nih.gov/articles/PMC8075197/|very good
2845622|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
2845623|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
2845624|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.
2845625|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.
2845626|NCT01495013|115317|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845627|NCT01495013|115317|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845628|NCT01495013|115317|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845629|NCT01495013|115317|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845630|NCT01495013|115317|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845631|NCT01495013|115317|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845632|NCT01128569|113090|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845633|NCT01128569|113090|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845634|NCT01128569|113090|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845635|NCT01128569|113090|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852258|NCT04744636||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2847747|NCT00372112|B2C108562|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847748|NCT00356369|107386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847749|NCT00356369|107386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847750|NCT00356369|107386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847751|NCT00356369|107386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847752|NCT00356369|107386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847753|NCT00356369|107386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847754|NCT01411111|112362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847755|NCT01411111|112362|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845636|NCT01128569|113090|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845637|NCT01128569|113090|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845638|NCT01128569|113090|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845639|NCT03150264||Study Protocol|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161575/|
2845640|NCT07161297||Study Protocol|https://www.humanitas-research.com/|Requests should be submitted to: ibd@humanitas.it Subject: REMI-IBD
2845641|NCT00445094||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845642|NCT00325143|217744/100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845643|NCT00325143|217744/100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845644|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
2845645|NCT00325143|217744/100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845646|NCT00325143|217744/100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845647|NCT00325143|217744/100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845648|NCT00652743|111443|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845649|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.
2845650|NCT00652743|111443|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845651|NCT00652743|111443|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845652|NCT00652743|111443|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847756|NCT01411111|112362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847757|NCT01411111|112362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847758|NCT01411111|112362|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847759|NCT01411111|112362|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847760|NCT01411111|112362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847761|NCT04221009||Informed Consent Form|https://arc.research.usf.edu/Prod/sd/Doc/0/DDRU7K2KMHLK9ECT12FPTMA60B/3S78A88933BKN7869JO1NSMT62.pdf|
2847762|NCT04221009||Study Protocol|https://arc.research.usf.edu/Prod/sd/Doc/0/06USV5NTK2VKJ06CUK3TQJR578/Protocol%20v01%202019-10-24.docx|
2847763|NCT00044278|LAM20007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847764|NCT00044278|LAM20007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847765|NCT00044278|LAM20007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847766|NCT00044278|LAM20007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847767|NCT00044278|LAM20007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847768|NCT00044278|LAM20007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847769|NCT00044278|LAM20007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847770|NCT01124422|113877|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847771|NCT01124422|113877|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847772|NCT01124422|113877|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847773|NCT01124422|113877|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847774|NCT01124422|113877|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847775|NCT01124422|113877|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847776|NCT01124422|113877|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847777|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.
2847778|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.
2847779|NCT03012802||Study Protocol|http://www.grupogerm.es/power|
2847780|NCT03012802||Statistical Analysis Plan|http://www.grupogerm.es/power|
2847781|NCT03012802||Clinical Study Report|http://www.grupogerm.es/power|
2847782|NCT00609492|109621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847783|NCT00609492|109621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847784|NCT00609492|109621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847785|NCT00609492|109621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847786|NCT00609492|109621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847787|NCT00609492|109621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847788|NCT00609492|109621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847789|NCT01018186|106839|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847790|NCT01018186|106839|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847791|NCT01018186|106839|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847792|NCT01018186|106839|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847793|NCT01018186|106839|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847794|NCT01018186|106839|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847795|NCT01018186|106839|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847796|NCT01428453|114458|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847797|NCT01428453|114458|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847798|NCT01428453|114458|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847799|NCT01428453|114458|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847800|NCT01428453|114458|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847801|NCT01428453|114458|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847802|NCT01428453|114458|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847803|NCT01702454|116023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847804|NCT01702454|116023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847805|NCT01702454|116023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847806|NCT01702454|116023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852259|NCT01153841|113151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852260|NCT01153841|113151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852261|NCT01153841|113151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852262|NCT01153841|113151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852263|NCT01153841|113151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852264|NCT01153841|113151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852265|NCT00044486||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852266|NCT00240539|100449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852267|NCT00240539|100449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852268|NCT00240539|100449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852269|NCT00240539|100449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852270|NCT00240539|100449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852271|NCT00971425|113572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852272|NCT00971425|113572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852273|NCT00971425|113572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852274|NCT00971425|113572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847807|NCT01702454|116023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847808|NCT01702454|116023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847809|NCT01702454|116023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847810|NCT01030939|112861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847811|NCT01030939|112861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847812|NCT01030939|112861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847813|NCT01030939|112861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847814|NCT01030939|112861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847815|NCT01030939|112861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847816|NCT01030939|112861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847817|NCT01077856||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-033&kw=V501-033&tab=access|
2847818|NCT01607086|111649|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847819|NCT01607086|111649|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847820|NCT01607086|111649|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847821|NCT01607086|111649|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847822|NCT01607086|111649|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847823|NCT01607086|111649|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847824|NCT01607086|111649|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847825|NCT00877877|111375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847826|NCT00877877|111375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847827|NCT00877877|111375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847828|NCT00877877|111375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847829|NCT00877877|111375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847830|NCT00877877|111375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847831|NCT00877877|111375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847832|NCT00256893|ROF102100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847833|NCT00256893|ROF102100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847834|NCT00256893|ROF102100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847835|NCT00256893|ROF102100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847836|NCT00256893|ROF102100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847837|NCT00256893|ROF102100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847838|NCT00256893|ROF102100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847839|NCT00369993|SAS104449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847840|NCT00369993|SAS104449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847841|NCT00369993|SAS104449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847842|NCT00369993|SAS104449|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847843|NCT00369993|SAS104449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847844|NCT00369993|SAS104449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847845|NCT00369993|SAS104449|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847846|NCT00496093||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847847|NCT04464369|LPDSItopride study|Study Protocol|http://www.targid.eu|
2847848|NCT02028065||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-101&kw=8616-101&tab=access|
2847849|NCT04631081||Individual Participant Data Set|https://www.project-redcap.org/|
2847850|NCT01847417|116498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847851|NCT01847417|116498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847852|NCT01847417|116498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847853|NCT01847417|116498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847854|NCT01847417|116498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847855|NCT01847417|116498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847856|NCT03715166||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2847857|NCT03715166||Study Protocol|https://clinicaltrials.servier.com/|
2847858|NCT03715166||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2847859|NCT03715166||Informed Consent Form|https://clinicaltrials.servier.com/|
2847860|NCT03715166||Clinical Study Report|https://clinicaltrials.servier.com/|
2847861|NCT03715166||study-level clinical trial data|https://clinicaltrials.servier.com/|
2847862|NCT00412854|104567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847863|NCT00412854|104567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847864|NCT00412854|104567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847865|NCT00412854|104567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847866|NCT00412854|104567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847867|NCT00412854|104567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847868|NCT00412854|104567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847869|NCT03019133|201609843|Informed Consent Form|http://hawkirb.research.uiowa.edu|
2847870|NCT01777256|115919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847871|NCT01777256|115919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847872|NCT01777256|115919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847873|NCT01777256|115919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847874|NCT01777256|115919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847875|NCT01777256|115919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847876|NCT01777256|115919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847877|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)
2847878|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf|CDC/NHSN Surveillance Definitions for Specific Types of Infections
2847879|NCT01949051|200285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852275|NCT00971425|113572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852276|NCT00971425|113572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852277|NCT00971425|113572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852278|NCT00406211|208136/039|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852279|NCT00406211|208136/039|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852280|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
2852281|NCT00406211|208136/039|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852282|NCT00406211|208136/039|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852283|NCT00406211|208136/039|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852284|NCT00118729|FFR101816|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852285|NCT00118729|FFR101816|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852286|NCT00118729|FFR101816|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852287|NCT00118729|FFR101816|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852288|NCT00118729|FFR101816|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852289|NCT00118729|FFR101816|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852290|NCT00118729|FFR101816|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852291|NCT00438022|Study ID is SDY4|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
2852292|NCT00438022|Study ID is SDY4|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
2852293|NCT00438022|Study ID is SDY4|Study details, -download packages, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
2852294|NCT02979366||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2852295|NCT02979366||Study Protocol|https://clinicaltrials.servier.com/|
2852296|NCT02979366||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2852297|NCT02979366||Informed Consent Form|https://clinicaltrials.servier.com/|
2852298|NCT02979366||Clinical Study Report|https://clinicaltrials.servier.com/|
2852299|NCT02979366||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2852300|NCT00866515|112205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852301|NCT00866515|112205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852302|NCT00866515|112205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852303|NCT00866515|112205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852304|NCT00866515|112205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852305|NCT00866515|112205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852306|NCT00866515|112205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852307|NCT01376245|113684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852308|NCT01376245|113684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852309|NCT01376245|113684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852310|NCT01376245|113684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852311|NCT01376245|113684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852312|NCT01376245|113684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852313|NCT01376245|113684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852314|NCT01357889|114856|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852315|NCT01357889|114856|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852316|NCT01357889|114856|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852317|NCT01357889|114856|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852318|NCT01357889|114856|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852319|NCT01357889|114856|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852320|NCT01357889|114856|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852321|NCT00533611||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852322|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.
2852323|NCT00964158|113528|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852324|NCT00964158|113528|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852325|NCT00964158|113528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852326|NCT00964158|113528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852327|NCT00964158|113528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852328|NCT00964158|113528|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852329|NCT00964158|113528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852330|NCT01021813||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-009&kw=4305-009&tab=access|
2852331|NCT00546286||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852332|NCT02141217|117044|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852333|NCT02141217|117044|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852334|NCT02141217|117044|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852335|NCT02141217|117044|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852336|NCT02141217|117044|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852337|NCT02141217|117044|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852338|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.
2852339|NCT04392869|clinicaltrialsCRAFT|Human Subjects Review|https://drive.ugr.es/index.php/s/DGKxnBhZfm058DA|Human Subjects Review approval and its translation into English
2852340|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.
2852341|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.
2852342|NCT05184309|Principle investigator|Statistical Analysis Plan|https://pubmed.ncbi.nlm.nih.gov/28446376/|
2852343|NCT02800720||Embedded Qualitative Study|http://link.springer.com/article/10.1007/s12671-015-0458-8|
2852344|NCT01319019|115032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852345|NCT01319019|115032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852346|NCT01319019|115032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852347|NCT01319019|115032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852348|NCT01319019|115032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852349|NCT01319019|115032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852350|NCT01319019|115032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852351|NCT07091838||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28179436/|
2852352|NCT01315847||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-067&kw=0974-067&tab=access|
2852353|NCT03336827||Study design|http://pdf.lu/YtWd|
2852354|NCT03336827||List of questionnaires|http://pdf.lu/TJ4c|
2852355|NCT03336827||Informed Consent Form|http://pdf.lu/dN2P|
2852356|NCT03336827||Informed Consent Form|http://pdf.lu/07Xz|
2847880|NCT01949051|200285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847881|NCT01949051|200285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847882|NCT01949051|200285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847883|NCT01949051|200285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847884|NCT01949051|200285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847885|NCT01949051|200285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847886|NCT00268996|SB-480848/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849920|NCT05075499|PMID|Study Protocol|http://products.sanofi.us/aubagio/aubagio.html|Aubagio (teriflunomide) \[prescribing information\]. Cambridge (MA): Genzyme Corporation; September 2012.
2849921|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/31898276/|Aubagio (teriflunomide) medication
2849922|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/29275977/|Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria.
2849923|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.
2849924|NCT07044193||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521375-31-00|
2849925|NCT00972686|112826|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849926|NCT00972686|112826|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849927|NCT00972686|112826|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849928|NCT00972686|112826|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849929|NCT00972686|112826|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849930|NCT00972686|112826|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849931|NCT00972686|112826|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849932|NCT00718120|110584|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849933|NCT00718120|110584|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849934|NCT00718120|110584|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849935|NCT00718120|110584|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849936|NCT00718120|110584|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849937|NCT00718120|110584|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849938|NCT00718120|110584|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849939|NCT00929526|112949|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849940|NCT00929526|112949|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849941|NCT00929526|112949|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849942|NCT00929526|112949|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849943|NCT00929526|112949|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849944|NCT00929526|112949|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849945|NCT03928665||DDLS - reference|https://www.sign.ac.uk/assets/sign144_disc_chart_colour.pdf|
2849946|NCT00035048||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849947|NCT04526171||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/Q3P4WX|
2849948|NCT04205669||Individual Participant Data Set|https://www.kaggle.com/julianmatthewman/grattigratta-data|
2849949|NCT01316913|113374|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849950|NCT01316913|113374|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849951|NCT01316913|113374|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843616|NCT01195792|111850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843617|NCT01195792|111850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843618|NCT00169481|103488|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843619|NCT00169481|103488|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843620|NCT00169481|103488|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843621|NCT00169481|103488|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843622|NCT00169481|103488|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843623|NCT00307034|105539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843624|NCT00307034|105539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843625|NCT00307034|105539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843626|NCT00307034|105539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843627|NCT00307034|105539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843628|NCT00307034|105539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843629|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"
2843630|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.
2843631|NCT00273039|NKF100110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843632|NCT00273039|NKF100110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843633|NCT00273039|NKF100110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843634|NCT00273039|NKF100110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843635|NCT00273039|NKF100110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843636|NCT00273039|NKF100110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843637|NCT00273039|NKF100110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843638|NCT00763438|2007-002160-10|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-002160-10/results|
2843639|NCT00197288|104437|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843640|NCT00197288|104437|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843641|NCT00197288|104437|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843642|NCT00197288|104437|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843643|NCT00197288|104437|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843644|NCT00197288|104437|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843645|NCT00197288|104437|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843646|NCT03324321||Funder|http://dunhillmedical.org.uk/|Dunhill RTF Grant (RTF97/0117)
2843647|NCT00548171|110804|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843648|NCT00548171|110804|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843649|NCT00548171|110804|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843650|NCT00548171|110804|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843651|NCT00548171|110804|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843652|NCT00548171|110804|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849952|NCT01316913|113374|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849953|NCT01316913|113374|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849954|NCT01316913|113374|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849955|NCT01316913|113374|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849956|NCT07013123|2025-521258-41-00|Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en|avalable after authorization of competent authorities
2849957|NCT06699511||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34847915/|
2849958|NCT01072149|110946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849959|NCT01072149|110946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849960|NCT01072149|110946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849961|NCT01072149|110946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849962|NCT01072149|110946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849963|NCT01072149|110946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849964|NCT01072149|110946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849965|NCT06477549|Protocol version 1.0|Study Protocol|https://cloud.mail.ru/public/wQ1q/8amGwZdMb|Study protocol signed
2849966|NCT01602900|116038|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849967|NCT01602900|116038|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849968|NCT01602900|116038|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849969|NCT01602900|116038|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849970|NCT01602900|116038|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849971|NCT01602900|116038|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849972|NCT01602900|116038|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849973|NCT00470483|TMT106386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849974|NCT00470483|TMT106386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849975|NCT00470483|TMT106386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849976|NCT00470483|TMT106386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849977|NCT00470483|TMT106386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843653|NCT00548171|110804|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849978|NCT00470483|TMT106386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849979|NCT05400525||Study Protocol|https://discoverthesecretofgoodhealth.weebly.com|
2849980|NCT04338568||Clinical Study Report|https://www.castoredc.com/|
2849981|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
2849982|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"
2849983|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
2849984|NCT00424476|HGS1006-C1057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849985|NCT00424476|HGS1006-C1057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849986|NCT00424476|HGS1006-C1057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849987|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
2849988|NCT00424476|HGS1006-C1057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849989|NCT00424476|HGS1006-C1057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852357|NCT00092482||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852358|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.
2852359|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.
2852360|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.
2852361|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.
2852362|NCT00141037|SDY132|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
2852363|NCT00141037|SDY132|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
2852364|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
2852365|NCT00704431|LPL111814|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852366|NCT00704431|LPL111814|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852367|NCT00704431|LPL111814|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852368|NCT00704431|LPL111814|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852369|NCT00704431|LPL111814|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852370|NCT00704431|LPL111814|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852371|NCT00334152|NKT102552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852372|NCT00334152|NKT102552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852373|NCT00334152|NKT102552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852374|NCT00334152|NKT102552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852375|NCT00334152|NKT102552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852376|NCT00334152|NKT102552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852377|NCT00334152|NKT102552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852378|NCT01527110|115215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852379|NCT01527110|115215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852380|NCT01527110|115215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843654|NCT00069836|712753/009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843655|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
2843656|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
2843657|NCT00069836|712753/009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843658|NCT00069836|712753/009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843659|NCT00069836|712753/009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843660|NCT00069836|712753/009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843661|NCT00541970|110659|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843662|NCT00541970|110659|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843663|NCT00541970|110659|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843664|NCT00541970|110659|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843665|NCT00541970|110659|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843666|NCT00541970|110659|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843667|NCT00541970|110659|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843668|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.
2843669|NCT00000476||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dig/|
2843670|NCT00000476||Study Forms|http://biolincc.nhlbi.nih.gov/studies/dig/|
2843671|NCT03274882||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2843672|NCT03274882||Study Protocol|https://clinicaltrials.servier.com/|
2843673|NCT03274882||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2843674|NCT03274882||Informed Consent Form|https://clinicaltrials.servier.com/|
2843675|NCT03274882||Clinical Study Report|https://clinicaltrials.servier.com/|
2843676|NCT03274882||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2843677|NCT00117325|FFR30006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843678|NCT00117325|FFR30006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843679|NCT00117325|FFR30006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843680|NCT00117325|FFR30006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843681|NCT00117325|FFR30006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843682|NCT00117325|FFR30006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843683|NCT00117325|FFR30006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843684|NCT03762486||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/citmatch|
2843685|NCT01335997||CSR Synsopsi Link|http://www.merck.com/clinical-trials/study.html?id=0524B-143&kw=0524B-143&tab=access|
2843686|NCT00811356|111319|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843687|NCT00811356|111319|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843688|NCT00811356|111319|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843689|NCT00811356|111319|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843690|NCT00811356|111319|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843691|NCT00811356|111319|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843692|NCT00811356|111319|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843693|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.
2845220|NCT01610388|113376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845221|NCT01610388|113376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845222|NCT01610388|113376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845223|NCT01610388|113376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845224|NCT01610388|113376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845225|NCT01245933||general information|http://www.asconet.net|
2845226|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.
2845227|NCT00005123||Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/hhp/|
2845228|NCT01899703|117213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845229|NCT01899703|117213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845230|NCT01899703|117213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845231|NCT01899703|117213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845232|NCT01899703|117213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852381|NCT01527110|115215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852382|NCT01527110|115215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852383|NCT01527110|115215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852384|NCT03427138|C2495|Individual Participant Data Set|http://ndar.nih.gov|
2852385|NCT00290303|100478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852386|NCT00290303|100478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852387|NCT00290303|100478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852388|NCT00290303|100478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852389|NCT00290303|100478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852390|NCT00290303|100478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852391|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
2852392|NCT03909672||Study Protocol|http://facisa.ufrn.br|
2852393|NCT02542813|201558|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852394|NCT02542813|201558|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852395|NCT02542813|201558|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852396|NCT02542813|201558|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852397|NCT02542813|201558|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852398|NCT02542813|201558|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852399|NCT02542813|201558|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852400|NCT05885048||Study Protocol|https://www.researchprotocols.org/2024/1/e51145|
2845653|NCT00652743|111443|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852401|NCT01235728||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-022&kw=0873-022&tab=access|
2852402|NCT00996593|104507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852403|NCT00996593|104507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852404|NCT00996593|104507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852405|NCT00996593|104507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852406|NCT00996593|104507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852407|NCT00996593|104507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852408|NCT00996593|104507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852409|NCT05752786||Study Protocol|https://osf.io/3gts8/|
2852410|NCT05752786||Statistical Analysis Plan|https://osf.io/3gts8/|
2852411|NCT05752786||Individual Participant Data Set|https://osf.io/3gts8/|
2852412|NCT00702910|B2C111401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852413|NCT00702910|B2C111401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852414|NCT00702910|B2C111401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852415|NCT00702910|B2C111401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852416|NCT00702910|B2C111401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852417|NCT00702910|B2C111401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852418|NCT00702910|B2C111401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852419|NCT00306241|106001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852420|NCT00306241|106001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852421|NCT00306241|106001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852422|NCT00306241|106001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852423|NCT00306241|106001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852424|NCT00306241|106001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852425|NCT05464472||BECK DEPRESSION INVENTORY|https://www.ismanet.org/doctoryourspirit/pdfs/Beck-Depression-Inventory-BDI.pdf|
2852426|NCT05464472||SF-36 QUESTIONNAIRE|https://clinmedjournals.org/articles/jmdt/jmdt-2-023-figure-1.pdf|
2852427|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.
2852428|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.
2843694|NCT04838522||Breast Milk At the Dawn of New Discoveries|https://betterbeginnings.org/what-we-do/research/breast-milk/|
2843695|NCT02904824||Clinical Study Report|http://www.dynasolutions.com|CRO data base
2843696|NCT00196924|580299/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843697|NCT00196924|580299/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843698|NCT00196924|580299/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843699|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.
2852429|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
2852430|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
2852431|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
2852432|NCT02697058||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2852433|NCT02697058||Study Protocol|https://clinicaltrials.servier.com/|
2852434|NCT02697058||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2852435|NCT02697058||Informed Consent Form|https://clinicaltrials.servier.com/|
2852436|NCT02697058||Clinical Study Report|https://clinicaltrials.servier.com/|
2852437|NCT02697058||study-level clinical trial data|https://clinicaltrials.servier.com/|
2852438|NCT01376388|115362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852439|NCT01376388|115362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852440|NCT01376388|115362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852441|NCT01376388|115362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852442|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.
2852443|NCT00005306||Study Forms|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|
2852444|NCT00383227|208129/032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852445|NCT00383227|208129/032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852446|NCT00383227|208129/032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852447|NCT00383227|208129/032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852448|NCT00383227|208129/032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852449|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
2852450|NCT00937326|113160|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852451|NCT00937326|113160|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852452|NCT00937326|113160|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852453|NCT00937326|113160|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849990|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
2849991|NCT00103857||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849992|NCT01381445|113435|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849993|NCT01381445|113435|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849994|NCT01381445|113435|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849995|NCT01381445|113435|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849996|NCT01381445|113435|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849997|NCT01381445|113435|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849998|NCT01381445|113435|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849999|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.
2852454|NCT00937326|113160|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852455|NCT00937326|113160|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852456|NCT00937326|113160|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852457|NCT02197598|2014-000413-31|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-000413-31/results|
2852458|NCT00264667|ADG103440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852459|NCT00264667|ADG103440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852460|NCT00264667|ADG103440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852461|NCT00264667|ADG103440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845654|NCT06379828||Study Protocol|https://newborn-health-standards.org/about/project-overview/|
2850000|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
2850001|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
2850002|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
2850003|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
2850004|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
2850005|NCT05214248||Study Protocol|https://doi.org/10.1016/S0377-1237(10)80131-5|Article Title: Meconium Aspiration Syndrome: An Insight
2850006|NCT00346398|SDY545|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY545|ImmPort study identifier is SDY545.
2850007|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.
2850008|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.
2850009|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.
2850010|NCT03884478||Study Protocol|https://www.researchprotocols.org/2021/4/e24647|available open access at URL provided
2850011|NCT00197262|FFR104861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850012|NCT00197262|FFR104861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850013|NCT00197262|FFR104861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850014|NCT00197262|FFR104861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850015|NCT00197262|FFR104861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852462|NCT00264667|ADG103440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852463|NCT00264667|ADG103440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852464|NCT00264667|ADG103440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852465|NCT06120192|10.6084/m9.figshare.23994768|Informed Consent Form|https://doi.org/10.6084/m9.figshare.23994768|
2852466|NCT06120192|10.6084/m9.figshare.23994768|Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.23994768|
2852467|NCT01031108|114089|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852468|NCT01031108|114089|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852469|NCT01031108|114089|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852470|NCT01031108|114089|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852471|NCT01031108|114089|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852472|NCT01031108|114089|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852473|NCT01031108|114089|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852474|NCT00092404||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852475|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.
2852476|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
2852477|NCT00654420||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0646-007&kw=0646-007&tab=access|
2852478|NCT01594749||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-031&kw=0517-031&tab=access|
2852479|NCT05837000|MKSU 51- 2 _ 16|Study Protocol|http://kfs.edu.eg/engkfs/|
2852480|NCT00750178||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852481|NCT01177826|111426|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852482|NCT01177826|111426|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852483|NCT01177826|111426|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852484|NCT01177826|111426|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852485|NCT01177826|111426|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852486|NCT01177826|111426|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852487|NCT02798640||Informed Consent Form|https://mega.nz/#!C5U1HZwI!7XB2jar-JDElrnYOZTbwg0RD5T1WPQEv3HkzT0XPXz8|
2852488|NCT02798640||Clinical Investigation plan|https://mega.nz/#!3gEnFCDK!DK911mpjGBw_bAKdfsR4F2RgzCQG7mYR3oBqrVkRtpA|
2850016|NCT00197262|FFR104861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852489|NCT02798640||Clinical Study Report|https://mega.nz/#!S1tThKrL!gaWPII28P3I0BLBrLD9iZJYRqb2R1x-uZT5djgV4ML8|
2852490|NCT01366534|114460|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852491|NCT01366534|114460|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852492|NCT01366534|114460|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852493|NCT01366534|114460|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852494|NCT01366534|114460|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843700|NCT00196924|580299/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843701|NCT00196924|580299/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843702|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
2843703|NCT00883909|103094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843704|NCT00883909|103094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850017|NCT00197262|FFR104861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850018|NCT04883541||PhD thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
2850019|NCT02404012||Website|https://ngletsum.wixsite.com/nito|
2850020|NCT00787371||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850021|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
2850022|NCT00632736|101468/248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850023|NCT00632736|101468/248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850024|NCT00632736|101468/248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850025|NCT00632736|101468/248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850026|NCT00632736|101468/248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850027|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
2850028|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.
2850029|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.
2850030|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
2850031|NCT03151694||Peer-Reviewed Article|http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12646/full|
2850032|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529982|
2850033|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529983|
2850034|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.
2850035|NCT00866619|110021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850036|NCT00866619|110021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850037|NCT00866619|110021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850038|NCT00866619|110021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852495|NCT01366534|114460|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852496|NCT00329784|SDY660|Individual Participant Data Set|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
2852497|NCT00329784|SDY660|Study summary, -design, -adverse event(s), -demographics, -study files|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
2852498|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)
2852499|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)
2852500|NCT00684463||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2843705|NCT00883909|103094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843706|NCT00883909|103094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850039|NCT00866619|110021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852501|NCT00076856||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852502|NCT00911144|112933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850040|NCT00866619|110021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850041|NCT04419571|285260|Individual Participant Data Set|https://www.myresearchproject.org.uk/|Data collection template available on IRAS (Integrated Research Application System) registration
2850042|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
2850043|NCT04419571|285260|Study Protocol|https://www.myresearchproject.org.uk/|Protocol available on IRAS (Integrated Research Application System) registration
2850044|NCT00879827|217744/049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850045|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
2850046|NCT00879827|217744/049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850047|NCT00879827|217744/049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850048|NCT00879827|217744/049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850049|NCT00092378||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850050|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.
2850051|NCT00000492||Study Forms|http://biolincc.nhlbi.nih.gov/studies/bhat/|
2850052|NCT02384122|27619827|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27619827|
2850053|NCT06700161|Study Protocol|Study Protocol|https://tipfakultesi.ksu.edu.tr/Default.aspx?SId=24451|
2850054|NCT04503434||Informed Consent Form|https://enquesta.clinic.cat/index.php/admin/survey/sa/view/surveyid/818692|
2850055|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.
2850056|NCT02907489||Study Protocol|https://www.scribd.com/document/328018560/Protocol-Omaia-Repaired-Autosaved|
2850057|NCT00227422|102394|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850058|NCT00227422|102394|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850059|NCT00227422|102394|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850060|NCT00227422|102394|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850061|NCT00227422|102394|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850062|NCT00227422|102394|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850063|NCT00733577|111829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852503|NCT00911144|112933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852504|NCT00911144|112933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852505|NCT00911144|112933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852506|NCT00911144|112933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852507|NCT00911144|112933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852508|NCT00911144|112933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852509|NCT00111891||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845655|NCT01697085||Clinical Study Report|http://www.maturitas.org/article/S0378-5122%2814%2900239-4/abstract?cc=y=|
2850064|NCT00733577|111829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852510|NCT03612674||Analytic Code|http://www.epiclin.it|
2852511|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).
2852512|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.
2843707|NCT00883909|103094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843708|NCT00883909|103094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843709|NCT00883909|103094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843710|NCT00871741|111761|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843711|NCT00871741|111761|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843712|NCT00871741|111761|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843713|NCT00871741|111761|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847887|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
2847888|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
2843714|NCT00871741|111761|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843715|NCT00871741|111761|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847889|NCT00268996|SB-480848/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847890|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
2847891|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
2847892|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
2847893|NCT00102882|SFA100062|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847894|NCT00102882|SFA100062|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847895|NCT00102882|SFA100062|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847896|NCT00102882|SFA100062|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847897|NCT00102882|SFA100062|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847898|NCT00102882|SFA100062|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847899|NCT00102882|SFA100062|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843716|NCT00871741|111761|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843717|NCT01711463|115199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843718|NCT01711463|115199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843719|NCT01711463|115199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843720|NCT01711463|115199|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843721|NCT01711463|115199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847900|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
2847901|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
2847902|NCT03577743|BMTN|Study Protocol|http://clinicaltrials.gov/NCT03577743|Phase 2 study to evaluate the effect of bevacizumab in metastatic triple negative breast cancer patients
2847903|NCT01686633|116863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847904|NCT01686633|116863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847905|NCT01686633|116863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847906|NCT01686633|116863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847907|NCT01686633|116863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847908|NCT01686633|116863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847909|NCT01686633|116863|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847910|NCT00503009|HZA109895|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847911|NCT00503009|HZA109895|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847912|NCT00503009|HZA109895|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847913|NCT00503009|HZA109895|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847914|NCT00503009|HZA109895|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847915|NCT00503009|HZA109895|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847916|NCT05069454||Study Protocol|http://www.isim.az|
2847917|NCT00608283|SDY289|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
2847918|NCT00608283|SDY289|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
2847919|NCT00608283|SDY289|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
2847920|NCT00451321|115493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847921|NCT00451321|115493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847922|NCT00451321|115493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847923|NCT00451321|115493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847924|NCT00451321|115493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847925|NCT00451321|115493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847926|NCT00451321|115493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847927|NCT02982967||Individual Participant Data Set|https://figshare.com/s/8f238bd02ca631cfe5fd|
2847928|NCT02369341|201959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847929|NCT02369341|201959|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847930|NCT02369341|201959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847931|NCT02369341|201959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847932|NCT02369341|201959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847933|NCT02369341|201959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847934|NCT02369341|201959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847935|NCT02626520||Study Protocol|https://docs.google.com/viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxyZWFsd29ybGRvbmNvbG9neXxneDo2OGI0ZDgxMzdkZDIxYWJh|
2847936|NCT02045797|116704|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847937|NCT02045797|116704|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847938|NCT02045797|116704|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847939|NCT02045797|116704|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847940|NCT02045797|116704|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847941|NCT02045797|116704|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847942|NCT02045797|116704|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847943|NCT00527943||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04736&kw=P04736&tab=access|
2847944|NCT00056407|ARI40006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847945|NCT00056407|ARI40006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847946|NCT00056407|ARI40006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847947|NCT00056407|ARI40006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847948|NCT00056407|ARI40006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847949|NCT00056407|ARI40006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847950|NCT00056407|ARI40006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847951|NCT00873509||Individual Participant Data Set|https://ndar.nih.gov|
2850065|NCT00733577|111829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850066|NCT00733577|111829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850067|NCT00733577|111829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847952|NCT04742101||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2847953|NCT04742101||Study Protocol|https://clinicaltrials.servier.com/|
2847954|NCT04742101||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2847955|NCT04742101||Informed Consent Form|https://clinicaltrials.servier.com/|
2847956|NCT04742101||Clinical Study Report|https://clinicaltrials.servier.com/|
2847957|NCT04742101||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2847958|NCT03578081||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|
2847959|NCT04999150|B0710118|Study Protocol|https://irbrcm.rcm.upr.edu/|
2847960|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
2847961|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
2847962|NCT00197041|257049/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847963|NCT00197041|257049/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847964|NCT00197041|257049/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847965|NCT00197041|257049/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847966|NCT00197041|257049/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847967|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.
2847968|NCT00060476||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847969|NCT03141281|https://osf.io/dp8n5/|Statistical Analysis Plan|https://osf.io/kq8yz/register/565fb3678c5e4a66b5582f67|Open Science Foundation registration of Data Analysis Plan
2847970|NCT01641692|116402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847971|NCT01641692|116402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847972|NCT01641692|116402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847973|NCT01641692|116402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847974|NCT01641692|116402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847975|NCT01641692|116402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847976|NCT01641692|116402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847977|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.
2847978|NCT01107587|113518|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847979|NCT01107587|113518|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847980|NCT01107587|113518|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847981|NCT01107587|113518|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847982|NCT01107587|113518|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847983|NCT01107587|113518|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847984|NCT04608500||Study Protocol|http://foamix.co.il/|
2847985|NCT01010906||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-005&kw=7009-005&tab=access|
2847986|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.
2847987|NCT00000560||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/best/|
2847988|NCT00000560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/best/|
2847989|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.
2847990|NCT00000586||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/MSH/|
2847991|NCT00000586||Study Forms|http://biolincc.nhlbi.nih.gov/studies/MSH/|
2847992|NCT04644614||Study Protocol|https://doi.org/10.1016/j.urols.2015.06.286|
2847993|NCT00454987|109664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847994|NCT00454987|109664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847995|NCT00454987|109664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847996|NCT00454987|109664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847997|NCT00454987|109664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847998|NCT01756495|116628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847999|NCT01756495|116628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848000|NCT01756495|116628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848001|NCT01756495|116628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848002|NCT01756495|116628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848003|NCT01756495|116628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848004|NCT01756495|116628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850068|NCT00733577|111829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848005|NCT01782664|116679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848006|NCT01782664|116679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848007|NCT01782664|116679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848008|NCT01782664|116679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848009|NCT01782664|116679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848010|NCT01782664|116679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848011|NCT01782664|116679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848012|NCT01948739||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25570900|
2848013|NCT00048607||CSR Synospis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848014|NCT04187560||Clinical Study Report|http://lbpharma.us/wp-content/uploads/2020/12/lb-102-001-clinical-study-report-final.pdf|
2848015|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.
2848016|NCT00751348|110876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848017|NCT00751348|110876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848018|NCT00751348|110876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848019|NCT00751348|110876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848020|NCT00751348|110876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848021|NCT00751348|110876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848022|NCT01462669|115860|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848023|NCT01462669|115860|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848024|NCT01462669|115860|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848025|NCT01462669|115860|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848026|NCT01462669|115860|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848027|NCT01462669|115860|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848028|NCT01462669|115860|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848029|NCT06906133||Information site for participants (in Icelandic)|https://www.unak.is/is/rannsoknir/rannsoknir-vid-ha/svefn|
2848030|NCT07171762||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/18166260/|
2848031|NCT07180485|t780927t@yahoo.com.tw|Study Protocol|https://orcid.org/0000-0002-8823-6901|t780927t@yahoo.com.tw
2848032|NCT01147861|114187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848033|NCT01147861|114187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848034|NCT01147861|114187|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848035|NCT01147861|114187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848036|NCT01147861|114187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848037|NCT01147861|114187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848038|NCT01147861|114187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848039|NCT00451386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848040|NCT01984775|117191|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848041|NCT01984775|117191|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848042|NCT01984775|117191|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848043|NCT01984775|117191|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848044|NCT01984775|117191|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848045|NCT01984775|117191|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848046|NCT00129129|101858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848047|NCT00129129|101858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848048|NCT00129129|101858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848049|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.
2848050|NCT00129129|101858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848051|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
2843722|NCT01711463|115199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845656|NCT00730756|FFR111158|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845657|NCT00730756|FFR111158|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845658|NCT00730756|FFR111158|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852513|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.
2852514|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.
2852515|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/|
2852516|NCT05394363||Current GenV collaborations|https://www.genv.org.au/for-researchers/current-genv-collaborations/|
2852517|NCT05394363||Working Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/working-papers/|
2852518|NCT05394363||Published Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/published-papers/|
2852519|NCT01431521||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4074-008&kw=4074-008&tab=access|
2852520|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
2845659|NCT00730756|FFR111158|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845660|NCT00730756|FFR111158|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845661|NCT00730756|FFR111158|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845662|NCT00730756|FFR111158|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845663|NCT01073293||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-007&kw=V503-007&tab=access|
2845664|NCT00335881|106745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845665|NCT00335881|106745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845666|NCT00335881|106745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845667|NCT00335881|106745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845668|NCT00335881|106745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845669|NCT00335881|106745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845670|NCT06187857||Study Protocol|https://osf.io/cavkf/?view_only=cc219af15f614756b43742875b6b0b39|
2845671|NCT01978145|115646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845672|NCT01978145|115646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845673|NCT01978145|115646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845674|NCT01978145|115646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845675|NCT01978145|115646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845676|NCT01978145|115646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845677|NCT01978145|115646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845678|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
2845679|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
2845680|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
2845681|NCT00421148||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845682|NCT01436110|115285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845683|NCT01436110|115285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845684|NCT01436110|115285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845685|NCT01436110|115285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845686|NCT01436110|115285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845687|NCT01436110|115285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845688|NCT01436110|115285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845689|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"
2845690|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.
2845691|NCT00688467||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05363&kw=P05363&tab=access|
2845692|NCT03750019|10.5255/UKDA-SN-853370|Individual Participant Data Set|http://dx.doi.org/10.5255/UKDA-SN-853370|
2845693|NCT03750019|10.17605/OSF.IO/WYCKJ|Study Protocol|https://doi.org/10.17605/OSF.IO/WYCKJ|
2845694|NCT00538057|HZA105871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845695|NCT00538057|HZA105871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845696|NCT00538057|HZA105871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845697|NCT00538057|HZA105871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845698|NCT00538057|HZA105871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845699|NCT00538057|HZA105871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845700|NCT00538057|HZA105871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845701|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
2845702|NCT00363311|AVO105948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845703|NCT00363311|AVO105948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845704|NCT00363311|AVO105948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845705|NCT00363311|AVO105948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845706|NCT00363311|AVO105948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845707|NCT00363311|AVO105948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845708|NCT00363311|AVO105948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845709|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.
2845710|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.
2845711|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.
2845712|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.
2845713|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
2845714|NCT05173376||Study Protocol|https://osf.io/scjn6/|Protocol on the Open Science Framework (OSF)
2845715|NCT05173376||Statistical Analysis Plan|https://osf.io/scjn6/|
2845716|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.
2845717|NCT05223673||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2845718|NCT05223673||Study Protocol|https://clinicaltrials.servier.com/|
2845719|NCT05223673||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2845720|NCT05223673||Informed Consent Form|https://clinicaltrials.servier.com/|
2845721|NCT05223673||Clinical Study Report|https://clinicaltrials.servier.com/|
2848052|NCT00779012||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848053|NCT01330485||Individual Participant Data Set|https://osf.io/426pd|
2848054|NCT01330485||All study files|https://osf.io/uhwnb|
2848055|NCT00907985|112676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845722|NCT05223673||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2845723|NCT00488514|TXA107977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845724|NCT00488514|TXA107977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845725|NCT00488514|TXA107977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845726|NCT00488514|TXA107977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845727|NCT00488514|TXA107977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845728|NCT00488514|TXA107977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845729|NCT00488514|TXA107977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845730|NCT05711875|Sridhar A, Shiliang Z, Woodson|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/33140989/|web site is provided
2845731|NCT01030822|112909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845732|NCT01030822|112909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845733|NCT01030822|112909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845734|NCT01030822|112909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845735|NCT01030822|112909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845736|NCT01030822|112909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845737|NCT01030822|112909|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845738|NCT01475721|115359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845739|NCT01475721|115359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845740|NCT01475721|115359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845741|NCT01475721|115359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845742|NCT01475721|115359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845743|NCT01475721|115359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845744|NCT01475721|115359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845745|NCT00225862|100310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845746|NCT00225862|100310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845747|NCT00225862|100310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845748|NCT00225862|100310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845749|NCT00225862|100310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845750|NCT00225862|100310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845751|NCT00225862|100310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845752|NCT01000506|112997|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845753|NCT01000506|112997|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845754|NCT01000506|112997|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845755|NCT01000506|112997|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845756|NCT01000506|112997|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845757|NCT01000506|112997|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845758|NCT01000506|112997|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845759|NCT03910075||Study Protocol|http://www.nihstrokenet.org/i-acquire/resources|
2845760|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.
2848056|NCT00907985|112676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848057|NCT00907985|112676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848058|NCT00907985|112676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848059|NCT00907985|112676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848060|NCT00907985|112676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848061|NCT00907985|112676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850069|NCT00733577|111829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850070|NCT00475436|AC4106889|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850071|NCT00475436|AC4106889|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850072|NCT00475436|AC4106889|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850073|NCT00475436|AC4106889|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850074|NCT00475436|AC4106889|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850075|NCT00475436|AC4106889|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850076|NCT00475436|AC4106889|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850077|NCT00733551|MOT109681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850078|NCT00733551|MOT109681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850079|NCT00733551|MOT109681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850080|NCT00733551|MOT109681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850081|NCT00733551|MOT109681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850082|NCT00733551|MOT109681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850083|NCT00352963|217744/097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850084|NCT00352963|217744/097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850085|NCT00352963|217744/097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850086|NCT00352963|217744/097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850087|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
2850088|NCT00352963|217744/097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850089|NCT06200480|NorHead|Study Protocol|https://www.ntnu.no/norhead/om|English Study protocol available by request to the Norwegian Centre of Headache Research (NorHead)
2850090|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)
2850091|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
2850092|NCT01031186|113324|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850093|NCT01031186|113324|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850094|NCT01031186|113324|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850095|NCT01031186|113324|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850096|NCT01031186|113324|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850097|NCT01031186|113324|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850098|NCT01031186|113324|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852521|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
2852522|NCT00964249|112017|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852523|NCT00964249|112017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852524|NCT00964249|112017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852525|NCT00964249|112017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852526|NCT00964249|112017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845761|NCT00127855|792014/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845762|NCT00127855|792014/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845763|NCT00127855|792014/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845764|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
2845765|NCT00127855|792014/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845766|NCT00400855|SIG103337|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845767|NCT00400855|SIG103337|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845768|NCT00400855|SIG103337|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845769|NCT00400855|SIG103337|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845770|NCT00400855|SIG103337|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845771|NCT00400855|SIG103337|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845772|NCT00400855|SIG103337|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845773|NCT01453491|115951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845774|NCT01453491|115951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845775|NCT01453491|115951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845776|NCT01453491|115951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845777|NCT01453491|115951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845778|NCT01453491|115951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845779|NCT01453491|115951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845780|NCT00289172|103792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845781|NCT00289172|103792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845782|NCT00289172|103792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845783|NCT00289172|103792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845784|NCT00289172|103792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845785|NCT00289172|103792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845786|NCT01999842|201072|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845787|NCT01999842|201072|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845788|NCT01999842|201072|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845789|NCT01999842|201072|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845790|NCT01999842|201072|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845791|NCT01999842|201072|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845792|NCT01999842|201072|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848064|NCT00322335|106672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848065|NCT00322335|106672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848066|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.
2848067|NCT00322335|106672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848068|NCT00322335|106672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848069|NCT00322335|106672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848070|NCT00380393|106464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848071|NCT00380393|106464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848072|NCT00380393|106464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848073|NCT00380393|106464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848074|NCT00380393|106464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852527|NCT00783549|111596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852528|NCT00783549|111596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852529|NCT00783549|111596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852530|NCT00783549|111596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852531|NCT00783549|111596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852532|NCT00783549|111596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852533|NCT00783549|111596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852534|NCT01160224|114312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852535|NCT01160224|114312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852536|NCT01160224|114312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852537|NCT01160224|114312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852538|NCT01160224|114312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852539|NCT01160224|114312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852540|NCT01160224|114312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852541|NCT00469040|B2C108784|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852542|NCT00469040|B2C108784|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852543|NCT00469040|B2C108784|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852544|NCT00469040|B2C108784|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852545|NCT00469040|B2C108784|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852546|NCT00469040|B2C108784|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852547|NCT00469040|B2C108784|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852548|NCT00732472|105211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852549|NCT00732472|105211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852550|NCT00732472|105211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852551|NCT00732472|105211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852552|NCT00732472|105211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852553|NCT00732472|105211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852554|NCT00732472|105211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852555|NCT01962467|200284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852556|NCT01962467|200284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852557|NCT01962467|200284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852558|NCT01962467|200284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852559|NCT01962467|200284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852560|NCT01962467|200284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852561|NCT01962467|200284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852562|NCT01899768|117270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852563|NCT01899768|117270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852564|NCT01899768|117270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852565|NCT01899768|117270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852566|NCT01899768|117270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852567|NCT01899768|117270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852568|NCT01899768|117270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852569|NCT03582969||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
2852570|NCT01808365|114991|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852571|NCT01808365|114991|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845793|NCT00920556|113222|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845794|NCT00920556|113222|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845795|NCT00920556|113222|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845796|NCT00920556|113222|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845797|NCT00920556|113222|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845798|NCT00920556|113222|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845799|NCT01366573|115256|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845800|NCT01366573|115256|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845801|NCT01366573|115256|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845802|NCT01366573|115256|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845803|NCT01366573|115256|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845804|NCT01366573|115256|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845805|NCT01366573|115256|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845806|NCT00005739||Abstract|http://ajph.aphapublications.org/doi/pdf/10.2105/AJPH.86.8_Pt_1.1146|
2845807|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.
