id|nct_id|document_id|document_type|url|comment
3052993|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
3055207|NCT02084316|CTN0056|Study Protocol|http://ctndisseminationlibrary.org/protocols/ctn0056.htm|
3052994|NCT00537654|ARI109882|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052995|NCT00537654|ARI109882|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052996|NCT00537654|ARI109882|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052997|NCT00537654|ARI109882|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052998|NCT00537654|ARI109882|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055208|NCT00090246||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055209|NCT00591786||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055210|NCT00965458|SDY797|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797.
3055211|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.
3055212|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.
3055213|NCT00965458|T1DAL ITN045AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
3055214|NCT00965458|T1DAL ITN045AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
3055215|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.
3055216|NCT01733758|113121|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055217|NCT01733758|113121|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055218|NCT01733758|113121|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055219|NCT01733758|113121|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052999|NCT00537654|ARI109882|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053000|NCT00537654|ARI109882|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055220|NCT01733758|113121|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055221|NCT01733758|113121|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057402|NCT00197002|208109/220|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057403|NCT00197002|208109/220|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057404|NCT00197002|208109/220|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057405|NCT00197002|208109/220|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053001|NCT01353768|115008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053002|NCT01353768|115008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053003|NCT01353768|115008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055222|NCT01733758|113121|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055223|NCT00517634|HZA109912|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057406|NCT00197002|208109/220|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059580|NCT00383162|TRX106571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050809|NCT00420680||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050810|NCT00289796|210602-002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050811|NCT00289796|210602-002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053004|NCT01353768|115008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053005|NCT01353768|115008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053006|NCT01353768|115008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053007|NCT01353768|115008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053008|NCT05931913||Individual Participant Data Set|https://nda.nih.gov/|
3053009|NCT00225823|FFR103184|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053010|NCT00225823|FFR103184|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053011|NCT00225823|FFR103184|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053012|NCT00225823|FFR103184|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053013|NCT00225823|FFR103184|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053014|NCT00225823|FFR103184|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053015|NCT00225823|FFR103184|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053016|NCT00659178|ILI108621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053017|NCT00659178|ILI108621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055224|NCT00517634|HZA109912|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055225|NCT00517634|HZA109912|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055226|NCT00517634|HZA109912|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057407|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
3059581|NCT00383162|TRX106571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059582|NCT00383162|TRX106571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059583|NCT00383162|TRX106571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059584|NCT00383162|TRX106571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059585|NCT00383162|TRX106571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059586|NCT00383162|TRX106571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059587|NCT01053988|112206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050812|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
3050813|NCT00289796|210602-002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050814|NCT00289796|210602-002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050815|NCT00289796|210602-002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059588|NCT01053988|112206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059589|NCT01053988|112206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059590|NCT01053988|112206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059591|NCT01053988|112206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059592|NCT01053988|112206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057408|NCT03347734||Clinical Study Report|https://en.wikipedia.org/wiki/Bates_method|
3053018|NCT00659178|ILI108621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053019|NCT00659178|ILI108621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055227|NCT00517634|HZA109912|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053020|NCT00659178|ILI108621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059593|NCT01053988|112206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059594|NCT00326248|NKT102553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053021|NCT00659178|ILI108621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053022|NCT00659178|ILI108621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050816|NCT02207829|201316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050817|NCT02207829|201316|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053023|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
3055228|NCT00517634|HZA109912|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055229|NCT00517634|HZA109912|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055230|NCT00635804||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3281-002&kw=3281-002&tab=access|
3059595|NCT00326248|NKT102553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053024|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
3053025|NCT01198756|113314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053026|NCT01198756|113314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059596|NCT00326248|NKT102553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059597|NCT00326248|NKT102553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059598|NCT00326248|NKT102553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059599|NCT00326248|NKT102553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059600|NCT00326248|NKT102553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059601|NCT03191227||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22984148|Cohort profile
3059602|NCT03214068||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282811/|
3050818|NCT02207829|201316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050819|NCT02207829|201316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053027|NCT01198756|113314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053028|NCT01198756|113314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055231|NCT02250586|awtg7|Individual Participant Data Set|https://osf.io|The trial's outcome data and scripts are available for download: https://osf.io/awtg7/
3055232|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.
3055233|NCT00000565||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ippb/|
3055234|NCT00000565||Study Forms|http://biolincc.nhlbi.nih.gov/studies/ippb/|
3055235|NCT00000565||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/ippb/|
3055236|NCT00346775|FFR105693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055237|NCT00346775|FFR105693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055238|NCT00346775|FFR105693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053029|NCT01198756|113314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057409|NCT00460707|NKV109990|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057410|NCT00460707|NKV109990|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057411|NCT00460707|NKV109990|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057412|NCT00460707|NKV109990|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057413|NCT00460707|NKV109990|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057414|NCT00460707|NKV109990|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057415|NCT00460707|NKV109990|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055239|NCT00346775|FFR105693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057416|NCT05336292||Individual Participant Data Set|https://drive.google.com/drive/folders/1Z6K71rEcfJHXIzsurwREdgHRweFwgFW3|Data will be made available upon reasonable request
3057417|NCT05376241||Individual Participant Data Set|https://osf.io/y8stc/|
3057418|NCT01453478|115550|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057419|NCT01453478|115550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057420|NCT01453478|115550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057421|NCT01453478|115550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057422|NCT01453478|115550|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057423|NCT01453478|115550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057424|NCT01453478|115550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057425|NCT05544773||Study Protocol|https://drive.google.com/file/d/1gKwThkhpbD7eQxFYL4CkTEhzWtcLS1jZ/view?usp=sharing|
3050820|NCT02207829|201316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050821|NCT02207829|201316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050822|NCT02207829|201316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050823|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."
3050824|NCT00605241|DAN106593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050825|NCT00605241|DAN106593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050826|NCT00605241|DAN106593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050827|NCT00605241|DAN106593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050828|NCT00605241|DAN106593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050829|NCT00605241|DAN106593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055240|NCT00346775|FFR105693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055241|NCT00346775|FFR105693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055242|NCT00346775|FFR105693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057426|NCT00831545||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057427|NCT05442606||Full Paper|https://www.e-arm.org/journal/view.php?doi=10.5535/arm.23058|
3059603|NCT00240500|100448|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050830|NCT00605241|DAN106593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050831|NCT00379613||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055243|NCT00539825|AC6108697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057428|NCT02920541||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050832|NCT00797667||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-049&kw=0974-049&tab=access|
3050833|NCT00774995|110073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057429|NCT02920541||Study Protocol|https://clinicaltrials.servier.com/|
3059604|NCT00240500|100448|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050834|NCT00774995|110073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055244|NCT00539825|AC6108697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057430|NCT02920541||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3057431|NCT02920541||Informed Consent Form|https://clinicaltrials.servier.com/|
3057432|NCT02920541||study-level clinical trial data|https://clinicaltrials.servier.com/|
3057433|NCT02920541||Clinical Study Report|https://clinicaltrials.servier.com/|
3057434|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.
3057435|NCT00036491|SDY625|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|ImmPort study identifier is SDY625.
3057436|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.
3057437|NCT06623838|HNYZ6|Study Protocol|https://doi.org/10.17605/OSF.IO/HNYZ6|
3057438|NCT00345878|105926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057439|NCT00345878|105926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057440|NCT00345878|105926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057441|NCT00345878|105926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059605|NCT00240500|100448|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059606|NCT00240500|100448|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059607|NCT00240500|100448|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050835|NCT00774995|110073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050836|NCT00774995|110073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053030|NCT01198756|113314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053031|NCT01198756|113314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053032|NCT00599911|2007-001071-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001071-11/results|
3053033|NCT00359983|107824|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057442|NCT00345878|105926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057443|NCT00345878|105926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057444|NCT00092339||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057445|NCT00984139|112682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057446|NCT00984139|112682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057447|NCT00984139|112682|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057448|NCT00984139|112682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057449|NCT00984139|112682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057450|NCT00984139|112682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057451|NCT00984139|112682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057452|NCT01639066|25800784|pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25800784|Publication for the primary study results
3050837|NCT00774995|110073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050838|NCT00774995|110073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050839|NCT00996996|104517|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053034|NCT00359983|107824|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055245|NCT00539825|AC6108697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055246|NCT00539825|AC6108697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055247|NCT00539825|AC6108697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057453|NCT00742508|CRV110734|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057454|NCT00742508|CRV110734|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055248|NCT00539825|AC6108697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055249|NCT00539825|AC6108697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057455|NCT00742508|CRV110734|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057456|NCT00742508|CRV110734|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057457|NCT00742508|CRV110734|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057458|NCT00514904|109495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057459|NCT00514904|109495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057460|NCT00514904|109495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057461|NCT00514904|109495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057462|NCT00514904|109495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057463|NCT00514904|109495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059608|NCT01140061||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-020&kw=0873-020&tab=access|
3059609|NCT00274677|SCA100223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059610|NCT00274677|SCA100223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059611|NCT00274677|SCA100223|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059612|NCT00274677|SCA100223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059613|NCT00274677|SCA100223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059614|NCT00274677|SCA100223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059615|NCT00274677|SCA100223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059616|NCT02371603|200229|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059617|NCT02371603|200229|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059618|NCT02371603|200229|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059619|NCT02371603|200229|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059620|NCT02371603|200229|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059621|NCT02371603|200229|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059622|NCT06040853|doi: 10.1371|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28282425/|
3059623|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.
3059624|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.