2845808|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.
2845809|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
2845810|NCT02771405||Informed Consent Form|http://www.megafileupload.com/f3sT/Attachments_201656.zip|
2845811|NCT00292071||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845812|NCT01484496|112341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845813|NCT01484496|112341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845814|NCT01484496|112341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845815|NCT01484496|112341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845816|NCT01484496|112341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845817|NCT01484496|112341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845818|NCT01484496|112341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845819|NCT00412191|LAM105379|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845820|NCT00412191|LAM105379|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845821|NCT00412191|LAM105379|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845822|NCT00412191|LAM105379|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845823|NCT00412191|LAM105379|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845824|NCT00412191|LAM105379|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845825|NCT00412191|LAM105379|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845826|NCT00943761||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-028&kw=7009-028&tab=access|
2845827|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|
2845828|NCT03202433|ISSN 0124-8146|Study Protocol|http://scielo.org.co/scielo.php?script=sci_arttext&pid=S0124-81462013000200010|
2845829|NCT03202433||Clinical Practice Guide|http://www.criscancer.org|
2845830|NCT00540592|110847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852572|NCT01808365|114991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848075|NCT00380393|106464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848076|NCT00228917|103812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848077|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.
2848078|NCT00228917|103812|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848079|NCT00228917|103812|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848080|NCT00228917|103812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848081|NCT00228917|103812|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848082|NCT01075698||Study Protocol|https://prsinfo.clinicaltrials.gov/definitions.html|
2848083|NCT01391065||Published article|https://doi.org/10.1016/j.ijrobp.2019.10.037|
2848084|NCT02735083||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2848085|NCT02735083||Study Protocol|https://clinicaltrials.servier.com/|
2848086|NCT02735083||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2848087|NCT02735083||Informed Consent Form|https://clinicaltrials.servier.com/|
2848088|NCT02735083||Clinical Study Report|https://clinicaltrials.servier.com/|
2848089|NCT02735083||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2848090|NCT00896558|112668|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848091|NCT00896558|112668|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848092|NCT00896558|112668|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848093|NCT00896558|112668|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848094|NCT00896558|112668|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848095|NCT00896558|112668|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848096|NCT00896558|112668|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848097|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.
2848098|NCT00000514||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/shep/|
2848099|NCT00000514||Study Forms|http://biolincc.nhlbi.nih.gov/studies/shep/|
2848100|NCT00000514||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/shep/|
2848101|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
2848102|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
2848103|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
2850099|NCT02214017|doi: 10.1177/1357633X15608984|publication|https://www.ncbi.nlm.nih.gov/pubmed/26468213|
2850100|NCT00092365||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850101|NCT00356564|106744|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843723|NCT01711463|115199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845831|NCT00540592|110847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845832|NCT00540592|110847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845833|NCT00540592|110847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845834|NCT00540592|110847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845835|NCT00540592|110847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845836|NCT00540592|110847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845837|NCT06085235||Individual Participant Data Set|https://osf.io/y8e2r/|
2845838|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.
2845839|NCT01018017|114010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845840|NCT01018017|114010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845841|NCT01018017|114010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845842|NCT01018017|114010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845843|NCT01018017|114010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845844|NCT01018017|114010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845845|NCT01018017|114010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845846|NCT03160456|IPG598|"NICE guidance Hypoglossal Nerve Stimulation"|https://www.nice.org.uk/guidance/ipg598|National Institute for Health and Care Excellence
2845847|NCT02052661|106793|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845848|NCT02052661|106793|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845849|NCT02052661|106793|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845850|NCT02052661|106793|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845851|NCT02052661|106793|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845852|NCT02052661|106793|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845853|NCT02052661|106793|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845854|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
2845855|NCT02833129||Study Protocol|http://arxiv.org/abs/1607.01756|
2845856|NCT00742131|MET111647|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845857|NCT00742131|MET111647|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845858|NCT00742131|MET111647|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845859|NCT00742131|MET111647|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845860|NCT00742131|MET111647|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845861|NCT00742131|MET111647|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845862|NCT00742131|MET111647|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845863|NCT00906178||Intervention website|http://www.cybersenga.com|
2845864|NCT01277705|711866/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845865|NCT01277705|711866/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845866|NCT01277705|711866/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845867|NCT01277705|711866/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845868|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
2845869|NCT01277705|711866/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850102|NCT00356564|106744|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850103|NCT00356564|106744|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850104|NCT00356564|106744|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850105|NCT00356564|106744|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850106|NCT00356564|106744|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850107|NCT00938041|393229/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850108|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
2850109|NCT00938041|393229/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850110|NCT00938041|393229/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850111|NCT00938041|393229/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850112|NCT00938041|393229/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850113|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
2843724|NCT02664935||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/lung-matrix/index.aspx|
2850114|NCT00434577|108494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850115|NCT00434577|108494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850116|NCT00434577|108494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850117|NCT00434577|108494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852573|NCT01808365|114991|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852574|NCT01808365|114991|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852575|NCT01808365|114991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852576|NCT01808365|114991|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852577|NCT00772889|111738|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852578|NCT00772889|111738|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852579|NCT00772889|111738|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852580|NCT00772889|111738|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852581|NCT00772889|111738|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852582|NCT00772889|111738|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852583|NCT00772889|111738|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852584|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.
2852585|NCT02968966||Synopsis|http://www.medizin.uni-tuebingen.de/kinder/de/abteilungen/cpcs/projekte/|
2852586|NCT00345956|105722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852587|NCT00345956|105722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852588|NCT00345956|105722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852589|NCT00345956|105722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852590|NCT00345956|105722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852591|NCT00345956|105722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852592|NCT00419237|FFA10013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852593|NCT00419237|FFA10013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852594|NCT00419237|FFA10013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852595|NCT00419237|FFA10013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852596|NCT00419237|FFA10013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852597|NCT00419237|FFA10013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852598|NCT00419237|FFA10013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852599|NCT00067444|29060/874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852600|NCT00067444|29060/874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852601|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
2852602|NCT00067444|29060/874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852603|NCT00067444|29060/874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852604|NCT00067444|29060/874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852605|NCT04704206|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
2852606|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
2850118|NCT00434577|108494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843725|NCT00678886|115495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843726|NCT00678886|115495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843727|NCT00678886|115495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843728|NCT00678886|115495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843729|NCT00678886|115495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843730|NCT00678886|115495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843731|NCT00678886|115495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843732|NCT06613204||data set|http://www.ohsu.edu/alzheimers-disease-research-center/data-resources|
2843733|NCT04815889||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35704376/|
2843734|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
2843735|NCT00258700|103974 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843736|NCT00258700|103974 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843737|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
2843738|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
2843739|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
2843740|NCT06989255|doi: 10.5281/zenodo.11371924|Study Protocol|https://zenodo.org/records/11371924|Study protocol including ICF
2843741|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
2843742|NCT01371812|114660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843743|NCT01371812|114660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843744|NCT01371812|114660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843745|NCT01371812|114660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843746|NCT01371812|114660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843747|NCT01371812|114660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843748|NCT01371812|114660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843749|NCT06982014|lecturer|Individual Participant Data Set|https://kocaelisaglik.edu.tr/|
2843750|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"
2843751|NCT00474266|109670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843752|NCT00474266|109670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843753|NCT00474266|109670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843754|NCT00474266|109670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843755|NCT00474266|109670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843756|NCT00474266|109670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843757|NCT00474266|109670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843758|NCT00426361|108464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843759|NCT00426361|108464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843760|NCT00426361|108464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843761|NCT00426361|108464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848104|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.
2848105|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.
2848106|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.
2848107|NCT00133874|TOC100224|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848108|NCT00133874|TOC100224|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848109|NCT00133874|TOC100224|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848110|NCT00133874|TOC100224|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848111|NCT00133874|TOC100224|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848112|NCT00133874|TOC100224|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848113|NCT00133874|TOC100224|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848114|NCT07044180||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521373-13-00|
2848115|NCT00116831|AVD100521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848116|NCT00116831|AVD100521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848117|NCT00116831|AVD100521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848118|NCT00116831|AVD100521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848119|NCT00116831|AVD100521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848120|NCT00116831|AVD100521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848121|NCT00116831|AVD100521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848122|NCT00578175|110058|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848123|NCT00578175|110058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848124|NCT00578175|110058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848125|NCT00578175|110058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848126|NCT00578175|110058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848127|NCT00578175|110058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848128|NCT00578175|110058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848129|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.
2848130|NCT02319031|PMID: 26822022|Primary Publication|http://www.ncbi.nlm.nih.gov/pubmed/26822022|
2848131|NCT01165138|106827|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848132|NCT01165138|106827|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845870|NCT02993627|18039384|Clinical Study Report|http://lipidworld.biomedcentral.com/articles/10.1186/1476-511X-6-33/|
2845871|NCT01165125|105548|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845872|NCT01165125|105548|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845873|NCT01165125|105548|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845874|NCT01165125|105548|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845875|NCT01165125|105548|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845876|NCT01165125|105548|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845877|NCT01165125|105548|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845878|NCT02947802||Study Instrument (Online Survey)|https://hbs.qualtrics.com/SE/?SID=SV_1LdkKR5P4DyCevH|This is the online survey participants will complete.
2845879|NCT02397915|201474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845880|NCT02397915|201474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845881|NCT02397915|201474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845882|NCT02397915|201474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845883|NCT02397915|201474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845884|NCT02397915|201474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845885|NCT02397915|201474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845886|NCT02726464||Patient Brochure|http://www.lightintegra.com/prism-study|
2845887|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.
2845888|NCT00883948||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/eden/|
2845889|NCT00883948||Study Forms|http://biolincc.nhlbi.nih.gov/studies/eden/|
2845890|NCT00097929||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845891|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
2845892|NCT00140712|101468/253|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845893|NCT00140712|101468/253|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845894|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
2845895|NCT00140712|101468/253|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845896|NCT00140712|101468/253|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845897|NCT00140712|101468/253|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845898|NCT01536561|104728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845899|NCT01536561|104728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845900|NCT01536561|104728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845901|NCT01536561|104728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845902|NCT01536561|104728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845903|NCT01536561|104728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845904|NCT01536561|104728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845905|NCT00329576|106640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845906|NCT00329576|106640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848133|NCT01165138|106827|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848134|NCT01165138|106827|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848135|NCT01165138|106827|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848136|NCT01165138|106827|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848137|NCT01165138|106827|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848138|NCT03672435||Individual Participant Data Set|http://www.abcd-vision.org/OCR/OCR%20proparacaine%20de-identified.pdf|deidentified OCR topical anesthetic recovery outcomes
2848139|NCT04164901||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2848140|NCT00603746|FFA109684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848141|NCT00603746|FFA109684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848142|NCT00603746|FFA109684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848143|NCT00603746|FFA109684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848144|NCT00603746|FFA109684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848145|NCT00603746|FFA109684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848146|NCT00603746|FFA109684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850119|NCT00434577|108494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850120|NCT00434577|108494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850121|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.
2850122|NCT00197119|100566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850123|NCT00197119|100566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850124|NCT00197119|100566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850125|NCT00197119|100566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850126|NCT00197119|100566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850127|NCT00603278|FFA109685|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850128|NCT00603278|FFA109685|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850129|NCT00603278|FFA109685|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850130|NCT00603278|FFA109685|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850131|NCT00603278|FFA109685|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848147|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.
2848148|NCT02016963|HGS1021-C1069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848149|NCT02016963|HGS1021-C1069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848150|NCT02016963|HGS1021-C1069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848151|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
2848152|NCT02016963|HGS1021-C1069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845907|NCT00329576|106640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845908|NCT00329576|106640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845909|NCT00329576|106640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845910|NCT00972517|113638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845911|NCT00972517|113638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845912|NCT00972517|113638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845913|NCT00972517|113638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845914|NCT00972517|113638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845915|NCT00972517|113638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845916|NCT00972517|113638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845917|NCT00456625|108984|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845918|NCT00456625|108984|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845919|NCT00456625|108984|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845920|NCT00456625|108984|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845921|NCT00456625|108984|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845922|NCT00456625|108984|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845923|NCT00456625|108984|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845924|NCT02218697|117276|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845925|NCT02218697|117276|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845926|NCT02218697|117276|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845927|NCT02218697|117276|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845928|NCT02218697|117276|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845929|NCT02218697|117276|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845930|NCT02218697|117276|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845931|NCT01899638|115380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845932|NCT01899638|115380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845933|NCT01899638|115380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845934|NCT01899638|115380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845935|NCT01899638|115380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845936|NCT01899638|115380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845937|NCT01899638|115380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843762|NCT00426361|108464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843763|NCT00426361|108464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843764|NCT00426361|108464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843765|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.
2843766|NCT00609180||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/omega/|
2843767|NCT00609180||Study Forms|http://biolincc.nhlbi.nih.gov/studies/omega/|
2843768|NCT02152605|201211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843769|NCT02152605|201211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843770|NCT02152605|201211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843771|NCT02152605|201211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843772|NCT02152605|201211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843773|NCT02152605|201211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843774|NCT02152605|201211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843775|NCT00224471|208141/042|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843776|NCT00224471|208141/042|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843777|NCT00224471|208141/042|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843778|NCT00224471|208141/042|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843779|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
2843780|NCT00224471|208141/042|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843781|NCT01160003|113209|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843782|NCT01160003|113209|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843783|NCT01160003|113209|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843784|NCT01160003|113209|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843785|NCT01160003|113209|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843786|NCT01160003|113209|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843787|NCT01160003|113209|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843788|NCT02549027||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-003&kw=1064-003&tab=access|
2843789|NCT01590797||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-254&kw=0431-254&tab=access|
2843790|NCT02105974|200820|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843791|NCT02105974|200820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843792|NCT02105974|200820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843793|NCT02105974|200820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843794|NCT02105974|200820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843795|NCT02105974|200820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843796|NCT02105974|200820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843797|NCT02000765|115774|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843798|NCT02000765|115774|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843799|NCT02000765|115774|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843800|NCT02000765|115774|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845938|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.
2845939|NCT00434993||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/alta/|
2845940|NCT00434993||Study Forms|http://biolincc.nhlbi.nih.gov/studies/alta/|
2845941|NCT00104416|LAM100036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845942|NCT00104416|LAM100036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845943|NCT00104416|LAM100036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845944|NCT00104416|LAM100036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845945|NCT00104416|LAM100036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845946|NCT00104416|LAM100036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845947|NCT00104416|LAM100036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850132|NCT00603278|FFA109685|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850133|NCT00603278|FFA109685|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850134|NCT02033668|116891|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850135|NCT02033668|116891|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850136|NCT02033668|116891|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850137|NCT02033668|116891|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850138|NCT02033668|116891|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850139|NCT02033668|116891|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850140|NCT02033668|116891|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845948|NCT00758069||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850141|NCT00383903|444563/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850142|NCT00383903|444563/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845949|NCT01534351||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0906A-149&kw=0906A-149&tab=access|
2848153|NCT02016963|HGS1021-C1069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848154|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
2852607|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
2852608|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
2852609|NCT00748306|111834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852610|NCT00748306|111834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852611|NCT00748306|111834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852612|NCT00748306|111834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852613|NCT00748306|111834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852614|NCT00748306|111834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852615|NCT00748306|111834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852616|NCT01086449|113819|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852617|NCT01086449|113819|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852618|NCT01086449|113819|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852619|NCT01086449|113819|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852620|NCT01086449|113819|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852621|NCT01086449|113819|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852622|NCT01086449|113819|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852623|NCT05859906||Clinical Study Report|http://doi.org/10.1093/bjaceaccp/mkh037|
2843801|NCT02000765|115774|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843802|NCT02000765|115774|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843803|NCT02000765|115774|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843804|NCT00385008|TRX105848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843805|NCT00385008|TRX105848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843806|NCT00385008|TRX105848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843807|NCT00385008|TRX105848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843808|NCT00385008|TRX105848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852624|NCT01722903||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25807199|
2843809|NCT00385008|TRX105848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843810|NCT00385008|TRX105848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843811|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.
2843812|NCT00000620||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/accord|
2843813|NCT00000620||Study Forms|http://biolincc.nhlbi.nih.gov/studies/accord|
2843814|NCT00000620||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/accord|
2843815|NCT00979641||Clinical Study Report|http://www.anticancerresearch.com|
2843816|NCT00315731|393229/027|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843817|NCT00315731|393229/027|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843818|NCT00315731|393229/027|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852625|NCT00829010|111634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852626|NCT00829010|111634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852627|NCT00829010|111634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852628|NCT00829010|111634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852629|NCT00829010|111634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852630|NCT00829010|111634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852631|NCT00829010|111634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852632|NCT00290355|249553/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852633|NCT00290355|249553/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852634|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
2852635|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
2852636|NCT00290355|249553/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852637|NCT00290355|249553/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852638|NCT00290355|249553/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843819|NCT00315731|393229/027|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843820|NCT00315731|393229/027|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843821|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
2843822|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
2843823|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.
2843824|NCT00000474||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/paths/|
2843825|NCT00000474||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/paths/|
2852639|NCT02202161|201351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852640|NCT02202161|201351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852641|NCT02202161|201351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852642|NCT02202161|201351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852643|NCT02202161|201351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852644|NCT02202161|201351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852645|NCT02202161|201351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852646|NCT01021553|109059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852647|NCT01021553|109059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852648|NCT01021553|109059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852649|NCT01021553|109059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852650|NCT01021553|109059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852651|NCT01021553|109059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852652|NCT01021553|109059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852653|NCT00518336|109616 (Y7)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852654|NCT00518336|109616 (Y7)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852655|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.
2852656|NCT00518336|109616 (Y7)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852657|NCT00518336|109616 (Y7)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852658|NCT00518336|109616 (Y7)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852659|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
2852660|NCT00034697||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2843826|NCT02006602|201011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843827|NCT02006602|201011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843828|NCT02006602|201011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843829|NCT02006602|201011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843830|NCT02006602|201011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843831|NCT02006602|201011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843832|NCT02006602|201011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843833|NCT00366366|217744/075|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843834|NCT00366366|217744/075|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843835|NCT00366366|217744/075|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843836|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
2843837|NCT00366366|217744/075|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843838|NCT00366366|217744/075|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843839|NCT02257385|116961|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843840|NCT02257385|116961|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843841|NCT02257385|116961|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843842|NCT02257385|116961|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843843|NCT02257385|116961|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843844|NCT02257385|116961|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843845|NCT02257385|116961|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843846|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
2843847|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.
2843848|NCT00000591||Study Forms|http://biolincc.nhlbi.nih.gov/studies/tcd/|
2843849|NCT01890863|200260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843850|NCT01890863|200260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843851|NCT01890863|200260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843852|NCT01890863|200260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843853|NCT01890863|200260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843854|NCT01890863|200260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843855|NCT01890863|200260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843856|NCT05088135||Clinical Study Report|https://doi.org/10.3389/fphys.2023.1215757|
2843857|NCT02872376||Study Protocol|https://sites.google.com/site/ridartstudy/|
2843858|NCT02872376||Informed Consent Form|https://sites.google.com/site/ridartstudy/|
2843859|NCT00086593|101464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848155|NCT00196950|134612/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848156|NCT00196950|134612/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848157|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.
2848158|NCT00196950|134612/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848159|NCT00196950|134612/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848160|NCT00196950|134612/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848161|NCT00394030|GLP107724|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848162|NCT00394030|GLP107724|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848163|NCT00394030|GLP107724|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848164|NCT00394030|GLP107724|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848165|NCT00394030|GLP107724|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848166|NCT00394030|GLP107724|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848167|NCT00394030|GLP107724|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848168|NCT07110077|vanesssatob@gmail.com|Study Protocol|https://drive.google.com/drive/folders/1oaz8ewLKW--cX5Nm7Y0I_j0jPhJzwzVS?usp=sharing|
2848169|NCT01494610|114334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848170|NCT01494610|114334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848171|NCT01494610|114334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848172|NCT01494610|114334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848173|NCT01494610|114334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848174|NCT01494610|114334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848175|NCT01494610|114334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848176|NCT03900299||Study Protocol|http://www.med.alexu.edu.eg/ethics-committee/|
2848177|NCT04126785|CAAE 96882818.3.0000.5398|Brazil Research Ethics Committees|http://plataformabrasil.saude.gov.br/|
2848178|NCT00924911|112034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848179|NCT00924911|112034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848180|NCT00924911|112034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848181|NCT00924911|112034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848182|NCT00924911|112034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848183|NCT00924911|112034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843860|NCT00086593|101464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843861|NCT00086593|101464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848184|NCT00924911|112034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848185|NCT03672695||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2848186|NCT03672695||Study Protocol|https://clinicaltrials.servier.com/|
2852661|NCT00329459|TRX105850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852662|NCT00329459|TRX105850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852663|NCT00329459|TRX105850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852664|NCT00329459|TRX105850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852665|NCT00329459|TRX105850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852666|NCT00329459|TRX105850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852667|NCT00329459|TRX105850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852668|NCT05399836||Study Protocol|https://osf.io/hx75k/|Protocol on the Open Science Framework (OSF)
2852669|NCT05399836||Statistical Analysis Plan|https://osf.io/hx75k/|
2852670|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.
2852671|NCT00686699||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04628&kw=P04628&tab=access|
2852672|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
2852673|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.
2852674|NCT00998985||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-004&kw=5172-004&tab=access|
2852675|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
2852676|NCT07100288||preprint|https://www.researchsquare.com/article/rs-283444/v1|
2852677|NCT01619176|GSE59526|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/geo|
2852678|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.
2843862|NCT00086593|101464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843863|NCT00086593|101464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843864|NCT00086593|101464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843865|NCT01499446|FFA20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843866|NCT01499446|FFA20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843867|NCT01499446|FFA20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852679|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.
2852680|NCT05327309||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/22456397/|
2852681|NCT02685839||Clinical Study Report|http://goo.gl/FilVtL|
2852682|NCT05386641|18192154|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2852683|NCT05386641|25977305|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2843868|NCT01499446|FFA20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843869|NCT01499446|FFA20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843870|NCT01499446|FFA20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843871|NCT01499446|FFA20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843872|NCT00533312||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852684|NCT05386641|26079868|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2852685|NCT05386641|29332760|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2852686|NCT05386641|32031629|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2843873|NCT00323050|102547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852687|NCT05386641|32767329|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2848187|NCT03672695||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2852688|NCT05386641||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2852689|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)
2852690|NCT01371799|113746|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850143|NCT00383903|444563/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850144|NCT00383903|444563/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850145|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
2850146|NCT00383903|444563/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850147|NCT00591409||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850148|NCT01697592||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=3102-015&kw=3102-015&tab=access|
2850149|NCT01772147|116136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850150|NCT01772147|116136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850151|NCT01772147|116136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850152|NCT01772147|116136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850153|NCT01772147|116136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850154|NCT01772147|116136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850155|NCT01772147|116136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850156|NCT00684203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04772&kw=P04772&tab=access|
2850157|NCT01742234|SDY292|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292|ImmPort study identifier is SDY292
2850158|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.
2850159|NCT04018547||Individual Participant Data Set|http://www.oxitone.com|De-identified data for primary and secondary outcome measures
2850160|NCT03013725||Study Protocol|http://husk.b.uib.no/prototest/|Protocol
2850161|NCT00522678|HZA102928|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850162|NCT00522678|HZA102928|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850163|NCT00522678|HZA102928|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850164|NCT00522678|HZA102928|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850165|NCT00522678|HZA102928|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850166|NCT00522678|HZA102928|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850167|NCT00522678|HZA102928|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850168|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."
2850169|NCT03037814|26161601|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/26161601|
2850170|NCT03037814|19953810|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/19953810|
2850171|NCT03037814|12542617|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/12542617|
2850172|NCT03116672|UABC|Clinical Study Report|http://www.uabc.mx|Clinical trial that evaluate drug and placebo
2850173|NCT03116672|protocol guide|Individual Participant Data Set|http://www.uabc.mx|Clinical Guide
2850174|NCT00144846|SB030002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850175|NCT00144846|SB030002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850176|NCT00144846|SB030002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848188|NCT03672695||Informed Consent Form|https://clinicaltrials.servier.com/|
2848189|NCT03672695||Clinical Study Report|https://clinicaltrials.servier.com/|
2848190|NCT00945503|109731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848191|NCT00945503|109731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848192|NCT00945503|109731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848193|NCT00945503|109731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848194|NCT00945503|109731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852691|NCT01371799|113746|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852692|NCT01371799|113746|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852693|NCT01371799|113746|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852694|NCT01371799|113746|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848195|NCT00945503|109731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852695|NCT01371799|113746|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852696|NCT04746027||Study Protocol|https://www.stmarys.ac.uk/staff-directory/jonathan-nixon|
2852697|NCT00354991||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852698|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.
2848196|NCT00945503|109731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848197|NCT02632708||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2852699|NCT00005128||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrcps/|
2852700|NCT04340804||Study Protocol|https://osf.io/k369t/|
2852701|NCT04340804||Statistical Analysis Plan|https://osf.io/k369t/|
2852702|NCT04340804||Informed Consent Form|https://osf.io/k369t/|
2852703|NCT04340804||Individual Participant Data Set|https://osf.io/k369t/|When results will be published
2852704|NCT01021293|112679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852705|NCT01021293|112679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852706|NCT01021293|112679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852707|NCT01021293|112679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852708|NCT01021293|112679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852709|NCT01021293|112679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852710|NCT00104299|SDY91|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY91|ImmPort study identifier is SDY91.
2852711|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.
2852712|NCT00104299|ITN021AI|Individual Participant Data Set|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
2852713|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.
2852714|NCT01428479|115070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852715|NCT01428479|115070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852716|NCT01428479|115070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852717|NCT01428479|115070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852718|NCT01428479|115070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852719|NCT01428479|115070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852720|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
2852721|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
2852722|NCT01213849|102932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852723|NCT01213849|102932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852724|NCT01213849|102932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848198|NCT02632708||Study Protocol|https://clinicaltrials.servier.com/|
2848199|NCT02632708||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2848200|NCT02632708||Informed Consent Form|https://clinicaltrials.servier.com/|
2848201|NCT02632708||Clinical Study Report|https://clinicaltrials.servier.com/|
2848202|NCT02632708||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2845950|NCT00703846|114568|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845951|NCT00703846|114568|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850177|NCT00144846|SB030002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850178|NCT00144846|SB030002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845952|NCT00703846|114568|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850179|NCT00144846|SB030002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850180|NCT00144846|SB030002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850181|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
2850182|NCT00064428|103413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850183|NCT00064428|103413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850184|NCT00064428|103413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850185|NCT00064428|103413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850186|NCT00064428|103413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850187|NCT00064428|103413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850188|NCT00064428|103413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850189|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.
2850190|NCT02991781|neurofeedback-auth|Individual Participant Data Set|http://ckan.smokefreebrain.eu/|
2850191|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.
2850192|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.
2850193|NCT00005278|REDS-HTLV|Study Forms|http://biolincc.nhlbi.nih.gov/studies/reds/|
2850194|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.
2850195|NCT00721812|111406|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850196|NCT00721812|111406|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850197|NCT00721812|111406|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850198|NCT00721812|111406|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850199|NCT00721812|111406|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850200|NCT00721812|111406|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845953|NCT00703846|114568|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850201|NCT00721812|111406|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850202|NCT01274559||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0524A-133&kw=0524A-133&tab=access|
2850203|NCT06244693|aparral|Individual Participant Data Set|http://www.redcap.med.uchile.cl|Data registry online system provided by sponsor
2850204|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 \[CIP\_PhD Rampidis Georgios\_1.1\]"
2850205|NCT00372255|106252|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850206|NCT00372255|106252|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850207|NCT00372255|106252|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850208|NCT00372255|106252|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850209|NCT00372255|106252|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850210|NCT00372255|106252|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850211|NCT00118703|FFR30007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850212|NCT00118703|FFR30007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850213|NCT00118703|FFR30007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850214|NCT00118703|FFR30007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850215|NCT00118703|FFR30007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850216|NCT00118703|FFR30007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845954|NCT00703846|114568|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845955|NCT00703846|114568|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845956|NCT00703846|114568|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845957|NCT03511508||Study Protocol|http://doi.org/10.1186/s13063-019-3405-5|Study Protocol
2845958|NCT00466947|109563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845959|NCT00466947|109563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845960|NCT00466947|109563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845961|NCT00466947|109563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850217|NCT00118703|FFR30007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848203|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).
2850218|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.
2850219|NCT00005541||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/heirs/|
2850220|NCT00005541||Study Forms|http://biolincc.nhlbi.nih.gov/studies/heirs/|
2850221|NCT00005541||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/heirs/|
2850222|NCT04882748||Individual Participant Data Set|https://www.frontiersin.org/articles/10.3389/fnbot.2021.715632/full#supplementary-material|
2850223|NCT00038961|103414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850224|NCT00038961|103414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850225|NCT00038961|103414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850226|NCT00038961|103414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850227|NCT00038961|103414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850228|NCT00038961|103414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850229|NCT04629443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2850230|NCT04629443||Study Protocol|https://clinicaltrials.servier.com/|
2848204|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.
2850231|NCT04629443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2850232|NCT04629443||Informed Consent Form|https://clinicaltrials.servier.com/|
2850233|NCT04629443||Clinical Study Report|https://clinicaltrials.servier.com/|
2850234|NCT04629443||study-level clinical trial data|https://clinicaltrials.servier.com/|
2850235|NCT05907317||Study Protocol|https://www.rigshospitalet.dk/english/departments/juliane-marie-centre/department-of-neonatology/research/safeboosc-iiiv/Pages/protocol.aspx|
2850236|NCT02348372|115385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850237|NCT02348372|115385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850238|NCT02348372|115385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850239|NCT02348372|115385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850240|NCT02348372|115385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850241|NCT02348372|115385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850242|NCT02348372|115385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850243|NCT00197223|104438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850244|NCT00197223|104438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850245|NCT00197223|104438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850246|NCT00197223|104438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850247|NCT00197223|104438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850248|NCT00197223|104438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850249|NCT00197223|104438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850250|NCT06254755||Individual Participant Data Set|http://competetrials@gmail.com|
2850251|NCT04498988||Official study group website|https://tu-dresden.de/bereichsuebergreifendes/sfb940/|
2850252|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).
2850253|NCT01138098|113954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850254|NCT01138098|113954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850255|NCT01138098|113954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850256|NCT01138098|113954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850257|NCT01138098|113954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850258|NCT01138098|113954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850259|NCT00719043|110624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850260|NCT00719043|110624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850261|NCT00719043|110624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850262|NCT00719043|110624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850263|NCT00719043|110624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850264|NCT00719043|110624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850265|NCT01192776||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25536254|
2850266|NCT01086384|106837|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850267|NCT01086384|106837|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850268|NCT01086384|106837|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850269|NCT01086384|106837|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850270|NCT01086384|106837|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850271|NCT01086384|106837|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850272|NCT01086384|106837|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850273|NCT01006616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05575&kw=7123-019&tab=access|
2850274|NCT00749359|PCR111656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850275|NCT00749359|PCR111656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845962|NCT00466947|109563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845963|NCT00466947|109563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845964|NCT00875485|110699|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845965|NCT00875485|110699|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845966|NCT00875485|110699|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845967|NCT00875485|110699|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845968|NCT00875485|110699|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845969|NCT03030352||Pilot Study of the How-to trial|http://link.springer.com/article/10.1007/s10826-013-9751-0|
2845970|NCT00500461|AC2106213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845971|NCT00500461|AC2106213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845972|NCT00500461|AC2106213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845973|NCT00500461|AC2106213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845974|NCT00500461|AC2106213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845975|NCT00500461|AC2106213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845976|NCT00500461|AC2106213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845977|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.
2845978|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.
2845979|NCT02060344||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
2845980|NCT02060344||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
2845981|NCT01822899|116134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845982|NCT01822899|116134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845983|NCT01822899|116134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845984|NCT01822899|116134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845985|NCT01822899|116134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845986|NCT01822899|116134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845987|NCT01822899|116134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845988|NCT00344318|107007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845989|NCT00344318|107007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845990|NCT00344318|107007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845991|NCT00344318|107007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845992|NCT00344318|107007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845993|NCT00344318|107007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845994|NCT00404378|NKV105093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845995|NCT00404378|NKV105093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845996|NCT00404378|NKV105093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852725|NCT01213849|102932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852726|NCT01213849|102932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852727|NCT01213849|102932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852728|NCT01213849|102932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852729|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
2852730|NCT00381472|101468/169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852731|NCT00381472|101468/169|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852732|NCT00381472|101468/169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852733|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
2852734|NCT00381472|101468/169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852735|NCT00381472|101468/169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852736|NCT00989664|104504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852737|NCT00989664|104504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852738|NCT00989664|104504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852739|NCT00989664|104504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852740|NCT00989664|104504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852741|NCT00989664|104504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852742|NCT00989664|104504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852743|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.
2848205|NCT06876779||Study Protocol|https://www.ugc.edu.hk/eng/rgc/funding_opport/fds/funded%20research/fds2425.html|
2852744|NCT02356770|PMID: 28107560|2. publicaton|https://www.ncbi.nlm.nih.gov/pubmed/28107560|2\. publication concerning the volumetric changes of the soft tissue
2852745|NCT02896686||Study Protocol|https://cirurgiahj23.wordpress.com|
2852746|NCT02084316|CTN0056|Study Protocol|http://ctndisseminationlibrary.org/protocols/ctn0056.htm|
2852747|NCT00115622|FFR30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852748|NCT00115622|FFR30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852749|NCT00115622|FFR30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852750|NCT00115622|FFR30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852751|NCT00115622|FFR30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852752|NCT00115622|FFR30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852753|NCT00115622|FFR30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852754|NCT00750360|218352/054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852755|NCT00750360|218352/054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852756|NCT00750360|218352/054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852757|NCT00750360|218352/054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852758|NCT00750360|218352/054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852759|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
2852760|NCT02671786||Pilot Study Research Paper|http://www.worldwidejournals.com/ijar/file.php?val=April_2015_1427896145__152.pdf|
2852761|NCT02135848|114272|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852762|NCT02135848|114272|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852763|NCT02135848|114272|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850276|NCT00749359|PCR111656|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850277|NCT00749359|PCR111656|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850278|NCT00749359|PCR111656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850279|NCT00749359|PCR111656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850280|NCT00749359|PCR111656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850281|NCT00157898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850282|NCT01691547|116415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850283|NCT01691547|116415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850284|NCT01691547|116415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850285|NCT01691547|116415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850286|NCT01691547|116415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850287|NCT01691547|116415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850288|NCT01691547|116415|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850289|NCT01648153|116378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850290|NCT01648153|116378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850291|NCT01648153|116378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850292|NCT01648153|116378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850293|NCT01648153|116378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850294|NCT01648153|116378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850295|NCT01648153|116378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850296|NCT02075619|200561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850297|NCT02075619|200561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850298|NCT02075619|200561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850299|NCT02075619|200561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850300|NCT02075619|200561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850301|NCT02075619|200561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850302|NCT02075619|200561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850303|NCT01015677||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6913-004&kw=6913-004&tab=access|
2850304|NCT00823836|106066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850305|NCT00823836|106066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850306|NCT00823836|106066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850307|NCT00823836|106066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850308|NCT00823836|106066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850309|NCT03034850||Study Protocol|https://drive.google.com/open?id=0B0qo2hDQpXhncWZFZkNfZXhZMjVuUGcxc0IzZll5TEtjaXdn|
2850310|NCT03034850|eudract/B-nr B37120154199|Advice Ethical Committee|https://drive.google.com/open?id=0B0qo2hDQpXhnU3AzRHY0d1NtVmlsSmx1cFhKOGtKLTVscno0|
2850311|NCT01777334|117115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850312|NCT01777334|117115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850313|NCT01777334|117115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848206|NCT01934153|117157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848207|NCT01934153|117157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848208|NCT01934153|117157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848209|NCT01934153|117157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848210|NCT01934153|117157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848211|NCT01934153|117157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848212|NCT01934153|117157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848213|NCT00519649|110474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848214|NCT00519649|110474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848215|NCT00519649|110474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848216|NCT00519649|110474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848217|NCT00519649|110474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848218|NCT00519649|110474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848219|NCT00519649|110474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848220|NCT01573624|115938|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848221|NCT01573624|115938|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848222|NCT01573624|115938|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848223|NCT01573624|115938|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848224|NCT01573624|115938|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848225|NCT01573624|115938|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848226|NCT01573624|115938|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848227|NCT00689481|114742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848228|NCT00689481|114742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848229|NCT00689481|114742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848230|NCT00689481|114742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848231|NCT00689481|114742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848232|NCT00689481|114742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848233|NCT00637195|111567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848234|NCT00637195|111567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848235|NCT00637195|111567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848236|NCT00637195|111567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848237|NCT00637195|111567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848238|NCT00637195|111567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848239|NCT00637195|111567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848240|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.
2848241|NCT01462357|115411|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848242|NCT01462357|115411|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848243|NCT01462357|115411|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852764|NCT02135848|114272|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852765|NCT02135848|114272|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852766|NCT02135848|114272|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852767|NCT02135848|114272|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852768|NCT00090246||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852769|NCT04308668||Individual Participant Data Set|http://www.covidpep.umn.edu/data|
2852770|NCT00517634|HZA109912|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852771|NCT00517634|HZA109912|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852772|NCT00517634|HZA109912|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852773|NCT00517634|HZA109912|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852774|NCT00517634|HZA109912|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852775|NCT00517634|HZA109912|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852776|NCT00517634|HZA109912|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852777|NCT01681004|INSITE|Individual Participant Data Set|http://yoda.yale.edu/|
2852778|NCT01979250||Manuscript|http://www.ncbi.nlm.nih.gov/pubmed/27273977|To acces the results, please go to the above mentioned manuscript.
2852779|NCT00539825|AC6108697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852780|NCT00539825|AC6108697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852781|NCT00539825|AC6108697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852782|NCT00539825|AC6108697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852783|NCT00539825|AC6108697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852784|NCT00539825|AC6108697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852785|NCT00539825|AC6108697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852786|NCT00591786||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852787|NCT00965458|SDY797|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797.
2852788|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.
2852789|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.
2852790|NCT00965458|T1DAL ITN045AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
2852791|NCT00965458|T1DAL ITN045AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
2852792|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.
2852793|NCT02619942||Study Protocol|http://www.trialsjournal.com/content/17/1/582|
2852794|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.
2852795|NCT00000565||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ippb/|
2852796|NCT00000565||Study Forms|http://biolincc.nhlbi.nih.gov/studies/ippb/|
2852797|NCT00000565||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/ippb/|
2852798|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.
2852799|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.
2852800|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.
2852801|NCT02250586|awtg7|Individual Participant Data Set|https://osf.io|The trial's outcome data and scripts are available for download: https://osf.io/awtg7/
2852802|NCT01733758|113121|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852803|NCT01733758|113121|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852804|NCT01733758|113121|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852805|NCT01733758|113121|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852806|NCT01733758|113121|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852807|NCT01733758|113121|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852808|NCT01733758|113121|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852809|NCT00955682|112036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852810|NCT00955682|112036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852811|NCT00955682|112036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852812|NCT00955682|112036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852813|NCT00955682|112036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852814|NCT00955682|112036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852815|NCT00635804||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3281-002&kw=3281-002&tab=access|
2852816|NCT00950755|104505|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852817|NCT00950755|104505|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852818|NCT00950755|104505|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852819|NCT00950755|104505|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852820|NCT00950755|104505|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852821|NCT00950755|104505|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852822|NCT00950755|104505|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852823|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
2852824|NCT00422955|49653/376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852825|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
2852826|NCT00422955|49653/376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852827|NCT00422955|49653/376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852828|NCT00422955|49653/376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852829|NCT00422955|49653/376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852830|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
2852831|NCT00346775|FFR105693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852832|NCT00346775|FFR105693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852833|NCT00346775|FFR105693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852834|NCT00346775|FFR105693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852835|NCT00346775|FFR105693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852836|NCT00346775|FFR105693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848244|NCT01462357|115411|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848245|NCT01462357|115411|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848246|NCT01462357|115411|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848247|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).
2848248|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)
2848249|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.
2848250|NCT01114841|114572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848251|NCT01114841|114572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848252|NCT01114841|114572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848253|NCT01114841|114572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848254|NCT01114841|114572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848255|NCT01114841|114572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848256|NCT01114841|114572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848257|NCT00812929|112025|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848258|NCT00812929|112025|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848259|NCT00812929|112025|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848260|NCT00812929|112025|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848261|NCT00812929|112025|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848262|NCT00812929|112025|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848263|NCT00812929|112025|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848264|NCT01930058||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8876-003&kw=8876-003|
2848265|NCT06919185|2025-01028-01|Study Protocol|https://slmf.se/forskning/lungmedicinsk-forskning/sparc/|
2848266|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|
2848267|NCT05007457|Benedetta Isani|Study Protocol|http://aosp.bo.it|
2848268|NCT03125265||Study Protocol|http://bmjopen.bmj.com/content/5/3/e006897.long|
2848269|NCT00779766|107638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848270|NCT00779766|107638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848271|NCT00779766|107638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848272|NCT00779766|107638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848273|NCT00779766|107638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848274|NCT00779766|107638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850314|NCT01777334|117115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850315|NCT01777334|117115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850316|NCT01777334|117115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850317|NCT01777334|117115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850318|NCT01316887|113359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850319|NCT01316887|113359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850320|NCT01316887|113359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850321|NCT01316887|113359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850322|NCT01316887|113359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850323|NCT01316887|113359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850324|NCT01316887|113359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850325|NCT02446613|204509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850326|NCT02446613|204509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850327|NCT02446613|204509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850328|NCT02446613|204509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850329|NCT02446613|204509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850330|NCT02446613|204509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850331|NCT02446613|204509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850332|NCT00516139|LEP105972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850333|NCT00516139|LEP105972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850334|NCT00516139|LEP105972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850335|NCT00516139|LEP105972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850336|NCT00516139|LEP105972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850337|NCT00516139|LEP105972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850338|NCT00516139|LEP105972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850339|NCT01841697||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-026&kw=3102-026&tab=access|
2850340|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFNnVaQWlTakh5dEU|
2850341|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFazRhT1hZVm41RzA|05.01.2017 updated because of an amendment of ethnic proposal.
2850342|NCT02242643|201234|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850343|NCT02242643|201234|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850344|NCT02242643|201234|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845997|NCT00404378|NKV105093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850345|NCT02242643|201234|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850346|NCT02242643|201234|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850347|NCT02242643|201234|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850348|NCT02242643|201234|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850349|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
2850350|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
2850351|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
2845998|NCT00404378|NKV105093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845999|NCT00404378|NKV105093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846000|NCT00404378|NKV105093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846001|NCT01762774|114068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846002|NCT01762774|114068|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846003|NCT01762774|114068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846004|NCT01762774|114068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846005|NCT01762774|114068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846006|NCT01762774|114068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846007|NCT01762774|114068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846008|NCT00633074|111454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846009|NCT00633074|111454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846010|NCT00633074|111454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846011|NCT00633074|111454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846012|NCT00633074|111454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846013|NCT00633074|111454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846014|NCT00633074|111454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846015|NCT00758264|111393|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846016|NCT00758264|111393|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846017|NCT00758264|111393|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846018|NCT00758264|111393|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846019|NCT00758264|111393|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846020|NCT00758264|111393|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846021|NCT00758264|111393|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846022|NCT00306293|VLX105832|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846023|NCT00306293|VLX105832|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846024|NCT00306293|VLX105832|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846025|NCT00306293|VLX105832|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846026|NCT00306293|VLX105832|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846027|NCT00306293|VLX105832|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846028|NCT00306293|VLX105832|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846029|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
2846030|NCT01431937|114347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846031|NCT01431937|114347|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846032|NCT01431937|114347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846033|NCT01431937|114347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846034|NCT01431937|114347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846035|NCT01431937|114347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846036|NCT01431937|114347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846037|NCT00473668|104977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846038|NCT00473668|104977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846039|NCT00473668|104977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846040|NCT00473668|104977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846041|NCT00473668|104977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846042|NCT00473668|104977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846043|NCT04569136|DOI：10.6315/2009.37(4)06|Clinical Study Report|http://www.airitilibrary.com/Publication/alDetailedMesh?DocID=10253009-200912-201002050027-201002050027-261-268|
2846044|NCT03257202|HS-17-00319|Study Protocol|http://istar.usc.edu|
2846045|NCT03257202|HS-17-00319|Informed Consent Form|http://istar.usc.edu|
2846046|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
2846047|NCT05896098||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/14616599/|
2846048|NCT00697866|208129/037|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846049|NCT00697866|208129/037|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846050|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
2846051|NCT00697866|208129/037|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846052|NCT00697866|208129/037|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846053|NCT00697866|208129/037|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846054|NCT00519376|B2C110165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846055|NCT00519376|B2C110165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846056|NCT00519376|B2C110165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846057|NCT00519376|B2C110165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846058|NCT00519376|B2C110165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846059|NCT00519376|B2C110165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846060|NCT00519376|B2C110165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846061|NCT00625196|HZA102940|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846062|NCT00625196|HZA102940|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846063|NCT00625196|HZA102940|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846064|NCT00625196|HZA102940|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846065|NCT00625196|HZA102940|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846066|NCT00625196|HZA102940|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846067|NCT00625196|HZA102940|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846068|NCT00500058|ILI105618|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846069|NCT00500058|ILI105618|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846070|NCT00500058|ILI105618|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846071|NCT00500058|ILI105618|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846072|NCT00500058|ILI105618|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848275|NCT00779766|107638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846073|NCT00500058|ILI105618|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846074|NCT00500058|ILI105618|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852837|NCT00346775|FFR105693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852838|NCT00407979|SDY5|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY5|ImmPort study identifier is SDY5
2852839|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
2852840|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.