3053035|NCT00359983|107824|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053036|NCT00359983|107824|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057464|NCT00514904|109495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057465|NCT00322361||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057466|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
3057467|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
3057468|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
3059625|NCT05347836||Study Protocol|https://www.degruyter.com/document/doi/10.1515/jpem-2015-0340/html|
3059626|NCT01870115||Publication|http://www.aging-us.com/article/101158|
3057469|NCT01573767|106853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057470|NCT01573767|106853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050840|NCT00996996|104517|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057471|NCT01573767|106853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053037|NCT00359983|107824|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055250|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
3057472|NCT01573767|106853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057473|NCT01573767|106853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057474|NCT01573767|106853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053038|NCT00359983|107824|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053039|NCT00640081||Clinical Study Report|http://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(14)70106-8/abstract|
3053040|NCT01978327|200592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053041|NCT01978327|200592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053042|NCT01978327|200592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053043|NCT01978327|200592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053044|NCT01978327|200592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053045|NCT01978327|200592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053046|NCT01978327|200592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053047|NCT01035645|110040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057475|NCT01573767|106853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057476|NCT00954512||CSR Synospsi Links|http://www.merck.com/clinical-trials/study.html?id=P04722&kw=P04722&tab=access|
3059627|NCT01324362|SAM40065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050841|NCT00996996|104517|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057477|NCT05546216||REFERENCE|https://doi.org/10.1016/j.ctcp.2019.101068|
3057478|NCT05546216||REFERENCE|http://dx.doi.org/10.1016/j.ijcard.2016.11.043|
3057479|NCT05546216||REFERENCE|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540812/|
3057480|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30367542/|
3057481|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/18065335/|
3057482|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/35307131/|
3057483|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/17056770/|
3057484|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/27252099/|
3057485|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/33632127/|
3057486|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/26171374/|
3057487|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/29476940/|
3057488|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.
3057489|NCT00005300||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/csscd/|
3057490|NCT00005300||Study Forms|http://biolincc.nhlbi.nih.gov/studies/csscd/|
3057491|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.
3057492|NCT04928469||Statistical Analysis Plan|https://docs.google.com/document/d/11uN0slg6N6K_10vm4BuXVtB7_QcZOAf5M6P0I-okGkU/edit#|
3057493|NCT02262689|201402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057494|NCT02262689|201402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057495|NCT02262689|201402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057496|NCT02262689|201402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057497|NCT02262689|201402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057498|NCT02262689|201402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053048|NCT01035645|110040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050842|NCT00996996|104517|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050843|NCT00996996|104517|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053049|NCT01035645|110040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053050|NCT01035645|110040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050844|NCT00996996|104517|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050845|NCT00996996|104517|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050846|NCT02019719|116099|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050847|NCT02019719|116099|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053051|NCT01035645|110040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053052|NCT01035645|110040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055251|NCT00422955|49653/376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050848|NCT02019719|116099|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053053|NCT03091231|mpUS2016|Study Protocol|http://www.martini-klinik.de|to request an electronic copy send an email to a.renter@uke.de
3053054|NCT01498679|113719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053055|NCT01498679|113719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053056|NCT01498679|113719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053057|NCT01498679|113719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053058|NCT01498679|113719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053059|NCT01498679|113719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053060|NCT01498679|113719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053061|NCT00603252|111149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053062|NCT00603252|111149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053063|NCT00603252|111149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053064|NCT00603252|111149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053065|NCT00603252|111149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055204|NCT01213849|102932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055205|NCT01213849|102932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055206|NCT01213849|102932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057499|NCT02262689|201402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057500|NCT00553397|SDY293|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
3057501|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.
3057502|NCT00553397|SDY293|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
3057503|NCT04909372||Study Protocol|https://osf.io/du58k/|
3057504|NCT04909372||Statistical Analysis Plan|https://osf.io/du58k/|
3057505|NCT04909372||Individual Participant Data Set|https://osf.io/du58k/|
3057506|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.
3057507|NCT00005159|NLMS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nlms/|Public-use IPD through BioLINCC. Registration is required for access.
3059628|NCT01324362|SAM40065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059629|NCT01324362|SAM40065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053066|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.
3053067|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.
3055252|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
3055253|NCT00422955|49653/376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053068|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.
3053069|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.
3053070|NCT01139580|114743|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053071|NCT01139580|114743|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053072|NCT01139580|114743|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053073|NCT01139580|114743|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057508|NCT01009255|110651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059630|NCT01324362|SAM40065|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059631|NCT01324362|SAM40065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059632|NCT01324362|SAM40065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059633|NCT01324362|SAM40065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059634|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|
3053074|NCT01139580|114743|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053075|NCT01139580|114743|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053076|NCT01139580|114743|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053077|NCT02688218|STUDY00015452|Study Protocol|http://eirb.ohsu.edu|Institutionally reviewed and accepted protocol for this study.
3053078|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
3053079|NCT03789448||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2128-8|
3053080|NCT00092352||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057509|NCT01009255|110651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057510|NCT01009255|110651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057511|NCT01009255|110651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057512|NCT01009255|110651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057513|NCT01009255|110651|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059635|NCT04119180||Study Protocol|https://bmcoralhealth.biomedcentral.com/articles/10.1186/s12903-021-01594-0|
3059636|NCT00398099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050849|NCT02019719|116099|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050850|NCT02019719|116099|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050851|NCT02019719|116099|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050852|NCT02019719|116099|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050853|NCT01476046|110951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059637|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:"
3059638|NCT01957202|200286|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059639|NCT01957202|200286|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059640|NCT01957202|200286|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059641|NCT01957202|200286|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050854|NCT01476046|110951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053081|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.
3053082|NCT00552929||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053083|NCT00306696|49653/342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053084|NCT00306696|49653/342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053085|NCT00306696|49653/342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053086|NCT00306696|49653/342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053087|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
3053088|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
3057514|NCT01009255|110651|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053089|NCT00306696|49653/342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053090|NCT00158860|HS2100275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053091|NCT00158860|HS2100275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053092|NCT00158860|HS2100275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055254|NCT00422955|49653/376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055255|NCT00422955|49653/376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057515|NCT00483704||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-031&kw=0974-031&tab=access|
3057516|NCT03273465||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
3057517|NCT01485445|115440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057518|NCT01485445|115440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057519|NCT01485445|115440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059642|NCT01957202|200286|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059643|NCT01957202|200286|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050855|NCT01476046|110951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050856|NCT01476046|110951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059644|NCT01957202|200286|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059645|NCT02636205|25014045|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25014045|
3059646|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|
3050857|NCT01476046|110951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050858|NCT01476046|110951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053093|NCT00158860|HS2100275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059647|NCT01196026|114451|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059648|NCT01196026|114451|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059649|NCT01196026|114451|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059650|NCT01196026|114451|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059651|NCT01196026|114451|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059652|NCT01196026|114451|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059653|NCT07061483||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/JKAXZ|
3059654|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
3050859|NCT01476046|110951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050860|NCT01319006|114703|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050861|NCT01319006|114703|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050862|NCT01319006|114703|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050863|NCT01319006|114703|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050864|NCT01319006|114703|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050865|NCT01319006|114703|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050866|NCT01319006|114703|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050867|NCT06635343||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28990891|
3050868|NCT00560833||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06459&kw=P06459&tab=access|
3050869|NCT01059617|113483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050870|NCT01059617|113483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050871|NCT01059617|113483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050872|NCT01059617|113483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050873|NCT01059617|113483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053094|NCT00158860|HS2100275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053095|NCT00158860|HS2100275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053096|NCT00158860|HS2100275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055256|NCT00422955|49653/376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059655|NCT00799903|100601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059656|NCT00799903|100601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050874|NCT01059617|113483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050875|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.
3050876|NCT00345579|105987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050877|NCT00345579|105987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050878|NCT00345579|105987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050879|NCT00345579|105987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057520|NCT01485445|115440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059657|NCT00799903|100601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059658|NCT00799903|100601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059659|NCT00799903|100601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059660|NCT00799903|100601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059661|NCT00799903|100601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050880|NCT00345579|105987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050881|NCT00345579|105987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050882|NCT00550225|MAB108115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050883|NCT00550225|MAB108115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050884|NCT00550225|MAB108115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050885|NCT00550225|MAB108115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050886|NCT00550225|MAB108115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050887|NCT00550225|MAB108115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050888|NCT00550225|MAB108115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050889|NCT06333444||Informed Consent Form|https://docs.google.com/forms/d/e/1FAIpQLScX9N2R8xP62390ly7vV8Ixyy_yfQsUUmUG3QCm_M-ZriXAnA/viewform|
3050890|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
3059662|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.
3059663|NCT00000526||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/cast/|
3059664|NCT00000526||Study Forms|http://biolincc.nhlbi.nih.gov/studies/cast/|
3059665|NCT06921174||Study Protocol|https://www.isemu.es|
3059666|NCT04205721||Individual Participant Data Set|http://dataverse.unc.edu/dataverse/cpc|Search for South Africa Impact Evaluation
3059667|NCT00250276|104772|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050891|NCT02701218|ENT-2558-03601|Study Protocol|http://ros.med.cmu.ac.th/Security/SignIn.aspx|Research administration section website
3050892|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
3050893|NCT00941603||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05675&kw=P05675&tab=access|
3059668|NCT00250276|104772|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059669|NCT00250276|104772|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059670|NCT00250276|104772|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059671|NCT00250276|104772|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059672|NCT00250276|104772|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059673|NCT00250276|104772|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059674|NCT02744092|AFT-28|Study Protocol|https://www.allianceforclinicaltrialsinoncology.org/main/public/standard.xhtml?path=%2FPublic%2FAFT|Email the study team at CANVAS@AllianceFoundationTrials.org.