2846075|NCT01245738||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-204&kw=0000-204&tab=access|
2846076|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.
2846077|NCT00000593||Study Forms|http://biolincc.nhlbi.nih.gov/studies/vats/|
2846078|NCT05446792||Approval of the Ethics Committee for Research with Human Beings in Brazil|https://plataformabrasil.saude.gov.br/login.jsf|
2846079|NCT02998203||Manuscript and supplementary files|https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0219420|
2846080|NCT00964340|113312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846081|NCT00964340|113312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846082|NCT00964340|113312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846083|NCT00964340|113312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846084|NCT00964340|113312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846085|NCT00964340|113312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846086|NCT06660953||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37971133/|
2846087|NCT00316693|104798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846088|NCT00316693|104798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846089|NCT00316693|104798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846090|NCT00316693|104798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846091|NCT00316693|104798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846092|NCT00316693|104798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846093|NCT00908115|208355/128|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846094|NCT00908115|208355/128|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846095|NCT00908115|208355/128|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846096|NCT00908115|208355/128|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852841|NCT00000610||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/magic/|
2846097|NCT00908115|208355/128|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846098|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
2846099|NCT01165320||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0991-074&kw=0991-074&tab=access|
2846100|NCT01155466||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04938&kw=P04938&tab=access|
2846101|NCT03192020||Study Protocol|http://bmjopen.bmj.com/content/8/3/e019054|Protocol in BMJ Open access
2846102|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.
2846103|NCT00896363|109035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846104|NCT00896363|109035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846105|NCT00896363|109035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846106|NCT00896363|109035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846107|NCT00896363|109035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846108|NCT00896363|109035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852842|NCT00000610||Study Forms|http://biolincc.nhlbi.nih.gov/studies/magic/|
2852843|NCT06047886||Prodigy technical sheet|https://www.miltenyibiotec.com/US-en/products/clinimacs-prodigy.html|
2852844|NCT00540228|110794|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852845|NCT00540228|110794|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846109|NCT00896363|109035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852846|NCT00540228|110794|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846110|NCT01691885|116601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846111|NCT01691885|116601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846112|NCT01691885|116601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846113|NCT01691885|116601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846114|NCT01691885|116601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846115|NCT01691885|116601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846116|NCT01691885|116601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846117|NCT00559468||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846118|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
2846119|NCT00871117|111852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846120|NCT00871117|111852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852847|NCT00540228|110794|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852848|NCT00540228|110794|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850352|NCT00379769|BRL-049653/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850353|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
2850354|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
2850355|NCT00379769|BRL-049653/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850356|NCT00725712|MET111643|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850357|NCT00725712|MET111643|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850358|NCT00725712|MET111643|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850359|NCT00725712|MET111643|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850360|NCT00725712|MET111643|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850361|NCT00725712|MET111643|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850362|NCT00725712|MET111643|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850363|NCT05394090||Individual Participant Data Set|http://www.pum.edu.pl|
2850364|NCT01453023|112777|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850365|NCT01453023|112777|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850366|NCT01453023|112777|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850367|NCT01453023|112777|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850368|NCT01453023|112777|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850369|NCT01453023|112777|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850370|NCT01453023|112777|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850371|NCT00443209||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-012&kw=0974-012&tab=access|
2852849|NCT00540228|110794|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852850|NCT00403962|NKP103401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852851|NCT00403962|NKP103401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852852|NCT00403962|NKP103401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852853|NCT00403962|NKP103401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852854|NCT00403962|NKP103401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852855|NCT00403962|NKP103401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852856|NCT00403962|NKP103401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852857|NCT00329225|49653/347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852858|NCT00329225|49653/347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852859|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
2843874|NCT00323050|102547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843875|NCT00323050|102547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843876|NCT00323050|102547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843877|NCT00323050|102547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843878|NCT00323050|102547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852860|NCT00329225|49653/347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852861|NCT00329225|49653/347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852862|NCT00329225|49653/347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852863|NCT00570492|FFR101782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850372|NCT01245140|117221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850373|NCT01245140|117221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850374|NCT01245140|117221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850375|NCT01245140|117221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850376|NCT01245140|117221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850377|NCT01245140|117221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850378|NCT01245140|117221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850379|NCT01407276||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-009&kw=3102-009&tab=access|
2850380|NCT00092183||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850381|NCT04240249||Individual Participant Data Set|https://github.com/hmep/r2fu/|
2850382|NCT04240249||Analytic Code|https://github.com/hmep/r2fu/|
2850383|NCT00546078|109628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850384|NCT00546078|109628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850385|NCT00546078|109628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850386|NCT00546078|109628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850387|NCT00546078|109628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850388|NCT00546078|109628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850389|NCT00546078|109628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850390|NCT01431950|114496|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850391|NCT01431950|114496|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850392|NCT01431950|114496|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850393|NCT01431950|114496|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850394|NCT01431950|114496|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850395|NCT01431950|114496|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850396|NCT01431950|114496|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850397|NCT01381575|114700|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850398|NCT01381575|114700|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850399|NCT01381575|114700|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850400|NCT01381575|114700|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850401|NCT01381575|114700|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850402|NCT01381575|114700|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850403|NCT05688618||Study Protocol|https://drive.google.com/drive/u/0/folders/1JG22lkEchQULxW79ktlsVcM5uGNB4iVh|
2850404|NCT00383123|104858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850405|NCT00383123|104858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850406|NCT00383123|104858|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850407|NCT00383123|104858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850408|NCT00383123|104858|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850409|NCT00383123|104858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850410|NCT00383123|104858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850411|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.
2846121|NCT00871117|111852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846122|NCT00871117|111852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846123|NCT00871117|111852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846124|NCT00871117|111852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846125|NCT00871117|111852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846126|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27179664|
2846127|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27629371|
2846128|NCT06896500|Ethics Committee Application|Clinical Study Report|https://drive.google.com/file/d/19dj7wMiq4mPOobklxuHQObULyObAOvgc/view?usp=sharing|
2846129|NCT06896500|informed consent form|Informed Consent Form|https://docs.google.com/document/d/1PuTtTRr_LxSuZvbzWyvw3EQZYQ0VyA7b/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
2846130|NCT06896500|Vaginal flatus status form|Forms|https://docs.google.com/document/d/1kFejPnvwa_N52yM8A2UKoAgZ3s1uPYuw/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
2846131|NCT06896500|study main data|Study Protocol|https://drive.google.com/file/d/1yPsrrEh2E2eVLPD-_QtWy8F0rgT0dM9g/view?usp=sharing|
2846132|NCT06891469|https://doi.org/10.6084/m9.fig|Individual Participant Data Set|https://figshare.com|figshare
2846133|NCT03207321||Individual Participant Data Set|http://apcaps.lshtm.ac.uk/|
2846134|NCT00549900|107336|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846135|NCT00549900|107336|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846136|NCT00549900|107336|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846137|NCT00549900|107336|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848276|NCT01310413|114464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848277|NCT01310413|114464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848278|NCT01310413|114464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848279|NCT01310413|114464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848280|NCT01310413|114464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848281|NCT01310413|114464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848282|NCT01957189|200254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848283|NCT01957189|200254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848284|NCT01957189|200254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848285|NCT01957189|200254|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848286|NCT01957189|200254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848287|NCT01957189|200254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848288|NCT01957189|200254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848289|NCT01837316|116592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848290|NCT01837316|116592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848291|NCT01837316|116592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848292|NCT01837316|116592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848293|NCT01837316|116592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848294|NCT01837316|116592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848295|NCT01837316|116592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846138|NCT00549900|107336|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848296|NCT01706250|114550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846139|NCT00549900|107336|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846140|NCT00937404|112581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846141|NCT00937404|112581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846142|NCT00937404|112581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846143|NCT00937404|112581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846144|NCT00937404|112581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846145|NCT00937404|112581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846146|NCT02014480|116132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846147|NCT02014480|116132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846148|NCT02014480|116132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846149|NCT02014480|116132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846150|NCT02014480|116132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846151|NCT02014480|116132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846152|NCT02014480|116132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846153|NCT00624819|111345 (Mth 12)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846154|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
2846155|NCT00624819|111345 (Mth 12)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846156|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
2846157|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
2846158|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
2846159|NCT01224821|104731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846160|NCT01224821|104731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846161|NCT01224821|104731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846162|NCT01224821|104731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846163|NCT01224821|104731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846164|NCT01224821|104731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846165|NCT01224821|104731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846166|NCT06357091||results can be obtained from principal investigator|https://www.kh-schwaz.at/|results can be obtained from the principle investigator
2846167|NCT03630744||web page|http://fluidday.com|
2846168|NCT00379977|106345|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846169|NCT00379977|106345|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846170|NCT00379977|106345|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846171|NCT00379977|106345|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846172|NCT00379977|106345|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846173|NCT00379977|106345|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846174|NCT00035360||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846175|NCT03029078||Study Protocol|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003048-11/FR|
2846176|NCT00355342|SCO40041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846177|NCT00355342|SCO40041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850412|NCT06509360||Individual Participant Data Set|https://www.castoredc.com/|Individual participant data is collected anonymously in Castor EDC.
2850413|NCT00263653|103954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850414|NCT00263653|103954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850415|NCT00263653|103954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843879|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.
2850416|NCT00263653|103954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850417|NCT00263653|103954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850418|NCT00263653|103954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850419|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.
2850420|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.
2850421|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.
2850422|NCT01160237|114454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850423|NCT01160237|114454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850424|NCT01160237|114454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850425|NCT01160237|114454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850426|NCT01160237|114454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850427|NCT01160237|114454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850428|NCT01160237|114454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850429|NCT00344032|104479|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850430|NCT00344032|104479|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850431|NCT00344032|104479|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850432|NCT00344032|104479|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850433|NCT00344032|104479|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850434|NCT00344032|104479|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850435|NCT00390260||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850436|NCT00968526|113459|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848297|NCT01706250|114550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848298|NCT01706250|114550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848299|NCT01706250|114550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848300|NCT01706250|114550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848301|NCT05262205||Study Protocol|http://irb.mans.edu.eg|
2850437|NCT00968526|113459|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850438|NCT00968526|113459|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850439|NCT00968526|113459|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850440|NCT00968526|113459|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850441|NCT00968526|113459|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850442|NCT00968526|113459|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850443|NCT00479882||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-063&kw=0524B-063&tab=access|
2850444|NCT00334334|107005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850445|NCT00334334|107005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850446|NCT00334334|107005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850447|NCT00334334|107005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850448|NCT00334334|107005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850449|NCT00334334|107005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850450|NCT00632502||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05365&kw=7123-017&tab=access|
2850451|NCT04954326||Individual Participant Data Set|https://clinicaltrials.servier.com|
2850452|NCT04954326||Study Protocol|https://clinicaltrials.servier.com|
2850453|NCT04954326||Statistical Analysis Plan|https://clinicaltrials.servier.com|
2850454|NCT04954326||Informed Consent Form|https://clinicaltrials.servier.com|
2850455|NCT04954326||Clinical Study Report|https://clinicaltrials.servier.com|
2850456|NCT04954326||Study-level clinical trial data|https://clinicaltrials.servier.com|
2850457|NCT03567629||Individual Participant Data Set|https://en.wikipedia.org/wiki/United_States_National_Library_of_Medicine|
2850458|NCT00090155||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850459|NCT05555745||Statistical Analysis Plan|https://osf.io/zw5cq|
2850460|NCT00388440|209762/147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850461|NCT00388440|209762/147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850462|NCT00388440|209762/147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850463|NCT00388440|209762/147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850464|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
2850465|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
2850466|NCT03260478||Study Protocol|https://bmjopen.bmj.com/content/12/10/e067117.info|
2850467|NCT02718261|NCT02467621|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT02467621?term=SUP-ICU&rank=1|SUP-ICU Website
2850468|NCT00770744|2008-000479-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-000479-11/results|
2850469|NCT00678301|110521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850470|NCT00678301|110521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850471|NCT00678301|110521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850472|NCT00678301|110521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850473|NCT00678301|110521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850474|NCT00678301|110521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846178|NCT00355342|SCO40041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846179|NCT00355342|SCO40041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846180|NCT00355342|SCO40041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846181|NCT00355342|SCO40041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846182|NCT00355342|SCO40041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846183|NCT01357135||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-201&kw=0431-201&tab=access|
2846184|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.
2846185|NCT05455008||Individual Participant Data Set|https://iro.uiowa.edu/esploro/outputs/dataset/9984236057502771|
2846186|NCT01360398|114378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846187|NCT01360398|114378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846188|NCT01360398|114378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846189|NCT01360398|114378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846190|NCT01360398|114378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846191|NCT01360398|114378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846192|NCT01360398|114378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846193|NCT03745183||Study Protocol|https://drive.google.com/open?id=1ial1puH4ar075LyGcoWIrU1AXclt3FO-|
2846194|NCT03745183||Tables 1-5|https://drive.google.com/open?id=1pmZyUhTfoOPWRDJgEFjMsa_K9bvQ_Lon|
2846195|NCT03745183||Figure 1. Flow chart of the study procedure|https://drive.google.com/open?id=1MpUGMeNkzeOlThYZ_Zur4xTgt5cOvQNN|
2846196|NCT03745183||Informed Consent Form|https://drive.google.com/open?id=1kV91jvmtUDi_BA2paf-iszXb7bCnKHZO|
2846197|NCT03745183||Individual Participant Data Set|https://drive.google.com/open?id=1n3y-FDFc63KGyGfbkNBlpLJ-6HE9BBUZ|
2846198|NCT03745183||Appendix E. Illustrated checklist for the T'boli|https://drive.google.com/open?id=1t2b-wyQsJaTEy6qqJCiL4Opg-Hdvdxzj|
2846199|NCT03745183||Appendix F. Illustrated instruction on Senna alata decoction preparation|https://drive.google.com/open?id=17hMRr2-GhROnq7Gdw0Skd1KFApCpCgzy|
2846200|NCT00642148|MKI102428|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846201|NCT00642148|MKI102428|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846202|NCT00642148|MKI102428|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846203|NCT00642148|MKI102428|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846204|NCT00642148|MKI102428|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846205|NCT00642148|MKI102428|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846206|NCT00642148|MKI102428|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846207|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.
2846208|NCT00000558||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/peace/|
2846209|NCT00000558||Study Forms|http://biolincc.nhlbi.nih.gov/studies/peace/|
2846210|NCT00307567|105555|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846211|NCT00307567|105555|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846212|NCT00307567|105555|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846213|NCT00307567|105555|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846214|NCT00307567|105555|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846215|NCT00307567|105555|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846216|NCT01480609|115214|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846217|NCT01480609|115214|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846218|NCT01480609|115214|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846219|NCT01480609|115214|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846220|NCT01480609|115214|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846221|NCT01480609|115214|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846222|NCT01480609|115214|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846223|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
2846224|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
2846225|NCT00343915|101695 Ext. Mth30|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846226|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
2846227|NCT00343915|101695 Ext. Mth30|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846228|NCT00134732|103478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848302|NCT00586469|111258|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848303|NCT00586469|111258|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848304|NCT00586469|111258|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848305|NCT00586469|111258|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848306|NCT00586469|111258|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848307|NCT00586469|111258|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848308|NCT00586469|111258|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848309|NCT00482079||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848310|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.
2848311|NCT00075829|BMT CTN-0102|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
2848312|NCT00075829|BMT CTN-0102|Study Forms|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
2848313|NCT00263692|213503/047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848314|NCT00263692|213503/047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848315|NCT00263692|213503/047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848316|NCT00263692|213503/047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848317|NCT00263692|213503/047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848318|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
2848319|NCT00094380|SDY798|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY798|ImmPort study identifier is SDY798.
2848320|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.
2848321|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.
2848322|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.
2848323|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.
2848324|NCT07086287|rhBNP|Study Protocol|https://www.chictr.org.cn/|China Clinical Trial Registration Center
2848325|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.
2848326|NCT01978119|115645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846229|NCT00134732|103478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846230|NCT00134732|103478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846231|NCT00134732|103478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846232|NCT00134732|103478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846233|NCT00134732|103478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846234|NCT00289198|FFR106080|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846235|NCT00289198|FFR106080|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846236|NCT00289198|FFR106080|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846237|NCT00289198|FFR106080|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846238|NCT00289198|FFR106080|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846239|NCT00289198|FFR106080|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846240|NCT00289198|FFR106080|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846241|NCT04786418||Study Protocol|http://www.directclinicaltrial.org.uk|
2846242|NCT06367907|SM 68/6-1|Study Protocol|https://gepris.dfg.de/gepris/projekt/424869737|
2846243|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
2846244|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
2846245|NCT00363727|101468/228|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846246|NCT00363727|101468/228|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846247|NCT00363727|101468/228|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846248|NCT00363727|101468/228|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846249|NCT00363727|101468/228|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846250|NCT00474617||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846251|NCT07041424||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28955539/|
2846252|NCT00354666|B2E101312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846253|NCT00354666|B2E101312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846254|NCT00354666|B2E101312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846255|NCT00354666|B2E101312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846256|NCT00354666|B2E101312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846257|NCT01636713|114634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846258|NCT01636713|114634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846259|NCT01636713|114634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846260|NCT01636713|114634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846261|NCT01636713|114634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848327|NCT01978119|115645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846262|NCT01636713|114634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846263|NCT01636713|114634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846264|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
2846265|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
2846266|NCT00126984|104703 (Primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848328|NCT01978119|115645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848329|NCT01978119|115645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848330|NCT01978119|115645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848331|NCT01978119|115645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848332|NCT00812812|112487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848333|NCT00812812|112487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848334|NCT00812812|112487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848335|NCT00812812|112487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848336|NCT04891679|PATIENT INFORMATION SHEET|Informed Consent Form|https://figshare.com/s/a6c10a2a4be65f30144b|
2848337|NCT04891679|STUDY PROTOCOL|Study Protocol|https://figshare.com/s/3f978a10eee4e90173bb|
2848338|NCT01181895|112060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848339|NCT01181895|112060|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848340|NCT01181895|112060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848341|NCT01181895|112060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852864|NCT00570492|FFR101782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852865|NCT00570492|FFR101782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852866|NCT00570492|FFR101782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852867|NCT00570492|FFR101782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852868|NCT00570492|FFR101782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852869|NCT00570492|FFR101782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852870|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.
2852871|NCT01711736|116926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852872|NCT01711736|116926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852873|NCT01711736|116926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852874|NCT01711736|116926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852875|NCT01711736|116926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852876|NCT01711736|116926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852877|NCT01852565|115679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852878|NCT01852565|115679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852879|NCT01852565|115679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852880|NCT01852565|115679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852881|NCT01852565|115679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852882|NCT01852565|115679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852883|NCT01852565|115679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852884|NCT01590810||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-001&kw=8150-001&tab=access|
2852885|NCT01231620|114373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852886|NCT01231620|114373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852887|NCT01231620|114373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848342|NCT01181895|112060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848343|NCT01181895|112060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848344|NCT01181895|112060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848345|NCT00338351|106208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848346|NCT00338351|106208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848347|NCT00338351|106208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848348|NCT00338351|106208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848349|NCT00338351|106208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848350|NCT00338351|106208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848351|NCT00701389||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-026&kw=0974-026&tab=access|
2848352|NCT00298831||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848353|NCT01003418|113629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848354|NCT01003418|113629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848355|NCT01003418|113629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848356|NCT01003418|113629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848357|NCT01003418|113629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848358|NCT01003418|113629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848359|NCT02143518||Clinical Study Report|https://gwvru.smhs.gwu.edu/clinical|
2848360|NCT02696850|CGI scale|Questionnaire|https://www.psywellness.com.sg/docs/CGI.pdf|
2848361|NCT01814722||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-266&kw=0518-266&tab=access|
2848362|NCT00432380|109216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848363|NCT00432380|109216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848364|NCT00432380|109216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848365|NCT00432380|109216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848366|NCT00432380|109216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848367|NCT00432380|109216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848368|NCT00432380|109216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848369|NCT01267071|114136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848370|NCT01267071|114136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848371|NCT01267071|114136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848372|NCT01267071|114136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848373|NCT01267071|114136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848374|NCT01267071|114136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848375|NCT01267071|114136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848376|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
2848377|NCT00774995|110073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848378|NCT00774995|110073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848379|NCT00774995|110073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848380|NCT00774995|110073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843880|NCT01295320|114825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843881|NCT01295320|114825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843882|NCT01295320|114825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843883|NCT01295320|114825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843884|NCT01295320|114825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843885|NCT01295320|114825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843886|NCT01295320|114825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843887|NCT01887171|10.15825/1995-1191-2015-3-24|Clinical Study Report|http://journal.transpl.ru/vtio/article/view/561/488|
2843888|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|
2843889|NCT00463697|B2C106996|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843890|NCT00463697|B2C106996|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843891|NCT00463697|B2C106996|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843892|NCT00463697|B2C106996|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843893|NCT00463697|B2C106996|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843894|NCT00463697|B2C106996|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843895|NCT00463697|B2C106996|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843896|NCT00306995|102499|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843897|NCT00306995|102499|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843898|NCT00306995|102499|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843899|NCT00306995|102499|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843900|NCT00306995|102499|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843901|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
2843902|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
2843903|NCT05063708||Analytic Code|http://zenodo.org|
2843904|NCT05063708||Statistical Analysis Plan|http://zenodo.org|
2843905|NCT00307021|105874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843906|NCT00307021|105874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843907|NCT00307021|105874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843908|NCT00307021|105874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843909|NCT00307021|105874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843910|NCT00307021|105874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846267|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
2846268|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.
2846269|NCT00126984|104703 (Primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846270|NCT06979739||Informed Consent Form|https://www.hku.edu.tr/iletisim/|
2846271|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
2846272|NCT02011490||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-105&kw=8616-105&tab=access|
2846273|NCT00306644|49653/334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846274|NCT00306644|49653/334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846275|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
2846276|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
2846277|NCT00306644|49653/334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846278|NCT00306644|49653/334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846279|NCT00306644|49653/334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846280|NCT00320463|105910|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846281|NCT00320463|105910|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846282|NCT00320463|105910|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846283|NCT00320463|105910|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846284|NCT00320463|105910|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846285|NCT00320463|105910|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846286|NCT00422994|RRL103628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852888|NCT01231620|114373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852889|NCT01231620|114373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852890|NCT01231620|114373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852891|NCT01231620|114373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852892|NCT06724874||Individual Participant Data Set|https://www.stat.ubc.ca/~rollin/stats/ssize/n2.html|
2846287|NCT00422994|RRL103628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846288|NCT00422994|RRL103628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846289|NCT00422994|RRL103628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846290|NCT00422994|RRL103628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846291|NCT00422994|RRL103628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846292|NCT00422994|RRL103628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846293|NCT00969436|109995|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846294|NCT00969436|109995|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846295|NCT00969436|109995|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846296|NCT00969436|109995|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852893|NCT00455572|107240|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846297|NCT00969436|109995|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846298|NCT00969436|109995|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846299|NCT00969436|109995|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846300|NCT01762813||Study Protocol|http://translational-medicine.biomedcentral.com/articles/10.1186/s12967-016-0951-4|
2846301|NCT00353873|SAM104926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846302|NCT00353873|SAM104926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846303|NCT00353873|SAM104926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846304|NCT00353873|SAM104926|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846305|NCT00353873|SAM104926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846306|NCT00353873|SAM104926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846307|NCT00353873|SAM104926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846308|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/0310250742582348|
2846309|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/1823080587913061|
2846310|NCT01669083|116741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846311|NCT01669083|116741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846312|NCT01669083|116741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846313|NCT01669083|116741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846314|NCT01669083|116741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846315|NCT01669083|116741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846316|NCT01669083|116741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846317|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
2846318|NCT06103929||Individual Participant Data Set|https://le.ac.uk/people/sam-tromans|
2846319|NCT06103929||Study Protocol|https://le.ac.uk/people/sam-tromans|
2846320|NCT06103929||Statistical Analysis Plan|https://le.ac.uk/people/sam-tromans|
2846321|NCT06103929||Informed Consent Form|https://le.ac.uk/people/sam-tromans|
2846322|NCT00475215||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846323|NCT00307554|105553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846324|NCT00307554|105553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846325|NCT00307554|105553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846326|NCT00307554|105553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846327|NCT00307554|105553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846328|NCT00307554|105553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846329|NCT05936528||Individual Participant Data Set|https://drive.google.com/drive/folders/1CBAPVtAVYsi2x1iLQdWl48b9OowGSxw9|
2846330|NCT01521377|114635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846331|NCT01521377|114635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846332|NCT01521377|114635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846333|NCT01521377|114635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846334|NCT01521377|114635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846335|NCT01521377|114635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846336|NCT01521377|114635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846337|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
2846338|NCT00652951|110142|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850475|NCT00678301|110521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850476|NCT01939353||Poster Abstracts|https://apsard.org/wp-content/uploads/2016/11/Poster-Abstracts-Compiled1.pdf|Poster number 25
2850477|NCT03266926||Study Protocol|https://www.scribd.com/document/344597619/Study-Protocol|
2850478|NCT03266926||Informed Consent Form|https://www.scribd.com/document/344597523/Consent-Form|
2850479|NCT03266926||Individual Participant Data Set|https://www.scribd.com/document/344597573/Data-Collection-Spreadsheet|
2850480|NCT03266926||Participant Documents|https://www.scribd.com/document/344597424/Participant-Documents|
2850481|NCT07124052|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
2852894|NCT00455572|107240|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843911|NCT01332292|102942|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843912|NCT01332292|102942|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843913|NCT01332292|102942|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843914|NCT01332292|102942|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843915|NCT01332292|102942|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843916|NCT01332292|102942|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843917|NCT01332292|102942|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843918|NCT00511823|NKV110483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843919|NCT00511823|NKV110483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843920|NCT00511823|NKV110483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843921|NCT00511823|NKV110483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843922|NCT00511823|NKV110483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843923|NCT00511823|NKV110483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843924|NCT00511823|NKV110483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843925|NCT00562848|MOT107043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843926|NCT00562848|MOT107043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843927|NCT00562848|MOT107043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843928|NCT00562848|MOT107043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843929|NCT00562848|MOT107043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843930|NCT00562848|MOT107043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843931|NCT00562848|MOT107043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850482|NCT00972322||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8245-012&kw=8245-012&tab=access|
2850483|NCT01132443|115902|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850484|NCT01132443|115902|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850485|NCT01132443|115902|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850486|NCT01132443|115902|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850487|NCT01132443|115902|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850488|NCT01132443|115902|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850489|NCT01132443|115902|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850490|NCT01725126|116623|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850491|NCT01725126|116623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850492|NCT01725126|116623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848381|NCT00774995|110073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848382|NCT00774995|110073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848383|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.
2848384|NCT00264615|LEP103944|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848385|NCT00264615|LEP103944|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848386|NCT00264615|LEP103944|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848387|NCT00264615|LEP103944|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848388|NCT00264615|LEP103944|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848389|NCT00264615|LEP103944|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848390|NCT00264615|LEP103944|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848391|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.
2848392|NCT00129259|SDY524|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY524|ImmPort study identifier is SDY524.
2848393|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.
2848394|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.
2848395|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.
2848396|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
2848397|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
2848398|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.
2848399|NCT00797667||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-049&kw=0974-049&tab=access|
2848400|NCT00420680||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848401|NCT02207829|201316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843932|NCT01198769|114351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843933|NCT01198769|114351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843934|NCT01198769|114351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843935|NCT01198769|114351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843936|NCT01198769|114351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843937|NCT01198769|114351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843938|NCT01198769|114351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843939|NCT03718832|doi:10.7910/DVN/LZUTU0|Individual Participant Data Set|https://doi.org/10.7910/DVN/LZUTU0|
2843940|NCT03718832|doi:10.7910/DVN/LZUTU0|Analytic Code|https://doi.org/10.7910/DVN/LZUTU0|
2843941|NCT00810667|2008-001441-26|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-001441-26/results|
2843942|NCT07192640||Study Protocol|https://doi.org/10.1590/acb370702|https://doi.org/10.1590/acb370702
2843943|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.
2843944|NCT03173209|Calm Moments Cards program|intervention materials|http://www.everymomentcounts.org|Calm Moments Cards program
2843945|NCT00696423|111535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846339|NCT00652951|110142|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846340|NCT00652951|110142|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846341|NCT00652951|110142|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846342|NCT00652951|110142|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846343|NCT00652951|110142|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846344|NCT01462617|115117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846345|NCT01462617|115117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846346|NCT01462617|115117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846347|NCT01462617|115117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846348|NCT01462617|115117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846349|NCT01462617|115117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846350|NCT01462617|115117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846351|NCT00945932|112851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846352|NCT00945932|112851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846353|NCT00945932|112851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846354|NCT00945932|112851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846355|NCT00945932|112851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846356|NCT00945932|112851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846357|NCT00945932|112851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846358|NCT00231413|102115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846359|NCT00231413|102115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846360|NCT00231413|102115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846361|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.
2846362|NCT00231413|102115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846363|NCT00231413|102115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846364|NCT03696901|Xydalba|Study Protocol|https://awbdb.bfarm.de/ords/f?p=101:STARTSEITE::::::|BfArM AWB Datenbank
2846365|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
2846366|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.
2846367|NCT01381536|114243|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846368|NCT01381536|114243|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846369|NCT01381536|114243|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846370|NCT01381536|114243|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846371|NCT01381536|114243|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846372|NCT01381536|114243|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846373|NCT00771615|111729|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846374|NCT00771615|111729|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846375|NCT00771615|111729|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846376|NCT00771615|111729|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846377|NCT00771615|111729|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846378|NCT00771615|111729|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846379|NCT00771615|111729|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846380|NCT01300455||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-036&kw=4305-036&tab=access|
2846381|NCT01147900|113055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846382|NCT01147900|113055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846383|NCT01147900|113055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846384|NCT01147900|113055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846385|NCT01147900|113055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846386|NCT01147900|113055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846387|NCT01209078|113414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846388|NCT01209078|113414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846389|NCT01209078|113414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846390|NCT01209078|113414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846391|NCT01209078|113414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846392|NCT01209078|113414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846393|NCT01209078|113414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846394|NCT06583694||Clinical Study Report|https://www.bangkoknoimodel.com/stat.|
2846395|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
2846396|NCT01600092||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-035&kw=V260-035&tab=access|
2846397|NCT04303299|Thai government data|Data references|https://ddc.moph.go.th|
2846398|NCT04303299||News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
2846399|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)
2846400|NCT04303299||Reference News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
2846401|NCT04892108||Study Protocol|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
2846402|NCT04892108||Statistical Analysis Plan|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
2846403|NCT04892108||Informed Consent Form|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
2846404|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.
2846405|NCT00343707|NKP102280|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846406|NCT00343707|NKP102280|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846407|NCT00343707|NKP102280|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846408|NCT00343707|NKP102280|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848402|NCT02207829|201316|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848403|NCT02207829|201316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846409|NCT00343707|NKP102280|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846410|NCT00343707|NKP102280|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846411|NCT00778895|111635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846412|NCT00778895|111635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846413|NCT00778895|111635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846414|NCT00778895|111635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843946|NCT00696423|111535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843947|NCT00696423|111535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843948|NCT00696423|111535|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843949|NCT00696423|111535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843950|NCT00696423|111535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843951|NCT00696423|111535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843952|NCT07192172|No. 1611-124-811|Study Protocol|http://cris.snuh.org|http://cris.snuh.org
2843953|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.
2843954|NCT01847404|116480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843955|NCT01847404|116480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843956|NCT01847404|116480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843957|NCT01847404|116480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843958|NCT01847404|116480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843959|NCT01847404|116480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843960|NCT00695305|LP2105521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843961|NCT00695305|LP2105521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843962|NCT00695305|LP2105521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843963|NCT00695305|LP2105521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843964|NCT00695305|LP2105521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843965|NCT00695305|LP2105521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843966|NCT00695305|LP2105521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843967|NCT01110018|112008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843968|NCT01110018|112008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843969|NCT01110018|112008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843970|NCT01110018|112008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843971|NCT01110018|112008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843972|NCT01110018|112008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843973|NCT01110018|112008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843974|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.
2843975|NCT01557504||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-296&kw=0431A-296&tab=access|
2843976|NCT01254643||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-008&kw=V503-008&tab=access|
2843977|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.
2852895|NCT00455572|107240|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852896|NCT00455572|107240|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843978|NCT03411161||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2843979|NCT03411161||Study Protocol|https://clinicaltrials.servier.com/|
2843980|NCT03411161||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2843981|NCT03411161||Informed Consent Form|https://clinicaltrials.servier.com/|
2843982|NCT03411161||Clinical Study Report|https://clinicaltrials.servier.com/|
2843983|NCT03411161||study-level clinical trial data|https://clinicaltrials.servier.com/|
2843984|NCT01563042|114594|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850493|NCT01725126|116623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850494|NCT01725126|116623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850495|NCT01725126|116623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850496|NCT01725126|116623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850497|NCT01734239||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V110-018&kw=V110-018&tab=access|
2850498|NCT04728139||Study Protocol|http://rehamhany809@gmail.com|
2850499|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.
2850500|NCT00586612|110215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850501|NCT00586612|110215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850502|NCT00586612|110215|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850503|NCT00586612|110215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850504|NCT00586612|110215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850505|NCT00586612|110215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852897|NCT00455572|107240|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852898|NCT00455572|107240|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852899|NCT00455572|107240|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852900|NCT01587716|115658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852901|NCT01587716|115658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852902|NCT01587716|115658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852903|NCT01587716|115658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852904|NCT01587716|115658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852905|NCT01587716|115658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852906|NCT01587716|115658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852907|NCT05814744||Individual Participant Data Set|https://drive.google.com/file/d/12gNVWYJj8dyy6Bh-6G59rFn2AQzjHycS/view?usp=share_link|
2852908|NCT05814744||Informed Consent Form|https://drive.google.com/file/d/1qPpYheG63CcWJqwWAD3ma3jFmmqCPWgm/view?usp=share_link|
2852909|NCT05814744||Study Protocol|https://drive.google.com/file/d/16x_dHL6GsO6V-K3p13T9EluZi20l4WtN/view?usp=share_link|
2852910|NCT01366846|LEAP-On (ITN049AD)|Individual Participant Data Set|https://www.itntrialshare.org/|
2852911|NCT01366846|LEAP-On (ITN049AD)|Study protocol synopsis; datasets and figures from published NEJM 2016 article|https://www.itntrialshare.org/|
2852912|NCT03350880||Clinical Study Report|https://periodicos.unicesumar.edu.br/index.php/saudpesq/article/view/9938|
2852913|NCT01439308|111925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852914|NCT01439308|111925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852915|NCT01439308|111925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852916|NCT01439308|111925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852917|NCT01439308|111925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852918|NCT01439308|111925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852919|NCT01439308|111925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852920|NCT06934421||Study Protocol|https://osf.io/8ywq6/|
2852921|NCT06934421||Statistical Analysis Plan|https://osf.io/8ywq6/|
2852922|NCT06934421||Informed Consent Form|https://osf.io/8ywq6/|
2852923|NCT06934421||Analytic Code|https://osf.io/8ywq6/|
2852924|NCT06934421||Individual Participant Data Set|https://osf.io/8ywq6/|
2852925|NCT03626337||Statistical Analysis Plan|https://osf.io/jfke3/|
2852926|NCT03473821||Statistical Analysis Plan|https://lucris.lub.lu.se/admin/files/138815992/MOTIFS_Data_Management_Protocol_1.6_2023_02_24.pdf|
2852927|NCT00968539|113456|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846415|NCT00778895|111635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846416|NCT00778895|111635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846417|NCT01147848|113091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846418|NCT01147848|113091|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846419|NCT01147848|113091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846420|NCT01147848|113091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846421|NCT01147848|113091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846422|NCT01147848|113091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846423|NCT01147848|113091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846424|NCT02891382||Individual Participant Data Set|https://figshare.com/articles/REDEEM_Study_Feasibility_pilot_study/7180802|
2846425|NCT00148941|213503/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846426|NCT00148941|213503/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846427|NCT00148941|213503/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846428|NCT00148941|213503/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846429|NCT00148941|213503/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846430|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
2846431|NCT04904848||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/25437107/|
2846432|NCT02747017||Study Protocol|http://insight.ccbr.umn.edu/official_documents/CDIFF/protocol_documents/I7-Protocol.pdf|
2846433|NCT05502510||Analytic Code|https://osf.io/bty8n/?view_only=f8bb6e5a7698443494d4c3788a45cc0f|The analytic code will be uploaded to OSF upon publishing the manuscript.
2846434|NCT04657783||Study Protocol|https://drive.google.com/drive/my-drive|
2846435|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
2846436|NCT01431963|115376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846437|NCT01431963|115376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846438|NCT01431963|115376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846439|NCT01431963|115376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846440|NCT01431963|115376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846441|NCT02964767||Epidemiological report|http://www.who.int|
2846442|NCT02964767||Clinical Study Report|http://www.Wiley.com|
2846443|NCT01000324|112267|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846444|NCT01000324|112267|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846445|NCT01000324|112267|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846446|NCT01000324|112267|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846447|NCT01000324|112267|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846448|NCT01000324|112267|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846449|NCT01000324|112267|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846450|NCT01853878|116389|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846451|NCT01853878|116389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846452|NCT01853878|116389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846453|NCT01853878|116389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846454|NCT01853878|116389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843985|NCT01563042|114594|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843986|NCT01563042|114594|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848404|NCT02207829|201316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848405|NCT02207829|201316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848406|NCT02207829|201316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848407|NCT02207829|201316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848408|NCT01476046|110951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848409|NCT01476046|110951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848410|NCT01476046|110951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848411|NCT01476046|110951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848412|NCT01476046|110951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848413|NCT01476046|110951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848414|NCT01476046|110951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848415|NCT01319006|114703|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848416|NCT01319006|114703|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848417|NCT01319006|114703|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848418|NCT01319006|114703|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848419|NCT01319006|114703|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848420|NCT01319006|114703|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848421|NCT01319006|114703|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848422|NCT00289796|210602-002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848423|NCT00289796|210602-002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848424|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
2848425|NCT00289796|210602-002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848426|NCT00289796|210602-002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848427|NCT00289796|210602-002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848428|NCT00560833||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06459&kw=P06459&tab=access|
2848429|NCT01059617|113483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848430|NCT01059617|113483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848431|NCT01059617|113483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848432|NCT01059617|113483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848433|NCT01059617|113483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848434|NCT01059617|113483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848435|NCT00605241|DAN106593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848436|NCT00605241|DAN106593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848437|NCT00605241|DAN106593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848438|NCT00605241|DAN106593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848439|NCT00605241|DAN106593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852928|NCT00968539|113456|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852929|NCT00968539|113456|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852930|NCT00968539|113456|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852931|NCT00968539|113456|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852932|NCT00968539|113456|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852933|NCT00968539|113456|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852934|NCT04631432||Statistical Analysis Plan|https://docs.google.com/document/d/16IlMPOgJMoh8tLIhB4JK5yeHI-0MfJVvRnQ8PdNp8-o/edit?usp=sharing|
2852935|NCT04631432||Study Protocol|https://drive.google.com/file/d/1YoXgB4ifoeu2Z8OnG6_hVWP4sBLRp9wP/view?usp=sharing|
2852936|NCT04631432||Informed Consent Form|https://drive.google.com/file/d/1WHJz01_y_b-gO4ZpZNAQsnqNf_SwdwNX/view?usp=sharing|
2852937|NCT01867996|116073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852938|NCT01867996|116073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852939|NCT01867996|116073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852940|NCT01867996|116073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852941|NCT01867996|116073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852942|NCT01867996|116073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852943|NCT01867996|116073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852944|NCT00326118|106445|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852945|NCT00326118|106445|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852946|NCT00326118|106445|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852947|NCT00326118|106445|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852948|NCT00326118|106445|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852949|NCT00326118|106445|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852950|NCT00938392|112662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852951|NCT00938392|112662|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852952|NCT00938392|112662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852953|NCT00938392|112662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852954|NCT00938392|112662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852955|NCT00938392|112662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852956|NCT00938392|112662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852957|NCT01817764|114930|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852958|NCT01817764|114930|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852959|NCT01817764|114930|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852960|NCT01817764|114930|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852961|NCT01817764|114930|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852962|NCT01817764|114930|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852963|NCT01817764|114930|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852964|NCT01453296|112776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852965|NCT01453296|112776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852966|NCT01453296|112776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850506|NCT00635128|110947|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850507|NCT00635128|110947|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850508|NCT00635128|110947|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850509|NCT00635128|110947|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850510|NCT00635128|110947|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850511|NCT00635128|110947|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850512|NCT00635128|110947|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850513|NCT04110704|IRAS 261294|Study Protocol|http://preview-kcl.cloud.contensis.com/Preview/1/research/project?id=478a6e61-4446-4a12-945e-c41a3879371d|
2850514|NCT01333813|112688|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850515|NCT01333813|112688|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850516|NCT01333813|112688|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850517|NCT01333813|112688|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850518|NCT01333813|112688|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850519|NCT01333813|112688|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850520|NCT01376232|113634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850521|NCT01376232|113634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850522|NCT01376232|113634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850523|NCT01376232|113634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850524|NCT01376232|113634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850525|NCT01376232|113634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850526|NCT01376232|113634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850527|NCT02145468|116197|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850528|NCT02145468|116197|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850529|NCT02145468|116197|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850530|NCT02145468|116197|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850531|NCT02145468|116197|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850532|NCT02145468|116197|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850533|NCT02145468|116197|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850534|NCT02963025||Study Protocol|http://prothor.info|
2850535|NCT00091559||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850536|NCT01353768|115008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850537|NCT01353768|115008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850538|NCT01353768|115008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850539|NCT01353768|115008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850540|NCT01353768|115008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850541|NCT01353768|115008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850542|NCT01353768|115008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850543|NCT00109330|776423/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852967|NCT01453296|112776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846455|NCT01853878|116389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846456|NCT01853878|116389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846457|NCT00871338|111709|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846458|NCT00871338|111709|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846459|NCT00871338|111709|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846460|NCT00871338|111709|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846461|NCT00871338|111709|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846462|NCT00871338|111709|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846463|NCT00871338|111709|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846464|NCT00383162|TRX106571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846465|NCT00383162|TRX106571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846466|NCT00383162|TRX106571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846467|NCT00383162|TRX106571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846468|NCT00383162|TRX106571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846469|NCT00383162|TRX106571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846470|NCT00383162|TRX106571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846471|NCT00348309|AVA102672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846472|NCT00348309|AVA102672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846473|NCT00348309|AVA102672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846474|NCT00348309|AVA102672|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846475|NCT00348309|AVA102672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846476|NCT00348309|AVA102672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846477|NCT00348309|AVA102672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846478|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
2846479|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
2846480|NCT00500955|BRL-49653/137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846481|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
2846482|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
2846483|NCT00500955|BRL-49653/137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846484|NCT00954993||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-029&kw=7009-029&tab=access|
2846485|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
2846486|NCT00326248|NKT102553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846487|NCT00326248|NKT102553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846488|NCT00326248|NKT102553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846489|NCT00326248|NKT102553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846490|NCT00326248|NKT102553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846491|NCT00326248|NKT102553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846492|NCT00326248|NKT102553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848440|NCT00605241|DAN106593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848441|NCT00605241|DAN106593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848442|NCT06633263||Study Protocol|https://osf.io/dhmj8/|
2848443|NCT06633263||Individual Participant Data Set|https://osf.io/dhmj8/|
2852968|NCT01453296|112776|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852969|NCT01453296|112776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852970|NCT01453296|112776|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852971|NCT00005009|SDY357|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357.