3050894|NCT05166018|SUMO|Individual Participant Data Set|https://sumo.doc.cortexxmi.com/|
3050895|NCT02679690||Informed Consent Form|http://www.osiris.pitt.edu|
3057521|NCT01485445|115440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050896|NCT00263666|444563/022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059675|NCT03110471||Publications|http://orcid.org/0000-0002-5691-2987|Prof Sue Jordan- publication list
3055257|NCT00955682|112036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055258|NCT00955682|112036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059676|NCT00127023|104389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059677|NCT00127023|104389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059678|NCT00127023|104389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059679|NCT00127023|104389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059680|NCT00127023|104389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059681|NCT00127023|104389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050897|NCT00263666|444563/022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050898|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
3050899|NCT00263666|444563/022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059682|NCT00812773|112356|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059683|NCT00812773|112356|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059684|NCT00812773|112356|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050900|NCT00263666|444563/022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050901|NCT00263666|444563/022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050902|NCT06633263||Study Protocol|https://osf.io/dhmj8/|
3050903|NCT06633263||Individual Participant Data Set|https://osf.io/dhmj8/|
3050904|NCT03793101||Clinical Study Report|http://eyemed.pl|
3050905|NCT01827904||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
3050906|NCT00920192|111645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050907|NCT00920192|111645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050908|NCT00920192|111645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050909|NCT00920192|111645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050910|NCT00920192|111645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050911|NCT00920192|111645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050912|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
3053097|NCT02615002||Study website|http://www.recognitionstudy.com|
3053098|NCT00852540|110978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059685|NCT00812773|112356|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050913|NCT00345904|107507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050914|NCT00345904|107507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059686|NCT00812773|112356|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053099|NCT00852540|110978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055259|NCT00955682|112036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050915|NCT00345904|107507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050916|NCT00345904|107507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050917|NCT00345904|107507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050918|NCT02676479||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/4037016|
3050919|NCT02322671|200107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050920|NCT02322671|200107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050921|NCT02322671|200107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050922|NCT02322671|200107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059687|NCT00812773|112356|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059688|NCT00812773|112356|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059689|NCT00892775|108760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050923|NCT02322671|200107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050924|NCT02322671|200107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057522|NCT01485445|115440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059690|NCT00892775|108760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059691|NCT00892775|108760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059692|NCT00892775|108760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059693|NCT00892775|108760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059694|NCT00892775|108760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059695|NCT00857857|110762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059696|NCT00857857|110762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059697|NCT00857857|110762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059698|NCT00857857|110762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050925|NCT02322671|200107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050926|NCT00833989|111539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050927|NCT00833989|111539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050928|NCT00833989|111539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050929|NCT00833989|111539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050930|NCT00833989|111539|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050931|NCT00833989|111539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050932|NCT00833989|111539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055260|NCT00955682|112036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059699|NCT00857857|110762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050933|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."
3050934|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. \[Epub ahead of print\]"
3053100|NCT00852540|110978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053101|NCT00852540|110978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055261|NCT00955682|112036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059700|NCT00857857|110762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059701|NCT00857857|110762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059702|NCT00992758|104512|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057523|NCT01485445|115440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057524|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.\[http://dx.doi.org/10.1097/PRS.0000000000002852\] \[PMID: 28027253\]
3057525|NCT03707366||Individual Participant Data Set|https://osf.io/673eu/|
3059703|NCT00992758|104512|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059704|NCT00992758|104512|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059705|NCT00992758|104512|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059706|NCT00992758|104512|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059707|NCT00992758|104512|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050935|NCT02672631||Study Protocol|http://clinical-mri.com/mr-neurography-diagnostic-criteria-to-determine-lesions-of-peripheral-nerves/|
3050936|NCT01090453|113615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050937|NCT01090453|113615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050938|NCT01090453|113615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050939|NCT01090453|113615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050940|NCT01090453|113615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050941|NCT01090453|113615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053102|NCT00852540|110978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053103|NCT00852540|110978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053104|NCT00852540|110978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053105|NCT01156792|114255|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059708|NCT00992758|104512|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053106|NCT01156792|114255|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059709|NCT01358825|115375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059710|NCT01358825|115375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059711|NCT01358825|115375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059712|NCT01358825|115375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059713|NCT01358825|115375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059714|NCT01358825|115375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059715|NCT01358825|115375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059716|NCT00985673|113536|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050942|NCT00493818|AKT106757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050943|NCT00493818|AKT106757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053107|NCT01156792|114255|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050944|NCT00493818|AKT106757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053108|NCT01156792|114255|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055262|NCT00955682|112036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055263|NCT01681004|INSITE|Individual Participant Data Set|http://yoda.yale.edu/|
3055264|NCT00950755|104505|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055265|NCT00950755|104505|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057526|NCT05416645|post LSG GERD|Study Protocol|http://www.mans.edu.eg/|Postlaparoscopic sleeve gastrectomy
3053109|NCT01156792|114255|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053110|NCT01156792|114255|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053111|NCT01156792|114255|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053112|NCT02960750|4382156|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382156/?report=classic|
3053113|NCT02960750|4323230|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323230/?report=classic|
3053114|NCT02960750|4266209|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266209/|
3055266|NCT00950755|104505|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055267|NCT00950755|104505|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057527|NCT00849134|111383|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057528|NCT00849134|111383|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057529|NCT00849134|111383|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057530|NCT00849134|111383|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057531|NCT00849134|111383|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057532|NCT00849134|111383|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057533|NCT00849134|111383|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057534|NCT00282386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059717|NCT00985673|113536|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059718|NCT00985673|113536|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059719|NCT00985673|113536|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050945|NCT00493818|AKT106757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053115|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/.