2852972|NCT00005009|SDY357|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357
2852973|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
2852974|NCT01016366|2008-003662-25|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-003662-25/results|
2852975|NCT06107348|10.17605/OSF.IO/2MGJK|Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
2852976|NCT00109278||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2852977|NCT02437175||Methodology paper|https://www.dovepress.com/articles.php?article_id=25534|
2852978|NCT03196960||Scoring Sheet|https://docs.google.com/document/d/1pqYbMe4S-W-vgYRHzd1d4Is7s6ZbMt_MGDlWtndRRdM/edit?usp=sharing|Mobilization Quantification Score
2852979|NCT00471237|CR9108963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852980|NCT00471237|CR9108963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852981|NCT00471237|CR9108963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848444|NCT02019719|116099|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848445|NCT02019719|116099|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848446|NCT02019719|116099|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848447|NCT02019719|116099|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848448|NCT02019719|116099|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848449|NCT02019719|116099|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848450|NCT02019719|116099|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848451|NCT06635343||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28990891|
2848452|NCT06333444||Informed Consent Form|https://docs.google.com/forms/d/e/1FAIpQLScX9N2R8xP62390ly7vV8Ixyy_yfQsUUmUG3QCm_M-ZriXAnA/viewform|
2848453|NCT00941603||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05675&kw=P05675&tab=access|
2848454|NCT00345579|105987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848455|NCT00345579|105987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852982|NCT00471237|CR9108963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852983|NCT00471237|CR9108963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852984|NCT00471237|CR9108963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852985|NCT00471237|CR9108963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852986|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/106014|
2852987|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/143046|
2852988|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889771|
2852989|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889781|
2848456|NCT00345579|105987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852990|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889773|
2852991|NCT00538473|110223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848457|NCT00345579|105987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852992|NCT00538473|110223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846493|NCT01112787|114571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846494|NCT01112787|114571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846495|NCT01112787|114571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846496|NCT01112787|114571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846497|NCT01112787|114571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846498|NCT01112787|114571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846499|NCT01112787|114571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846500|NCT00532298|110620|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846501|NCT00532298|110620|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846502|NCT00532298|110620|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846503|NCT00532298|110620|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846504|NCT00532298|110620|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846505|NCT00532298|110620|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846506|NCT00532298|110620|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846507|NCT03191227||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22984148|Cohort profile
2846508|NCT00240500|100448|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846509|NCT00240500|100448|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846510|NCT00240500|100448|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846511|NCT00240500|100448|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846512|NCT00240500|100448|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846513|NCT01053988|112206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846514|NCT01053988|112206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846515|NCT01053988|112206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846516|NCT01053988|112206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846517|NCT01053988|112206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846518|NCT01053988|112206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846519|NCT01053988|112206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846520|NCT01324362|SAM40065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846521|NCT01324362|SAM40065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846522|NCT01324362|SAM40065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846523|NCT01324362|SAM40065|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846524|NCT01324362|SAM40065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846525|NCT01324362|SAM40065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846526|NCT01324362|SAM40065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846527|NCT01140061||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-020&kw=0873-020&tab=access|
2846528|NCT00274677|SCA100223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846529|NCT00274677|SCA100223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846530|NCT00274677|SCA100223|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846531|NCT00274677|SCA100223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846532|NCT00274677|SCA100223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846533|NCT00274677|SCA100223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846534|NCT00274677|SCA100223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846535|NCT02371603|200229|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846536|NCT02371603|200229|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846537|NCT02371603|200229|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846538|NCT02371603|200229|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846539|NCT02371603|200229|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846540|NCT02371603|200229|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846541|NCT03214068||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282811/|
2846542|NCT01870115||Publication|http://www.aging-us.com/article/101158|
2846543|NCT04119180||Study Protocol|https://bmcoralhealth.biomedcentral.com/articles/10.1186/s12903-021-01594-0|
2846544|NCT00398099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846545|NCT06040853|doi: 10.1371|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28282425/|
2846546|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|
2846547|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.
2846548|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.
2846549|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:"
2846550|NCT01957202|200286|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846551|NCT01957202|200286|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846552|NCT01957202|200286|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846553|NCT01957202|200286|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846554|NCT01957202|200286|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846555|NCT01957202|200286|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846556|NCT01957202|200286|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846557|NCT00250276|104772|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846558|NCT00250276|104772|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846559|NCT00250276|104772|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846560|NCT00250276|104772|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846561|NCT00250276|104772|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846562|NCT00250276|104772|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846563|NCT00250276|104772|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846564|NCT01196026|114451|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846565|NCT01196026|114451|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846566|NCT01196026|114451|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846567|NCT01196026|114451|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846568|NCT01196026|114451|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846569|NCT01196026|114451|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846570|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
2846571|NCT00799903|100601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846572|NCT00799903|100601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846573|NCT00799903|100601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846574|NCT00799903|100601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846575|NCT00799903|100601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850544|NCT00109330|776423/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850545|NCT00109330|776423/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850546|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
2850547|NCT00109330|776423/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850548|NCT00109330|776423/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850549|NCT00056277|SCA30924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850550|NCT00056277|SCA30924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850551|NCT00056277|SCA30924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850552|NCT00056277|SCA30924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846576|NCT00799903|100601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850553|NCT00056277|SCA30924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850554|NCT00056277|SCA30924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850555|NCT00056277|SCA30924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850556|NCT05931913||Individual Participant Data Set|https://nda.nih.gov/|
2850557|NCT04340791||Study Protocol|https://osf.io/kq9c8/|
2850558|NCT04340791||Statistical Analysis Plan|https://osf.io/kq9c8/|
2850559|NCT04340791||Informed Consent Form|https://osf.io/kq9c8/|
2850560|NCT04340791||Individual Participant Data Set|https://osf.io/kq9c8/|When results will be published
2850561|NCT00989625|108504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850562|NCT00989625|108504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852993|NCT00538473|110223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852994|NCT00538473|110223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852995|NCT00538473|110223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852996|NCT00538473|110223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843987|NCT01563042|114594|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843988|NCT01563042|114594|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843989|NCT01563042|114594|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843990|NCT01563042|114594|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843991|NCT00779935||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2843992|NCT00197171|100386 (EXT Y5)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843993|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
2843994|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.
2843995|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
2846577|NCT00799903|100601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846578|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.
2846579|NCT00000526||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/cast/|
2846580|NCT00000526||Study Forms|http://biolincc.nhlbi.nih.gov/studies/cast/|
2846581|NCT07061483||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/JKAXZ|
2846582|NCT05347836||Study Protocol|https://www.degruyter.com/document/doi/10.1515/jpem-2015-0340/html|
2846583|NCT02636205|25014045|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25014045|
2846584|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|
2846585|NCT00812773|112356|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846586|NCT00812773|112356|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846587|NCT00812773|112356|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2852997|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."
2852998|NCT03011385||Study Protocol|https://drive.google.com/file/d/1xGrVkCeXwUZbih7NuOujjlNJcWvQ4j6H/view?usp=sharing|The file includes the protocol for data collection and intervention sessions
2852999|NCT00297063|AVD104742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853000|NCT00297063|AVD104742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846588|NCT00812773|112356|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846589|NCT00812773|112356|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850563|NCT00989625|108504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850564|NCT00989625|108504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850565|NCT00989625|108504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850566|NCT00989625|108504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850567|NCT00989625|108504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850568|NCT00359983|107824|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850569|NCT00359983|107824|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850570|NCT00359983|107824|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843996|NCT00197171|100386 (EXT Y5)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2843997|NCT07097649||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/33946001/|
2843998|NCT06881329|GSE290201|Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE290201|Gene Expression Omnibus repository
2843999|NCT01551771|115802|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844000|NCT01551771|115802|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844001|NCT01551771|115802|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844002|NCT01551771|115802|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844003|NCT01551771|115802|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844004|NCT01551771|115802|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848458|NCT00345579|105987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848459|NCT00345579|105987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848460|NCT05166018|SUMO|Individual Participant Data Set|https://sumo.doc.cortexxmi.com/|
2848461|NCT00550225|MAB108115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848462|NCT00550225|MAB108115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848463|NCT00550225|MAB108115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848464|NCT00550225|MAB108115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848465|NCT00550225|MAB108115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848466|NCT00550225|MAB108115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848467|NCT00550225|MAB108115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848468|NCT02679690||Informed Consent Form|http://www.osiris.pitt.edu|
2848469|NCT00379613||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848470|NCT03793101||Clinical Study Report|http://eyemed.pl|
2848471|NCT00996996|104517|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848472|NCT00996996|104517|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848473|NCT00996996|104517|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848474|NCT00996996|104517|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848475|NCT00996996|104517|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848476|NCT00996996|104517|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848477|NCT00996996|104517|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848478|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
2848479|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."
2848480|NCT02701218|ENT-2558-03601|Study Protocol|http://ros.med.cmu.ac.th/Security/SignIn.aspx|Research administration section website
2848481|NCT00263666|444563/022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846590|NCT00812773|112356|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853001|NCT00297063|AVD104742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846591|NCT00812773|112356|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846592|NCT06921174||Study Protocol|https://www.isemu.es|
2846593|NCT03110471||Publications|http://orcid.org/0000-0002-5691-2987|Prof Sue Jordan- publication list
2846594|NCT02744092|AFT-28|Study Protocol|https://www.allianceforclinicaltrialsinoncology.org/main/public/standard.xhtml?path=%2FPublic%2FAFT|Email the study team at CANVAS@AllianceFoundationTrials.org.
2846595|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.
2853002|NCT00297063|AVD104742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846596|NCT00892775|108760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846597|NCT00892775|108760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846598|NCT00892775|108760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846599|NCT00892775|108760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846600|NCT00892775|108760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846601|NCT00892775|108760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846602|NCT00857857|110762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846603|NCT00857857|110762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846604|NCT00857857|110762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846605|NCT00857857|110762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846606|NCT00857857|110762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846607|NCT00857857|110762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846608|NCT00857857|110762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846609|NCT00938184|112811|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846610|NCT00938184|112811|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846611|NCT00938184|112811|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846612|NCT00938184|112811|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846613|NCT00481702||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846614|NCT01358825|115375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846615|NCT01358825|115375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846616|NCT01358825|115375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846617|NCT01358825|115375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846618|NCT01358825|115375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846619|NCT01358825|115375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846620|NCT01358825|115375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846621|NCT04205721||Individual Participant Data Set|http://dataverse.unc.edu/dataverse/cpc|Search for South Africa Impact Evaluation
2846622|NCT00985673|113536|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846623|NCT00985673|113536|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846624|NCT00985673|113536|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846625|NCT00985673|113536|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846626|NCT00985673|113536|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846627|NCT00985673|113536|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846628|NCT00985673|113536|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846629|NCT00127023|104389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846630|NCT00127023|104389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846631|NCT00127023|104389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846632|NCT00127023|104389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846633|NCT00127023|104389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846634|NCT00127023|104389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846635|NCT06239740||Study Protocol|https://doi.org/10.5281/zenodo.10488186|
2846636|NCT00992758|104512|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846637|NCT00992758|104512|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846638|NCT00992758|104512|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846639|NCT00992758|104512|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846640|NCT00992758|104512|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846641|NCT00992758|104512|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846642|NCT00992758|104512|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846643|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.
2846644|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.
2846645|NCT06342817||Study Protocol|https://drive.google.com/file/d/1YWyRsHac1y9eqsmQXVHCsmYArWwAdMoq/view?usp=sharing|
2848482|NCT00263666|444563/022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848483|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
2848484|NCT00263666|444563/022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848485|NCT00263666|444563/022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848486|NCT00263666|444563/022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848487|NCT01827904||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
2848488|NCT02676479||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/4037016|
2848489|NCT00833989|111539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848490|NCT00833989|111539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848491|NCT00833989|111539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848492|NCT00833989|111539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848493|NCT00833989|111539|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853003|NCT00297063|AVD104742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848494|NCT00833989|111539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848495|NCT00833989|111539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853004|NCT00297063|AVD104742|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844005|NCT01551771|115802|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844006|NCT03494712||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2844007|NCT03494712||Study Protocol|https://clinicaltrials.servier.com/|
2844008|NCT03494712||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2844009|NCT03494712||Informed Consent Form|https://clinicaltrials.servier.com/|
2844010|NCT03494712||Clinical Study Report|https://clinicaltrials.servier.com/|
2844011|NCT03494712||study-level clinical trial data|https://clinicaltrials.servier.com/|
2844012|NCT02836002||Individual Participant Data Set|https://datadryad.org//resource/doi:10.5061/dryad.60h41|
2844013|NCT06968286||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/39758269/|
2844014|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
2844015|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
2844016|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
2844017|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
2844018|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
2844019|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
2844020|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
2844021|NCT00422604|AC2106956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844022|NCT00422604|AC2106956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850571|NCT00359983|107824|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844023|NCT00422604|AC2106956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844024|NCT00422604|AC2106956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844025|NCT00422604|AC2106956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844026|NCT00422604|AC2106956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844027|NCT00422604|AC2106956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844028|NCT06676878||Study Protocol|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
2844029|NCT06676878||Informed Consent Form|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
2850572|NCT00359983|107824|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844030|NCT00811967||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846646|NCT06342817||Informed Consent Form|https://drive.google.com/file/d/1TfBgnmUMvF4tFJu-a1lGXlcawu0k5YeJ/view?usp=sharing|
2846647|NCT06122506||Statistical Analysis Plan|https://drive.google.com/file/d/16iZkdhVtT_pnExSoUhJV5iprYyA1JYhx/view?usp=sharing|
2846648|NCT06122506||Study Protocol|https://drive.google.com/file/d/1Z_nDas-Emj7x3OnbkcmRl3Pujy0tjlmM/view?usp=sharing|
2846649|NCT00985465|113166|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846650|NCT00985465|113166|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846651|NCT00985465|113166|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846652|NCT00985465|113166|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846653|NCT00985465|113166|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846654|NCT00985465|113166|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846655|NCT00985465|113166|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846656|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
2846657|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).
2846658|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/).
2846659|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_prep/|Source code for preprocessing prostate MRI data archives.
2846660|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_baseline|Source code for training baseline diagnostic AI models.
2846661|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.
2846662|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).
2853005|NCT00297063|AVD104742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846663|NCT00387881|TXA107563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846664|NCT00387881|TXA107563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846665|NCT00387881|TXA107563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853006|NCT00539006|FFU105924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853007|NCT00539006|FFU105924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853008|NCT00539006|FFU105924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853009|NCT00539006|FFU105924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853010|NCT00539006|FFU105924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853011|NCT00539006|FFU105924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853012|NCT00539006|FFU105924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853013|NCT00903409|111818|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853014|NCT00903409|111818|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853015|NCT00903409|111818|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853016|NCT00903409|111818|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853017|NCT00903409|111818|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853018|NCT00903409|111818|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853019|NCT03052374||Informed Consent Form|http://childstudies.ca/contact|
2853020|NCT03052374||Study Protocol|http://childstudies.ca/contact|
2853021|NCT03052374||Statistical Analysis Plan|http://childstudies.ca/contact|
2853022|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
2846666|NCT00387881|TXA107563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846667|NCT00387881|TXA107563|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853023|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
2853024|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
2846668|NCT00387881|TXA107563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846669|NCT00387881|TXA107563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846670|NCT00496015|107137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853025|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
2853026|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
2853027|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.
2853028|NCT00364273|B2F104300|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853029|NCT00364273|B2F104300|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853030|NCT00364273|B2F104300|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853031|NCT00364273|B2F104300|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846671|NCT00496015|107137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846672|NCT00496015|107137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846673|NCT00496015|107137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846674|NCT00496015|107137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846675|NCT00496015|107137|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846676|NCT00496015|107137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846677|NCT00102765|SFA103153|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846678|NCT00102765|SFA103153|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846679|NCT00102765|SFA103153|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846680|NCT00102765|SFA103153|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846681|NCT00102765|SFA103153|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846682|NCT00102765|SFA103153|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846683|NCT00102765|SFA103153|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846684|NCT01342913|113107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846685|NCT01342913|113107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846686|NCT01342913|113107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846687|NCT01342913|113107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846688|NCT01342913|113107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846689|NCT01342913|113107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846690|NCT01342913|113107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846691|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.
2846692|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/22original18.pdf|
2844031|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.
2853032|NCT00364273|B2F104300|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853033|NCT00364273|B2F104300|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853034|NCT00364273|B2F104300|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853035|NCT01153685|110628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853036|NCT01153685|110628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853037|NCT01153685|110628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853038|NCT01153685|110628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853039|NCT01153685|110628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853040|NCT01153685|110628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853041|NCT00938275|113261|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853042|NCT00938275|113261|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853043|NCT00938275|113261|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853044|NCT00938275|113261|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853045|NCT00938275|113261|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853046|NCT00938275|113261|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853047|NCT00938275|113261|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853048|NCT00479739|SAM40056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853049|NCT00479739|SAM40056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853050|NCT00479739|SAM40056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853051|NCT00479739|SAM40056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853052|NCT00479739|SAM40056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853053|NCT00479739|SAM40056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853054|NCT00479739|SAM40056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853055|NCT00381667|B2C104604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853056|NCT00381667|B2C104604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853057|NCT00381667|B2C104604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853058|NCT00381667|B2C104604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853059|NCT00381667|B2C104604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853060|NCT00381667|B2C104604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853061|NCT00381667|B2C104604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853062|NCT02446496|201529|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853063|NCT02446496|201529|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853064|NCT02446496|201529|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853065|NCT02446496|201529|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853066|NCT02446496|201529|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853067|NCT02446496|201529|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853068|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.
2853069|NCT00005274||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
2846693|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/23original19.pdf|
2853070|NCT00005274||Study Forms|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
2846694|NCT00988884||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-005&kw=V503-005&tab=access|
2846695|NCT00539994|ALB110247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846696|NCT00539994|ALB110247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846697|NCT00539994|ALB110247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846698|NCT00539994|ALB110247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846699|NCT00539994|ALB110247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846700|NCT00539994|ALB110247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846701|NCT00539994|ALB110247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846702|NCT00861705||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov|
2846703|NCT00938158|108370|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846704|NCT00938158|108370|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846705|NCT00938158|108370|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846706|NCT00938158|108370|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853071|NCT00005274||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
2853072|NCT02677675||Study Protocol|http://www.nmrr.gov.my|
2853073|NCT01563029|106855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853074|NCT01563029|106855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853075|NCT01563029|106855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853076|NCT01563029|106855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853077|NCT01563029|106855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853078|NCT01563029|106855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853079|NCT01563029|106855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853080|NCT01294709||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-014&kw=0974-014&tab=access|
2853081|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"
2853082|NCT01480271|114450|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853083|NCT01480271|114450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853084|NCT01480271|114450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846707|NCT00938158|108370|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846708|NCT00938158|108370|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846709|NCT00938158|108370|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846710|NCT01387217|114070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846711|NCT01387217|114070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846712|NCT01387217|114070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846713|NCT01387217|114070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853085|NCT01480271|114450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853086|NCT01480271|114450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853087|NCT01480271|114450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853088|NCT01480271|114450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853089|NCT02691312||FDA 501(k)|https://www.accessdata.fda.gov/cdrh_docs/pdf10/K101935.pdf|
2853090|NCT00981409|106206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844032|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.
2845233|NCT01899703|117213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848496|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."
2848497|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. \[Epub ahead of print\]"
2848498|NCT02322671|200107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848499|NCT02322671|200107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848500|NCT02322671|200107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848501|NCT02322671|200107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848502|NCT02322671|200107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848503|NCT02322671|200107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848504|NCT02322671|200107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848505|NCT01090453|113615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848506|NCT01090453|113615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848507|NCT01090453|113615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846714|NCT01387217|114070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846715|NCT01387217|114070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846716|NCT01387217|114070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846717|NCT06938126|TE-KEB/22/2023|Individual Participant Data Set|https://tf.hu/en/|For more information please email to: petridis.leonidas@tf.hu
2846718|NCT00689390||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05063&kw=P05063&tab=access|
2846719|NCT00605852|HH3110161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846720|NCT00605852|HH3110161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846721|NCT00605852|HH3110161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846722|NCT00605852|HH3110161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846723|NCT00605852|HH3110161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846724|NCT00605852|HH3110161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846725|NCT00605852|HH3110161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846726|NCT00550407|SCA104779|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846727|NCT00550407|SCA104779|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846728|NCT00550407|SCA104779|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846729|NCT00550407|SCA104779|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846730|NCT01928927||Grading table|https://rsc.tech-res.com/clinical-research-sites/safety-reporting/daids-grading-tables|
2846731|NCT03847766|31484523|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31484523/|Data can be accessed by request from the corresponding author
2846732|NCT01009060|113147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846733|NCT01009060|113147|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846734|NCT01009060|113147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846735|NCT01009060|113147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846736|NCT01009060|113147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846737|NCT01009060|113147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846738|NCT01009060|113147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846739|NCT00960063||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05883&kw=P05883&tab=access|
2846740|NCT01527123|115959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846741|NCT01527123|115959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853091|NCT00981409|106206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853092|NCT00981409|106206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853093|NCT00607906|AXO110461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853094|NCT00607906|AXO110461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853095|NCT00607906|AXO110461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844033|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.
2844034|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.
2844035|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.
2844036|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.
2846742|NCT01527123|115959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846743|NCT01527123|115959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846744|NCT01527123|115959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846745|NCT01527123|115959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844037|NCT07111143||Health-Damaging Climate Events Highlight the Need for Interdisciplinary, Engaged Research|https://pubmed.ncbi.nlm.nih.gov/38371354/|
2844038|NCT00005235||NCBI website|http://www.ncbi.nlm.nih.gov/pubmed/8353919|
2844039|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
2844040|NCT00226499|100388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844041|NCT00226499|100388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846746|NCT06357481|doi: 10.1111/iej.13304|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32266988/|
2846747|NCT06555185|10.17632/2cwcz2vx4v.1|Individual Participant Data Set|https://data.mendeley.com/datasets/2cwcz2vx4v/1|
2846748|NCT01969708|PB2016-103333|Study Protocol|https://ntrl.ntis.gov/NTRL/|SCORE2 Protocol Version 3.0 (the Identifier for the appendices is PB2016-103334)
2846749|NCT02481154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2846750|NCT02481154||Study Protocol|https://clinicaltrials.servier.com/|
2846751|NCT02481154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2846752|NCT02481154||Informed Consent Form|https://clinicaltrials.servier.com/|
2846753|NCT02481154||Clinical Study Report|https://clinicaltrials.servier.com/|
2846754|NCT02481154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2846755|NCT00405080|NKV105091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846756|NCT00405080|NKV105091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846757|NCT00405080|NKV105091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846758|NCT00405080|NKV105091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846759|NCT00405080|NKV105091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846760|NCT00405080|NKV105091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846761|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.
2846762|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
2846763|NCT00382772|107876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846764|NCT00382772|107876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846765|NCT00382772|107876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846766|NCT00382772|107876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846767|NCT00382772|107876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846768|NCT00382772|107876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846769|NCT02257398|115775|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846770|NCT02257398|115775|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844042|NCT00226499|100388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844043|NCT00226499|100388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846771|NCT02257398|115775|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846772|NCT02257398|115775|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844044|NCT00226499|100388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844045|NCT00226499|100388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846773|NCT02257398|115775|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846774|NCT02257398|115775|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846775|NCT02257398|115775|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853096|NCT00607906|AXO110461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846776|NCT02855476||Study Protocol|http://hdclarity.net/study-information/|
2846777|NCT02855476||Informed Consent Form|http://hdclarity.net/study-information/|Draft informed consent form, not yet approved by an Institutional Review Board for clinical use
2846778|NCT00506350|109817|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846779|NCT00506350|109817|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846780|NCT00506350|109817|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846781|NCT00506350|109817|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846782|NCT00506350|109817|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846783|NCT00506350|109817|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846784|NCT00506350|109817|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846785|NCT01673529|115246|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846786|NCT01673529|115246|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846787|NCT01673529|115246|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846788|NCT01673529|115246|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846789|NCT01673529|115246|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846790|NCT01673529|115246|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846791|NCT01673529|115246|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846792|NCT00551317|LPL110077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846793|NCT00551317|LPL110077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846794|NCT00551317|LPL110077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846795|NCT00551317|LPL110077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846796|NCT00551317|LPL110077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846797|NCT00551317|LPL110077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846798|NCT00551317|LPL110077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846799|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.
2846800|NCT00390143|108595 Mth18|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846801|NCT00390143|108595 Mth18|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846802|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
2846803|NCT00390143|108595 Mth18|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846804|NCT00390143|108595 Mth18|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846805|NCT00390143|108595 Mth18|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846806|NCT00379964||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846807|NCT01054885|112207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846808|NCT01054885|112207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846809|NCT01054885|112207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848508|NCT01090453|113615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848509|NCT01090453|113615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848510|NCT01090453|113615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848511|NCT04411290||Principal investigator data|https://scholar.google.com.tr/citations?user=6bFlCZwAAAAJ&hl=tr|
2848512|NCT00920192|111645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848513|NCT00920192|111645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848514|NCT00920192|111645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848515|NCT00920192|111645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848516|NCT00920192|111645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848517|NCT00920192|111645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848518|NCT01196975|112963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848519|NCT01196975|112963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848520|NCT01196975|112963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848521|NCT01196975|112963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848522|NCT01196975|112963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848523|NCT01196975|112963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848524|NCT01196975|112963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848525|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
2848526|NCT01462344|115358|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848527|NCT01462344|115358|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848528|NCT01462344|115358|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848529|NCT01462344|115358|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848530|NCT01462344|115358|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848531|NCT01462344|115358|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848532|NCT01462344|115358|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848533|NCT02672631||Study Protocol|http://clinical-mri.com/mr-neurography-diagnostic-criteria-to-determine-lesions-of-peripheral-nerves/|
2848534|NCT00345904|107507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846810|NCT01054885|112207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846811|NCT01054885|112207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846812|NCT01054885|112207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846813|NCT01054885|112207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846814|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
2846815|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
2846816|NCT00269217||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846817|NCT00674817|MAB110123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846818|NCT00674817|MAB110123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846819|NCT00674817|MAB110123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846820|NCT00674817|MAB110123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846821|NCT00674817|MAB110123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846822|NCT00674817|MAB110123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846823|NCT00674817|MAB110123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846824|NCT01424384|105012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846825|NCT01424384|105012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846826|NCT01424384|105012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846827|NCT01424384|105012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846828|NCT01424384|105012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846829|NCT01424384|105012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846830|NCT01424384|105012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853097|NCT00607906|AXO110461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853098|NCT00607906|AXO110461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846831|NCT03941470|IRB17200056|Study Protocol|http://Email:ethics_committee12@yahoo.com|
2853099|NCT00607906|AXO110461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853100|NCT00443131|107731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853101|NCT00443131|107731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853102|NCT00443131|107731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853103|NCT00443131|107731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853104|NCT00443131|107731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853105|NCT00443131|107731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853106|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.
2844046|NCT07089667||Study Protocol|https://drive.google.com/drive/folders/1QpzE6ACGieVNCGQ1nsLJHxUWtB-fUfLV?usp=sharing|
2844047|NCT00471081|109375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844048|NCT00471081|109375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844049|NCT00471081|109375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844050|NCT00471081|109375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844051|NCT00471081|109375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844052|NCT00471081|109375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846832|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)
2846833|NCT06644573|Virtual Consultation SOAP Note|Individual Participant Data Set|https://drive.google.com/file/d/1uAAbC0gRFOthwnUiWz3O2sDyLgkGkiKf/view?usp=sharing|Virtual Consultation SOAP Note
2846834|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
2846835|NCT06644573|PROSOMNIA Sleep Quiz|Individual Participant Data Set|https://drive.google.com/file/d/1XWzVYL0L2OR8FzFUGtd0vggjwBflBAFa/view?usp=sharing|PROSOMNIA Sleep Quiz
2846836|NCT06644573|Sleep Quiz Evaluation|Clinical Study Report|https://drive.google.com/file/d/1Hzw1OvpbAn44nCbvqbtPwC25clwCbclW/view?usp=sharing|PSHES Sleep Quiz Scoring System
2846837|NCT06644573|Mood/Emotion Quality Scale|Individual Participant Data Set|https://drive.google.com/file/d/1-UzkVbn7UG57aZMg9d1LRB9yoLkjUlWS/view?usp=sharing|Mood/Emotion Quality Scale
2846838|NCT00951353|SDY951|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study identifier is SDY951.
2846839|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."
2846840|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.
2846841|NCT00837434|SDY824|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|ImmPort study identifier is SDY824.
2846842|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.
2846843|NCT00360230|106367|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846844|NCT00360230|106367|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846845|NCT00360230|106367|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846846|NCT00360230|106367|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846847|NCT00360230|106367|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846848|NCT00360230|106367|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846849|NCT03435250||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2846850|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
2846851|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/18426039|
2846852|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/19952380|
2846853|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/20922783|
2846854|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/?term=In+vitro+effects+of+detergent+sclerosants+on+coagulation%2C+platelets+and+microparticles.|
2844053|NCT00471081|109375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844054|NCT07111780|example study protokol|Study Protocol|https://www.nature.com/articles/s41598-024-79811-3|
2844055|NCT06941233||Study Protocol|https://hjpwd.ahs.uic.edu|study protocol may be accessed by contacting the research team
2844056|NCT00485732|107291|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844057|NCT00485732|107291|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846855|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/21725957|
2846856|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/16226898|
2846857|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/11231246|
2844058|NCT00485732|107291|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846858|NCT06999954||Informed Consent Form|https://www.sdsalliance.org/sds-gps|Available from the SDS-GPS program team at gps@sdsalliance.org
2846859|NCT06602661||Study Protocol|https://docs.google.com/document/d/1-NMx1lP-_x1KHA0t49yEG7tNsFgepmyWPkbdFfWMPMc/edit?usp=sharing|
2846860|NCT06602661||Informed Consent Form|https://drive.google.com/file/d/1rON8VADRvws1J_I_rmqAAy2sNgL0I9c5/view?usp=sharing|
2846861|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
2846862|NCT01353898||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1972-003&kw=1972-003&tab=access|
2846863|NCT03038061||Informed Consent Form|http://ventilation.fbmi.cvut.cz/wp-content/uploads/2017/01/Informed-Consent-Form.pdf|Informed Consent
2846864|NCT06471972||Study Protocol|http://stepcare.org/biomarkers|Lab manuals and sample collection form
2846865|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|
2846866|NCT06473740||Individual Participant Data Set|https://patientdatabase.ishemii.net/login|
2846867|NCT01929317|116991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846868|NCT01929317|116991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846869|NCT06591234||Study Protocol|https://www.ausl.bologna.it/|To send a request by mail
2846870|NCT06700473|10.1097/JNR.0000000000000129.|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/28277391/|https://pubmed.ncbi.nlm.nih.gov/28277391/
2846871|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
2846872|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
2846873|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,
2846874|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)
2846875|NCT01357850|112670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846876|NCT01357850|112670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846877|NCT01357850|112670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846878|NCT01357850|112670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846879|NCT01357850|112670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846880|NCT01357850|112670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846881|NCT01357850|112670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846882|NCT01656408||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-002&kw=8150-002&tab=access|
2853107|NCT00549120|MAB104954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853108|NCT00549120|MAB104954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853109|NCT00549120|MAB104954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853110|NCT00549120|MAB104954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853111|NCT00549120|MAB104954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853112|NCT00549120|MAB104954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853113|NCT00549120|MAB104954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853114|NCT00627458|111344|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853115|NCT00627458|111344|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853116|NCT00627458|111344|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853117|NCT00627458|111344|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853118|NCT00627458|111344|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853119|NCT00627458|111344|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846883|NCT06081816|10.4314/ahs.v19i1.55|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
2846884|NCT06081816|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
2846885|NCT03584789||Study Protocol|https://www.researchprotocols.org/2021/4/e24342|
2846886|NCT00614731|SDY3|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
2846887|NCT00614731|SDY3|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
2846888|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.
2846889|NCT01416324|114985|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846890|NCT01416324|114985|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846891|NCT01416324|114985|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846892|NCT01416324|114985|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846893|NCT01416324|114985|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846894|NCT01416324|114985|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846895|NCT01416324|114985|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846896|NCT05345652||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31571625/|
2846897|NCT05350397|REFERENCE|REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30982782/|
2846898|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_35_70_76_127.pdf|
2846899|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/30982782/|
2846900|NCT05350397|REFERENCE|REFERENCE|http://dergipark.org.tr/tr/pub/ikcusbfd/issue/60165/705219|
2846901|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_37_60_1_10.pdf|
2846902|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/18992625/|
2846903|NCT05350397|REFERENCE|REFERENCE|http://www.ncbi.nlm.nih.gov/books/NBK72567/|
2846904|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1016/j.ctcp.2021.101304|
2846905|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1097/HNP.0000000000000384|
2846906|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/23981400/|
2846907|NCT00090207||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2846908|NCT01128634|113950|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846909|NCT01128634|113950|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846910|NCT01128634|113950|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846911|NCT01128634|113950|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846912|NCT01128634|113950|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846913|NCT01128634|113950|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846914|NCT01128634|113950|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846915|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.
2846916|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.
2846917|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.
2846918|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|
2846919|NCT00345358|107058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846920|NCT00345358|107058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844059|NCT00485732|107291|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846921|NCT00345358|107058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846922|NCT00345358|107058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846923|NCT00345358|107058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846924|NCT00345358|107058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844060|NCT00485732|107291|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844061|NCT00485732|107291|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844062|NCT00485732|107291|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844063|NCT00838903|112753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844064|NCT00838903|112753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844065|NCT00838903|112753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844066|NCT00838903|112753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844067|NCT00838903|112753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844068|NCT00838903|112753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844069|NCT00838903|112753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844070|NCT01822639|116798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844071|NCT01822639|116798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844072|NCT01822639|116798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844073|NCT01822639|116798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844074|NCT01822639|116798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844075|NCT01822639|116798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844076|NCT01822639|116798|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844077|NCT00661557|107408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846925|NCT06595771||Study Protocol|https://haydarpasanumuneah.saglik.gov.tr/|
2846926|NCT02094924|200957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846927|NCT02094924|200957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846928|NCT02094924|200957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846929|NCT02094924|200957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846930|NCT02094924|200957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846931|NCT02094924|200957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846932|NCT02094924|200957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844078|NCT00661557|107408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844079|NCT00661557|107408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844080|NCT00661557|107408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844081|NCT00661557|107408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844082|NCT00661557|107408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844083|NCT00661557|107408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844084|NCT01894386|200587|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846933|NCT00742261|MET111516|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846934|NCT00742261|MET111516|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846935|NCT00742261|MET111516|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846936|NCT00742261|MET111516|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846937|NCT00742261|MET111516|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846938|NCT00742261|MET111516|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844085|NCT01894386|200587|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844086|NCT01894386|200587|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844087|NCT01894386|200587|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844088|NCT01894386|200587|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844089|NCT01894386|200587|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844090|NCT01894386|200587|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844091|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.
2846939|NCT00742261|MET111516|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846940|NCT01587924|116582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846941|NCT01587924|116582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846942|NCT01587924|116582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846943|NCT01587924|116582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846944|NCT01587924|116582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846945|NCT01587924|116582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846946|NCT01587924|116582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844092|NCT06575504||Study Protocol|https://guides.lib.umich.edu/datamanagement/clinicaltrials|
2846947|NCT02581410|201198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846948|NCT02581410|201198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846949|NCT02581410|201198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846950|NCT02581410|201198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846951|NCT02581410|201198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846952|NCT02581410|201198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846953|NCT02581410|201198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846954|NCT00976560|113009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846955|NCT00976560|113009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846956|NCT00976560|113009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846957|NCT00976560|113009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846958|NCT00976560|113009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846959|NCT00976560|113009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846960|NCT00976560|113009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846961|NCT00760617|111737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846962|NCT00760617|111737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846963|NCT00760617|111737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846964|NCT00760617|111737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846965|NCT00760617|111737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846966|NCT00760617|111737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846967|NCT00760617|111737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846968|NCT04591808||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2846969|NCT04591808||Study Protocol|https://clinicaltrials.servier.com/|
2846970|NCT04591808||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2846971|NCT04591808||Informed Consent Form|https://clinicaltrials.servier.com/|
2846972|NCT04591808||Clinical Study Report|https://clinicaltrials.servier.com/|
2846973|NCT04591808||[study-level clinical trial data]|https://clinicaltrials.servier.com/|
2846974|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.
2846975|NCT00555061|TOC106489|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846976|NCT00555061|TOC106489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846977|NCT00555061|TOC106489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844093|NCT04579848||Study Protocol|https://drive.google.com/file/d/1AKuis2zJlqhUqY4OEPyVhQPpIiuPnnhr/view?usp=sharing|
2846978|NCT00555061|TOC106489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846979|NCT00555061|TOC106489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846980|NCT00555061|TOC106489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846981|NCT00555061|TOC106489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846982|NCT06947681|Not available at moment|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|Most of the informations available at This site and Google Scholar
2846983|NCT00951977|SDY290|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
2846984|NCT00951977|SDY290|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
2846985|NCT00951977|SDY290|Study summary, -design, -demographics, -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
2846986|NCT02914301|FWA00005945|Informed Consent Form|https://files.acrobat.com/a/preview/c262292c-6de1-4f73-bae3-689555b8c77f|
2846987|NCT02914301|Post-Partum Survey|Individual Participant Data Set|https://files.acrobat.com/a/preview/5ec925dd-52ad-4b07-b6fc-2084d2f751d5|
2846988|NCT02914301|Prenatal Participant Data -22|Individual Participant Data Set|https://files.acrobat.com/a/preview/984213bb-ccef-419b-8f56-87336004ec5a|
2846989|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
2846990|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."
2846991|NCT01485172|111662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846992|NCT01485172|111662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846993|NCT01485172|111662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846994|NCT01485172|111662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846995|NCT01485172|111662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846996|NCT01485172|111662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846997|NCT01192191|114156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846998|NCT01192191|114156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2846999|NCT01192191|114156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847000|NCT01192191|114156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847001|NCT01192191|114156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847002|NCT01192191|114156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847003|NCT01192191|114156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847004|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.
2847005|NCT01175083|114056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847006|NCT01175083|114056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847007|NCT01175083|114056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844094|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1mB2pEgRmuMhaVM_eNnnyXdqsyev4wev5/view?usp=sharing|
2847008|NCT01175083|114056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847009|NCT01175083|114056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847010|NCT01175083|114056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847011|NCT01175083|114056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847012|NCT01818011|116266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847013|NCT01818011|116266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847014|NCT01818011|116266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847015|NCT01818011|116266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847016|NCT01818011|116266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847017|NCT01818011|116266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847018|NCT01818011|116266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847019|NCT01049009|26285691|Publication|https://www.ncbi.nlm.nih.gov/pubmed/26285691|
2847020|NCT00329355|TRX105852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847021|NCT00329355|TRX105852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847022|NCT00329355|TRX105852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847023|NCT00329355|TRX105852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847024|NCT00329355|TRX105852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847025|NCT00329355|TRX105852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847026|NCT00329355|TRX105852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847027|NCT01318980|114604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847028|NCT01318980|114604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847029|NCT01318980|114604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847030|NCT01318980|114604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847031|NCT01318980|114604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847032|NCT01318980|114604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847033|NCT01318980|114604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847034|NCT00533676||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847035|NCT07156396|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
2847036|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
2847037|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
2847038|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
2847039|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
2847040|NCT00265148|BRL-49653/461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847041|NCT00265148|BRL-49653/461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847042|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
2847043|NCT00389987||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847044|NCT01015638|114546|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847045|NCT01015638|114546|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847046|NCT01015638|114546|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847047|NCT01015638|114546|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847048|NCT01015638|114546|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848535|NCT00345904|107507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848536|NCT00345904|107507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848537|NCT00345904|107507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848538|NCT00345904|107507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848539|NCT06426537||Study Protocol|http://drive.google.com/drive/u/3/folders/15qW39gHRtgwIuP8rGm8ukhXtYnLRCFNO|
2848540|NCT00695669|111626|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848541|NCT00695669|111626|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844095|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1oE_9J-5uwLpboVWEsUJL6tHn4st1ea9r/view?usp=sharing|
2844096|NCT00133848|TOC103469|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847049|NCT01449799|113423|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847050|NCT01449799|113423|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847051|NCT01449799|113423|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847052|NCT01449799|113423|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847053|NCT01449799|113423|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847054|NCT01449799|113423|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847055|NCT01449799|113423|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847056|NCT06940778|blenti|Study Protocol|https://hcor.com.br|blenti
2848542|NCT00695669|111626|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848543|NCT00695669|111626|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848544|NCT00695669|111626|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848545|NCT00695669|111626|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844097|NCT00133848|TOC103469|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848546|NCT00695669|111626|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848547|NCT00493818|AKT106757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848548|NCT00493818|AKT106757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848549|NCT00493818|AKT106757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848550|NCT00493818|AKT106757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848551|NCT00493818|AKT106757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848552|NCT00493818|AKT106757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848553|NCT00493818|AKT106757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848554|NCT01217073||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-006&kw=3102-006&tab=access|
2848555|NCT00515502|AC4108123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848556|NCT00515502|AC4108123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848557|NCT00515502|AC4108123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848558|NCT00515502|AC4108123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848559|NCT00515502|AC4108123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848560|NCT00515502|AC4108123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848561|NCT00515502|AC4108123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848562|NCT03058211|PI16/00486|Study Protocol|http://www.iispv.cat|Protocol in Spanish language
2848563|NCT03058211|PI16/00486|Informed Consent Form|http://www.iispv.cat|Informed consent form in Spanish language
2848564|NCT00355082|LAM30055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848565|NCT00355082|LAM30055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848566|NCT00355082|LAM30055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844098|NCT00133848|TOC103469|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848567|NCT00355082|LAM30055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848568|NCT00355082|LAM30055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848569|NCT00355082|LAM30055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848570|NCT00355082|LAM30055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848571|NCT00374842|108656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848572|NCT00374842|108656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844099|NCT00133848|TOC103469|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848573|NCT00374842|108656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848574|NCT00374842|108656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848575|NCT00374842|108656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848576|NCT00354874|B2C101762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847057|NCT06757920|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2847058|NCT07144891||article|https://pmc.ncbi.nlm.nih.gov/articles/PMC7488296/|
2847059|NCT00535288||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06472&kw=P06472&tab=access|
2847060|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.
2847061|NCT01696604|116715|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847062|NCT01696604|116715|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847063|NCT01696604|116715|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847064|NCT01696604|116715|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847065|NCT01696604|116715|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847066|NCT01696604|116715|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847067|NCT01696604|116715|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847068|NCT00776919|114677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847069|NCT00776919|114677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847070|NCT00776919|114677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847071|NCT00776919|114677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847072|NCT00776919|114677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847073|NCT00776919|114677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847074|NCT00776919|114677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847075|NCT00368199||Individual Participant Data Set|https://peerj.com/articles/2037/|
2847076|NCT01702493|117041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847077|NCT01702493|117041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847078|NCT01702493|117041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847079|NCT01702493|117041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847080|NCT01702493|117041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848577|NCT00354874|B2C101762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847081|NCT01702493|117041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847082|NCT01702493|117041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847083|NCT07145281||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/TCRUW|
2847084|NCT00435045|OM9L|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847085|NCT00435045|OM9L|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850573|NCT00359983|107824|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850574|NCT04445727|vitamin c|Clinical Study Report|http://www.bonusan.es/vademecum/vitamina_c1000_complejo_de_ascorbatos.html|
2850575|NCT00537654|ARI109882|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847086|NCT00435045|OM9L|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847087|NCT00435045|OM9L|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847088|NCT00435045|OM9L|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847089|NCT00435045|OM9L|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847090|NCT00435045|OM9L|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847091|NCT00470834|AVO108943|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850576|NCT00537654|ARI109882|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850577|NCT00537654|ARI109882|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850578|NCT00537654|ARI109882|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844100|NCT00133848|TOC103469|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847092|NCT00470834|AVO108943|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847093|NCT00470834|AVO108943|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847094|NCT00470834|AVO108943|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847095|NCT00470834|AVO108943|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850579|NCT00537654|ARI109882|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850580|NCT00537654|ARI109882|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850581|NCT00537654|ARI109882|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850582|NCT00599911|2007-001071-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001071-11/results|
2850583|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
2850584|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
2850585|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
2850586|NCT01978327|200592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850587|NCT01978327|200592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850588|NCT01978327|200592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850589|NCT01978327|200592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850590|NCT01978327|200592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850591|NCT01978327|200592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850592|NCT01978327|200592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850593|NCT01035645|110040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850594|NCT01035645|110040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850595|NCT01035645|110040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850596|NCT01035645|110040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850597|NCT01035645|110040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850598|NCT01035645|110040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850599|NCT00640081||Clinical Study Report|http://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(14)70106-8/abstract|
2850600|NCT00225823|FFR103184|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850601|NCT00225823|FFR103184|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850602|NCT00225823|FFR103184|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850603|NCT00225823|FFR103184|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850604|NCT00225823|FFR103184|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850605|NCT00225823|FFR103184|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850606|NCT00225823|FFR103184|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850607|NCT03091231|mpUS2016|Study Protocol|http://www.martini-klinik.de|to request an electronic copy send an email to a.renter@uke.de
2850608|NCT00659178|ILI108621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850609|NCT00659178|ILI108621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850610|NCT00659178|ILI108621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850611|NCT00659178|ILI108621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850612|NCT00659178|ILI108621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850613|NCT00659178|ILI108621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850614|NCT00659178|ILI108621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850615|NCT02688218|STUDY00015452|Study Protocol|http://eirb.ohsu.edu|Institutionally reviewed and accepted protocol for this study.
2850616|NCT01198756|113314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850617|NCT01198756|113314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850618|NCT01198756|113314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850619|NCT01198756|113314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850620|NCT01198756|113314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850621|NCT01198756|113314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850622|NCT01198756|113314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850623|NCT00603252|111149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850624|NCT00603252|111149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850625|NCT00603252|111149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850626|NCT00603252|111149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850627|NCT00603252|111149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850628|NCT02615002||Study website|http://www.recognitionstudy.com|
2850629|NCT06906354|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2850630|NCT03789448||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2128-8|
2847096|NCT00470834|AVO108943|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847097|NCT00470834|AVO108943|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847098|NCT02758483|63683417.1.0000.5257|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
2847099|NCT01115322|114573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847100|NCT01115322|114573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847101|NCT01115322|114573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847102|NCT01115322|114573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847103|NCT01115322|114573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847104|NCT01115322|114573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847105|NCT01115322|114573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847106|NCT07131241||Individual Participant Data Set|https://www.fjmu.edu.cn|For more information, please contact: dajunchai@126.com
2847107|NCT06947330||Study Protocol|https://www.ilovepdf.com/download/6bhl069fp1wzcttl2h9kympvwcw0z348Az4p933p7tx6gm77hss9dbx3gbxjvm9ypjzwt97hdptj659jxht28ybgh1m4lyj34sth4k980tx1wzvm0A2pjghl7rs70r7pk67kblvbcfl9fn68lp5c06pjtdd07x9jqh7grqdl8b1kkp3b6271/88w|
2847108|NCT01209104|113722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847109|NCT01209104|113722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847110|NCT01209104|113722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847111|NCT01209104|113722|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847112|NCT01209104|113722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847113|NCT01209104|113722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847114|NCT01209104|113722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847115|NCT03673397||Individual Participant Data Set|https://doi.org/10.7910/DVN/WASN36|
2847116|NCT01128621|113132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847117|NCT01128621|113132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847118|NCT01128621|113132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847119|NCT01128621|113132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847120|NCT01128621|113132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847121|NCT01128621|113132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847122|NCT01128621|113132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847123|NCT04727489||Study Protocol|http://www.inserm.fr|
2847124|NCT04727489||Informed Consent Form|http://www.inserm.fr|
2847125|NCT04570059|Booklet of recommendation|intervention material|https://hal.archives-ouvertes.fr/|Booklet of recommendation provided to the intervention group (in French)
2847126|NCT01328444|114417|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847127|NCT01328444|114417|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847128|NCT01328444|114417|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847129|NCT01328444|114417|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847130|NCT01328444|114417|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847131|NCT01328444|114417|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847132|NCT01328444|114417|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847133|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.
2847134|NCT00000590||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pactg/|
2847135|NCT00000590||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/pactg/|
2847136|NCT03111186|HS-15-00706|Study Protocol|http://istar.usc.edu|
2847137|NCT03111186|HS-15-00706|Informed Consent Form|http://istar.usc.edu|
2847138|NCT00363545|107077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847139|NCT00363545|107077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847140|NCT00363545|107077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847141|NCT00363545|107077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847142|NCT00363545|107077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847143|NCT00363545|107077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847144|NCT01106092|113264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847145|NCT01106092|113264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847146|NCT01106092|113264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847147|NCT01106092|113264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847148|NCT01106092|113264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847149|NCT01106092|113264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847150|NCT01106092|113264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847151|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
2847152|NCT00794898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847153|NCT01144299|114292|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847154|NCT01144299|114292|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847155|NCT01144299|114292|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847156|NCT01144299|114292|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847157|NCT01144299|114292|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847158|NCT01144299|114292|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847159|NCT01144299|114292|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847160|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)."
2847161|NCT00376714|AC2105333|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847162|NCT00376714|AC2105333|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847163|NCT00376714|AC2105333|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848578|NCT00354874|B2C101762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848579|NCT00354874|B2C101762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848580|NCT00354874|B2C101762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848581|NCT00354874|B2C101762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844101|NCT00133848|TOC103469|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847164|NCT00376714|AC2105333|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848582|NCT00354874|B2C101762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848583|NCT00951041|113574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848584|NCT00951041|113574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848585|NCT00951041|113574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848586|NCT00951041|113574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848587|NCT00951041|113574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848588|NCT00951041|113574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848589|NCT00951041|113574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848590|NCT00679939|AVD111179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847165|NCT00376714|AC2105333|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847166|NCT00376714|AC2105333|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847167|NCT00376714|AC2105333|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847168|NCT00406562|107924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847169|NCT00406562|107924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847170|NCT00406562|107924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847171|NCT00406562|107924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847172|NCT00406562|107924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847173|NCT00406562|107924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847174|NCT00406562|107924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847175|NCT02184624|200301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847176|NCT02184624|200301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847177|NCT02184624|200301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847178|NCT02184624|200301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847179|NCT02184624|200301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847180|NCT02184624|200301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847181|NCT02184624|200301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847182|NCT05053373||Individual Participant Data Set|http://www.medresman.org.cn/pub/en/proj/projectshow.aspx?proj=1282|
2847183|NCT02700087|Consent form cycle 3|Informed Consent Form|https://eprotocol.stanford.edu/irb/ControlServlet?updateFlag=Y|
2847184|NCT01451437||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=P07649&kw=P07649&tab=access|
2847185|NCT02691585||Study Protocol|http://rguhs.ac.in/|
2847186|NCT02003274||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov|
2847187|NCT00920803|113221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847188|NCT00920803|113221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847189|NCT00920803|113221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847190|NCT00920803|113221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847191|NCT00920803|113221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848591|NCT00679939|AVD111179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848592|NCT00679939|AVD111179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848593|NCT00679939|AVD111179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848594|NCT00679939|AVD111179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848595|NCT00679939|AVD111179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848596|NCT00679939|AVD111179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848597|NCT06520111|sice|Study Protocol|https://siceitalia.com/|SICE- Team di ricerca Endocrino-metabolica- crisal
2848598|NCT00319098|107064|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848599|NCT00319098|107064|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848600|NCT00319098|107064|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848601|NCT00319098|107064|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848602|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.
2848603|NCT00319098|107064|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847192|NCT00920803|113221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847193|NCT00627575|LEP108937|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847194|NCT00627575|LEP108937|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847195|NCT00627575|LEP108937|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847196|NCT00627575|LEP108937|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847197|NCT00627575|LEP108937|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847198|NCT00627575|LEP108937|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847199|NCT00627575|LEP108937|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847200|NCT00169442|104065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847201|NCT00169442|104065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847202|NCT00169442|104065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847203|NCT00169442|104065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847204|NCT00169442|104065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847205|NCT00169442|104065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847206|NCT00400608|SAS105519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847207|NCT00400608|SAS105519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847208|NCT00400608|SAS105519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847209|NCT00400608|SAS105519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847210|NCT00400608|SAS105519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847211|NCT00400608|SAS105519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847212|NCT00400608|SAS105519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847213|NCT00456807|109801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847214|NCT00456807|109801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847215|NCT00456807|109801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847216|NCT00456807|109801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847217|NCT00456807|109801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850631|NCT01498679|113719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847218|NCT00456807|109801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847219|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/34004390/|This article is from the National Library of Medicine.
2847220|NCT06078150||Systematic Review|https://pubmed.ncbi.nlm.nih.gov/32375184/|This article is from the National Library of Medicine.
2847221|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/24905451/|This article is from the National Library of Medicine.
2847222|NCT02045953|201092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847223|NCT02045953|201092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847224|NCT02045953|201092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847225|NCT02045953|201092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847226|NCT02045953|201092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847227|NCT02045953|201092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847228|NCT02045953|201092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847229|NCT00400478||Clinical Study Report|https://www.clinicaltrialsregister.eu/ctr-search/search;jsessionid=cJHnlkSBP30JjfQV2K-KXCK3mdjOE64o0FAsUcmzHmslzlaX5yhQ!675812678|
2847230|NCT05386628|26079868|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2847231|NCT05386628|16225693|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2847232|NCT05386628|12924842|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2847233|NCT05386628|31864435|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2847234|NCT05386628|22018755|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2847235|NCT05386628|18192154|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2847236|NCT05386628|25977305|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2847237|NCT05386628|20068255|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2850632|NCT01498679|113719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850633|NCT01498679|113719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847238|NCT01587898|116581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847239|NCT01587898|116581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847240|NCT01587898|116581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847241|NCT01587898|116581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847242|NCT01587898|116581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847243|NCT01587898|116581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847244|NCT01587898|116581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847245|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
2847246|NCT03009370||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26806685|
2847247|NCT00067938|SCA40917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847248|NCT00067938|SCA40917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847249|NCT00067938|SCA40917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847250|NCT00067938|SCA40917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850634|NCT01498679|113719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847251|NCT00067938|SCA40917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847252|NCT00067938|SCA40917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847253|NCT00197158|104387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847254|NCT00197158|104387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847255|NCT00197158|104387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847256|NCT00197158|104387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847257|NCT00197158|104387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847258|NCT00197158|104387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847259|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"
2847260|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.
2847261|NCT00000485||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hdfp/|
2847262|NCT00541463||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847263|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.
2847264|NCT00005132||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nghs/|
2847265|NCT00005132||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nghs/|
2847266|NCT03016676||Study Protocol|http://www.ijpbs.net/abstract.php?article=5240|
2847267|NCT00955383|112359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847268|NCT00955383|112359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847269|NCT00955383|112359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847270|NCT00955383|112359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847271|NCT00955383|112359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847272|NCT00955383|112359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847273|NCT00955383|112359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847274|NCT06995794||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/|
2847275|NCT06995794||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
2847276|NCT02393586||Link to Pubmed (Final publication)|https://www.ncbi.nlm.nih.gov/pubmed/28333342|
2847277|NCT01338779|ImmPort Study ID: SDY546|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
2847278|NCT01338779|ImmPort Study ID: SDY546|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
2847279|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|
2847280|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.
2847281|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.
2847282|NCT02848443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2847283|NCT02848443||Study Protocol|https://clinicaltrials.servier.com/|
2847284|NCT02848443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2847285|NCT02848443||Informed Consent Form|https://clinicaltrials.servier.com/|
2847286|NCT02848443||Clinical Study Report|https://clinicaltrials.servier.com/|
2847287|NCT02848443||study-level clinical trial data|https://clinicaltrials.servier.com/|
2847288|NCT07239076|AssitU|Informed Consent Form|https://pmc.ncbi.nlm.nih.gov/articles/PMC10049812/|For treatment
2850635|NCT01498679|113719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850636|NCT01498679|113719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847289|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
2847290|NCT00829985|SDY223|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
2847291|NCT00829985|SDY223|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
2847292|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.
2847293|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.
2847294|NCT01155479||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05664&kw=P05664&tab=access|
2847295|NCT04335422||references|https://www.ncbi.nlm.nih.gov/pubmed/28540536|
2847296|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."
2847297|NCT03121027||Individual Participant Data Set|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|Detail about sampling and BDHS 2011 report
2847298|NCT00042029||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847299|NCT01286831|106181|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847300|NCT01286831|106181|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847301|NCT01286831|106181|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847302|NCT01286831|106181|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847303|NCT01286831|106181|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847304|NCT01286831|106181|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847305|NCT01286831|106181|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847306|NCT01277042|114590|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847307|NCT01277042|114590|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847308|NCT01277042|114590|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847309|NCT01277042|114590|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847310|NCT01277042|114590|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847311|NCT01277042|114590|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847312|NCT04488107|ICH topic S9|ICH topic S9 - nonclinical evaluation for anticancer pharmaceuticals. 2009|https://database.ich.org/sites/default/files/S9_Guideline.pdf|
2847313|NCT04488107|IBRANCE® (palbociclib) capsule|label for IBRANCE® (palbociclib) capsules|https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/207103s000lbl.pdf|
2847314|NCT04488107|IBRANCE® (palbociclib) tablets|label for IBRANCE® (palbociclib) tablets,|https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf|
2847315|NCT04488107|KISQALI® (ribociclib) tablets|Label for KISQALI® (ribociclib) tablets|https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209092s005lbl.pdf|
2847316|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|
2847317|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|
2847318|NCT01067443||Study Protocol|http://journals.plos.org/plosntds/article/file?type=supplementary&id=info:doi/10.1371/journal.pntd.0004880.s002|Final Study Protocol
2847319|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 \[there-on other citations are referenced 1 citation later\]
2847320|NCT02777736||Study Protocol|http://www.lymphoma.cz/docs/studies/dlbcl/CLSG-CNS-01_en.pdf|
2847321|NCT00688207|AVA109941|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847322|NCT00688207|AVA109941|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847323|NCT00688207|AVA109941|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847324|NCT00688207|AVA109941|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847325|NCT00688207|AVA109941|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847326|NCT00688207|AVA109941|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847327|NCT00688207|AVA109941|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847328|NCT00371007||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2847329|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
2847330|NCT00101829|SDY961|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
2847331|NCT00101829|SDY961|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
2847332|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
2847333|NCT00510874|110028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847334|NCT00510874|110028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847335|NCT00510874|110028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847336|NCT00510874|110028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847337|NCT00510874|110028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847338|NCT00510874|110028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847339|NCT00510874|110028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847340|NCT01323946|109825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847341|NCT01323946|109825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847342|NCT01323946|109825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847343|NCT01323946|109825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847344|NCT01323946|109825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847345|NCT01323946|109825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847346|NCT01323946|109825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848604|NCT00989287|113866|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848605|NCT00989287|113866|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848606|NCT00989287|113866|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848607|NCT00989287|113866|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848608|NCT00989287|113866|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848609|NCT00989287|113866|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848610|NCT00989287|113866|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848611|NCT01258608|200149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848612|NCT01258608|200149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848613|NCT01258608|200149|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848614|NCT01258608|200149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848615|NCT01258608|200149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848616|NCT01258608|200149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848617|NCT00464815|109069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848618|NCT00464815|109069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848619|NCT00464815|109069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847347|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
2847348|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
2848620|NCT00464815|109069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848621|NCT00464815|109069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848622|NCT00464815|109069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848623|NCT00464815|109069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848624|NCT06485817||Analytic Code|https://osf.io/3jvw8/|Project directory where study relevant documentation can be found and data will be uploaded.
2848625|NCT00137930|104480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848626|NCT00137930|104480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848627|NCT00137930|104480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848628|NCT00137930|104480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848629|NCT00137930|104480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848630|NCT00137930|104480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848631|NCT05154279||Study Protocol|https://www.ijrcog.org/index.php/ijrcog/article/view/3925|
2848632|NCT05154279||Study Protocol|https://ebwhj.journals.ekb.eg/article_125772.html|
2848633|NCT00518115|GLP110125|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848634|NCT00518115|GLP110125|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848635|NCT00518115|GLP110125|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848636|NCT00518115|GLP110125|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848637|NCT00518115|GLP110125|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848638|NCT00518115|GLP110125|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848639|NCT00518115|GLP110125|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848640|NCT00697749|208129/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848641|NCT00697749|208129/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848642|NCT00697749|208129/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848643|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
2848644|NCT00697749|208129/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848645|NCT00697749|208129/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848646|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
2848647|NCT00428090|105640|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848648|NCT00428090|105640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847349|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
2847350|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
2847351|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
2848649|NCT00428090|105640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848650|NCT00428090|105640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848651|NCT00428090|105640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848652|NCT00428090|105640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847352|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
2847353|NCT03272230||Study Protocol|https://data.mendeley.com/datasets/mv8hndcd95/2|The ECOCAPTURE ethograms: apathy ethogram and disinhibition ethogram
2847354|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
2847355|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
2847356|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
2847357|NCT01266941|111789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847358|NCT01266941|111789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847359|NCT01266941|111789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847360|NCT01266941|111789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847361|NCT01266941|111789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847362|NCT01266941|111789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847363|NCT01266941|111789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847364|NCT02826850||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
2847365|NCT02826850||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
2847366|NCT00887406|104865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847367|NCT00887406|104865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847368|NCT00887406|104865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847369|NCT00887406|104865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847370|NCT00887406|104865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847371|NCT00887406|104865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847372|NCT01036061|108414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847373|NCT01036061|108414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847374|NCT01036061|108414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847375|NCT01036061|108414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847376|NCT01036061|108414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847377|NCT01036061|108414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847378|NCT05749770||Individual Participant Data Set|https://zenodo.org/records/5913009|
2847379|NCT01039974|112648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847380|NCT01039974|112648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847381|NCT01039974|112648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847382|NCT01039974|112648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847383|NCT01039974|112648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847384|NCT01039974|112648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847385|NCT01039974|112648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847386|NCT05377203|PMID: 37276913|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/37276913|
2847387|NCT05648071|[ PMID ]31560378|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31560378/|
2847388|NCT05648071|PMID:30285222|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30285222/|
2847389|NCT05648071|PMID:31378236|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31378236/|
2847390|NCT05648071|PMID:32997907|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32997907/|
2847391|NCT05648071|PMID:30955977|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30955977/|
2847392|NCT05648071|PMID:31402780|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31402780/|
2847393|NCT05648071|PMID:32781263|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32781263/|
2847394|NCT05648071|PMID: 34358724|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34358724/|
2844102|NCT00133848|TOC103469|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850637|NCT01498679|113719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844103|NCT00920439|112683|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850638|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.
2850639|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.
2844104|NCT00920439|112683|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844105|NCT00920439|112683|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844106|NCT00920439|112683|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844107|NCT00920439|112683|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847395|NCT05648071|PMID: 29229461|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29229461/|
2850640|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.
2850641|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.
2850642|NCT01139580|114743|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850643|NCT01139580|114743|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847396|NCT05648071|PMID: 30119083|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30119083/|
2847397|NCT06933992||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|
2847398|NCT03075046||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
2850644|NCT01139580|114743|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850645|NCT01139580|114743|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850646|NCT01139580|114743|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850647|NCT01139580|114743|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850648|NCT01139580|114743|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850649|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.
2850650|NCT00552929||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850651|NCT00092352||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850652|NCT00158860|HS2100275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850653|NCT00158860|HS2100275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850654|NCT00158860|HS2100275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850655|NCT00158860|HS2100275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850656|NCT00158860|HS2100275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844108|NCT00920439|112683|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844109|NCT06456775||Individual Participant Data Set|https://bit.ly/49RBPuQ|
2844110|NCT07152041|CAMS-Ph+B-ALL|Individual Participant Data Set|https://login.imedidata.com|CAMS-Ph+ALL-2025 DATASET
2844111|NCT01262872|114174|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847399|NCT00023244|SDY133|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
2847400|NCT00023244|SDY133|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
2850657|NCT00158860|HS2100275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850658|NCT00158860|HS2100275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847401|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
2847402|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.
2847403|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.
2847404|NCT00290277|104951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847405|NCT00290277|104951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847406|NCT00290277|104951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847407|NCT00290277|104951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847408|NCT00290277|104951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847409|NCT00290277|104951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847410|NCT00290277|104951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847411|NCT00135564|711202/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847412|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
2850659|NCT02960750|4382156|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382156/?report=classic|
2850660|NCT02960750|4323230|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323230/?report=classic|
2853120|NCT00627458|111344|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853121|NCT04845451|Cluster Headaches-Neuroma|Clinical Study Report|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
2853122|NCT04845451|Cluster Headaches-Neuroma|Statistical Analysis Plan|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
2853123|NCT05016765|2y7fs|Study Protocol|https://osf.io/2y7fs/|
2853124|NCT01336608|113108|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853125|NCT01336608|113108|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853126|NCT01336608|113108|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853127|NCT01336608|113108|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853128|NCT01336608|113108|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853129|NCT01336608|113108|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853130|NCT01336608|113108|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853131|NCT00633217|111117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853132|NCT00633217|111117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853133|NCT00633217|111117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847413|NCT00135564|711202/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847414|NCT00135564|711202/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847415|NCT00135564|711202/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847416|NCT00135564|711202/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847417|NCT00679055||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0736-006&kw=0736-006&tab=access|
2847418|NCT06934850||Clinical Study Report|https://etik.inonu.edu.tr/panel/index|
2853134|NCT00633217|111117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853135|NCT00633217|111117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853136|NCT00633217|111117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850661|NCT02960750|4266209|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266209/|
2850662|NCT00662818||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-034&kw=0974-034&tab=access|
2850663|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
2850664|NCT00852540|110978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850665|NCT00852540|110978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850666|NCT00852540|110978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850667|NCT00852540|110978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850668|NCT00852540|110978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850669|NCT00852540|110978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850670|NCT00852540|110978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850671|NCT02135354||Study Protocol|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
2853137|NCT00633217|111117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853138|NCT00803673|110106|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853139|NCT00803673|110106|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853140|NCT00803673|110106|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853141|NCT00803673|110106|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853142|NCT00803673|110106|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853143|NCT00803673|110106|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853144|NCT00803673|110106|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853145|NCT00552617||CSr Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2853146|NCT04688814||Study Protocol|http://www.med.alexu.edu.eg|
2853147|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
2853148|NCT06565754||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563562/|
2853149|NCT02524665|114553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853150|NCT02524665|114553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853151|NCT02524665|114553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853152|NCT02524665|114553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853153|NCT02524665|114553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853154|NCT02524665|114553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853155|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|
2853156|NCT01077531|111601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853157|NCT01077531|111601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853158|NCT01077531|111601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853159|NCT01077531|111601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853160|NCT01077531|111601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853161|NCT01077531|111601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848653|NCT00428090|105640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848654|NCT06182306||Study Protocol|https://www.pearbio.com/pearmet|Company website with background and information and links to protocol, etc.
2848655|NCT04605978||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2848656|NCT04605978||Study Protocol|https://clinicaltrials.servier.com/|
2848657|NCT04605978||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2848658|NCT04605978||Informed Consent Form|https://clinicaltrials.servier.com/|
2848659|NCT04605978||Clinical Study Report|https://clinicaltrials.servier.com/|
2848660|NCT04605978||study-level clinical trial data|https://clinicaltrials.servier.com/|
2848661|NCT01627327|115805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848662|NCT01627327|115805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848663|NCT01627327|115805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848664|NCT01627327|115805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848665|NCT01627327|115805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848666|NCT01627327|115805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848667|NCT01627327|115805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848668|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
2848669|NCT01825213|PMID: 25181365|Peer reviewed article|http://ieeexplore.ieee.org/document/6887313/?arnumber=6887313|
2848670|NCT01377480||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05267&kw=P05267&tab=access|
2848671|NCT02920697||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2848672|NCT02920697||Study Protocol|https://clinicaltrials.servier.com/|
2848673|NCT02920697||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2848674|NCT02920697||Informed Consent Form|https://clinicaltrials.servier.com/|
2848675|NCT02920697||study-level clinical trial data|https://clinicaltrials.servier.com/|
2848676|NCT02920697||Clinical Study Report|https://clinicaltrials.servier.com/|
2848677|NCT06038760||Study Protocol|https://www.pearbio.com/pearglio|
2848678|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"
2848679|NCT00306982|106622|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848680|NCT00306982|106622|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848681|NCT00306982|106622|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848682|NCT00306982|106622|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848683|NCT00306982|106622|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848684|NCT00306982|106622|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848685|NCT02254447|201713|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848686|NCT02254447|201713|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848687|NCT02254447|201713|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848688|NCT02254447|201713|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848689|NCT02254447|201713|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848690|NCT02254447|201713|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848691|NCT02254447|201713|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848692|NCT04322123||Study Protocol|https://www.medrxiv.org/content/10.1101/2020.05.19.20106997v1|Preprint of the Protocol
2848693|NCT06264479||Study Protocol|https://www.pearbio.com/peartree2|
2848694|NCT06670183||Individual Participant Data Set|https://www.ukbiobank.ac.uk/enable-your-research/apply-for-access|Apply for access to UK Biobank
2848695|NCT01337674||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4618-010&kw=4618-010&tab=access|
2848696|NCT00453986|109067|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848697|NCT00453986|109067|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848698|NCT00453986|109067|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847419|NCT00699764|208141/017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847420|NCT00699764|208141/017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847421|NCT00699764|208141/017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847422|NCT00699764|208141/017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847423|NCT00699764|208141/017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847424|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
2847425|NCT00857883|111314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847426|NCT00857883|111314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847427|NCT00857883|111314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847428|NCT00857883|111314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847429|NCT00857883|111314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847430|NCT00857883|111314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847431|NCT00857883|111314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848699|NCT00453986|109067|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848700|NCT00453986|109067|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848701|NCT00453986|109067|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848702|NCT00453986|109067|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850672|NCT02135354||Statistical Analysis Plan|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
2850673|NCT01156792|114255|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850674|NCT01156792|114255|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850675|NCT01156792|114255|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850676|NCT01156792|114255|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847432|NCT00543543||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-001&kw=V503-001&tab=access|
2847433|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)."
2847434|NCT00289718|100556 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847435|NCT00289718|100556 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847436|NCT00289718|100556 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847437|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.
2847438|NCT00289718|100556 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847439|NCT01926015||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-060&kw=V260-060&tab=access|
2847440|NCT01453725||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07642&kw=8259-006&tab=access|
2847441|NCT00334607|107531|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847442|NCT00334607|107531|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847443|NCT00334607|107531|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847444|NCT00334607|107531|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847445|NCT00334607|107531|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2847446|NCT00334607|107531|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848703|NCT01777321|116760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848704|NCT01777321|116760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848705|NCT01777321|116760|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848706|NCT01777321|116760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848707|NCT01777321|116760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848708|NCT01777321|116760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848709|NCT01777321|116760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848710|NCT01506895|115403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848711|NCT01506895|115403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848712|NCT01506895|115403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848713|NCT01506895|115403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848714|NCT01506895|115403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848715|NCT01506895|115403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848716|NCT01506895|115403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848717|NCT01218126|113006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848718|NCT01218126|113006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848719|NCT01218126|113006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848720|NCT01218126|113006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848721|NCT01218126|113006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848722|NCT01218126|113006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848723|NCT01218126|113006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848724|NCT06599567|sample size|Individual Participant Data Set|https://bmjopen.bmj.com/content/10/11/e039976|reference article to see sample size with g power
2848725|NCT06599567|Nintendo Wii protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28330586/|
2848726|NCT06599567|Graded motor imagery protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32003812/|
2848727|NCT06901193||Study Protocol|https://orapps.osu.edu/buck-irb/index/view/study/64513|
2848728|NCT01879423|115207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848729|NCT01879423|115207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848730|NCT01879423|115207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848731|NCT01879423|115207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848732|NCT01879423|115207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848733|NCT01879423|115207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848734|NCT01879423|115207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848735|NCT02614443|10.1186/s40814-016-0068-9|Study Protocol|https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-016-0068-9|
2848736|NCT01477853||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431E-211&kw=0431E-211&tab=access|
2848737|NCT00508261|109835|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848738|NCT00508261|109835|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848739|NCT00508261|109835|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848740|NCT00508261|109835|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848741|NCT00508261|109835|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848742|NCT00508261|109835|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848743|NCT00508261|109835|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848744|NCT05435352||Study Protocol|https://www.pearbio.com/peartnbc|
2848745|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."
2848746|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."
2848747|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."
2848748|NCT00361959|SCO40036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848749|NCT00361959|SCO40036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848750|NCT00361959|SCO40036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848751|NCT00361959|SCO40036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848752|NCT00361959|SCO40036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848753|NCT00361959|SCO40036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848754|NCT00361959|SCO40036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848755|NCT00796250||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850677|NCT01156792|114255|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848756|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
2848757|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.
2848758|NCT00118716|SFA100314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848759|NCT00118716|SFA100314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848760|NCT00118716|SFA100314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848761|NCT00118716|SFA100314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848762|NCT00118716|SFA100314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848763|NCT00118716|SFA100314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848764|NCT01376323|114728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848765|NCT01376323|114728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848766|NCT01376323|114728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848767|NCT01376323|114728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848768|NCT01376323|114728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848769|NCT01376323|114728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850678|NCT01156792|114255|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848770|NCT01376323|114728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848771|NCT00452686|108638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848772|NCT00452686|108638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848773|NCT00452686|108638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848774|NCT00452686|108638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848775|NCT00452686|108638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848776|NCT00452686|108638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848777|NCT00452686|108638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848778|NCT03117725|31098|Study Protocol|https://ezdrug.mfds.go.kr|
2848779|NCT06579820||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|pubmed
2848780|NCT06320626|37369395|Study Protocol|http://bmjopen.bmj.com/content/13/6/e072363.long|Published study protocol
2848781|NCT01678131||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-048&kw=7009-048&tab=access|
2848782|NCT03077464||preliminary results|http://hdl.handle.net/2097/19148|Rodicheva master's thesis document with preliminary analyses
2848783|NCT04699955||Individual Participant Data Set|https://osf.io/akef9/|
2848784|NCT06453655||Study Protocol|https://doi.org/10.1097/MEG.0b013e328333fca6|
2848785|NCT00441701||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04592&kw=7123-012&tab=access|
2848786|NCT03681574|study protocol|Study Protocol|https://www.justbeamit.com/k7ciq|study protocol
2848787|NCT03681574|data set|Individual Participant Data Set|https://www.justbeamit.com/nwxjr|individual participant data set
2848788|NCT03681574|informed consent form|Informed Consent Form|https://www.justbeamit.com/n2c2d|consert form
2848789|NCT03681574|statistical plan|Statistical Analysis Plan|https://www.justbeamit.com/43kxq|statistical plan
2848790|NCT05525936|University of Sydney|Individual Participant Data Set|https://redcap.sydney.edu.au/|
2848791|NCT00652938|111507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848792|NCT00652938|111507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848793|NCT00652938|111507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848794|NCT00652938|111507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848795|NCT00652938|111507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848796|NCT00652938|111507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848797|NCT00652938|111507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848798|NCT07165366||Informed Consent Form|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EalUzspTf7VClbHYAyBlJg4BVp2wl1gK8uHn7MzUbZ4tbA?e=1vfYnE|
2848799|NCT07165366||Statistical Analysis Plan|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EbDir0nT8JNAlpv4-vfnOxMBCBxsvrV2UjY2_ua4APTs2g?e=zJdPmF|
2848800|NCT03408275||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data available to researchers on application through the website
2848801|NCT04599686|NCT04599686|Study Protocol|http://clinicaltrials.gov/ct2/results?cond=&term=NCT04599686&cntry=&state=&city=&dist=|Please see the clinical trials NCT04599686
2848802|NCT02948881|BON103593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848803|NCT02948881|BON103593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848804|NCT02948881|BON103593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848805|NCT02948881|BON103593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848806|NCT02948881|BON103593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848807|NCT02948881|BON103593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848808|NCT02948881|BON103593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848809|NCT01691521|115588|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848810|NCT01691521|115588|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848811|NCT01691521|115588|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848812|NCT01691521|115588|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848813|NCT01691521|115588|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848814|NCT01691521|115588|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848815|NCT01691521|115588|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848816|NCT04599738||Study Protocol|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
2848817|NCT04599738||Informed Consent Form|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
2848818|NCT00979602|113480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848819|NCT00979602|113480|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848820|NCT00979602|113480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848821|NCT00979602|113480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848822|NCT00979602|113480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848823|NCT00979602|113480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848824|NCT00979602|113480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848825|NCT02786264||Statistical Analysis Plan|https://docs.google.com/document/d/1SUzYG_9aKT5sSkPXEmhvRTqvhXRflQLBiXJe59inDh4/edit?usp=sharing|
2848826|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.
2848827|NCT07165613||thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp
2848828|NCT00082537||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848829|NCT00327184|106388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848830|NCT00327184|106388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848831|NCT00327184|106388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848832|NCT00327184|106388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848833|NCT00327184|106388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848834|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.
2848835|NCT00116844|VLX103596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848836|NCT00116844|VLX103596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848837|NCT00116844|VLX103596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848838|NCT00116844|VLX103596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848839|NCT00116844|VLX103596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848840|NCT00116844|VLX103596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848841|NCT00116844|VLX103596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848842|NCT00682643|FFR110537|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848843|NCT00682643|FFR110537|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848844|NCT00682643|FFR110537|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848845|NCT00682643|FFR110537|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848846|NCT00682643|FFR110537|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848847|NCT00682643|FFR110537|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848848|NCT00682643|FFR110537|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848849|NCT01036022|111407|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848850|NCT01036022|111407|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848851|NCT01036022|111407|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848852|NCT01036022|111407|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848853|NCT01036022|111407|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848854|NCT01036022|111407|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848855|NCT01036022|111407|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848856|NCT00144872|LAM100118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848857|NCT00144872|LAM100118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848858|NCT00144872|LAM100118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848859|NCT00144872|LAM100118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848860|NCT00144872|LAM100118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848861|NCT00144872|LAM100118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848862|NCT00144872|LAM100118|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848863|NCT00980005|112999|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848864|NCT00980005|112999|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848865|NCT00980005|112999|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848866|NCT00980005|112999|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848867|NCT00980005|112999|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848868|NCT00980005|112999|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848869|NCT00980005|112999|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848870|NCT01590771||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-253&kw=0431-253&tab=access|
2848871|NCT00674635|104972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848872|NCT00674635|104972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848873|NCT00674635|104972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848874|NCT00674635|104972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848875|NCT00674635|104972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848876|NCT00674635|104972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848877|NCT00674635|104972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848878|NCT02726776||Study Protocol|https://cloud.scientificnet.org/index.php/s/7vKbCJ1vs0UOYNN|Unfortunately available only in German
2848879|NCT02726776||Informed Consent Form|https://cloud.scientificnet.org/index.php/s/9RXyWhRxEgUgbTd|Unfortunately available only in German or Italian
2848880|NCT02777996||Study Protocol|http://www.ispo.it|In Italian, available under request
2848881|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.
2848882|NCT06925763||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/?term=nitroglycerin+in+bone+regeneration|
2848883|NCT06900699|Not available at moment|papers|https://pubmed.ncbi.nlm.nih.gov/|Most of thé informations available at This site and Google Scholar
2848884|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
2848885|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
2848886|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
2848887|NCT00344006|CDA 714703/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848888|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
2848889|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
2848890|NCT00344006|CDA 714703/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848891|NCT00352898|105909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848892|NCT00352898|105909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848893|NCT00352898|105909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848894|NCT00352898|105909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848895|NCT00352898|105909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848896|NCT00352898|105909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848897|NCT05051332|NCT03545269|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Efficacy and Safety of Treatment of Articular Cartilage Lesions With CartiLife®
2848898|NCT05051332|NCT03517046|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Safety of Treatment of Articular Cartilage Lesions With CartiLife®
2848899|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
2848900|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.
2848901|NCT00289770|100551 (EXT Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848902|NCT00289770|100551 (EXT Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848903|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
2848904|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)
2848905|NCT01678820||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-266&kw=0431D-266&tab=access|
2848906|NCT01190215|114452|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848907|NCT01190215|114452|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848908|NCT01190215|114452|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848909|NCT01190215|114452|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848910|NCT01190215|114452|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848911|NCT01190215|114452|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848912|NCT01235975|113807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848913|NCT01235975|113807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848914|NCT01235975|113807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848915|NCT01235975|113807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848916|NCT01235975|113807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848917|NCT01235975|113807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848918|NCT01812382|117151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848919|NCT01812382|117151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848920|NCT01812382|117151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848921|NCT01812382|117151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848922|NCT01812382|117151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848923|NCT01812382|117151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850679|NCT01156792|114255|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850680|NCT00116883|FFR100012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850681|NCT00116883|FFR100012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850682|NCT00116883|FFR100012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850683|NCT00116883|FFR100012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850684|NCT00116883|FFR100012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850685|NCT00116883|FFR100012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850686|NCT00116883|FFR100012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850687|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.
2850688|NCT00005130||Study Protocol|http://www.cardia.dopm.uab.edu/exam-materials2/protocols|
2850689|NCT00005130||Informed Consent Form|http://www.cardia.dopm.uab.edu/exam-materials2/consent-forms|
2850690|NCT00005130||Data Collection Forms|http://www.cardia.dopm.uab.edu/exam-materials2/data-collection-forms|
2850691|NCT00005130||Study Manuals|http://www.cardia.dopm.uab.edu/exam-materials2/manual-of-operations|
2850692|NCT00353288|105908|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844112|NCT01262872|114174|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844113|NCT01262872|114174|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844114|NCT01262872|114174|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850693|NCT00353288|105908|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853162|NCT01077531|111601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853163|NCT00370396|107046|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853164|NCT00370396|107046|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853165|NCT00370396|107046|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853166|NCT00370396|107046|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853167|NCT00370396|107046|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853168|NCT00370396|107046|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853169|NCT02647554||Study Protocol|http://pan.baidu.com/s/1eQJUJDK|
2853170|NCT00975884|113630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853171|NCT00975884|113630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848924|NCT01812382|117151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848925|NCT00044460|49653/326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848926|NCT00044460|49653/326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848927|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
2848928|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
2848929|NCT00044460|49653/326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848930|NCT00044460|49653/326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848931|NCT00044460|49653/326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848932|NCT01017120|114576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848933|NCT01017120|114576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848934|NCT01017120|114576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848935|NCT01017120|114576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848936|NCT01017120|114576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848937|NCT01017120|114576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848938|NCT01017120|114576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848939|NCT01868035|393229/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848940|NCT01868035|393229/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848941|NCT01868035|393229/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848942|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
2848943|NCT01868035|393229/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848944|NCT01868035|393229/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848945|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
2848946|NCT03047122|P110006|U.S. Food and Drug Administration. somo-v Automated Breast Ultrasound System|http://www.accessdata.fda.gov/cdrh_docs/pdf11/P110006b.pdf|
2848947|NCT01929330|117342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848948|NCT01929330|117342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848949|NCT01929330|117342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848950|NCT01929330|117342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848951|NCT01929330|117342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848952|NCT01929330|117342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848953|NCT01929330|117342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848954|NCT00453479|AC2108378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848955|NCT00453479|AC2108378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848956|NCT00453479|AC2108378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848957|NCT00453479|AC2108378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848958|NCT00453479|AC2108378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848959|NCT00453479|AC2108378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848960|NCT00453479|AC2108378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848961|NCT00197028|103967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848962|NCT00197028|103967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848963|NCT00197028|103967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848964|NCT00197028|103967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848965|NCT00197028|103967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848966|NCT00197028|103967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848967|NCT01147692|108366|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848968|NCT01147692|108366|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848969|NCT01147692|108366|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848970|NCT01147692|108366|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848971|NCT01147692|108366|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848972|NCT01147692|108366|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848973|NCT01147692|108366|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848974|NCT00196989|ADG20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848975|NCT00196989|ADG20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848976|NCT00196989|ADG20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848977|NCT00196989|ADG20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848978|NCT00196989|ADG20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848979|NCT00196989|ADG20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848980|NCT00196989|ADG20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848981|NCT04020003|mengxinke|Individual Participant Data Set|http://www.chictr.org.cn|
2848982|NCT00451217||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848983|NCT00047983|SDY352|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
2848984|NCT00047983|SDY352|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
2848985|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.
2848986|NCT00535743||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2848987|NCT02378402|ClinicalTrials.gov/NCT02378402|Clinical Study Report|http://jcmr-online.biomedcentral.com/articles/10.1186/s12968-016-0228-3|
2848988|NCT03176446|1.941.369|Approval of the ethics committee|http://plataformabrasil.saude.gov.br|
2848989|NCT06233123||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/32021311/|
2848990|NCT06480682|RED-D|Individual Participant Data Set|https://figshare.com/account/home|All anonymised data will be published on figshare
2848991|NCT06480682|RED-D|Study Protocol|https://figshare.com/account/home|Study protocol will be published on figshare
2848992|NCT00460148|ROP109087|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848993|NCT00460148|ROP109087|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848994|NCT00460148|ROP109087|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848995|NCT00460148|ROP109087|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848996|NCT00460148|ROP109087|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848997|NCT00460148|ROP109087|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848998|NCT00460148|ROP109087|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2848999|NCT01607385|116511|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849000|NCT01607385|116511|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849001|NCT01607385|116511|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849002|NCT01607385|116511|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849003|NCT01607385|116511|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849004|NCT01607385|116511|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849005|NCT01607385|116511|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849006|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.
2849007|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
2849008|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
2849009|NCT00240526|100450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849010|NCT00240526|100450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849011|NCT00240526|100450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849012|NCT00240526|100450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849013|NCT00240526|100450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849014|NCT00240526|100450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849015|NCT01751113|116572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849016|NCT01751113|116572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849017|NCT01751113|116572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849018|NCT01751113|116572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849019|NCT01751113|116572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849020|NCT01424436|113043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849021|NCT01424436|113043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849022|NCT01424436|113043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849023|NCT01424436|113043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849024|NCT01424436|113043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849025|NCT01424436|113043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849026|NCT01424436|113043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849027|NCT00517309||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849028|NCT00092170||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849029|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
2849030|NCT00742885|111756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849031|NCT00742885|111756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849032|NCT00742885|111756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849033|NCT00742885|111756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849034|NCT00742885|111756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849035|NCT00742885|111756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849036|NCT00742885|111756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849037|NCT03877705|Pubmed|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/m/pubmed/30455769/?i=6&from=xylitol%20review|
2849038|NCT00224523|FFR104503|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849039|NCT00224523|FFR104503|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849040|NCT00224523|FFR104503|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849041|NCT00224523|FFR104503|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849042|NCT00224523|FFR104503|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849043|NCT00224523|FFR104503|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849044|NCT00224523|FFR104503|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849045|NCT00317174|759346/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849046|NCT00317174|759346/002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849047|NCT00317174|759346/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849048|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
2849049|NCT00317174|759346/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849050|NCT00317174|759346/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849051|NCT00034645||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849052|NCT00579982|LBI108884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849053|NCT00579982|LBI108884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849054|NCT00579982|LBI108884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849055|NCT00579982|LBI108884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849056|NCT00579982|LBI108884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849057|NCT00579982|LBI108884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849058|NCT00579982|LBI108884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849059|NCT00318149|104886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849060|NCT00318149|104886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849061|NCT00318149|104886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849062|NCT00318149|104886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849063|NCT00318149|104886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849064|NCT00318149|104886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849065|NCT01340911|115444|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849066|NCT01340911|115444|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849067|NCT01340911|115444|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849068|NCT01340911|115444|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849069|NCT01340911|115444|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849070|NCT01340911|115444|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849071|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.
2849072|NCT00000556||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/affirm/|
2849073|NCT00000556||Study Forms|http://biolincc.nhlbi.nih.gov/studies/affirm/|
2849074|NCT00551213||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04721&kw=P04721&tab=access|
2849075|NCT00432679|AVD105248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849076|NCT00432679|AVD105248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849077|NCT00432679|AVD105248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849078|NCT00432679|AVD105248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849079|NCT00432679|AVD105248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849080|NCT00432679|AVD105248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849081|NCT00432679|AVD105248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849082|NCT00605371|LEP111102|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849083|NCT00605371|LEP111102|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849084|NCT00605371|LEP111102|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849085|NCT00605371|LEP111102|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849086|NCT00605371|LEP111102|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849087|NCT00605371|LEP111102|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849088|NCT00605371|LEP111102|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849089|NCT01648179|116595|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849090|NCT01648179|116595|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849091|NCT01648179|116595|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849092|NCT01648179|116595|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849093|NCT01648179|116595|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849094|NCT01648179|116595|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849095|NCT01648179|116595|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849096|NCT00519636|FFU105927|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849097|NCT00519636|FFU105927|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849098|NCT00519636|FFU105927|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849099|NCT00519636|FFU105927|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849100|NCT00519636|FFU105927|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849101|NCT00519636|FFU105927|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849102|NCT00519636|FFU105927|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849103|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.
2849104|NCT00697554|208129/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849105|NCT00697554|208129/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849106|NCT00697554|208129/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849107|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
2849108|NCT00697554|208129/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849109|NCT04731714|mtbzf|Individual Participant Data Set|https://osf.io/mtbzf/|IPD, study protocol, SAP, and ICF will all be posted at this location.
2849110|NCT00090272||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850694|NCT00353288|105908|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850695|NCT00353288|105908|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850696|NCT00353288|105908|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850697|NCT00353288|105908|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850698|NCT00306696|49653/342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850699|NCT00306696|49653/342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850700|NCT00306696|49653/342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850701|NCT00306696|49653/342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850702|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
2850703|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
2850704|NCT00306696|49653/342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850705|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/.