3057535|NCT01440387|115418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050946|NCT00493818|AKT106757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057536|NCT01440387|115418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057537|NCT01440387|115418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057538|NCT01440387|115418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057539|NCT01440387|115418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057540|NCT01440387|115418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057541|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.
3057542|NCT00000589||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/trap/|
3057543|NCT00000589||Study Forms|http://biolincc.nhlbi.nih.gov/studies/trap/|
3050947|NCT00493818|AKT106757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057544|NCT01716520|116133|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057545|NCT01716520|116133|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057546|NCT01716520|116133|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053116|NCT00116883|FFR100012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053117|NCT00116883|FFR100012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057547|NCT01716520|116133|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053118|NCT00116883|FFR100012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055268|NCT00950755|104505|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055269|NCT00950755|104505|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057548|NCT01716520|116133|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057549|NCT01716520|116133|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055270|NCT00950755|104505|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055271|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
3057550|NCT01716520|116133|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057551|NCT03532815||Study Protocol|https://sites.google.com/view/lifestyle-intervention-/home|
3057552|NCT00103922|CIL103657|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059720|NCT00985673|113536|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059721|NCT00985673|113536|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057553|NCT00103922|CIL103657|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059722|NCT00985673|113536|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059723|NCT00481702||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050948|NCT00493818|AKT106757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050949|NCT01196975|112963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050950|NCT01196975|112963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050951|NCT01196975|112963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050952|NCT01196975|112963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053119|NCT00116883|FFR100012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053120|NCT00116883|FFR100012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053121|NCT00116883|FFR100012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053122|NCT00116883|FFR100012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053123|NCT02135354||Study Protocol|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
3055272|NCT01270139|doi: 10.13140/2.1.3109.5847|Study Protocol|https://www.researchgate.net/publication/273623828_Protocol_v31_of_NANOM-FIM_trial|The protocol of the trial (v. 3.1.) was released in ResearchGate in March 2015.
3057554|NCT00103922|CIL103657|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057555|NCT00103922|CIL103657|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059724|NCT00938184|112811|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059725|NCT00938184|112811|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050953|NCT01196975|112963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050954|NCT01196975|112963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050955|NCT01196975|112963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050956|NCT01462344|115358|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053124|NCT02135354||Statistical Analysis Plan|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
3053125|NCT00662818||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-034&kw=0974-034&tab=access|
3053126|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.
3053127|NCT00005130||Study Protocol|http://www.cardia.dopm.uab.edu/exam-materials2/protocols|
3053128|NCT00005130||Informed Consent Form|http://www.cardia.dopm.uab.edu/exam-materials2/consent-forms|
3059726|NCT00938184|112811|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059727|NCT00938184|112811|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059728|NCT06239740||Study Protocol|https://doi.org/10.5281/zenodo.10488186|
3059729|NCT06122506||Statistical Analysis Plan|https://drive.google.com/file/d/16iZkdhVtT_pnExSoUhJV5iprYyA1JYhx/view?usp=sharing|
3059730|NCT06122506||Study Protocol|https://drive.google.com/file/d/1Z_nDas-Emj7x3OnbkcmRl3Pujy0tjlmM/view?usp=sharing|
3050957|NCT01462344|115358|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050958|NCT01462344|115358|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050959|NCT01462344|115358|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050960|NCT01462344|115358|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050961|NCT01462344|115358|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050962|NCT01462344|115358|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050963|NCT00354874|B2C101762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050964|NCT00354874|B2C101762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050965|NCT00354874|B2C101762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050966|NCT00354874|B2C101762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050967|NCT00354874|B2C101762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050968|NCT00354874|B2C101762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050969|NCT00354874|B2C101762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050970|NCT00951041|113574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050971|NCT00951041|113574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050972|NCT00951041|113574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050973|NCT00951041|113574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050974|NCT00951041|113574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050975|NCT00951041|113574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050976|NCT00951041|113574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050977|NCT06426537||Study Protocol|http://drive.google.com/drive/u/3/folders/15qW39gHRtgwIuP8rGm8ukhXtYnLRCFNO|
3053129|NCT00005130||Data Collection Forms|http://www.cardia.dopm.uab.edu/exam-materials2/data-collection-forms|
3055273|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.