2850706|NCT02437253||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=28119823|
2850707|NCT00071747|SCA30926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844115|NCT01262872|114174|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849111|NCT00992160|111364|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849112|NCT00992160|111364|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849113|NCT00992160|111364|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849114|NCT00992160|111364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849115|NCT00992160|111364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849116|NCT00992160|111364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849117|NCT00992160|111364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849118|NCT00920374|113018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849119|NCT00920374|113018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849120|NCT00920374|113018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849121|NCT00920374|113018|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849122|NCT00920374|113018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849123|NCT00920374|113018|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849124|NCT00920374|113018|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849125|NCT03173248||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2849126|NCT03173248||Study Protocol|https://clinicaltrials.servier.com/|
2849127|NCT03173248||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2849128|NCT03173248||Informed Consent Form|https://clinicaltrials.servier.com/|
2849129|NCT03173248||Clinical Study Report|https://clinicaltrials.servier.com/|
2849130|NCT03173248||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2849131|NCT01627340|115918|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849132|NCT01627340|115918|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849133|NCT01627340|115918|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849134|NCT01627340|115918|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849135|NCT01627340|115918|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849136|NCT01627340|115918|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849137|NCT05776030||Statistical Analysis Plan|https://osf.io/87wfq/files/osfstorage|
2849138|NCT01577732|115389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849139|NCT01577732|115389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849140|NCT01577732|115389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849141|NCT01577732|115389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849142|NCT01577732|115389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849143|NCT01577732|115389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849144|NCT01323660|114418|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849145|NCT01323660|114418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849146|NCT01323660|114418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849147|NCT01323660|114418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849148|NCT01323660|114418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849149|NCT01323660|114418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849150|NCT01323660|114418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849151|NCT02985697|DEXProtocol|Study Protocol|https://drive.google.com/open?id=0BwBFaEmsvS0PYnlzVDUyMGREWFk|Protocol for the study; includes introduction, design, and references/citations.
2849152|NCT00933062|113140|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849153|NCT00933062|113140|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849154|NCT00933062|113140|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849155|NCT00933062|113140|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849156|NCT00933062|113140|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849157|NCT00933062|113140|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849158|NCT00933062|113140|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849159|NCT03904082||Clinical Study Report|http://doi.org/10.1016/j.jclinane.2018.06.033|
2849160|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.
2849161|NCT03205020||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25118503|
2849162|NCT01161160|114495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849163|NCT01161160|114495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849164|NCT01161160|114495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849165|NCT01161160|114495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849166|NCT01161160|114495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849167|NCT01161160|114495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849168|NCT01161160|114495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849169|NCT04610203||Study Protocol|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2849170|NCT04610203||Informed Consent Form|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2849171|NCT04610203||Clinical Study Report|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2849172|NCT04610203||Individual Participant Data Set|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2849173|NCT04610203||Statistical Analysis Plan|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|Included in the Study Protocol and Clinical Study report
2849174|NCT00410384|HGS1006-C1056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849175|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
2849176|NCT00410384|HGS1006-C1056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849177|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
2849178|NCT00410384|HGS1006-C1056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849179|NCT00410384|HGS1006-C1056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849180|NCT00410384|HGS1006-C1056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849181|NCT00119743|347414/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849182|NCT00119743|347414/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849183|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
2849184|NCT00119743|347414/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849185|NCT00119743|347414/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849186|NCT00119743|347414/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849187|NCT00578227|110886|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849188|NCT00578227|110886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849189|NCT00578227|110886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849190|NCT00578227|110886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849191|NCT00578227|110886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849192|NCT00578227|110886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849193|NCT00578227|110886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849194|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
2849195|NCT01114620|114270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849196|NCT01114620|114270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849197|NCT01114620|114270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849198|NCT01114620|114270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849199|NCT01114620|114270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849200|NCT01114620|114270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849201|NCT01114620|114270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849202|NCT00364442|SAS10019|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849203|NCT00364442|SAS10019|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849204|NCT00364442|SAS10019|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849205|NCT00364442|SAS10019|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849206|NCT00364442|SAS10019|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849207|NCT00364442|SAS10019|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849208|NCT00364442|SAS10019|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849209|NCT01125774||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-065&kw=0974-065&tab=access|
2849210|NCT00097370|100901|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849211|NCT00097370|100901|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849212|NCT00097370|100901|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849213|NCT00097370|100901|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849214|NCT00097370|100901|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849215|NCT00097370|100901|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849216|NCT00097370|100901|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849217|NCT06919211||Study Protocol|https://eyewiki.org/Retinal_Detachment|
2849218|NCT03668067||Individual Participant Data Set|http://www.abcd-vision.org/references/2WIN%20Bus%20de-identified%209-6-18.pdf|Public de-identified ongoing
2849219|NCT00263679|100406/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849220|NCT00263679|100406/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849221|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
2849222|NCT00263679|100406/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849223|NCT00263679|100406/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849224|NCT00263679|100406/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849225|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
2849226|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
2849227|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
2849228|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
2849229|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
2849230|NCT00197236|208109/232|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849231|NCT00197236|208109/232|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849232|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
2849233|NCT00197236|208109/232|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849234|NCT00197236|208109/232|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849235|NCT00197236|208109/232|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849236|NCT01096056|114182|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849237|NCT01096056|114182|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849238|NCT01096056|114182|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849239|NCT01096056|114182|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849240|NCT01096056|114182|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849241|NCT01096056|114182|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849242|NCT04553302||Clinical Study Report|http://ard.bmj.com/content/79/Suppl_1/555.2|
2849243|NCT01244984|113989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849244|NCT01244984|113989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850708|NCT00071747|SCA30926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849245|NCT01244984|113989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849246|NCT01244984|113989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849247|NCT01244984|113989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849248|NCT01244984|113989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849249|NCT01244984|113989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850709|NCT00071747|SCA30926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850710|NCT00071747|SCA30926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850711|NCT00071747|SCA30926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850712|NCT00071747|SCA30926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850713|NCT01323972|113398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850714|NCT01323972|113398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850715|NCT01323972|113398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850716|NCT01323972|113398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850717|NCT01323972|113398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850718|NCT01323972|113398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850719|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"
2850720|NCT06729515||Individual Participant Data Set|https://figshare.com/s/46ea85c406ec97afc17a|
2850721|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
2850722|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
2850723|NCT00321373|107022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850724|NCT00321373|107022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850725|NCT00321373|107022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844116|NCT01262872|114174|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850726|NCT00321373|107022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850727|NCT00321373|107022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850728|NCT01476098|114693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850729|NCT01476098|114693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850730|NCT01476098|114693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850731|NCT01476098|114693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850732|NCT01476098|114693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850733|NCT01476098|114693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850734|NCT01476098|114693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850735|NCT00950586|110792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850736|NCT00950586|110792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850737|NCT00950586|110792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849250|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.
2844117|NCT02637206|200920|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844118|NCT02637206|200920|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849251|NCT00004560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pad/|
2849252|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.
2849253|NCT01738867|116753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849254|NCT01738867|116753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849255|NCT01738867|116753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849256|NCT01738867|116753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849257|NCT01738867|116753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849258|NCT01738867|116753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849259|NCT01738867|116753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849260|NCT06103422||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/26935213/|
2849261|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/26935213/|
2849262|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/11078134/|
2850738|NCT00950586|110792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850739|NCT00950586|110792|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850740|NCT00950586|110792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850741|NCT00950586|110792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850742|NCT01711723|115676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850743|NCT01711723|115676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850744|NCT01711723|115676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850745|NCT01711723|115676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850746|NCT01711723|115676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850747|NCT01711723|115676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850748|NCT01711723|115676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850749|NCT00363870|108134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850750|NCT00363870|108134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850751|NCT00363870|108134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850752|NCT00363870|108134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844119|NCT02637206|200920|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850753|NCT00363870|108134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850754|NCT00363870|108134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850755|NCT00363870|108134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850756|NCT00196976|103533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850757|NCT00196976|103533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850758|NCT00196976|103533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850759|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.
2849263|NCT04405713|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
2849264|NCT00586339|107863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849265|NCT00586339|107863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849266|NCT00586339|107863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849267|NCT00586339|107863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849268|NCT00586339|107863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849269|NCT00586339|107863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849270|NCT01013974|113377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849271|NCT01013974|113377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849272|NCT01013974|113377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849273|NCT01013974|113377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849274|NCT01013974|113377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849275|NCT01013974|113377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849276|NCT01013974|113377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849277|NCT01196988|113275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849278|NCT01196988|113275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849279|NCT01196988|113275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849280|NCT01196988|113275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849281|NCT01196988|113275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849282|NCT01196988|113275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849283|NCT01196988|113275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849284|NCT04401722|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|through elnakeebayman@yahoo.com
2849285|NCT00140673|444563/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849286|NCT00140673|444563/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849287|NCT00140673|444563/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849288|NCT00140673|444563/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849289|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
2849290|NCT00140673|444563/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849291|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
2849292|NCT01457560|217744/060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849293|NCT01457560|217744/060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849294|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
2849295|NCT01457560|217744/060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849296|NCT01457560|217744/060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849297|NCT00843193|106870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849298|NCT00843193|106870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849299|NCT00843193|106870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849300|NCT00843193|106870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849301|NCT00843193|106870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849302|NCT00843193|106870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849303|NCT00843193|106870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849304|NCT01078233||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-058&kw=0518-058&tab=access|
2849305|NCT00502593|107066|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849306|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.
2849307|NCT00502593|107066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849308|NCT00502593|107066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849309|NCT00502593|107066|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849310|NCT00502593|107066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849311|NCT00502593|107066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849312|NCT01984086|200921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849313|NCT01984086|200921|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844120|NCT02637206|200920|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849314|NCT01984086|200921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849315|NCT01984086|200921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849316|NCT01984086|200921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849317|NCT01984086|200921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849318|NCT01984086|200921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849319|NCT02808442||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2849320|NCT02808442||Study Protocol|https://clinicaltrials.servier.com/|
2849321|NCT02808442||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2849322|NCT02808442||Informed Consent Form|https://clinicaltrials.servier.com/|
2849323|NCT02808442||Clinical Study Report|https://clinicaltrials.servier.com/|
2849324|NCT02808442||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2849325|NCT00420316|109810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849326|NCT00420316|109810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849327|NCT00420316|109810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849328|NCT00420316|109810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849329|NCT00420316|109810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849330|NCT00420316|109810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849331|NCT00420316|109810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849332|NCT02281318|200862|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849333|NCT02281318|200862|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849334|NCT02281318|200862|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849335|NCT02281318|200862|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849336|NCT02281318|200862|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849337|NCT02281318|200862|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849338|NCT02281318|200862|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849339|NCT01651949||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-003&kw=V503-003&tab=access|
2849340|NCT00937846|110771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849341|NCT00937846|110771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849342|NCT00937846|110771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849343|NCT00937846|110771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849344|NCT00937846|110771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849345|NCT00937846|110771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849346|NCT00937846|110771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849347|NCT00501020|49653/284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849348|NCT00501020|49653/284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849349|NCT00501020|49653/284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849350|NCT00501020|49653/284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849351|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
2849352|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
2844121|NCT02637206|200920|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844122|NCT02637206|200920|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844123|NCT02637206|200920|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849353|NCT00501020|49653/284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849354|NCT00197015|208109/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849355|NCT00197015|208109/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849356|NCT00197015|208109/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849357|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
2849358|NCT00197015|208109/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849359|NCT00197015|208109/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849360|NCT06615128||Study Protocol|https://doi.org/10.4049/jimmunol.182.3.1541|
2849361|NCT06615128||Study Protocol|https://doi.org/10.1371/journal.pone.0047748|
2849362|NCT06706882||INFORMATION SHEET|https://drive.google.com/file/d/1Y90Fr8O30tFqNL_OjAjMfrayrK8-KKxt/view?usp=sharing|
2849363|NCT06706882|Informed Consent Form|Informed Consent Form|https://drive.google.com/file/d/1eQLHRV80sIPlZNoHR5HFS4uauF8RWoDI/view?usp=sharing|
2849364|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.
2849365|NCT00538213|110263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849366|NCT00538213|110263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849367|NCT00538213|110263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849368|NCT00538213|110263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849369|NCT00538213|110263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849370|NCT00538213|110263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849371|NCT00538213|110263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849372|NCT01025843||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5478-001&kw=5478-001&tab=access|
2849373|NCT02683811||Study Protocol|http://www.diariodellasalute.it|Study protocol (Italian version) can be requested by contacting the project manager (lmarinaro@aslcn2.it)
2849374|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.
2849375|NCT02289560||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
2849376|NCT00961142||Results|https://www.clinicaltrialsregister.eu/ctr-search/search?query=2007-006016-33|
2844124|NCT02006589|200956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849377|NCT01235949|112921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849378|NCT01235949|112921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849379|NCT01235949|112921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849380|NCT01235949|112921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849381|NCT01235949|112921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849382|NCT01235949|112921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849383|NCT00972504|112864|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849384|NCT00972504|112864|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849385|NCT00972504|112864|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849386|NCT00972504|112864|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849387|NCT00972504|112864|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849388|NCT00972504|112864|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849389|NCT00972504|112864|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849390|NCT00970307|112157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849391|NCT00970307|112157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849392|NCT00970307|112157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849393|NCT00970307|112157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849394|NCT00970307|112157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849395|NCT00970307|112157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849396|NCT00970307|112157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849397|NCT00711126|B2C106180|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849398|NCT00711126|B2C106180|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849399|NCT00711126|B2C106180|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853172|NCT00975884|113630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853173|NCT00975884|113630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853174|NCT00975884|113630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853175|NCT00975884|113630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853176|NCT04355767||Individual Participant Data Set|https://biodatacatalyst.nhlbi.nih.gov/|
2849400|NCT00711126|B2C106180|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849401|NCT00711126|B2C106180|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849402|NCT00711126|B2C106180|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849403|NCT00711126|B2C106180|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849404|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
2849405|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25939657|Report of vascular function testing
2849406|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/24548114|Report of platelet function and physiology
2849407|NCT03912948||Web site for patient information on studies bases on patients data (RGPD)|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|
2849408|NCT05888155|01095697530|Clinical Study Report|http://Shaimaa4796@gmail.com|
2849409|NCT01123083|115494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849410|NCT01123083|115494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849411|NCT01123083|115494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849412|NCT01123083|115494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849413|NCT01123083|115494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849414|NCT01123083|115494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849415|NCT01123083|115494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849416|NCT06210334||Clinical Study Report|https://www.researchdata.org.cn/|
2849417|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.
2849418|NCT00241644|102248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849419|NCT00241644|102248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849420|NCT00241644|102248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849421|NCT00241644|102248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849422|NCT00241644|102248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849423|NCT00241644|102248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849424|NCT01370694||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=8808-001&kw=8808-001&tab=access|
2849425|NCT01648140|115879|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849426|NCT01648140|115879|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849427|NCT01648140|115879|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849428|NCT01648140|115879|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849429|NCT01648140|115879|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849430|NCT01648140|115879|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849431|NCT00622830|LPL110736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849432|NCT00622830|LPL110736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849433|NCT00622830|LPL110736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849434|NCT00622830|LPL110736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849435|NCT00622830|LPL110736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849436|NCT00622830|LPL110736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849437|NCT00622830|LPL110736|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849438|NCT01406262|107085|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849439|NCT01406262|107085|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849440|NCT01406262|107085|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849441|NCT01406262|107085|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849442|NCT01406262|107085|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844125|NCT02006589|200956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849443|NCT01406262|107085|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849444|NCT01406262|107085|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849445|NCT01405924||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-030&kw=0517-030&tab=access|
2849446|NCT02918916||Tables. Training program, Phototherapy parameters, Time point of outcomes|https://pt.scribd.com/document/325401697/Documents-ClinicalTrials-ID-2015-25219-0|
2849447|NCT05171218||Individual Participant Data Set|https://osf.io/efya2/|
2849448|NCT05171218||Study Protocol|https://doi.org/10.17605/OSF.IO/VHCA5|
2849449|NCT05171218||Statistical Analysis Plan|https://doi.org/10.17605/OSF.IO/VHCA5|
2849450|NCT05171218||Informed Consent Form|https://osf.io/efya2/|
2849451|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.
2849452|NCT01930045||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-295&kw=0518-295&tab=access|
2849453|NCT00688519|114741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849454|NCT00688519|114741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849455|NCT00688519|114741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849456|NCT00688519|114741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849457|NCT00688519|114741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849458|NCT00688519|114741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849459|NCT00688519|114741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849460|NCT04893213||Study Protocol|https://osf.io/yku5q/|Protocol on the Open Science Framework (OSF)
2849461|NCT04893213||Statistical Analysis Plan|https://osf.io/yku5q/|
2849462|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.
2849463|NCT00465816|109063|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849464|NCT00465816|109063|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849465|NCT00465816|109063|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853177|NCT00289731|100382|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853178|NCT00289731|100382|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853179|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.
2853180|NCT00289731|100382|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853181|NCT00289731|100382|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853182|NCT00289731|100382|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853183|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.
2853184|NCT01440595||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-012&kw=5172-012&tab=access|
2844126|NCT02006589|200956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849466|NCT00465816|109063|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849467|NCT00465816|109063|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849468|NCT00465816|109063|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849469|NCT00465816|109063|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849470|NCT00723450|SCA102833|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849471|NCT00723450|SCA102833|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849472|NCT00723450|SCA102833|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849473|NCT00723450|SCA102833|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849474|NCT00723450|SCA102833|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849475|NCT00723450|SCA102833|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849476|NCT00723450|SCA102833|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849477|NCT00202865||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849478|NCT00327665|106068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849479|NCT00327665|106068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849480|NCT00327665|106068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849481|NCT00327665|106068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849482|NCT00327665|106068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849483|NCT00327665|106068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849484|NCT01831791|114264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849485|NCT01831791|114264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849486|NCT01831791|114264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849487|NCT01831791|114264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849488|NCT01831791|114264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849489|NCT01831791|114264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849490|NCT01831791|114264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849491|NCT02744521|Study protocol|Study Protocol|https://sites.google.com/site/relevantdocuments2016|I shared this protocol on Google Plus.
2849492|NCT00478738|MAB104958|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849493|NCT00478738|MAB104958|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849494|NCT00478738|MAB104958|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849495|NCT00478738|MAB104958|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849496|NCT00478738|MAB104958|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850760|NCT00196976|103533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850761|NCT00196976|103533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850762|NCT01016977|114566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850763|NCT01016977|114566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850764|NCT01016977|114566|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850765|NCT01016977|114566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850766|NCT01016977|114566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850767|NCT01016977|114566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850768|NCT01016977|114566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850769|NCT00704405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-009&kw=7009-009&tab=access|
2850770|NCT01395888|115247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850771|NCT01395888|115247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850772|NCT01395888|115247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850773|NCT01395888|115247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850774|NCT01395888|115247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850775|NCT01395888|115247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850776|NCT01395888|115247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850777|NCT01498653|113714|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850778|NCT01498653|113714|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850779|NCT01498653|113714|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850780|NCT01498653|113714|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850781|NCT01498653|113714|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850782|NCT01498653|113714|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850783|NCT01498653|113714|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850784|NCT01602562|116100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850785|NCT01602562|116100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850786|NCT01602562|116100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850787|NCT01602562|116100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850788|NCT01323647|114306|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850789|NCT01323647|114306|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850790|NCT01323647|114306|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850791|NCT01323647|114306|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850792|NCT01323647|114306|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850793|NCT01323647|114306|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850794|NCT02549014||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-001&kw=1064-001&tab=access|
2850795|NCT00675090|H3B109689|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850796|NCT00675090|H3B109689|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850797|NCT00675090|H3B109689|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850798|NCT00675090|H3B109689|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850799|NCT00675090|H3B109689|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850800|NCT00675090|H3B109689|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850801|NCT00675090|H3B109689|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850802|NCT01362257|112014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850803|NCT01362257|112014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850804|NCT01362257|112014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850805|NCT01362257|112014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844127|NCT02006589|200956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849497|NCT00478738|MAB104958|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849498|NCT00478738|MAB104958|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849499|NCT00880477|217744/069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849500|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
2849501|NCT00880477|217744/069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849502|NCT00880477|217744/069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849503|NCT00880477|217744/069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849504|NCT00891176|112830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849505|NCT00891176|112830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849506|NCT00891176|112830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849507|NCT00891176|112830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849508|NCT00891176|112830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849509|NCT00891176|112830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849510|NCT00346151|SDY674|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674
2849511|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.
2849512|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
2849513|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.
2849514|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.
2849515|NCT02916758||Individual Participant Data Set|http://grad.kean.edu/ot/faculty|Please contact cmulry@kean.edu to request the data set
2849516|NCT00687011||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2849517|NCT01424397|111924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849518|NCT01424397|111924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849519|NCT01424397|111924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849520|NCT01424397|111924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849521|NCT01424397|111924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849522|NCT01424397|111924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849523|NCT01424397|111924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849524|NCT03343197||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2849525|NCT03343197||Study Protocol|https://clinicaltrials.servier.com/|
2849526|NCT03343197||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2849527|NCT03343197||Informed Consent Form|https://clinicaltrials.servier.com/|
2849528|NCT03343197||Clinical Study Report|https://clinicaltrials.servier.com/|
2849529|NCT03343197||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2849530|NCT01607372|116392|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849531|NCT01607372|116392|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849532|NCT01607372|116392|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849533|NCT01607372|116392|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850806|NCT01362257|112014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844128|NCT02006589|200956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849534|NCT01607372|116392|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849535|NCT01607372|116392|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849536|NCT01607372|116392|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849537|NCT06972433||Study Protocol|http://www.scd.edu.pk|
2849538|NCT00126997|104020|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849539|NCT00126997|104020|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849540|NCT00126997|104020|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849541|NCT00126997|104020|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849542|NCT00126997|104020|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849543|NCT00126997|104020|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849544|NCT06973135||Statistical Analysis Plan|https://dent.alexu.edu.eg/index.php/ar/|
2849545|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.
2849546|NCT00704184||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-007&kw=7009-007&tab=access|
2849547|NCT01780298||Individual Participant Data Set|https://doi.org/10.12688/f1000research.11698.2|
2849548|NCT06783530||Study Protocol|https://dentfac.mans.edu.eg|Faculty of Dentistry, Mansoura University - Ethical Committee Information.
2849549|NCT00802464|112077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849550|NCT00802464|112077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849551|NCT00802464|112077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849552|NCT00802464|112077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849553|NCT00802464|112077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849554|NCT00802464|112077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849555|NCT00802464|112077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849556|NCT00529516|109821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849557|NCT00529516|109821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849558|NCT00529516|109821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849559|NCT00529516|109821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849560|NCT00529516|109821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849561|NCT00529516|109821|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849562|NCT00529516|109821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849563|NCT04641741|FGBMEP202001|Study Protocol|https://www.idisantiago.es/|The study protocol was added to clinicaltrials.gov
2849564|NCT00000936|SDY354|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
2849565|NCT00000936|SDY354|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
2849566|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.
2849567|NCT02439827||Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-015-2543-2|Study design paper
2849568|NCT02439827||Individual Participant Data Set|http://www.scielo.br/scielo.php?pid=S1980-00372016000200207&script=sci_arttext|Instrument validation study
2849569|NCT02439827||Individual Participant Data Set|http://journals.humankinetics.com/doi/abs/10.1123/jpah.2016-0113|Intervention results
2849570|NCT05489250||Informed Consent Form|https://platon-network.de/contact|
2849571|NCT05489250||See Use & Access Regulation|https://platon-network.de/contact|
2849572|NCT05782231|VIV0001019|Individual Participant Data Set|https://doi.org/10.25934/PR00010109|
2850807|NCT01362257|112014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850808|NCT01362257|112014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850809|NCT01055379|2009-011144-19|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2009-011144-19/results|
2850810|NCT01636960||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08556&kw=P08556&tab=access|
2850811|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.
2850812|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.
2850813|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.
2850814|NCT01313637|113361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850815|NCT01313637|113361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850816|NCT01313637|113361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850817|NCT01313637|113361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850818|NCT01313637|113361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849573|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.
2849574|NCT01673555|116008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849575|NCT01673555|116008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850819|NCT01313637|113361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850820|NCT01313637|113361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849576|NCT01673555|116008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850821|NCT01751074|115677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850822|NCT01751074|115677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850823|NCT01751074|115677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850824|NCT01751074|115677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850825|NCT01751074|115677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850826|NCT01751074|115677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850827|NCT01751074|115677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850828|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Hand Shape Representation in Parietal Reach Region. The Journal of Neuroscience."
2850829|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Decoding motor imagery from the posterior parietal cortex of a tetraplegic human. Science"
2850830|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.
2850831|NCT00839657||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coag/|
2850832|NCT00839657||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coag/|
2850833|NCT00839657||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coag/|
2850834|NCT04817761||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2850835|NCT04817761||Study Protocol|https://clinicaltrials.servier.com/|
2850836|NCT04817761||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2850837|NCT04817761||Informed Consent Form|https://clinicaltrials.servier.com/|
2850838|NCT04817761||Clinical Study Report|https://clinicaltrials.servier.com/|
2850839|NCT04817761||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2850840|NCT01287065|114624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849577|NCT01673555|116008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849578|NCT01673555|116008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849579|NCT01673555|116008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850841|NCT01287065|114624|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850842|NCT01287065|114624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850843|NCT01287065|114624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850844|NCT01287065|114624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850845|NCT01287065|114624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850846|NCT01287065|114624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850847|NCT01808482|116702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850848|NCT01808482|116702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850849|NCT01808482|116702|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850850|NCT01808482|116702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850851|NCT01808482|116702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849580|NCT01673555|116008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850852|NCT01808482|116702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850853|NCT01808482|116702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853185|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."
2849581|NCT01000597|113477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849582|NCT01000597|113477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849583|NCT01000597|113477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849584|NCT01000597|113477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849585|NCT01000597|113477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849586|NCT01000597|113477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849587|NCT01000597|113477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849588|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|
2849589|NCT04649008||Individual Participant Data Set|https://www.ieeg.org/|
2849590|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"
2849591|NCT01808339|117156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849592|NCT01808339|117156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849593|NCT01808339|117156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849594|NCT01808339|117156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849595|NCT01808339|117156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850854|NCT00710021|SDY474|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474.
2850855|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.
2850856|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.
2850857|NCT06727760|Survey in efficacy of probioti|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
2850858|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|
2850859|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|
2850860|NCT06727760|0-1 Yaş Arası Bebekler|rewiev|https://dergipark.org.tr/tr/pub/firattip/issue/6338/84544|
2850861|NCT06727760|kangroo care guide|Guide|https://www.who.int/publications/i/item/9241590351|
2850862|NCT06727760|The Effects of Kangaroo Mother|article|https://ijn.mums.ac.ir/article_4152.html|
2850863|NCT06727760|efficacy of probiotic|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
2850864|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|
2850865|NCT06727760|The Effect of Aromatherapy|doctora thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
2850866|NCT00451100||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2850867|NCT01138007|113351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850868|NCT01138007|113351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850869|NCT01138007|113351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850870|NCT01138007|113351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850871|NCT01138007|113351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850872|NCT01457547|217744/094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850873|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
2850874|NCT01457547|217744/094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850875|NCT01457547|217744/094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850876|NCT01457547|217744/094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850877|NCT01457547|217744/094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850878|NCT00398645|FFA106783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850879|NCT00398645|FFA106783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850880|NCT00398645|FFA106783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850881|NCT00398645|FFA106783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850882|NCT00398645|FFA106783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850883|NCT00398645|FFA106783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850884|NCT00398645|FFA106783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850885|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)
2850886|NCT01323634|113109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850887|NCT01323634|113109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850888|NCT01323634|113109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850889|NCT01323634|113109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850890|NCT01323634|113109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850891|NCT01323634|113109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850892|NCT01323634|113109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850893|NCT04140383||Clinical Study Report|http://rdcu.be/bUabz|
2850894|NCT00407069|SDY10|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
2850895|NCT00407069|SDY10|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
2850896|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.
2850897|NCT01294683||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-118&kw=0524B-118&tab=access|
2850898|NCT03434782|60622416.1.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
2850899|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
2850900|NCT05981599||Clinical Study Report|https://doi.org/10.1371/journal.pone.0281544|
2850901|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
2850902|NCT01128894|114179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850903|NCT01128894|114179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850904|NCT01128894|114179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850905|NCT01128894|114179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850906|NCT01128894|114179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850907|NCT01128894|114179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850908|NCT01128894|114179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850909|NCT00402363|OM8 Afib|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850910|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
2850911|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
2850912|NCT00402363|OM8 Afib|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850913|NCT00402363|OM8 Afib|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850914|NCT00402363|OM8 Afib|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850915|NCT00402363|OM8 Afib|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850916|NCT00753272|106372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850917|NCT00753272|106372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850918|NCT00753272|106372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850919|NCT00753272|106372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850920|NCT00753272|106372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850921|NCT00753272|106372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850922|NCT00753272|106372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850923|NCT05512637||Study Protocol|https://bmjopen.bmj.com/content/14/11/e084110|
2850924|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
2850925|NCT01177787||Individual Participant Data Set|http://dx.doi.org/10.4172/2165-7904.1000203|
2850926|NCT03761511|NICOFA|Study Protocol|https://ukaachen.sharepoint.com/:b:/s/NICOFA/ESUAT8h1fTBHlTcsdu48LrQBbvvAABdsy81bvQ4Egq696g?e=8Xliis|
2850927|NCT01323621|112352|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850928|NCT01323621|112352|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850929|NCT01323621|112352|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850930|NCT01323621|112352|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850931|NCT01323621|112352|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850932|NCT01323621|112352|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850933|NCT01323621|112352|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853186|NCT01294605|263855/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853187|NCT01294605|263855/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853188|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
2853189|NCT01294605|263855/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853190|NCT01294605|263855/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853191|NCT01294605|263855/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853192|NCT03284073|NCT01844362|Study Protocol|http://clinicaltrials.gov|
2853193|NCT03567330||Study Protocol|https://link-springer-com.udel.idm.oclc.org/article/10.1186/s12885-018-5052-8|
2853194|NCT00140738|100633|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853195|NCT00140738|100633|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853196|NCT00140738|100633|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853197|NCT00140738|100633|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853198|NCT00140738|100633|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853199|NCT00140738|100633|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853200|NCT00969059|112967|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853201|NCT00969059|112967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853202|NCT00969059|112967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850934|NCT05905003||Individual Participant Data Set|https://nda.nih.gov/ampscz/|
2850935|NCT00390910|107737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850936|NCT00390910|107737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850937|NCT00390910|107737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850938|NCT00390910|107737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850939|NCT00390910|107737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850940|NCT00390910|107737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850941|NCT00390910|107737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850942|NCT00530868||Clinical Study Report|https://doi.org/10.1186/s13058-020-01258-x|Bevacizumab and Letrozole
2850943|NCT01372410|115321|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850944|NCT01372410|115321|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850945|NCT01372410|115321|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850946|NCT01372410|115321|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850947|NCT01372410|115321|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850948|NCT01372410|115321|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850949|NCT01372410|115321|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850950|NCT00992511|113809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850951|NCT00992511|113809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850952|NCT00992511|113809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850953|NCT00992511|113809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850954|NCT00992511|113809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850955|NCT00992511|113809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850956|NCT00992511|113809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850957|NCT05833087||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08079-9|
2850958|NCT05833087||Statistical Analysis Plan|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
2850959|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
2853203|NCT00969059|112967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853204|NCT00969059|112967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853205|NCT00969059|112967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853206|NCT00969059|112967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853207|NCT00386100|AVT105913|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853208|NCT00386100|AVT105913|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853209|NCT00386100|AVT105913|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853210|NCT00386100|AVT105913|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850960|NCT05833087||Analytic Code|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
2850961|NCT01313650|113373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850962|NCT01313650|113373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850963|NCT01313650|113373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850964|NCT01313650|113373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850965|NCT01313650|113373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850966|NCT01313650|113373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850967|NCT01313650|113373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850968|NCT03992469||Individual Participant Data Set|https://vivli.org/|
2850969|NCT01387230|115408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850970|NCT01387230|115408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850971|NCT01387230|115408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850972|NCT01387230|115408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850973|NCT01387230|115408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850974|NCT01387230|115408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850975|NCT01387230|115408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850976|NCT00437671||FDA approved labeling information|http://www.talecris-pi.info/inserts/hypertet.pdf|
2850977|NCT01405937||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-044&kw=7009-044&tab=access|
2850978|NCT01545570|114403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850979|NCT01545570|114403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850980|NCT01545570|114403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850981|NCT01545570|114403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850982|NCT01545570|114403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850983|NCT01545570|114403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850984|NCT01545570|114403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850985|NCT04561804||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/MOH_2017-06-07_000470.aspx|Israel Ministry of Health registration number
2850986|NCT00863109||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05278&kw=P05278&tab=access|
2850987|NCT04024644|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
2850988|NCT04024644|10.1016/j.joms.2011.09.034|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
2850989|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.
2850990|NCT01829360||Treatment & Testing Scripts|http://doi.org/10.23641/asha.9745181|See item S4 and S7.
2850991|NCT01829360||Published report of findings|http://doi.org/10.1044/2019_LSHSS-VOIA-18-0131|This article is open access
2850992|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.
2850993|NCT04100629||Study Protocol|https://drive.google.com/open?id=1vNjwT5j9Y32e7vdayZAMBp-3PvJWCiSK|
2850994|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.
2850995|NCT07060235|fascial tarining|statics|https://www.anatomytrains.com/fascialfitness/fascial_fitness1.pdf|fascia and mobile app
2850996|NCT01153802|112773|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850997|NCT01153802|112773|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850998|NCT01153802|112773|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2850999|NCT01153802|112773|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851000|NCT01153802|112773|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851001|NCT01153802|112773|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851002|NCT01153802|112773|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851003|NCT01436071|115283|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851004|NCT01436071|115283|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851005|NCT01436071|115283|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851006|NCT01436071|115283|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851007|NCT01436071|115283|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851008|NCT01436071|115283|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851009|NCT01436071|115283|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851010|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.
2851011|NCT00378833||CSR synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851012|NCT01013766|111823|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851013|NCT01013766|111823|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851014|NCT01013766|111823|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851015|NCT01013766|111823|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851016|NCT01013766|111823|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851017|NCT01013766|111823|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851018|NCT01013766|111823|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851019|NCT01667107||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5592-105&kw=5592-105&tab=access|
2851020|NCT01086410|106851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851021|NCT01086410|106851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851022|NCT01086410|106851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851023|NCT01086410|106851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851024|NCT01086410|106851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851025|NCT01086410|106851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851026|NCT01086410|106851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851027|NCT02509104|201897|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851028|NCT02509104|201897|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851029|NCT02509104|201897|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851030|NCT02509104|201897|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851031|NCT02509104|201897|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851032|NCT02509104|201897|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851033|NCT02509104|201897|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851034|NCT02689531|VIV00008648|Individual Participant Data Set|https://doi.org/10.25934/PR00008648|
2851035|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.
2851036|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.
2851037|NCT00108914|FFR30008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851038|NCT00108914|FFR30008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851039|NCT00108914|FFR30008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851040|NCT00108914|FFR30008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851041|NCT00108914|FFR30008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851042|NCT00108914|FFR30008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851043|NCT00108914|FFR30008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851044|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
2851045|NCT00766090|112202|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851046|NCT00766090|112202|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851047|NCT00766090|112202|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851048|NCT00766090|112202|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851049|NCT00766090|112202|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851050|NCT00766090|112202|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851051|NCT00766090|112202|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851052|NCT00067951|712753/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851053|NCT00067951|712753/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851054|NCT00067951|712753/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851055|NCT00067951|712753/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851056|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
2851057|NCT00067951|712753/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851058|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
2851059|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
2851060|NCT00139347|444563/024|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851061|NCT00139347|444563/024|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851062|NCT00139347|444563/024|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851063|NCT00139347|444563/024|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851064|NCT00139347|444563/024|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851065|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
2851066|NCT05689970|PubMed ID: 34763217|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/34763217/|
2851067|NCT01177384||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-130&kw=0431-130&tab=access|
2851068|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
2851069|NCT00279019|AC2103473|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851070|NCT00279019|AC2103473|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851071|NCT00279019|AC2103473|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851072|NCT00279019|AC2103473|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851073|NCT00279019|AC2103473|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851074|NCT00279019|AC2103473|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851075|NCT00279019|AC2103473|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851076|NCT01159912|112059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844129|NCT02006589|200956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844130|NCT02006589|200956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844131|NCT01154114|480848/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851077|NCT01159912|112059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851078|NCT01159912|112059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851079|NCT01159912|112059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851080|NCT01159912|112059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851081|NCT01159912|112059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851082|NCT01159912|112059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851083|NCT06725225||Individual Participant Data Set|https://vivli.org|
2851084|NCT04160169|doi:10.15139/S3/XEXQXO|Individual Participant Data Set|https://dataverse.unc.edu/dataset.xhtml?persistentId=doi:10.15139/S3/XEXQXO|
2851085|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.
2851086|NCT00000551||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/act/|
2851087|NCT00000551||Study Forms|http://biolincc.nhlbi.nih.gov/studies/act/|
2851088|NCT00000551||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/act/|
2851089|NCT00376584||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851090|NCT01086462|114041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851091|NCT01086462|114041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851092|NCT01086462|114041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844132|NCT01154114|480848/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844133|NCT01154114|480848/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844134|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
2844135|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
2844136|NCT01154114|480848/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844137|NCT01154114|480848/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851093|NCT01086462|114041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851094|NCT01086462|114041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851095|NCT01086462|114041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851096|NCT01086462|114041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851097|NCT00370227|107706|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851098|NCT00370227|107706|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851099|NCT00370227|107706|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851100|NCT00370227|107706|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851101|NCT00370227|107706|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851102|NCT00370227|107706|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851103|NCT01717287||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-248&kw=0518-248&tab=access|
2851104|NCT01973777||Clinical Study Report|http://www.contraceptionjournal.org/article/S0010-7824%2815%2930125-6/abstract|
2844138|NCT00812981|111954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851105|NCT00330395||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851106|NCT00768326|2006-003739-57|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2006-003739-57/results|
2851107|NCT00082524||CSRSynopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851108|NCT00169455|103477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851109|NCT00169455|103477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851110|NCT00169455|103477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851111|NCT00169455|103477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851112|NCT00169455|103477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851113|NCT00169455|103477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851114|NCT00449670|109630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851115|NCT00449670|109630|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851116|NCT00449670|109630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851117|NCT00449670|109630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851118|NCT00449670|109630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851119|NCT00449670|109630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851120|NCT00449670|109630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851121|NCT00309634|106750|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851122|NCT00309634|106750|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851123|NCT00309634|106750|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851124|NCT00309634|106750|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851125|NCT00309634|106750|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851126|NCT00309634|106750|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851127|NCT03662165||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/UULS6T|
2851128|NCT00674583|111414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851129|NCT00674583|111414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851130|NCT00674583|111414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851131|NCT00674583|111414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851132|NCT00674583|111414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851133|NCT00674583|111414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851134|NCT00674583|111414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851135|NCT00861250||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25303369|First study article: http://www.ncbi.nlm.nih.gov/pubmed/23206270
2851136|NCT00111800|100925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851137|NCT00111800|100925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851138|NCT00111800|100925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851139|NCT00111800|100925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851140|NCT00111800|100925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851141|NCT00111800|100925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851142|NCT00111800|100925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851143|NCT00714285|111295|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851144|NCT00714285|111295|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851145|NCT00714285|111295|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851146|NCT00714285|111295|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851147|NCT00714285|111295|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851148|NCT00714285|111295|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851149|NCT00714285|111295|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851150|NCT00789880|SDY14|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
2851151|NCT00789880|SDY14|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
2851152|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.
2851153|NCT05820633||Study Protocol|https://www.sealedenvelope.com/simple-randomiser/v1/lists|
2851154|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)
2851155|NCT06935656||Study Protocol|https://osf.io/9mp83|
2851156|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.
2851157|NCT00282295|105753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851158|NCT00282295|105753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851159|NCT00282295|105753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851160|NCT00282295|105753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851161|NCT00282295|105753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851162|NCT00282295|105753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851163|NCT00346073|106316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851164|NCT00346073|106316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851165|NCT00346073|106316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851166|NCT00346073|106316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851167|NCT00346073|106316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851168|NCT00346073|106316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851169|NCT00980200|113310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851170|NCT00980200|113310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851171|NCT00980200|113310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851172|NCT00980200|113310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851173|NCT00980200|113310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851174|NCT00980200|113310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851175|NCT00980200|113310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851176|NCT07171515||Study Protocol|https://data.doi.or.kr/10.22694/CANCERDATA032018070101|1\. 1. Guidelines for the Pancreatic Cancer Registry, National Cancer Center Big Data
2851177|NCT07171515||Study Protocol|https://cancerportal.kr/ncc/clinicalLibraryInfo.do|2\. CONNECT Cancer Big Data Library: Pancreatic Cancer Section
2851178|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
2851179|NCT00122681|580299/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851180|NCT00122681|580299/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851181|NCT00122681|580299/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851182|NCT00122681|580299/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851183|NCT00122681|580299/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851184|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
2851185|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
2851186|NCT02938884||Study Protocol|https://oncore.umn.edu/login/|
2851187|NCT03715153||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2851188|NCT03715153||Study Protocol|https://clinicaltrials.servier.com/|
2851189|NCT03715153||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2851190|NCT03715153||Informed Consent Form|https://clinicaltrials.servier.com/|
2851191|NCT03715153||Clinical Study Report|https://clinicaltrials.servier.com/|
2851192|NCT03715153||study-level clinical trial data]|https://clinicaltrials.servier.com/|
2851193|NCT01147744|112186|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851194|NCT01147744|112186|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851195|NCT01147744|112186|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851196|NCT01147744|112186|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851197|NCT01147744|112186|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851198|NCT01147744|112186|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851199|NCT01147744|112186|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851200|NCT05705609|Kim H, Kim S, Choe K, Kim JS|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/29579508/|web site is provided
2851201|NCT00315744|102318|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851202|NCT00315744|102318|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851203|NCT00315744|102318|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851204|NCT00315744|102318|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851205|NCT00315744|102318|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851206|NCT00315744|102318|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851207|NCT00290342|104871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851208|NCT00290342|104871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851209|NCT00290342|104871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851210|NCT00290342|104871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851211|NCT00290342|104871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851212|NCT00290342|104871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851213|NCT06089148|Cairo unversity|Study Protocol|https://medicine.cu.edu.eg/index.php/en/postgraduate/32-research/161-research-ethics-committee|upon requirement
2851214|NCT02257372|201314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851215|NCT02257372|201314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851216|NCT02257372|201314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851217|NCT02257372|201314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851218|NCT02257372|201314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851219|NCT02257372|201314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851220|NCT02257372|201314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851221|NCT00316680|104489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851222|NCT00316680|104489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851223|NCT00316680|104489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851224|NCT00316680|104489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851225|NCT00316680|104489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851226|NCT00316680|104489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851227|NCT03686436||Study Protocol|https://www.clinicaltrials.gov|
2851228|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.
2851229|NCT01669070|115441|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851230|NCT01669070|115441|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851231|NCT01669070|115441|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851232|NCT01669070|115441|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851233|NCT01669070|115441|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851234|NCT01669070|115441|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851235|NCT01669070|115441|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851236|NCT02134483||Article|https://www.ncbi.nlm.nih.gov/pubmed/26375142|
2851237|NCT02699957|Data Collection Form|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|
2851238|NCT02699957|Data Dictionary|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|Element definitions and coding instructions.
2851239|NCT00490568|AVA102675|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851240|NCT00490568|AVA102675|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851241|NCT00490568|AVA102675|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851242|NCT00490568|AVA102675|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851243|NCT00490568|AVA102675|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851244|NCT00490568|AVA102675|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851245|NCT00490568|AVA102675|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851246|NCT00695448|PIK111051|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851247|NCT00695448|PIK111051|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851248|NCT00695448|PIK111051|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851249|NCT00695448|PIK111051|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851250|NCT00695448|PIK111051|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851251|NCT00695448|PIK111051|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853211|NCT00386100|AVT105913|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853212|NCT00386100|AVT105913|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853213|NCT00386100|AVT105913|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853214|NCT01332513|114552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853215|NCT01332513|114552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853216|NCT01332513|114552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851252|NCT00695448|PIK111051|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851253|NCT04630587||Study Protocol|http://www.oulu.fi/medicine/node/52771|
2851254|NCT00996268|113412|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851255|NCT00996268|113412|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851256|NCT00996268|113412|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851257|NCT00996268|113412|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851258|NCT00996268|113412|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851259|NCT00996268|113412|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851260|NCT00996268|113412|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851261|NCT01018628|114011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851262|NCT01018628|114011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851263|NCT01018628|114011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851264|NCT01018628|114011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851265|NCT01018628|114011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851266|NCT01018628|114011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851267|NCT01018628|114011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851268|NCT00996944|113079|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851269|NCT00996944|113079|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851270|NCT00996944|113079|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851271|NCT00996944|113079|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851272|NCT00034658||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851273|NCT00385255|106323|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851274|NCT00385255|106323|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851275|NCT00385255|106323|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851276|NCT00385255|106323|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851277|NCT00385255|106323|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851278|NCT00385255|106323|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851279|NCT01225731||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05495&kw=P05495&tab=access|
2851280|NCT00513409|110031|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851281|NCT00513409|110031|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851282|NCT00513409|110031|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851283|NCT00513409|110031|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851284|NCT00513409|110031|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851285|NCT00513409|110031|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851286|NCT03177772|dtp38|Study Protocol|https://osf.io/dtp38/|Open Science Framework. we are registered
2851287|NCT02467933|449|Study Protocol|https://www.socialscienceregistry.org/trials/729|Study protocol archived on American Economic Association Social Science Registry page.
2851288|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)"
2851289|NCT00382993|TRX106573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851290|NCT00382993|TRX106573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851291|NCT00382993|TRX106573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851292|NCT00382993|TRX106573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851293|NCT00382993|TRX106573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851294|NCT00382993|TRX106573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851295|NCT00382993|TRX106573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851296|NCT04411355|10128359|National Thesis Center|https://tez.yok.gov.tr/UlusalTezMerkezi|thesis Number: 494582
2851297|NCT00835237|111413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851298|NCT00835237|111413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851299|NCT00835237|111413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851300|NCT00835237|111413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851301|NCT00835237|111413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851302|NCT00835237|111413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851303|NCT00835237|111413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851304|NCT02692495|10.17632/8bk6h6bmkr.1|Individual Participant Data Set|https://data.mendeley.com/datasets/8bk6h6bmkr/1|
2851305|NCT02692495||Clinical Study Report|http://www.aurametrix.com/nct02692495|
2851306|NCT02692495|10.1101/139014|Preprint|http://biorxiv.org/content/early/2017/05/19/139014|Study results
2851307|NCT00092846||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851308|NCT00548496|CR9108914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851309|NCT00548496|CR9108914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851310|NCT00548496|CR9108914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851311|NCT00548496|CR9108914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851312|NCT00548496|CR9108914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851313|NCT00548496|CR9108914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851314|NCT00548496|CR9108914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851315|NCT00090194|SDY356|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
2851316|NCT00090194|SDY356|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
2851317|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
2851318|NCT02931058||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2366-9|
2851319|NCT02931058||Clinical Study Report|https://www.clinicalkey.com/#!/content/journal/1-s2.0-S1063458422007154|
2851320|NCT04106648||Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/|
2851321|NCT02700490|10.17863/CAM.43399|Complete Data Set|https://doi.org/10.17863/CAM.43399|
2851322|NCT00976066|111848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851323|NCT00976066|111848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851324|NCT00976066|111848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851325|NCT00976066|111848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851326|NCT00976066|111848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851327|NCT00976066|111848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851328|NCT00976066|111848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851329|NCT01425203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08160&kw=P08160&tab=access|
2851330|NCT01857869|117014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851331|NCT01857869|117014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851332|NCT01857869|117014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851333|NCT01857869|117014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851334|NCT01857869|117014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851335|NCT01857869|117014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851336|NCT01857869|117014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851337|NCT00790907|108888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851338|NCT00790907|108888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851339|NCT00790907|108888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851340|NCT00790907|108888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851341|NCT00790907|108888|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851342|NCT00790907|108888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851343|NCT00790907|108888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851344|NCT00452699|ADA109055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851345|NCT00452699|ADA109055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851346|NCT00452699|ADA109055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851347|NCT00452699|ADA109055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851348|NCT00452699|ADA109055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851349|NCT00452699|ADA109055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851350|NCT00452699|ADA109055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851351|NCT00731250|111611|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851352|NCT00731250|111611|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851353|NCT00731250|111611|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851354|NCT00731250|111611|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851355|NCT00731250|111611|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851356|NCT00731250|111611|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851357|NCT00731250|111611|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851358|NCT00092430||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851359|NCT00317109|104756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851360|NCT00317109|104756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851361|NCT00317109|104756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851362|NCT00317109|104756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851363|NCT00317109|104756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851364|NCT00317109|104756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851365|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
2851366|NCT01627587|115893|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851367|NCT01627587|115893|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851368|NCT01627587|115893|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851369|NCT01627587|115893|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851370|NCT01627587|115893|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851371|NCT01627587|115893|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851372|NCT01627587|115893|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851373|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
2851374|NCT00861744|111870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851375|NCT00861744|111870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851376|NCT00861744|111870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851377|NCT00861744|111870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851378|NCT00861744|111870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851379|NCT00861744|111870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851380|NCT00861744|111870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851381|NCT01014117|114009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851382|NCT01014117|114009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851383|NCT01014117|114009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851384|NCT01014117|114009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851385|NCT01014117|114009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851386|NCT01014117|114009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851387|NCT00972673|112018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851388|NCT00972673|112018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851389|NCT00972673|112018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853217|NCT01332513|114552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853218|NCT01332513|114552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853219|NCT01332513|114552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853220|NCT01332513|114552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853221|NCT00879970|111960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853222|NCT00879970|111960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853223|NCT00879970|111960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853224|NCT00879970|111960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853225|NCT00879970|111960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853226|NCT00879970|111960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853227|NCT00879970|111960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853228|NCT02094937|201135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853229|NCT02094937|201135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853230|NCT02094937|201135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853231|NCT02094937|201135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853232|NCT02094937|201135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853233|NCT00550420|AVA102677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853234|NCT00550420|AVA102677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853235|NCT00550420|AVA102677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853236|NCT00550420|AVA102677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853237|NCT00550420|AVA102677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853238|NCT00550420|AVA102677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853239|NCT00550420|AVA102677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853240|NCT01416376|115830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853241|NCT01416376|115830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853242|NCT01416376|115830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853243|NCT01416376|115830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853244|NCT01416376|115830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853245|NCT01416376|115830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853246|NCT00411697|106789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853247|NCT00411697|106789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853248|NCT00411697|106789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853249|NCT00411697|106789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853250|NCT00411697|106789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853251|NCT00411697|106789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853252|NCT00524576|108988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853253|NCT00524576|108988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853254|NCT00524576|108988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851390|NCT00972673|112018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851391|NCT01110200|113874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851392|NCT01110200|113874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851393|NCT01110200|113874|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851394|NCT01110200|113874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851395|NCT01110200|113874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851396|NCT01110200|113874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851397|NCT01110200|113874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851398|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
2851399|NCT02889458|BrCA.risk.001|Study Protocol|http://www.hkuctr.com/Study/Show/b122235f3995420a97d570a85d03b542|
2851400|NCT00505453|110502|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851401|NCT00505453|110502|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851402|NCT00505453|110502|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851403|NCT00505453|110502|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851404|NCT00505453|110502|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851405|NCT00505453|110502|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851406|NCT00505453|110502|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851407|NCT00808444|111654|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851408|NCT00808444|111654|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851409|NCT00808444|111654|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851410|NCT00808444|111654|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851411|NCT00808444|111654|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851412|NCT00808444|111654|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851413|NCT00808444|111654|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851414|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.
2851415|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
2851416|NCT00368576|LPL107629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851417|NCT00368576|LPL107629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851418|NCT00368576|LPL107629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851419|NCT00368576|LPL107629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851420|NCT00368576|LPL107629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851421|NCT00368576|LPL107629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851422|NCT00368576|LPL107629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851423|NCT01209026|102936|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851424|NCT01209026|102936|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851425|NCT01209026|102936|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851426|NCT01209026|102936|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851427|NCT01209026|102936|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851428|NCT01209026|102936|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844139|NCT00812981|111954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844140|NCT00812981|111954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844141|NCT00812981|111954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844142|NCT00812981|111954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851429|NCT01209026|102936|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851430|NCT00039988|Study identifier is SDY471|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
2851431|NCT00039988|Study identifier is SDY471|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
2851432|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|
2851433|NCT01353703|111157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851434|NCT01353703|111157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851435|NCT01353703|111157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851436|NCT01353703|111157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851437|NCT01353703|111157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851438|NCT01353703|111157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851439|NCT01353742|114957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853255|NCT00524576|108988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853256|NCT00524576|108988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853257|NCT05163379||Study Protocol|https://khgmekodemedb.saglik.gov.tr/Eklenti/23273/0/fizik-tedavi-ve-rehabilitasyon-islemleri-degerlendirme-olcekleripdf.pdf|
2853258|NCT00297206|HS210914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853259|NCT00297206|HS210914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853260|NCT00297206|HS210914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853261|NCT00297206|HS210914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853262|NCT00297206|HS210914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853263|NCT00297206|HS210914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853264|NCT00297206|HS210914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853265|NCT02496221|201834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853266|NCT02496221|201834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853267|NCT02496221|201834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853268|NCT02496221|201834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853269|NCT02496221|201834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853270|NCT02496221|201834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853271|NCT02496221|201834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853272|NCT02879747||Study Protocol|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
2853273|NCT02879747||Statistical Analysis Plan|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
2853274|NCT01663714|104514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853275|NCT01663714|104514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853276|NCT01663714|104514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853277|NCT01663714|104514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853278|NCT01663714|104514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853279|NCT01663714|104514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853280|NCT01663714|104514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853281|NCT01165242|114249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853282|NCT01165242|114249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853283|NCT01165242|114249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853284|NCT01165242|114249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853285|NCT01165242|114249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853286|NCT01165242|114249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853287|NCT01162590|113545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853288|NCT01162590|113545|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853289|NCT01162590|113545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853290|NCT01162590|113545|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853291|NCT01162590|113545|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853292|NCT01162590|113545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851440|NCT01353742|114957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851441|NCT01353742|114957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851442|NCT01353742|114957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851443|NCT01353742|114957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851444|NCT01353742|114957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851445|NCT01353742|114957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851446|NCT02480933|https://doi.org/10.3892/mco.20|Study Protocol|http://www.spandidos-publications.com/mco|feasibility of the protocol paper
2851447|NCT01471665|115134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851448|NCT01471665|115134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851449|NCT01471665|115134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851450|NCT01471665|115134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851451|NCT01471665|115134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851452|NCT01471665|115134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851453|NCT01471665|115134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851454|NCT00684515||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05005&kw=P05005&tab=access|
2851455|NCT03194984|27045285|Metanalysis, systematic review|https://www.ncbi.nlm.nih.gov/pubmed/?term=27045285|
2851456|NCT03194984|21740236|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21740236|
2851457|NCT03194984|21488723|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21488723|
2851458|NCT03194984|27007348|Informed Consent Form|https://www.ncbi.nlm.nih.gov/pubmed/?term=27007348|
2851459|NCT00814957|110269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851460|NCT00814957|110269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851461|NCT00814957|110269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851462|NCT00814957|110269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851463|NCT00814957|110269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851464|NCT00814957|110269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851465|NCT00814957|110269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851466|NCT00920660|113161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851467|NCT00920660|113161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851468|NCT00920660|113161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844143|NCT00812981|111954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844144|NCT00812981|111954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851469|NCT00920660|113161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851470|NCT00920660|113161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851471|NCT00920660|113161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844145|NCT00996125|112022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844146|NCT00996125|112022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844147|NCT00996125|112022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844148|NCT00996125|112022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851472|NCT00920660|113161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851473|NCT01017952|102970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851474|NCT01017952|102970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851475|NCT01017952|102970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851476|NCT01017952|102970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851477|NCT01017952|102970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851478|NCT01017952|102970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851479|NCT01017952|102970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851480|NCT03276611||Statistical Analysis Plan|http://www.ncbi.nlm.nih.gov/|
2851481|NCT00132730||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-005&kw=0873-005&tab=access|
2851482|NCT01827631|116416|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851483|NCT01827631|116416|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851484|NCT01827631|116416|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851485|NCT01827631|116416|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851486|NCT01827631|116416|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851487|NCT01827631|116416|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851488|NCT01827631|116416|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851489|NCT01462266||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-260&kw=0431-260&tab=access|
2853293|NCT00950833|112801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853294|NCT00950833|112801|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853295|NCT00950833|112801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853296|NCT00950833|112801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853297|NCT00950833|112801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853298|NCT00950833|112801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853299|NCT00950833|112801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853300|NCT03189797||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed|
2853301|NCT02169583|201022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853302|NCT02169583|201022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853303|NCT02169583|201022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853304|NCT02169583|201022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853305|NCT02169583|201022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853306|NCT02169583|201022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853307|NCT02169583|201022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853308|NCT06538168||Informed Consent Form|https://www.facebook.com/gghgmabadfsd/?paipv=0&eav=AfbwgEmoehvAkH8F8E-KZ9WClHEgcLyNQwBOij0PYLNHpvrJZ1KZbTJdZYuWB21J8rA&_rdr|
2853309|NCT00964223|114547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844149|NCT00996125|112022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851490|NCT01475734|108372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851491|NCT01475734|108372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851492|NCT01475734|108372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851493|NCT01475734|108372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851494|NCT01475734|108372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851495|NCT01475734|108372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851496|NCT01475734|108372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851497|NCT02000804|117326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851498|NCT02000804|117326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851499|NCT02000804|117326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851500|NCT02000804|117326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851501|NCT02000804|117326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851502|NCT02000804|117326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851503|NCT02000804|117326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851504|NCT00982904||Publication of results|http://www.dndi.org/wp-content/uploads/2009/06/ClinicalPK_Tarral_FexinidazoleHAT_2014.pdf|Publication of results
2851505|NCT05506397||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/|
2851506|NCT01097629||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-029&kw=4305-029&tab=access|
2851507|NCT04106622||Pubmed|https://www.ncbi.nlm.nih.gov/pubmed/|
2851508|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
2851509|NCT00137917|710158/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851510|NCT00137917|710158/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851511|NCT00137917|710158/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853310|NCT00964223|114547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853311|NCT00964223|114547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853312|NCT00964223|114547|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853313|NCT00964223|114547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853314|NCT00964223|114547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853315|NCT00964223|114547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853316|NCT05709054||Clinical Study Report|https://doi.org/10.1016/j.ijosm.2018.07.006|
2853317|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.
2853318|NCT00000606||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nett/|
2853319|NCT00000606||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nett/|
2853320|NCT00345683|105988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853321|NCT00345683|105988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853322|NCT00345683|105988|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853323|NCT00345683|105988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853324|NCT00345683|105988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853325|NCT00345683|105988|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853326|NCT00345683|105988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853327|NCT00606684|B2C111045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853328|NCT00606684|B2C111045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853329|NCT00606684|B2C111045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853330|NCT00606684|B2C111045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853331|NCT00606684|B2C111045|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853332|NCT00606684|B2C111045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853333|NCT00606684|B2C111045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853334|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.
2853335|NCT00000531||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/avid/|
2853336|NCT00000531||Study Forms|http://biolincc.nhlbi.nih.gov/studies/avid/|
2853337|NCT00000531||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/avid/|
2853338|NCT04716673||Individual Participant Data Set|https://info.swissubase.ch|
2853339|NCT02224521|112071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853340|NCT02224521|112071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853341|NCT02224521|112071|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853342|NCT02224521|112071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853343|NCT02224521|112071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853344|NCT02224521|112071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853345|NCT02224521|112071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853346|NCT00551564|DIX110434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853347|NCT00551564|DIX110434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853348|NCT00551564|DIX110434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853349|NCT00551564|DIX110434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853350|NCT00551564|DIX110434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853351|NCT00551564|DIX110434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853352|NCT00551564|DIX110434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853353|NCT00616928|110464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853354|NCT00616928|110464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853355|NCT00616928|110464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853356|NCT00616928|110464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853357|NCT00616928|110464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851512|NCT00137917|710158/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851513|NCT04719351||Individual Participant Data Set|https://osf.io/uz3b7/?view_only=ba37189d0b594529b159ba27564dfb81|
2851514|NCT02899858|140503|Study Protocol|https://www4.vanderbilt.edu/irb/|
2851515|NCT00600171|B2C109575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851516|NCT00600171|B2C109575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851517|NCT00600171|B2C109575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851518|NCT00600171|B2C109575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851519|NCT00600171|B2C109575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851520|NCT00600171|B2C109575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851521|NCT00600171|B2C109575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851522|NCT00783393||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851523|NCT01879410|114951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851524|NCT01879410|114951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851525|NCT01879410|114951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851526|NCT01879410|114951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851527|NCT01879410|114951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851528|NCT01879410|114951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851529|NCT01879410|114951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851530|NCT03311048|Sistema Nacional de Informação|Informed Consent Form|http://portal2.saude.gov.br/sisnep/pesquisador|
2851531|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
2851532|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.
2851533|NCT00379951||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851534|NCT01086436|113552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851535|NCT01086436|113552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851536|NCT01086436|113552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851537|NCT01086436|113552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851538|NCT01086436|113552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851539|NCT01086436|113552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851540|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.
2851541|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.
2851542|NCT01428466|114849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851543|NCT01428466|114849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851544|NCT01428466|114849|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853358|NCT00616928|110464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853359|NCT00616928|110464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853360|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
2853361|NCT00229112||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2853362|NCT01001169|113847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853363|NCT01001169|113847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853364|NCT01001169|113847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853365|NCT01001169|113847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853366|NCT01001169|113847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853367|NCT01001169|113847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853368|NCT01001169|113847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853369|NCT01626820|116664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853370|NCT01626820|116664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853371|NCT01626820|116664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853372|NCT01626820|116664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853373|NCT01626820|116664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853374|NCT01626820|116664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853375|NCT01626820|116664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853376|NCT00743067|MET111648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853377|NCT00743067|MET111648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853378|NCT00743067|MET111648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853379|NCT00743067|MET111648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853380|NCT00743067|MET111648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853381|NCT00743067|MET111648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844150|NCT00996125|112022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844151|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
2844152|NCT00617890||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04720&kw=P04720&tab=access|
2844153|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/22118062/|
2844154|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/20673234/|
2844155|NCT00095420||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076578/|
2844156|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/27620949/|
2844157|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.
2844158|NCT00288626||Study summary, -design, -demographics, and -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY549|ImmPort study identifier is SDY549
2844159|NCT01777282|116170|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844160|NCT01777282|116170|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844161|NCT01777282|116170|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844162|NCT01777282|116170|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844163|NCT01777282|116170|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844164|NCT01777282|116170|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844165|NCT00566020|SCA106052|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853382|NCT00743067|MET111648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853383|NCT01000857|112812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853384|NCT01000857|112812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844166|NCT00566020|SCA106052|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844167|NCT00566020|SCA106052|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844168|NCT00566020|SCA106052|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844169|NCT02476578||Study Protocol|https://goo.gl/B6j1oF|LIMIT HEBREW PROTOCOL Version 3 (Final)
2844170|NCT04132323||Study Protocol|https://www.venousregistry.org/index.php?f=1&id=97|
2853385|NCT01000857|112812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853386|NCT01000857|112812|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853387|NCT02058628|200398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853388|NCT02058628|200398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853389|NCT02058628|200398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853390|NCT02058628|200398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853391|NCT02058628|200398|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853392|NCT02058628|200398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853393|NCT02058628|200398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853394|NCT04413747|guest_1|Study Protocol|http://giardinostlucia.it|
2853395|NCT04413747|guest_2|Informed Consent Form|http://giardinostlucia.it|
2853396|NCT04413747|guest_3|Individual Participant Data Set|http://giardinostlucia.it|
2853397|NCT01209052|112483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853398|NCT01209052|112483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853399|NCT01209052|112483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853400|NCT01209052|112483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853401|NCT01209052|112483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853402|NCT01209052|112483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853403|NCT01209052|112483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853404|NCT04517006||Individual Participant Data Set|https://osf.io/63yg9/|Not yet available, but will be posted once study is complete.
2853405|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.
2853406|NCT04517006||Informed Consent Form|https://osf.io/63yg9/|
2853407|NCT04517006||Analytic Code|https://osf.io/63yg9/|Will be posted after study is complete.
2853408|NCT00035009||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2853409|NCT01928914|114582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853410|NCT01928914|114582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853411|NCT01928914|114582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853412|NCT01928914|114582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853413|NCT01928914|114582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853414|NCT01928914|114582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853415|NCT01928914|114582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853416|NCT00946257|112438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853417|NCT00946257|112438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853418|NCT00946257|112438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853419|NCT00946257|112438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853420|NCT00946257|112438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853421|NCT00946257|112438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853422|NCT00946257|112438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853423|NCT00996671|113581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853424|NCT00996671|113581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853425|NCT00996671|113581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853426|NCT00996671|113581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853427|NCT00996671|113581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853428|NCT00996671|113581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853429|NCT00996671|113581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853430|NCT00684671|111572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853431|NCT00684671|111572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853432|NCT00684671|111572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853433|NCT00684671|111572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853434|NCT00684671|111572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853435|NCT00684671|111572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853436|NCT01691508|115575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853437|NCT01691508|115575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853438|NCT01691508|115575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853439|NCT01691508|115575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853440|NCT01691508|115575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853441|NCT01691508|115575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853442|NCT01691508|115575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853443|NCT00274703|MEE103226|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853444|NCT00274703|MEE103226|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853445|NCT00274703|MEE103226|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853446|NCT00274703|MEE103226|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853447|NCT00274703|MEE103226|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853448|NCT00197275|104733|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853449|NCT00197275|104733|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853450|NCT00197275|104733|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853451|NCT00197275|104733|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853452|NCT00197275|104733|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853453|NCT00197275|104733|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853454|NCT04956666||Individual Participant Data Set|https://clinicaltrials.servier.com|
2853455|NCT04956666||Study Protocol|https://clinicaltrials.servier.com|
2853456|NCT04956666||Statistical Analysis Plan|https://clinicaltrials.servier.com|
2853457|NCT04956666||Informed Consent Form|https://clinicaltrials.servier.com|
2853458|NCT04956666||Clinical Study Report|https://clinicaltrials.servier.com|
2853459|NCT04956666||Study-level clinical trial data|https://clinicaltrials.servier.com|
2853460|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
2853461|NCT00425737|444563/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853462|NCT00425737|444563/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853463|NCT00425737|444563/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853464|NCT00425737|444563/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853465|NCT00425737|444563/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853466|NCT03974633||Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1dEjSUmhIkqAOvh30WaJ0svs6jrdEGDyU5FXHeBuTOF8/edit?usp=sharing|
2853467|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/33036555/|
2853468|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/32247709/|
2853469|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/34252034/|
2853470|NCT01974895|200806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853471|NCT01974895|200806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853472|NCT01974895|200806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853473|NCT01974895|200806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853474|NCT01974895|200806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853475|NCT01974895|200806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853476|NCT01974895|200806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853477|NCT00317161|100480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853478|NCT00317161|100480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853479|NCT00317161|100480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853480|NCT00317161|100480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853481|NCT00317161|100480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853482|NCT00317161|100480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853483|NCT00376779|106786|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853484|NCT00376779|106786|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853485|NCT00376779|106786|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853486|NCT00376779|106786|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853487|NCT00376779|106786|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853488|NCT00376779|106786|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853489|NCT00329602|ROR104836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853490|NCT00329602|ROR104836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853491|NCT00329602|ROR104836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853492|NCT00329602|ROR104836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853493|NCT00329602|ROR104836|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853494|NCT00329602|ROR104836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853495|NCT00329602|ROR104836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853496|NCT01047345||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-006&kw=V503-006&tab=access|
2853497|NCT04025034||Informed Consent Form|http://microsoftwindows.com|Navigator
2853498|NCT00404274|NKV105097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853499|NCT00404274|NKV105097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853500|NCT00404274|NKV105097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853501|NCT00404274|NKV105097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853502|NCT00404274|NKV105097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853503|NCT00404274|NKV105097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853504|NCT00404274|NKV105097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853505|NCT00502775|FFU109047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853506|NCT00502775|FFU109047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853507|NCT00502775|FFU109047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853508|NCT00502775|FFU109047|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853509|NCT00502775|FFU109047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853510|NCT00502775|FFU109047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853511|NCT00502775|FFU109047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853512|NCT01385033||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3328-002&kw=3328-002&tab=access|
2853513|NCT00569062|PKI108574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853514|NCT00569062|PKI108574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853515|NCT00569062|PKI108574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853516|NCT00569062|PKI108574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853517|NCT00569062|PKI108574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853518|NCT00394056|NKP106254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853519|NCT00394056|NKP106254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853520|NCT00394056|NKP106254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853521|NCT00394056|NKP106254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853522|NCT00394056|NKP106254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853523|NCT00394056|NKP106254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853524|NCT02746952||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2853525|NCT02746952||Study Protocol|https://clinicaltrials.servier.com/|
2853526|NCT02746952||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2853527|NCT02746952||Informed Consent Form|https://clinicaltrials.servier.com/|
2853528|NCT02746952||Clinical Study Report|https://clinicaltrials.servier.com/|
2853529|NCT02746952||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2853530|NCT00861809|111809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853531|NCT00861809|111809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853532|NCT00861809|111809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853533|NCT00861809|111809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853534|NCT00861809|111809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853535|NCT00861809|111809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853536|NCT00861809|111809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853537|NCT00436007|106369|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853538|NCT00436007|106369|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853539|NCT00436007|106369|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853540|NCT00436007|106369|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853541|NCT00436007|106369|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853542|NCT00436007|106369|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853543|NCT00442936||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-011&kw=0974-011&tab=access|
2844171|NCT01863667||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3102-027&kw=3102-027&tab=access|
2853544|NCT00622609|MAG103114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853545|NCT00622609|MAG103114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853546|NCT00622609|MAG103114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853547|NCT00622609|MAG103114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853548|NCT00622609|MAG103114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853549|NCT00622609|MAG103114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853550|NCT00109109||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2853551|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.
2853552|NCT00000619||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/escape/|
2853553|NCT00000619||Study Forms|http://biolincc.nhlbi.nih.gov/studies/escape/|
2853554|NCT00950807|113073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853555|NCT00950807|113073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853556|NCT00950807|113073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853557|NCT00950807|113073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853558|NCT00950807|113073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853559|NCT00950807|113073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853560|NCT00950807|113073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853561|NCT02197468||Clinical Study Report|https://www.frontiersin.org/articles/10.3389/fped.2018.00347/full|Publication from this study
2853562|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.
2853563|NCT00000566||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pioped/|
2853564|NCT00000566||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pioped/|
2853565|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.
2853566|NCT00269048|LPL104884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853567|NCT00269048|LPL104884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853568|NCT00269048|LPL104884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853569|NCT00269048|LPL104884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853570|NCT00269048|LPL104884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853571|NCT00269048|LPL104884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853572|NCT00269048|LPL104884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853573|NCT07217353|IRB 2025-158|Study Protocol|https://www.axiommentor.com/pages/irb/sectionsOfProtocol.cfm?id=977&b=MP|
2853574|NCT06000280|Repositorio|Informed Consent Form|http://repositorio.bc.ufg.br|Repositorio da Biblioteca Central da Universidade Federal de Goias
2853575|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.
2853576|NCT01974999|SDY1094|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|ImmPort study identifier is SDY1094.
2853577|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.
2853578|NCT01295372|2010-022181-28|EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2010-022181-28/result|
2853579|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, \[osf.io/d5t4m/\].
2853580|NCT01866319||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3475-006&kw=3475-006&tab=access|
2853581|NCT01019603|114565|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853582|NCT01019603|114565|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853583|NCT01019603|114565|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853584|NCT01019603|114565|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853585|NCT01019603|114565|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853586|NCT01019603|114565|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853587|NCT01019603|114565|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853588|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."
2853589|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
2853590|NCT01030965|113589|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853591|NCT01030965|113589|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853592|NCT01030965|113589|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844172|NCT00116818|FFR20002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853593|NCT01030965|113589|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853594|NCT01030965|113589|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853595|NCT01030965|113589|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853596|NCT01030965|113589|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853597|NCT03044171|57655916.3.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
2853598|NCT01954264|200187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853599|NCT01954264|200187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853600|NCT01954264|200187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853601|NCT01954264|200187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853602|NCT01954264|200187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853603|NCT01954264|200187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853604|NCT03167671|ISBN-10: 1886039224|Book|https://www.amazon.com/Prescription-Drug-Abuse-Epidemic-Understanding/dp/1886039224|
2853605|NCT00062790|ARI40014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853606|NCT00062790|ARI40014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853607|NCT00062790|ARI40014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853608|NCT00062790|ARI40014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853609|NCT00062790|ARI40014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853610|NCT00062790|ARI40014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853611|NCT00062790|ARI40014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853612|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
2853613|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
2853614|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
2853615|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.
2853616|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
2853617|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
2853618|NCT00993187||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-202&kw=NCT00993187&tab=access|
2853619|NCT03579303|123|Individual Participant Data Set|http://bethesda.org?data-id=123|De-identified data for primary and secondary outcome measures
2853620|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).
2853621|NCT00693966|580299/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853622|NCT00693966|580299/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853623|NCT00693966|580299/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853624|NCT00693966|580299/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853625|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
2853626|NCT00693966|580299/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853627|NCT04437693||Clinical Study Report|https://www.worldometers.info/coronavirus/|https://www.worldometers.info/coronavirus/
2853628|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
2853629|NCT07025395|28 May 2025|Study Protocol|https://youtu.be/ql8SD07abnI|Core Training Protocol by Ioannis Tsartsapakis Ph.D.
2853630|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
2853631|NCT03222765||Study Protocol|http://www.epredice.eu|Study Protocol Version 5.0
2853632|NCT00076934|SDY661|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661|ImmPort study identifier is SDY661
2853633|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
2853634|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.
2853635|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.
2853636|NCT00358449|MEE103219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853637|NCT00358449|MEE103219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853638|NCT00358449|MEE103219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853639|NCT00358449|MEE103219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853640|NCT00358449|MEE103219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853641|NCT00358449|MEE103219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853642|NCT00358449|MEE103219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853643|NCT00454909|109377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853644|NCT00454909|109377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853645|NCT00454909|109377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853646|NCT00454909|109377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853647|NCT00454909|109377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853648|NCT00454909|109377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853649|NCT00454909|109377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853650|NCT01171963|113808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853651|NCT01171963|113808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853652|NCT01171963|113808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853653|NCT01171963|113808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853654|NCT01171963|113808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853655|NCT01171963|113808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853656|NCT01171963|113808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853657|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"
2853658|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"
2853659|NCT01171989|113978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853660|NCT01171989|113978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853661|NCT01171989|113978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853662|NCT01171989|113978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853663|NCT01171989|113978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853664|NCT01171989|113978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853665|NCT01171989|113978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853666|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.
2853667|NCT00302952|SDY473|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473
2853668|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
2853669|NCT00624065|COR111096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853670|NCT00624065|COR111096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853671|NCT00624065|COR111096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853672|NCT00624065|COR111096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853673|NCT00624065|COR111096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853674|NCT00624065|COR111096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853675|NCT00624065|COR111096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853676|NCT01376167|112582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853677|NCT01376167|112582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853678|NCT01376167|112582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853679|NCT01376167|112582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853680|NCT01376167|112582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853681|NCT01376167|112582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853682|NCT01472341||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-113&kw=0000-113&tab=access|
2853683|NCT00379600|ARA102198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853684|NCT00379600|ARA102198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853685|NCT00379600|ARA102198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853686|NCT00379600|ARA102198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853687|NCT00379600|ARA102198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853688|NCT00379600|ARA102198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853689|NCT00379600|ARA102198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853690|NCT02578953|204646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853691|NCT02578953|204646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853692|NCT02578953|204646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853693|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
2853694|NCT04391933|CPR|Informed Consent Form|https://komite.regionsyddanmark.dk/wm258128|
2853695|NCT01536405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V221-027&kw=V221-027&tab=access|
2853696|NCT03306394||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2853697|NCT03306394||Study Protocol|https://clinicaltrials.servier.com/|
2853698|NCT03306394||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2853699|NCT03306394||Informed Consent Form|https://clinicaltrials.servier.com/|
2853700|NCT03306394||Clinical Study Report|https://clinicaltrials.servier.com/|
2853701|NCT03306394||study-level clinical trial data|https://clinicaltrials.servier.com/|
2853702|NCT02841488||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
2853703|NCT02605395|201528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853704|NCT02605395|201528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853705|NCT02605395|201528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853706|NCT02605395|201528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853707|NCT01639092|25596179|Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25596179|Publication for the primary study results
2853708|NCT04752592||Study Protocol|https://www.seroselecttb.org/resources|
2853709|NCT01037114|112266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853710|NCT01037114|112266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853711|NCT01037114|112266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853712|NCT01037114|112266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853713|NCT01037114|112266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853714|NCT01037114|112266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853715|NCT01037114|112266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853716|NCT01421277||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-076&kw=0974-076&tab=access|
2853717|NCT00609674|FFU111439|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853718|NCT00609674|FFU111439|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853719|NCT00609674|FFU111439|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853720|NCT00609674|FFU111439|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853721|NCT00609674|FFU111439|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853722|NCT00609674|FFU111439|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853723|NCT00609674|FFU111439|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853724|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
2853725|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
2853726|NCT00385320|444563/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844173|NCT00116818|FFR20002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853727|NCT00385320|444563/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853728|NCT00385320|444563/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853729|NCT00385320|444563/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853730|NCT00385320|444563/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853731|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
2853732|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|
2853733|NCT02197481|PMID:25925431|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25925431|
2853734|NCT00268203|BEX104545|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853735|NCT00268203|BEX104545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853736|NCT00268203|BEX104545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853737|NCT00268203|BEX104545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853738|NCT03192163||Survey|http://j.mp/2qdz7P2|This is the RedCap survey that subjects will take.
2853739|NCT01899755|116987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853740|NCT01899755|116987|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853741|NCT01899755|116987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853742|NCT01899755|116987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853743|NCT01899755|116987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853744|NCT01899755|116987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853745|NCT01899755|116987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853746|NCT01929863|200185|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853747|NCT01929863|200185|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853748|NCT01929863|200185|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853749|NCT01929863|200185|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853750|NCT01929863|200185|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853751|NCT01929863|200185|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853752|NCT01929863|200185|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853753|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/31353554/|
2853754|NCT07067515||PMC article.|https://pubmed.ncbi.nlm.nih.gov/30734608/|
2853755|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/35508275/|
2853756|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
2853757|NCT01818024|116343|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853758|NCT01818024|116343|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853759|NCT01818024|116343|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853760|NCT01818024|116343|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853761|NCT01818024|116343|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853762|NCT01818024|116343|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853763|NCT01818024|116343|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853764|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.
2853765|NCT00005292||Study Forms|https://biolincc.nhlbi.nih.gov/studies/aadr/Forms/|
2853766|NCT02045849|117349|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853767|NCT02045849|117349|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853768|NCT02045849|117349|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853769|NCT02045849|117349|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853770|NCT02045849|117349|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853771|NCT02045849|117349|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853772|NCT02045849|117349|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853773|NCT01039961|113022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853774|NCT01039961|113022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853775|NCT01039961|113022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853776|NCT01039961|113022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853777|NCT01039961|113022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853778|NCT01039961|113022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844174|NCT00116818|FFR20002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853779|NCT01039961|113022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853780|NCT05866263||Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/23405164/|
2853781|NCT05866263||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/23405164/|
2853782|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.
2853783|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).
2853784|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).
2853785|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).
2853786|NCT00429481|444563/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853787|NCT00429481|444563/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853788|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
2853789|NCT00429481|444563/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853790|NCT00429481|444563/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853791|NCT00429481|444563/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853792|NCT00363077|107975|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853793|NCT00363077|107975|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853794|NCT00363077|107975|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853795|NCT00363077|107975|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853796|NCT00363077|107975|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853797|NCT01934205|116666|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853798|NCT01934205|116666|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853799|NCT01934205|116666|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853800|NCT01934205|116666|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853801|NCT01934205|116666|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853802|NCT01934205|116666|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853803|NCT01934205|116666|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853804|NCT00294047|104820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853805|NCT00294047|104820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853806|NCT00294047|104820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853807|NCT00294047|104820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853808|NCT00294047|104820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853809|NCT00294047|104820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853810|NCT00196963|103532|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853811|NCT00196963|103532|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853812|NCT00196963|103532|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853813|NCT00196963|103532|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853814|NCT00196963|103532|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853815|NCT00197249|270362/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853816|NCT00197249|270362/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853817|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
2853818|NCT00197249|270362/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851545|NCT01428466|114849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851546|NCT04523532||Study Protocol|http://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s13148-017-0407-6|
2851547|NCT00976144|113208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851548|NCT00976144|113208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851549|NCT00976144|113208|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851550|NCT00976144|113208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851551|NCT00976144|113208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851552|NCT00976144|113208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851553|NCT00976144|113208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851554|NCT05521737||Protocol reapproval report|https://drive.google.com/file/d/1P3sbgleW3murWJq_FIaerBlFU12aga9z/view?usp=sharing|
2851555|NCT02698098||Study Protocol|http://dx.doi.org/10.7910/DVN/RO34OK|
2851556|NCT02698098||Individual Participant Data Set|http://dx.doi.org/10.7910/DVN/RO34OK|
2851557|NCT02698098||Analytic Code|http://dx.doi.org/10.7910/DVN/RO34OK|
2851558|NCT00348140|AVA102670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851559|NCT00348140|AVA102670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851560|NCT00348140|AVA102670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851561|NCT00348140|AVA102670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851562|NCT00348140|AVA102670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851563|NCT00348140|AVA102670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851564|NCT00348140|AVA102670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851565|NCT00609596|ARI111402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851566|NCT00609596|ARI111402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851567|NCT00609596|ARI111402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851568|NCT00609596|ARI111402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851569|NCT00609596|ARI111402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851570|NCT00609596|ARI111402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851571|NCT00609596|ARI111402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851572|NCT01648231|116797|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851573|NCT01648231|116797|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851574|NCT01648231|116797|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851575|NCT01648231|116797|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851576|NCT01648231|116797|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851577|NCT01648231|116797|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851578|NCT01648231|116797|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851579|NCT00849017|112756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851580|NCT00849017|112756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851581|NCT00849017|112756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851582|NCT00849017|112756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851583|NCT00849017|112756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851584|NCT00849017|112756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853819|NCT00197249|270362/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853820|NCT01494532|111569|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853821|NCT01494532|111569|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853822|NCT01494532|111569|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853823|NCT01494532|111569|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853824|NCT01494532|111569|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853825|NCT01494532|111569|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853826|NCT01717950||Clinical Study Report|https://smhs.gwu.edu/mitm-crg/|
2853827|NCT00985751|113171|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853828|NCT00985751|113171|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853829|NCT00985751|113171|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853830|NCT00985751|113171|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853831|NCT00985751|113171|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853832|NCT00268216|SCO30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853833|NCT00268216|SCO30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853834|NCT00268216|SCO30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853835|NCT00268216|SCO30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853836|NCT00268216|SCO30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853837|NCT00268216|SCO30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853838|NCT00268216|SCO30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2853839|NCT06729164|Open Science Framework|The study's relevant instructional context measures. Supporting materials include the assessment instrument, protocols, etc.|https://osf.io/eq5s8/overview|
2853840|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.
2844175|NCT00116818|FFR20002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844176|NCT00116818|FFR20002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844177|NCT00116818|FFR20002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844178|NCT00116818|FFR20002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844179|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.
2844180|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
2844181|NCT00291876|100571 (M138)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844182|NCT00291876|100571 (M138)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844183|NCT00291876|100571 (M138)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844184|NCT00291876|100571 (M138)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844185|NCT00291876|100571 (M138)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844186|NCT04068129||Individual Participant Data Set|http://www.abcd-vision.org/references/index.html|
2844187|NCT01521390|115487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844188|NCT01521390|115487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844189|NCT01521390|115487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844190|NCT01521390|115487|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844191|NCT01521390|115487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844192|NCT01521390|115487|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851585|NCT00849017|112756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851586|NCT03289130||Individual Participant Data Set|https://pcap.bioinf.unc.edu/|
2851587|NCT02706938|Clinical Trial Protocol|Study Protocol|https://drive.google.com/open?id=0B6Uam9x9PtiiV2xUcDBKU3RHYU0|
2844193|NCT01521390|115487|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844194|NCT06575127||Informed Consent Form|https://drive.google.com/file/d/1_CG_0wzCH_ZUxWXsfARsyWlcx37fOcRq/view?usp=drive_link|
2844195|NCT05497518||Study Protocol|https://tuftsmedicalcenter.box.com/s/bplcm9clgjsnnq23zcwwwuze6up368q4|
2844196|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
2844197|NCT05664360||Individual Participant Data Set|https://www.doi.org/10.17605/OSF.IO/TRU4N|
2844198|NCT00839527|112757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844199|NCT00839527|112757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844200|NCT00839527|112757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844201|NCT00839527|112757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844202|NCT00839527|112757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844203|NCT00839527|112757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851588|NCT00868790||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3577-009&kw=3577-009&tab=access|
2851589|NCT01154101|114296|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844204|NCT00839527|112757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844205|NCT02064504|201010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844206|NCT02064504|201010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851590|NCT01154101|114296|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851591|NCT01154101|114296|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844207|NCT02064504|201010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844208|NCT02064504|201010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844209|NCT02064504|201010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844210|NCT02064504|201010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844211|NCT02064504|201010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844212|NCT06968169||Study Protocol|https://doi.org/10.17605/OSF.IO/AJDZS|
2844213|NCT01014988|113678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844214|NCT01014988|113678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844215|NCT01014988|113678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844216|NCT01014988|113678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844217|NCT01014988|113678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844218|NCT01014988|113678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844219|NCT01014988|113678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844220|NCT00347139|B2C106093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844221|NCT00347139|B2C106093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844222|NCT00347139|B2C106093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844223|NCT00347139|B2C106093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844224|NCT00347139|B2C106093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844225|NCT00347139|B2C106093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844226|NCT00347139|B2C106093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844227|NCT00115492|SCO100250|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844228|NCT00115492|SCO100250|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844229|NCT00115492|SCO100250|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844230|NCT00115492|SCO100250|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844231|NCT00115492|SCO100250|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844232|NCT00115492|SCO100250|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844233|NCT00115492|SCO100250|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844234|NCT00268177|SCO30005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844235|NCT00268177|SCO30005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844236|NCT00268177|SCO30005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844237|NCT00268177|SCO30005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844238|NCT00268177|SCO30005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844239|NCT00268177|SCO30005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844240|NCT00268177|SCO30005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844241|NCT00256854|ROX104805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844242|NCT00256854|ROX104805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844243|NCT00256854|ROX104805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844244|NCT00256854|ROX104805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844245|NCT00256854|ROX104805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844246|NCT00256854|ROX104805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844247|NCT00256854|ROX104805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844248|NCT02004886||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0893-005&kw=0893-005&tab=access|
2844249|NCT00370318|107017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844250|NCT00370318|107017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844251|NCT00370318|107017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844252|NCT00370318|107017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844253|NCT00370318|107017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844254|NCT00370318|107017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845234|NCT01899703|117213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845235|NCT01371682|112771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845236|NCT01371682|112771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845237|NCT01371682|112771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845238|NCT01371682|112771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845239|NCT01371682|112771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844255|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
2844256|NCT00325156|100917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851592|NCT01154101|114296|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851593|NCT01154101|114296|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851594|NCT01154101|114296|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851595|NCT04067518||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2851596|NCT04067518||Study Protocol|https://clinicaltrials.servier.com/|
2851597|NCT04067518||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2851598|NCT04067518||Informed Consent Form|https://clinicaltrials.servier.com/|
2851599|NCT04067518||Clinical Study Report|https://clinicaltrials.servier.com/|
2851600|NCT04067518||study-level clinical trial data|https://clinicaltrials.servier.com/|
2851601|NCT00792298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-006&kw=4305-006&tab=access|
2851602|NCT00707798|111651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851603|NCT00707798|111651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851604|NCT00707798|111651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851605|NCT00707798|111651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851606|NCT00707798|111651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851607|NCT04091347|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
2851608|NCT04091347|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
2851609|NCT00537719|GLP107030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851610|NCT00537719|GLP107030|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851611|NCT00537719|GLP107030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851612|NCT00537719|GLP107030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851613|NCT00537719|GLP107030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851614|NCT00537719|GLP107030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851615|NCT00537719|GLP107030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851616|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."