3055274|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.
3057347|NCT01571999|114636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057348|NCT01571999|114636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059731|NCT00387881|TXA107563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059732|NCT00387881|TXA107563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059733|NCT00387881|TXA107563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059734|NCT00387881|TXA107563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050978|NCT03058211|PI16/00486|Study Protocol|http://www.iispv.cat|Protocol in Spanish language
3057349|NCT01571999|114636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057350|NCT01571999|114636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057351|NCT01571999|114636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057352|NCT01571999|114636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057556|NCT00103922|CIL103657|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057557|NCT00103922|CIL103657|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055275|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.
3055276|NCT00407979|SDY5|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY5|ImmPort study identifier is SDY5
3059735|NCT00387881|TXA107563|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059736|NCT00387881|TXA107563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059737|NCT00387881|TXA107563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050979|NCT03058211|PI16/00486|Informed Consent Form|http://www.iispv.cat|Informed consent form in Spanish language
3050980|NCT01217073||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-006&kw=3102-006&tab=access|
3050981|NCT00989287|113866|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057558|NCT02064465|200697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055277|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
3055278|NCT01711736|116926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055279|NCT01711736|116926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055280|NCT01711736|116926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057559|NCT02064465|200697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057560|NCT02064465|200697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057561|NCT02064465|200697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059738|NCT00496015|107137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055281|NCT01711736|116926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059739|NCT00496015|107137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059740|NCT00496015|107137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059741|NCT00496015|107137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055282|NCT01711736|116926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055283|NCT01711736|116926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057562|NCT02064465|200697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057563|NCT02064465|200697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059742|NCT00496015|107137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059743|NCT00496015|107137|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050982|NCT00989287|113866|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057564|NCT02064465|200697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057565|NCT00568334|109705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053130|NCT00005130||Study Manuals|http://www.cardia.dopm.uab.edu/exam-materials2/manual-of-operations|
3053131|NCT06906354|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3057566|NCT00568334|109705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057567|NCT00568334|109705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057568|NCT00568334|109705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059744|NCT00496015|107137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059745|NCT00985465|113166|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059746|NCT00985465|113166|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059747|NCT00985465|113166|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050983|NCT00989287|113866|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055284|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.
3055285|NCT00000610||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/magic/|
3055286|NCT00000610||Study Forms|http://biolincc.nhlbi.nih.gov/studies/magic/|
3055287|NCT06047886||Prodigy technical sheet|https://www.miltenyibiotec.com/US-en/products/clinimacs-prodigy.html|
3055288|NCT01852565|115679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055289|NCT01852565|115679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055290|NCT01852565|115679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055291|NCT01852565|115679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055292|NCT01852565|115679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055293|NCT01852565|115679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055294|NCT01852565|115679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055295|NCT00540228|110794|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055296|NCT00540228|110794|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055297|NCT00540228|110794|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055298|NCT00540228|110794|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055299|NCT00540228|110794|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055300|NCT00540228|110794|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055301|NCT00455572|107240|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055302|NCT00455572|107240|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055303|NCT00455572|107240|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055304|NCT00455572|107240|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057569|NCT00568334|109705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057570|NCT00568334|109705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057571|NCT00359177|NKT102785|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057572|NCT00359177|NKT102785|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057573|NCT00359177|NKT102785|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057574|NCT00359177|NKT102785|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057575|NCT00359177|NKT102785|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057576|NCT00359177|NKT102785|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050984|NCT00989287|113866|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050985|NCT00989287|113866|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050986|NCT00989287|113866|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050987|NCT00989287|113866|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050988|NCT00695669|111626|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057577|NCT00359177|NKT102785|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050989|NCT00695669|111626|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050990|NCT00695669|111626|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050991|NCT00695669|111626|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050992|NCT00695669|111626|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050993|NCT00695669|111626|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050994|NCT00695669|111626|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050995|NCT04411290||Principal investigator data|https://scholar.google.com.tr/citations?user=6bFlCZwAAAAJ&hl=tr|
3050996|NCT00515502|AC4108123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050997|NCT00515502|AC4108123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050998|NCT00515502|AC4108123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053132|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"
3053133|NCT00950586|110792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053134|NCT00950586|110792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053135|NCT00950586|110792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053136|NCT00950586|110792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053137|NCT00950586|110792|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053138|NCT00950586|110792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053139|NCT00950586|110792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055305|NCT00455572|107240|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055306|NCT00455572|107240|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055307|NCT00455572|107240|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055308|NCT00570492|FFR101782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055309|NCT00570492|FFR101782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055310|NCT00570492|FFR101782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055311|NCT00570492|FFR101782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055312|NCT00570492|FFR101782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057578|NCT02713438||Study Protocol|https://drive.google.com/file/d/1bosgzFmvKglMyMjhELiSg-fqzw1pn1nf/view?usp=sharing|The handbook with the protocol for experimenters (in English)