2851617|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)
2851618|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)
2851619|NCT07199218||Informed Consent Form|https://osf.io/f69ds/files/osf|
2851620|NCT07236723||Data Monitoring Committee Charter|https://pmc.ncbi.nlm.nih.gov/articles/PMC7571449/|https://pmc.ncbi.nlm.nih.gov/articles/PMC7571449/
2851621|NCT01495026|115708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851622|NCT01495026|115708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851623|NCT01495026|115708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851624|NCT01495026|115708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851625|NCT01495026|115708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851626|NCT01495026|115708|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844257|NCT00325156|100917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844258|NCT00325156|100917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844259|NCT00325156|100917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844260|NCT00325156|100917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844261|NCT00325156|100917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844262|NCT00784550|111114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844263|NCT00784550|111114|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844264|NCT00784550|111114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844265|NCT00784550|111114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844266|NCT00784550|111114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844267|NCT00784550|111114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844268|NCT00784550|111114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844269|NCT01424514|114974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844270|NCT01424514|114974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844271|NCT01424514|114974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844272|NCT01424514|114974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844273|NCT01424514|114974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844274|NCT01424514|114974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849596|NCT01808339|117156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849597|NCT01808339|117156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849598|NCT00123903|COR103560|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849599|NCT00123903|COR103560|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849600|NCT00123903|COR103560|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849601|NCT00123903|COR103560|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849602|NCT00123903|COR103560|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849603|NCT00123903|COR103560|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849604|NCT00123903|COR103560|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849605|NCT03181711||Study Protocol|http://mah.se|can be requested by mail Karin.Ridell@mah.se
2849606|NCT03997916||Individual Participant Data Set|http://redcap.uhhospitals.org/redcap|
2849607|NCT00314860|101468/204|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849608|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
2849609|NCT00314860|101468/204|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849610|NCT00314860|101468/204|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849611|NCT00314860|101468/204|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849612|NCT00314860|101468/204|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849613|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
2849614|NCT05909618||Nature Communications manuscript|https://www.nature.com/articles/s41467-021-22186-0|
2849615|NCT05179200||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08035-7|
2849616|NCT01017146|114575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849617|NCT01017146|114575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849618|NCT01017146|114575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851627|NCT01495026|115708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851628|NCT06896929|permethrin|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/21860157/|Comparison of permethrin and ivermectin in scabies was done
2851629|NCT00358813|NKT102783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851630|NCT00358813|NKT102783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851631|NCT00358813|NKT102783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851632|NCT00358813|NKT102783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851633|NCT00358813|NKT102783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849619|NCT01017146|114575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849620|NCT01017146|114575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844275|NCT01424514|114974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844276|NCT00035295||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844277|NCT00381238|AVA104617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844278|NCT00381238|AVA104617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844279|NCT00381238|AVA104617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844280|NCT00381238|AVA104617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844281|NCT00381238|AVA104617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844282|NCT00381238|AVA104617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844283|NCT00381238|AVA104617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844284|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.
2844285|NCT00005276||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/access|
2844286|NCT00005276||Study Forms|http://biolincc.nhlbi.nih.gov/studies/access|
2844287|NCT00005276||Procedures Manual|http://biolincc.nhlbi.nih.gov/studies/access|
2844288|NCT00976820|113482|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844289|NCT00976820|113482|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844290|NCT00976820|113482|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844291|NCT00976820|113482|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844292|NCT00976820|113482|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844293|NCT00976820|113482|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844294|NCT01571999|114636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844295|NCT01571999|114636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844296|NCT01571999|114636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844297|NCT01571999|114636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844298|NCT01571999|114636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844299|NCT01571999|114636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844300|NCT01571999|114636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844301|NCT02184585|117057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844302|NCT02184585|117057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844303|NCT02184585|117057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844304|NCT02184585|117057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844305|NCT02184585|117057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844306|NCT02184585|117057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844307|NCT02184585|117057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844308|NCT01899742|116960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844309|NCT01899742|116960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844310|NCT01899742|116960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844311|NCT01899742|116960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844312|NCT01899742|116960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844313|NCT01899742|116960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844314|NCT01899742|116960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844315|NCT01154088|114248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844316|NCT01154088|114248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844317|NCT01154088|114248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844318|NCT01154088|114248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844319|NCT01154088|114248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844320|NCT01154088|114248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844321|NCT03347734||Clinical Study Report|https://en.wikipedia.org/wiki/Bates_method|
2844322|NCT03228316||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/27208713|
2844323|NCT01446237|115576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844324|NCT01446237|115576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844325|NCT01446237|115576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844326|NCT01446237|115576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844327|NCT01446237|115576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844328|NCT01446237|115576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844329|NCT01446237|115576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844330|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
2844331|NCT00460707|NKV109990|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844332|NCT00460707|NKV109990|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844333|NCT00460707|NKV109990|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844334|NCT00460707|NKV109990|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844335|NCT00460707|NKV109990|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844336|NCT00460707|NKV109990|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844337|NCT00460707|NKV109990|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844338|NCT01453478|115550|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844339|NCT01453478|115550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844340|NCT01453478|115550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844341|NCT01453478|115550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844342|NCT01453478|115550|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844343|NCT01453478|115550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844344|NCT01453478|115550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844345|NCT05336292||Individual Participant Data Set|https://drive.google.com/drive/folders/1Z6K71rEcfJHXIzsurwREdgHRweFwgFW3|Data will be made available upon reasonable request
2844346|NCT00831545||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844347|NCT05544773||Study Protocol|https://drive.google.com/file/d/1gKwThkhpbD7eQxFYL4CkTEhzWtcLS1jZ/view?usp=sharing|
2844348|NCT00197002|208109/220|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844349|NCT00197002|208109/220|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844350|NCT00197002|208109/220|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844351|NCT00197002|208109/220|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844352|NCT00197002|208109/220|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851634|NCT00358813|NKT102783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851635|NCT00358813|NKT102783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851636|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
2851637|NCT00818259||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=0869-134&kw=0869-134&tab=access|
2851638|NCT00684177|TOC110977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851639|NCT00684177|TOC110977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851640|NCT00684177|TOC110977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851641|NCT00684177|TOC110977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851642|NCT00684177|TOC110977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851643|NCT00684177|TOC110977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851644|NCT00684177|TOC110977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851645|NCT02069002||Study Protocol|http://bmjopen.bmj.com/content/6/6/e011003.full.pdf+html|
2851646|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.
2851647|NCT00312013|FRX106365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851648|NCT00312013|FRX106365|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851649|NCT00312013|FRX106365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851650|NCT00312013|FRX106365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851651|NCT00312013|FRX106365|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851652|NCT00312013|FRX106365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851653|NCT00312013|FRX106365|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851654|NCT00996840|111592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851655|NCT00996840|111592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851656|NCT00996840|111592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851657|NCT00996840|111592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851658|NCT00996840|111592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851659|NCT00996840|111592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851660|NCT00996840|111592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851661|NCT01164878||Individual Participant Data Set|https://dfzljdn9uc3pi.cloudfront.net/2016/2483/1/SPSS_repa_et_al.sav|SPSS Data Set for Analysis
2844353|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
2844354|NCT05376241||Individual Participant Data Set|https://osf.io/y8stc/|
2844355|NCT00984139|112682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844356|NCT00984139|112682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844357|NCT00984139|112682|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844358|NCT00984139|112682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844359|NCT00984139|112682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844360|NCT00984139|112682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844361|NCT00984139|112682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844362|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.
2844363|NCT00036491|SDY625|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|ImmPort study identifier is SDY625.
2844364|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.
2844365|NCT00954512||CSR Synospsi Links|http://www.merck.com/clinical-trials/study.html?id=P04722&kw=P04722&tab=access|
2844366|NCT02920541||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2844367|NCT02920541||Study Protocol|https://clinicaltrials.servier.com/|
2844368|NCT02920541||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2844369|NCT02920541||Informed Consent Form|https://clinicaltrials.servier.com/|
2844370|NCT02920541||study-level clinical trial data|https://clinicaltrials.servier.com/|
2844371|NCT02920541||Clinical Study Report|https://clinicaltrials.servier.com/|
2844372|NCT01639066|25800784|pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25800784|Publication for the primary study results
2844373|NCT00345878|105926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844374|NCT00345878|105926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844375|NCT00345878|105926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844376|NCT00345878|105926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844377|NCT00345878|105926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844378|NCT00345878|105926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844379|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.
2844380|NCT06623838|HNYZ6|Study Protocol|https://doi.org/10.17605/OSF.IO/HNYZ6|
2844381|NCT00742508|CRV110734|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844382|NCT00742508|CRV110734|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844383|NCT00742508|CRV110734|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844384|NCT00742508|CRV110734|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844385|NCT00742508|CRV110734|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844386|NCT05442606||Full Paper|https://www.e-arm.org/journal/view.php?doi=10.5535/arm.23058|
2844387|NCT02262689|201402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844388|NCT02262689|201402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844389|NCT02262689|201402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844390|NCT02262689|201402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844391|NCT02262689|201402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844392|NCT02262689|201402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844393|NCT02262689|201402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844394|NCT00514904|109495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844395|NCT00514904|109495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844396|NCT00514904|109495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844397|NCT00514904|109495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844398|NCT00514904|109495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844399|NCT00514904|109495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844400|NCT00514904|109495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844401|NCT00553397|SDY293|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
2844402|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.
2844403|NCT00553397|SDY293|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
2844404|NCT01573767|106853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851662|NCT00463437|109507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851663|NCT00463437|109507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851664|NCT00463437|109507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851665|NCT00463437|109507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851666|NCT00463437|109507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851667|NCT00463437|109507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851668|NCT00463437|109507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851669|NCT02740309|Sala Institute|Sala Institute for Child & Family Centered Care|http://nyulangone.org/locations/hassenfeld-childrens-hospital/sala-institute-for-child-family-centered-care|
2851670|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.
2851671|NCT03094247||Individual Participant Data Set|https://openscholarship.wustl.edu/data/101/|
2851672|NCT03184948||Statistical Analysis Plan|http://ketkisheth.weebly.com/|
2851673|NCT00291343|105239 (mth24-30)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851674|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
2851675|NCT00291343|105239 (mth24-30)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851676|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
2851677|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.
2851678|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
2851679|NCT01471327|115705|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851680|NCT01471327|115705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851681|NCT01471327|115705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851682|NCT01471327|115705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851683|NCT01471327|115705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844405|NCT01573767|106853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844406|NCT01573767|106853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844407|NCT01573767|106853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844408|NCT01573767|106853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844409|NCT01573767|106853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851684|NCT01471327|115705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851685|NCT01471327|115705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851686|NCT00473694||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851687|NCT02184637|200951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851688|NCT02184637|200951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851689|NCT02184637|200951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844410|NCT01573767|106853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844411|NCT00092339||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844412|NCT00005159|NLMS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nlms/|Public-use IPD through BioLINCC. Registration is required for access.
2844413|NCT05546216||REFERENCE|https://doi.org/10.1016/j.ctcp.2019.101068|
2844414|NCT05546216||REFERENCE|http://dx.doi.org/10.1016/j.ijcard.2016.11.043|
2844415|NCT05546216||REFERENCE|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540812/|
2844416|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30367542/|
2844417|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/18065335/|
2844418|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/35307131/|
2844419|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/17056770/|
2844420|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/27252099/|
2844421|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/33632127/|
2844422|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/26171374/|
2844423|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/29476940/|
2844424|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.
2844425|NCT00005300||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/csscd/|
2844426|NCT00005300||Study Forms|http://biolincc.nhlbi.nih.gov/studies/csscd/|
2844427|NCT03273465||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
2844428|NCT00322361||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844429|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
2844430|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
2844431|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
2844432|NCT04909372||Study Protocol|https://osf.io/du58k/|
2844433|NCT04909372||Statistical Analysis Plan|https://osf.io/du58k/|
2844434|NCT04909372||Individual Participant Data Set|https://osf.io/du58k/|
2844435|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.
2844436|NCT04928469||Statistical Analysis Plan|https://docs.google.com/document/d/11uN0slg6N6K_10vm4BuXVtB7_QcZOAf5M6P0I-okGkU/edit#|
2844437|NCT00483704||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-031&kw=0974-031&tab=access|
2851690|NCT02184637|200951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849621|NCT01017146|114575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851691|NCT02184637|200951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844438|NCT05416645|post LSG GERD|Study Protocol|http://www.mans.edu.eg/|Postlaparoscopic sleeve gastrectomy
2844439|NCT02064465|200697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844440|NCT02064465|200697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844441|NCT02064465|200697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844442|NCT02064465|200697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844443|NCT02064465|200697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2849622|NCT01017146|114575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844444|NCT02064465|200697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844445|NCT02064465|200697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844446|NCT00282386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844447|NCT01009255|110651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844448|NCT01009255|110651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844449|NCT01009255|110651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844450|NCT01009255|110651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844451|NCT01009255|110651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844452|NCT01009255|110651|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844453|NCT01009255|110651|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844454|NCT00103922|CIL103657|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844455|NCT00103922|CIL103657|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844456|NCT00103922|CIL103657|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844457|NCT00103922|CIL103657|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844458|NCT00103922|CIL103657|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844459|NCT00103922|CIL103657|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844460|NCT03707366||Individual Participant Data Set|https://osf.io/673eu/|
2844461|NCT00849134|111383|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844462|NCT00849134|111383|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844463|NCT00849134|111383|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844464|NCT00849134|111383|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844465|NCT00849134|111383|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844466|NCT00849134|111383|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844467|NCT00849134|111383|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844468|NCT01440387|115418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844469|NCT01440387|115418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844470|NCT01440387|115418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844471|NCT01440387|115418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844472|NCT01440387|115418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844473|NCT01440387|115418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844474|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.\[http://dx.doi.org/10.1097/PRS.0000000000002852\] \[PMID: 28027253\]
2844475|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.
2844476|NCT00005131||Study Forms|http://www2.cscc.unc.edu/aric/cohort-forms|
2844477|NCT00005131||Study Manuals|http://www2.cscc.unc.edu/aric/cohort-forms|
2844478|NCT01362244|111782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844479|NCT01362244|111782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844480|NCT01362244|111782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844481|NCT01362244|111782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844482|NCT01362244|111782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844483|NCT01362244|111782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844484|NCT01362244|111782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844485|NCT01485445|115440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844486|NCT01485445|115440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844487|NCT01485445|115440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844488|NCT01485445|115440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844489|NCT01485445|115440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844490|NCT01485445|115440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844491|NCT01485445|115440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844492|NCT02713438||Study Protocol|https://drive.google.com/file/d/1bosgzFmvKglMyMjhELiSg-fqzw1pn1nf/view?usp=sharing|The handbook with the protocol for experimenters (in English)
2844493|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
2844494|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.
2844495|NCT00000589||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/trap/|
2844496|NCT00000589||Study Forms|http://biolincc.nhlbi.nih.gov/studies/trap/|
2844497|NCT00359177|NKT102785|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844498|NCT00359177|NKT102785|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844499|NCT00359177|NKT102785|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844500|NCT00359177|NKT102785|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844501|NCT00359177|NKT102785|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844502|NCT00359177|NKT102785|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844503|NCT00359177|NKT102785|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844504|NCT01636947||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-225&kw=0869-225&tab=access|
2844505|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
2844506|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
2844507|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
2844508|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
2844509|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
2844510|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
2844511|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
2844512|NCT01716520|116133|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844513|NCT01716520|116133|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844514|NCT01716520|116133|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844515|NCT01716520|116133|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844516|NCT01716520|116133|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844517|NCT01716520|116133|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844518|NCT01716520|116133|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844519|NCT02839564||Study Protocol|http://gmail.com|Study data can be requested by mailing to mjmolegraaf@gmail.com
2844520|NCT00568334|109705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844521|NCT00568334|109705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844522|NCT00568334|109705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844523|NCT00568334|109705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844524|NCT00568334|109705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844525|NCT00568334|109705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844526|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
2844527|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
2844528|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
2844529|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
2844530|NCT00411073|SB 480848/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844531|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
2844532|NCT00411073|SB 480848/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844533|NCT02983916||Clinical Study Report|https://doi.org/10.1038/s41395-018-0158-9|
2844534|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,
2844535|NCT03532815||Study Protocol|https://sites.google.com/view/lifestyle-intervention-/home|
2844536|NCT00530790|107846|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844537|NCT00530790|107846|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844538|NCT00530790|107846|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844539|NCT00530790|107846|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844540|NCT03449992||Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.5873190.v1|
2844541|NCT01648192|116681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844542|NCT01648192|116681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851692|NCT02184637|200951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851693|NCT02184637|200951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851694|NCT06935851||Study Protocol|https://osf.io|signing a data agreement
2851695|NCT04457921|Mary Colleen Simonelli|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/30102886/|web site is provided
2851696|NCT03322358||Individual Participant Data Set|https://www.sleepdata.org/datasets/urbanpoor|
2851697|NCT01583036|116216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851698|NCT01583036|116216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851699|NCT01583036|116216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851700|NCT01583036|116216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851701|NCT01583036|116216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851702|NCT01583036|116216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851703|NCT01583036|116216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851704|NCT00942162|111476|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851705|NCT00942162|111476|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851706|NCT00942162|111476|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851707|NCT00942162|111476|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851708|NCT00942162|111476|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844543|NCT01648192|116681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844544|NCT01648192|116681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844545|NCT01648192|116681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844546|NCT01648192|116681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844547|NCT01648192|116681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844548|NCT01370616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0826-061&kw=0826-061&tab=access|
2851709|NCT00942162|111476|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851710|NCT00942162|111476|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851711|NCT01772134|116135|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851712|NCT01772134|116135|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851713|NCT01772134|116135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851714|NCT01772134|116135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851715|NCT01772134|116135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851716|NCT01772134|116135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851717|NCT01772134|116135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851718|NCT00499707|712753/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851719|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
2851720|NCT00499707|712753/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851721|NCT00499707|712753/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851722|NCT00499707|712753/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851723|NCT00499707|712753/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851724|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
2851725|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.
2851726|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.
2851727|NCT05446675|EC/EH/220608-SK|Individual Participant Data Set|https://ehs-hernia-registry.com|
2851728|NCT07030387||Study Protocol|https://www.precis-2.org/Help/Documentation/Help|
2851729|NCT00920543|SAM40086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851730|NCT00920543|SAM40086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851731|NCT00920543|SAM40086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851732|NCT00920543|SAM40086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844549|NCT01119846|111598|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844550|NCT01119846|111598|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844551|NCT01119846|111598|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844552|NCT01119846|111598|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844553|NCT01119846|111598|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844554|NCT01119846|111598|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851733|NCT00920543|SAM40086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844555|NCT01119846|111598|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851734|NCT00920543|SAM40086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844556|NCT00034944||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844557|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
2844558|NCT00482599||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844559|NCT00603382|FFA109687|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844560|NCT00603382|FFA109687|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844561|NCT00603382|FFA109687|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844562|NCT00603382|FFA109687|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844563|NCT00603382|FFA109687|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844564|NCT00603382|FFA109687|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844565|NCT00603382|FFA109687|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844566|NCT01039805|112571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844567|NCT01039805|112571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844568|NCT01039805|112571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844569|NCT01039805|112571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844570|NCT01039805|112571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844571|NCT01039805|112571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844572|NCT01039805|112571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844573|NCT03075332|plataforma brasil|Ethics committee project|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|all project
2844574|NCT01088711||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-004&kw=3102-004&tab=access|
2844575|NCT00329745|107070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844576|NCT00329745|107070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844577|NCT00329745|107070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844578|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.
2844579|NCT00329745|107070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844580|NCT00329745|107070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844581|NCT02785562||Study Protocol|http://www.g-f-p-c.org|The login can be obtained directly on gfpc site.
2844582|NCT03602833||Summary of Product Characteristics|https://www.medicines.org.uk/emc/product/8453|
2844583|NCT05880095||Study Protocol|https://ensati.wixsite.com/ensati/qu%C3%A9-es-ensati|
2844584|NCT01148459|112745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844585|NCT01148459|112745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844586|NCT01148459|112745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844587|NCT01148459|112745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844588|NCT01148459|112745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844589|NCT01148459|112745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844590|NCT02696174||Study Protocol|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Total protocol FILE named protocol.pdf
2844591|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
2844592|NCT02696174||Questionnaires|https://www.flipdrive.com/site/login|Username: HMI Password: insurance All questionnaires (English) uploaded
2844593|NCT00657657|110071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844594|NCT00657657|110071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844595|NCT00657657|110071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844596|NCT00657657|110071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844597|NCT00657657|110071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844598|NCT00657657|110071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844599|NCT03126253||Report of the survey along with sampling plan|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|
2844600|NCT05543031||Study Protocol|http://dc.etsu.edu/etd/772|
2844601|NCT05543031||Study Protocol|http://encompass.eku.edu/honors_theses|
2844602|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."
2844603|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.
2844604|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.
2844605|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.
2844606|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.
2844607|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.
2844608|NCT00547248|109509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844609|NCT00547248|109509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844610|NCT00547248|109509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844611|NCT00547248|109509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844612|NCT00547248|109509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844613|NCT00547248|109509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844614|NCT00547248|109509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844615|NCT01147718|111680|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844616|NCT01147718|111680|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844617|NCT01147718|111680|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844618|NCT01147718|111680|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844619|NCT01147718|111680|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844620|NCT01147718|111680|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844621|NCT01147718|111680|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844622|NCT00435461|FFU109045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844623|NCT00435461|FFU109045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844624|NCT00435461|FFU109045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844625|NCT00435461|FFU109045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844626|NCT00435461|FFU109045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844627|NCT00435461|FFU109045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844628|NCT03249168||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/26705527|
2844629|NCT00370591|SAM40104|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844630|NCT00370591|SAM40104|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844631|NCT00370591|SAM40104|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844632|NCT00370591|SAM40104|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844633|NCT00370591|SAM40104|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844634|NCT00370591|SAM40104|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844635|NCT00370591|SAM40104|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844636|NCT01934127|115415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844637|NCT01934127|115415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844638|NCT01934127|115415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844639|NCT01934127|115415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844640|NCT01934127|115415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844641|NCT01934127|115415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844642|NCT00481767|106069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844643|NCT00481767|106069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844644|NCT00481767|106069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844645|NCT00481767|106069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844646|NCT00481767|106069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844647|NCT00481767|106069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844648|NCT00481767|106069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844649|NCT01400906|114748|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844650|NCT01400906|114748|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844651|NCT01400906|114748|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844652|NCT01400906|114748|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844653|NCT01400906|114748|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844654|NCT01400906|114748|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844655|NCT01400906|114748|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844656|NCT00406081|SDY2|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
2844657|NCT00406081|SDY2|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
2844658|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.
2844659|NCT02588664||Full Data Package|https://www.pcori.org/about-us/governance/policy-data-management-and-data-sharing|
2844660|NCT00519467|714703/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844661|NCT00519467|714703/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851735|NCT00920543|SAM40086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851736|NCT00814710|111188|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851737|NCT00814710|111188|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851738|NCT00814710|111188|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844662|NCT00519467|714703/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844663|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
2844664|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
2851739|NCT00814710|111188|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851740|NCT00814710|111188|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851741|NCT00814710|111188|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851742|NCT00814710|111188|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844665|NCT00519467|714703/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844666|NCT00519467|714703/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844667|NCT01158742|SDY291|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
2844668|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.
2844669|NCT01158742|SDY291|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
2844670|NCT00534638|106636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844671|NCT00534638|106636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844672|NCT00534638|106636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844673|NCT00534638|106636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844674|NCT00534638|106636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844675|NCT00534638|106636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844676|NCT00534638|106636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844677|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
2844678|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
2844679|NCT00693615|580299/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844680|NCT00693615|580299/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844681|NCT00693615|580299/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844682|NCT00693615|580299/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844683|NCT00693615|580299/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844684|NCT00461097|SDY218|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY218|ImmPort study identifier is SDY218
2844685|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
2844686|NCT00610168|110806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844687|NCT00610168|110806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844688|NCT00610168|110806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844689|NCT00610168|110806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844690|NCT00610168|110806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844691|NCT00610168|110806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844692|NCT00610168|110806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844693|NCT00370097|FAS106533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844694|NCT00370097|FAS106533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844695|NCT00370097|FAS106533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851743|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.
2851744|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
2851745|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
2844696|NCT00370097|FAS106533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844697|NCT00370097|FAS106533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844698|NCT00370097|FAS106533|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844699|NCT00370097|FAS106533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844700|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|
2844701|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.|
2844702|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.|
2844703|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|
2844704|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/15008827|
2844705|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|
2844706|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|
2844707|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|
2844708|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/20606205|
2844709|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22699609|
2844710|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|
2844711|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|
2844712|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|
2844713|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|
2844714|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.|
2844715|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/9794114|
2844716|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|
2844717|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Zinc+as+a+potential+coadjuvant+in+therapy+for+type+2+diabetes.|
2844718|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|
2844719|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/25284151|
2844720|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/27915988|
2844721|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Insulino-mimetic+and+anti-diabetic+effects+of+zinc|
2844722|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/28615382|
2844723|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/12502486|
2844724|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22375253|
2844725|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|
2844726|NCT01808261|104615|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844727|NCT01808261|104615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844728|NCT01808261|104615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844729|NCT01808261|104615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844730|NCT01808261|104615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844731|NCT01808261|104615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844732|NCT01808261|104615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844733|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.
2844734|NCT01046331||Study Forms|http://biolincc.nhlbi.nih.gov/studies/h1n1/|
2844735|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.
2844736|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.
2844737|NCT00346749|ADC105931|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844738|NCT00346749|ADC105931|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844739|NCT00346749|ADC105931|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844740|NCT00346749|ADC105931|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844741|NCT00346749|ADC105931|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844742|NCT00346749|ADC105931|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844743|NCT00107757|FFR100010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844744|NCT00107757|FFR100010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844745|NCT00107757|FFR100010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844746|NCT00107757|FFR100010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844747|NCT00107757|FFR100010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844748|NCT00107757|FFR100010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844749|NCT00107757|FFR100010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844750|NCT00268983|393229/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844751|NCT00268983|393229/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844752|NCT00268983|393229/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844753|NCT00268983|393229/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844754|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
2844755|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
2844756|NCT00268983|393229/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844757|NCT01236040|114371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844758|NCT01236040|114371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844759|NCT01236040|114371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844760|NCT01236040|114371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844761|NCT01236040|114371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844762|NCT01236040|114371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844763|NCT00230243||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844764|NCT01630135|116364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844765|NCT01630135|116364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844766|NCT01630135|116364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844767|NCT01630135|116364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844768|NCT01212094||Paper describing the results of interim analysis|http://onlinelibrary.wiley.com/doi/10.1002/acn3.293/full|
2844769|NCT03180203|Study Intensive Care|Study Protocol|https://www.catharinaziekenhuis.nl/contact.html|Contact can be made to request the study protocol (Dutch)
2844770|NCT02527629||Study results|https://pubmed.ncbi.nlm.nih.gov/32386409/|
2844771|NCT01061541|208108/091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845240|NCT01371682|112771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844772|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.
2844773|NCT01061541|208108/091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844774|NCT01061541|208108/091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844775|NCT01061541|208108/091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844776|NCT01061541|208108/091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844777|NCT00920959|SAS30021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844778|NCT00920959|SAS30021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844779|NCT00920959|SAS30021|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844780|NCT00920959|SAS30021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844781|NCT00920959|SAS30021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844782|NCT00920959|SAS30021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844783|NCT00920959|SAS30021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851746|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.
2851747|NCT01362322|114778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851748|NCT01362322|114778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851749|NCT01362322|114778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851750|NCT01362322|114778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851751|NCT01362322|114778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851752|NCT01362322|114778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851753|NCT01009463|102871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851754|NCT01009463|102871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851755|NCT01009463|102871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851756|NCT01009463|102871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851757|NCT01009463|102871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851758|NCT01009463|102871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851759|NCT01009463|102871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851760|NCT00693706|110127|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851761|NCT00693706|110127|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851762|NCT00693706|110127|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851763|NCT00693706|110127|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851764|NCT00693706|110127|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851765|NCT00693706|110127|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851766|NCT00693706|110127|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851767|NCT07228520|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
2851768|NCT07228520|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
2851769|NCT00410371|LBI108614|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851770|NCT00410371|LBI108614|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851771|NCT00410371|LBI108614|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844784|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.
2844785|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.
2844786|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
2844787|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
2844788|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.
2844789|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.
2844790|NCT03271593||Clinical Study Report|https://www.gsk-clinicalstudyregister.com/study/205369?search=study&search_terms=205369#csr|Results disclosed in the Clinical Study Report.
2844791|NCT00354965|AUG102821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844792|NCT00354965|AUG102821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844793|NCT00354965|AUG102821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844794|NCT00354965|AUG102821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844795|NCT00354965|AUG102821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844796|NCT00354965|AUG102821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844797|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.
2844798|NCT00612820|IPR110723|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844799|NCT00612820|IPR110723|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844800|NCT00612820|IPR110723|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844801|NCT00612820|IPR110723|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844802|NCT00612820|IPR110723|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844803|NCT00612820|IPR110723|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844804|NCT00612820|IPR110723|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844805|NCT02689804||Publication|http://dx.doi.org/10.1016/j.contraception.2017.01.004|Results Reference: Yes
2845241|NCT01371682|112771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845242|NCT01248975|114387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845243|NCT01248975|114387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845244|NCT01248975|114387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845245|NCT01248975|114387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845246|NCT01248975|114387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845247|NCT01248975|114387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845248|NCT01248975|114387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845249|NCT01059851||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-023&kw=4305-023&tab=access|
2845250|NCT01039675|113120|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845251|NCT01039675|113120|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845252|NCT01039675|113120|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845253|NCT01039675|113120|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844806|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.
2844807|NCT00933595||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
2844808|NCT00933595||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
2844809|NCT00933595||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
2844810|NCT01405560||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-045&kw=7009-045&tab=access|
2844811|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
2844812|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
2844813|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
2844814|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
2844815|NCT00371735|CDA 714703/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844816|NCT00371735|CDA 714703/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844817|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
2844818|NCT00731822|HZC111348|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844819|NCT00731822|HZC111348|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844820|NCT00731822|HZC111348|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844821|NCT00731822|HZC111348|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844822|NCT00731822|HZC111348|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844823|NCT00731822|HZC111348|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844824|NCT00731822|HZC111348|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844825|NCT00792909|111736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844826|NCT00792909|111736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844827|NCT00792909|111736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844828|NCT00792909|111736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844829|NCT00792909|111736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844830|NCT00792909|111736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844831|NCT01545388||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-136&kw=0431A-136&tab=access|
2844832|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.
2844833|NCT00097006|REDS II-CORE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/core/|
2844834|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.
2844835|NCT00097006|REDS II-LAPS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/laps/|
2844836|NCT00097006|REDS II-LAPS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/laps/|
2844837|NCT00097006|REDS II-LAPS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/laps/|
2844838|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.
2844839|NCT00097006|REDS II-MS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/redsms/|
2844840|NCT00097006|REDS II-MS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/redsms/|
2844841|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.
2844842|NCT00097006|REDS II-RISE|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rise/|
2844843|NCT00097006|REDS II-RISE|Study Forms|http://biolincc.nhlbi.nih.gov/studies/rise/|
2844844|NCT00097006|REDS II-RISE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/rise/|
2844845|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.
2844846|NCT00523913|AVD105720|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844847|NCT00523913|AVD105720|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844848|NCT00523913|AVD105720|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844849|NCT00523913|AVD105720|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844850|NCT00523913|AVD105720|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844851|NCT00523913|AVD105720|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844852|NCT00523913|AVD105720|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844853|NCT00358358|SCO104925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844854|NCT00358358|SCO104925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844855|NCT00358358|SCO104925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844856|NCT00358358|SCO104925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844857|NCT00358358|SCO104925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844858|NCT00358358|SCO104925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844859|NCT00358358|SCO104925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844860|NCT00427908|108658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844861|NCT00427908|108658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844862|NCT00427908|108658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844863|NCT00427908|108658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844864|NCT00427908|108658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844865|NCT00427908|108658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844866|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
2844867|NCT00903201|110399|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844868|NCT00903201|110399|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844869|NCT00903201|110399|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844870|NCT00903201|110399|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844871|NCT00903201|110399|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844872|NCT00903201|110399|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844873|NCT00903201|110399|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844874|NCT01299558|102934|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844875|NCT01299558|102934|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844876|NCT01299558|102934|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844877|NCT01299558|102934|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844878|NCT01299558|102934|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844879|NCT01299558|102934|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844880|NCT01299558|102934|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844881|NCT01573000|104515|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851772|NCT00410371|LBI108614|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851773|NCT00410371|LBI108614|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851774|NCT00410371|LBI108614|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851775|NCT00410371|LBI108614|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851776|NCT04406038|ID|Individual Participant Data Set|http://github.com/eusporg/spb_covid_study20|Please consult with the README.md for the repository.
2851777|NCT00971321|113462|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851778|NCT00971321|113462|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851779|NCT00971321|113462|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851780|NCT00971321|113462|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851781|NCT00971321|113462|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851782|NCT00971321|113462|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851783|NCT00971321|113462|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851784|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.
2851785|NCT01857895|200016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851786|NCT01857895|200016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851787|NCT01857895|200016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851788|NCT01857895|200016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851789|NCT01857895|200016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851790|NCT01857895|200016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851791|NCT01857895|200016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2851792|NCT04936672||Study Protocol|https://doi.org/10.1249/MSS.0b013e318213fefb|The protocol setting and data collection process is based on this reference
2851793|NCT06961422|0009-0009-61|Individual Participant Data Set|https://orcid.org/0009-0009-6142-6201|
2851794|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.
2851795|NCT00474253||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2851796|NCT01972425||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1442-x|
2851797|NCT05957562|orcid.org/0000-0003-0558-6402|Study Protocol|http://orcid.org/0000-0003-0558-6402|
2851798|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.
2851799|NCT04752787||Study Protocol|http://files.eric.ed.gov/fulltext/EJ1086361.pdf|
2851800|NCT04752787||Study Protocol|https://mhealth.jmir.org/2018/4/e109/|
2851801|NCT04160403||Study Protocol|https://www.ncbi.nlm.nih.gov/|
2851802|NCT03407391||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data is available for use by researchers on application through the website
2844882|NCT01573000|104515|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844883|NCT01573000|104515|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844884|NCT01573000|104515|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844885|NCT01573000|104515|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844886|NCT01573000|104515|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844887|NCT01573000|104515|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844888|NCT01702467|116698|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844889|NCT01702467|116698|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844890|NCT01702467|116698|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844891|NCT01702467|116698|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844892|NCT01702467|116698|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844893|NCT01702467|116698|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844894|NCT01702467|116698|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844895|NCT00896064|112993|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844896|NCT00896064|112993|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844897|NCT00896064|112993|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844898|NCT00896064|112993|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844899|NCT00896064|112993|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844900|NCT00969228|112269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844901|NCT00969228|112269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844902|NCT00969228|112269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844903|NCT00969228|112269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844904|NCT00969228|112269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844905|NCT00969228|112269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844906|NCT00969228|112269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844907|NCT01725685|116524|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844908|NCT01725685|116524|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844909|NCT01725685|116524|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844910|NCT01725685|116524|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844911|NCT01725685|116524|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844912|NCT01725685|116524|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844913|NCT01725685|116524|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844914|NCT00092196||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844915|NCT03074695|Pro00079368|Informed Consent Form|https://eirb.mc.duke.edu/|
2844916|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.
2844917|NCT00526474||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04737&kw=P04737&tab=access|
2844918|NCT04087239||Individual Participant Data Set|http://www.redcap.uzchs.ac.zw/redcap|Data being entered, now verification of enrolment case report forms
2844919|NCT01204671|114269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844920|NCT01204671|114269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844921|NCT01204671|114269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844922|NCT01204671|114269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844923|NCT01204671|114269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844924|NCT01204671|114269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844925|NCT01204671|114269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844926|NCT02944292||Study Protocol|https://drive.google.com/open?id=0B-XpW352z4ZJMFdseHNwTWI2clU|
2844927|NCT01494636|115419|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844928|NCT01494636|115419|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844929|NCT01494636|115419|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844930|NCT01494636|115419|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844931|NCT01494636|115419|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844932|NCT01494636|115419|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844933|NCT01494636|115419|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844934|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."
2844935|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
2844936|NCT00103454|FFR30002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844937|NCT00103454|FFR30002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844938|NCT00103454|FFR30002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844939|NCT00103454|FFR30002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844940|NCT00103454|FFR30002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844941|NCT00103454|FFR30002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844942|NCT00103454|FFR30002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844943|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
2844944|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
2844945|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
2844946|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
2844947|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.
2844948|NCT01218308|114541|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844949|NCT01218308|114541|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844950|NCT01218308|114541|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844951|NCT01218308|114541|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844952|NCT01218308|114541|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844953|NCT01218308|114541|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844954|NCT01218308|114541|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844955|NCT00023231|SDY131|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
2844956|NCT00023231|SDY131|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
2844957|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
2844958|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.
2844959|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
2844960|NCT00887484|114544|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844961|NCT00887484|114544|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844962|NCT00887484|114544|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844963|NCT00887484|114544|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844964|NCT00887484|114544|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844965|NCT04801251|Sarah bakry|Study Protocol|https://www.outlook.com/aun.edu.eg|All data or information will be uploaded on the website
2844966|NCT00413023|NKF100096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844967|NCT00413023|NKF100096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844968|NCT00413023|NKF100096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844969|NCT00413023|NKF100096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844970|NCT00413023|NKF100096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844971|NCT00413023|NKF100096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844972|NCT00413023|NKF100096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844973|NCT01035749|113883|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844974|NCT01035749|113883|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844975|NCT01035749|113883|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844976|NCT01035749|113883|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844977|NCT01035749|113883|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844978|NCT01035749|113883|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844979|NCT06523712||Informed Consent Form|https://schoolsplus.pk/schools/sharif-education-complex/|
2844980|NCT06523712||Informed Consent Form|https://apseducation123.wixsite.com/website|
2844981|NCT06523712||Informed Consent Form|https://apsaskarixi.pk/|
2844982|NCT01704261||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-022&kw=3102-022&tab=access|
2844983|NCT00481663||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2844984|NCT00423046|108933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844985|NCT00423046|108933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844986|NCT00423046|108933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844987|NCT00423046|108933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844988|NCT00423046|108933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844989|NCT00423046|108933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844990|NCT00423046|108933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844991|NCT01663389|112167|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844992|NCT01663389|112167|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844993|NCT01663389|112167|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844994|NCT01663389|112167|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844995|NCT01663389|112167|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844996|NCT01663389|112167|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844997|NCT01663389|112167|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844998|NCT00545025|110674|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2844999|NCT00545025|110674|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845000|NCT00545025|110674|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845001|NCT00545025|110674|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845002|NCT00545025|110674|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845003|NCT00545025|110674|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845004|NCT01027845|112640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845005|NCT01027845|112640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845006|NCT01027845|112640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845007|NCT01027845|112640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845008|NCT01027845|112640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845009|NCT01027845|112640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845010|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
2845011|NCT00355641|101468/206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845012|NCT00355641|101468/206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845013|NCT00355641|101468/206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845014|NCT00355641|101468/206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845015|NCT00355641|101468/206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845016|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
2845017|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
2845018|NCT00706563|111631|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845019|NCT00706563|111631|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845020|NCT00706563|111631|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845021|NCT00706563|111631|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845022|NCT00706563|111631|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845023|NCT00706563|111631|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845024|NCT00706563|111631|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845025|NCT04434508|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
2845026|NCT00764790|111751|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845027|NCT00764790|111751|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845028|NCT00764790|111751|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845029|NCT00764790|111751|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845030|NCT00764790|111751|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845031|NCT00764790|111751|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845032|NCT00764790|111751|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845033|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
2845034|NCT01725672|116806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845035|NCT01725672|116806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845036|NCT01725672|116806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845037|NCT01725672|116806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845038|NCT01725672|116806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845039|NCT01725672|116806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845040|NCT01725672|116806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845041|NCT00687700|MAB110553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845042|NCT00687700|MAB110553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845043|NCT00687700|MAB110553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845044|NCT00687700|MAB110553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845045|NCT00687700|MAB110553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845046|NCT00687700|MAB110553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845047|NCT00687700|MAB110553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845048|NCT00325169|104962|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845049|NCT00325169|104962|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845050|NCT00325169|104962|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845051|NCT00325169|104962|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845052|NCT00325169|104962|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845053|NCT00325169|104962|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845054|NCT00325169|104962|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845055|NCT00478621|109836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845056|NCT00478621|109836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845057|NCT00478621|109836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845058|NCT00478621|109836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845059|NCT00478621|109836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845060|NCT00478621|109836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845061|NCT00113165|LAM100034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845062|NCT00113165|LAM100034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845063|NCT00113165|LAM100034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845064|NCT00113165|LAM100034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845065|NCT00113165|LAM100034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845066|NCT00113165|LAM100034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845067|NCT00113165|LAM100034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845068|NCT00420745|106481|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845069|NCT00420745|106481|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845070|NCT00420745|106481|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845071|NCT00420745|106481|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845072|NCT00420745|106481|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845073|NCT00420745|106481|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845074|NCT00420745|106481|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845075|NCT00034632||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2845076|NCT00849056|112755|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845077|NCT00849056|112755|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845078|NCT00849056|112755|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845079|NCT00849056|112755|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845080|NCT00849056|112755|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845081|NCT00849056|112755|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845082|NCT00849056|112755|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845083|NCT00126945|104702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845084|NCT00126945|104702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845085|NCT00126945|104702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845086|NCT00126945|104702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845087|NCT00126945|104702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845088|NCT00126945|104702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845089|NCT01416571|112691|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845090|NCT01416571|112691|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845091|NCT01416571|112691|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845092|NCT01416571|112691|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845093|NCT01416571|112691|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845094|NCT01416571|112691|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845095|NCT07155863||Study Protocol|https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-024-06091-6|
2845096|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."
2845097|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.
2845098|NCT00544271|263855/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845099|NCT00544271|263855/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845100|NCT00544271|263855/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845101|NCT00544271|263855/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845102|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
2845103|NCT00544271|263855/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845104|NCT01524835|SDY294|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
2845105|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.
2845106|NCT01524835|SDY294|Study summary, -design, -demographics, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
2845107|NCT06956586|Research|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37330438/|"There is no additional information."
2845108|NCT00090103|ARI40005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845109|NCT00090103|ARI40005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845110|NCT00090103|ARI40005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845111|NCT00090103|ARI40005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845112|NCT00090103|ARI40005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845113|NCT00090103|ARI40005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845114|NCT00090103|ARI40005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845254|NCT01039675|113120|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845115|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.
2845116|NCT00453687|AC2108380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845117|NCT00453687|AC2108380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845118|NCT00453687|AC2108380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845119|NCT00453687|AC2108380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845120|NCT00453687|AC2108380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845121|NCT00453687|AC2108380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845122|NCT00453687|AC2108380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845123|NCT00358488|B2E106359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845124|NCT00358488|B2E106359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845125|NCT00358488|B2E106359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845126|NCT00358488|B2E106359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845127|NCT00358488|B2E106359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845128|NCT00358488|B2E106359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845129|NCT00358488|B2E106359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845130|NCT03641729||Study Protocol|http://aline.priori.fioritto@gmail.com|More information contact the principal investigator
2845131|NCT00321763|107192|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845132|NCT00321763|107192|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845133|NCT00321763|107192|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845134|NCT00321763|107192|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845135|NCT00321763|107192|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845136|NCT00689741|580299/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845137|NCT00689741|580299/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845138|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
2845139|NCT00689741|580299/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845140|NCT00689741|580299/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845141|NCT00689741|580299/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845142|NCT01134042|106829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845143|NCT01134042|106829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845144|NCT01134042|106829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845145|NCT01134042|106829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845146|NCT01134042|106829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845147|NCT01134042|106829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845148|NCT01134042|106829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845149|NCT06108921||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
2845150|NCT04744181||Individual Participant Data Set|https://redcap-irccs.policlinicogemelli.it/|
2845151|NCT02035540||Study results|http://pubmed.ncbi.nlm.nih.gov/30879050/|
2845152|NCT01431976|115377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845153|NCT01431976|115377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845154|NCT01431976|115377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845155|NCT01431976|115377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845156|NCT01431976|115377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845157|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.
2845158|NCT01192178|113872|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845159|NCT01192178|113872|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845160|NCT01192178|113872|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845161|NCT01192178|113872|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845162|NCT01192178|113872|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845163|NCT01192178|113872|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845164|NCT01192178|113872|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845165|NCT01405859||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983677/|Final Study Results, Published in Tremor and Other Hyperkinetic Disorders
2845166|NCT00000935|SDY355|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
2845167|NCT00000935|SDY355|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
2845168|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.
2845169|NCT01706328|116974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845170|NCT01706328|116974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845171|NCT01706328|116974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845172|NCT01706328|116974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845173|NCT01706328|116974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845174|NCT01706328|116974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845175|NCT01706328|116974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845176|NCT01014091|113810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845177|NCT01014091|113810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845178|NCT01014091|113810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845179|NCT01014091|113810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845180|NCT01014091|113810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845181|NCT01014091|113810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845182|NCT01014091|113810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845183|NCT07130370|fabatool@numl.edu.pk|Informed Consent Form|https://pakjmcr.com/index.php/1/article/view/67|It is not applicable at this time.
2845184|NCT05704309|DPPOS|Individual Participant Data Set|https://repository.niddk.nih.gov/studies/dppos/|
2845185|NCT05704309||Individual Participant Data Set|https://naccdata.org/requesting-data/data-request-process|will be available in 2025
2845186|NCT07011264||Study Protocol|https://reporter.nih.gov/search/xHobiVLiPU68u-6wSogmsA/project-details/11052906|
2845187|NCT00765076|112147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845188|NCT00765076|112147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845189|NCT00765076|112147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845190|NCT00765076|112147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845191|NCT00765076|112147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845192|NCT00765076|112147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845193|NCT00386698|104887|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845194|NCT00386698|104887|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845195|NCT00386698|104887|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845196|NCT00386698|104887|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845197|NCT00386698|104887|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845198|NCT00386698|104887|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845199|NCT00385840|108708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845200|NCT00385840|108708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845201|NCT00385840|108708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845202|NCT00385840|108708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845255|NCT01039675|113120|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845256|NCT01039675|113120|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2845257|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.
2845258|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.
2845259|NCT06882057|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