3057579|NCT01362244|111782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057580|NCT01362244|111782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057581|NCT01362244|111782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050999|NCT00515502|AC4108123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051000|NCT00515502|AC4108123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051001|NCT00515502|AC4108123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051002|NCT00515502|AC4108123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051003|NCT06520111|sice|Study Protocol|https://siceitalia.com/|SICE- Team di ricerca Endocrino-metabolica- crisal
3051004|NCT00319098|107064|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053140|NCT01476098|114693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053141|NCT01476098|114693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053142|NCT01476098|114693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053143|NCT01476098|114693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053144|NCT01476098|114693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053145|NCT01476098|114693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053146|NCT01476098|114693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053147|NCT00321373|107022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053148|NCT00321373|107022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053149|NCT00321373|107022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053150|NCT00321373|107022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053151|NCT00321373|107022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053152|NCT01323972|113398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053153|NCT01323972|113398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053154|NCT01323972|113398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053155|NCT01323972|113398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053156|NCT01323972|113398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059748|NCT00985465|113166|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059749|NCT00985465|113166|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053157|NCT01323972|113398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059750|NCT00985465|113166|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059751|NCT00985465|113166|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051005|NCT00319098|107064|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053158|NCT00353288|105908|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053159|NCT00353288|105908|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053160|NCT00353288|105908|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053161|NCT00353288|105908|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053162|NCT00353288|105908|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053163|NCT00353288|105908|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053164|NCT02437253||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=28119823|
3053165|NCT00363870|108134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053166|NCT00363870|108134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053167|NCT00363870|108134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053168|NCT00363870|108134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053169|NCT00363870|108134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055313|NCT00570492|FFR101782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051006|NCT00319098|107064|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059752|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.
3055314|NCT00570492|FFR101782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055315|NCT01587716|115658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055316|NCT01587716|115658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055317|NCT01587716|115658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055318|NCT01587716|115658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055319|NCT01587716|115658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057582|NCT01362244|111782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057583|NCT01362244|111782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057584|NCT01362244|111782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057585|NCT01362244|111782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057586|NCT02839564||Study Protocol|http://gmail.com|Study data can be requested by mailing to mjmolegraaf@gmail.com
3051007|NCT00319098|107064|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051008|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.
3051009|NCT00319098|107064|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051010|NCT00464815|109069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051011|NCT00464815|109069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051012|NCT00464815|109069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051013|NCT00464815|109069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053170|NCT00363870|108134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053171|NCT00363870|108134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053172|NCT00196976|103533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053173|NCT00196976|103533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053174|NCT00196976|103533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053175|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.
3051014|NCT00464815|109069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051015|NCT00464815|109069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053176|NCT00196976|103533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053177|NCT00196976|103533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053178|NCT00071747|SCA30926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053179|NCT00071747|SCA30926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053180|NCT00071747|SCA30926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055320|NCT01587716|115658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057587|NCT01636947||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-225&kw=0869-225&tab=access|
3057588|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.
3057589|NCT00005131||Study Forms|http://www2.cscc.unc.edu/aric/cohort-forms|
3057590|NCT00005131||Study Manuals|http://www2.cscc.unc.edu/aric/cohort-forms|
3051016|NCT00464815|109069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051017|NCT00355082|LAM30055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051018|NCT00355082|LAM30055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053181|NCT00071747|SCA30926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053182|NCT00071747|SCA30926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053183|NCT00071747|SCA30926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055321|NCT01587716|115658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055322|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.
3055323|NCT01231620|114373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055324|NCT01231620|114373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055325|NCT01231620|114373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055326|NCT01231620|114373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057591|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
3057592|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
3057593|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
3057594|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
3057595|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
3057596|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
3057597|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
3057598|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
3059753|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.
3059754|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.
3053184|NCT01016977|114566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059755|NCT00102765|SFA103153|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059756|NCT00102765|SFA103153|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053185|NCT01016977|114566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053186|NCT01016977|114566|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053187|NCT01016977|114566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059757|NCT00102765|SFA103153|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053188|NCT01016977|114566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053189|NCT01016977|114566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059758|NCT00102765|SFA103153|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059759|NCT00102765|SFA103153|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059760|NCT00102765|SFA103153|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059761|NCT00102765|SFA103153|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059762|NCT06342817||Study Protocol|https://drive.google.com/file/d/1YWyRsHac1y9eqsmQXVHCsmYArWwAdMoq/view?usp=sharing|
3059763|NCT06342817||Informed Consent Form|https://drive.google.com/file/d/1TfBgnmUMvF4tFJu-a1lGXlcawu0k5YeJ/view?usp=sharing|
3059764|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
3059765|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).
3059766|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/).
3051019|NCT00355082|LAM30055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053190|NCT01016977|114566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053191|NCT01602562|116100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053192|NCT01602562|116100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053193|NCT01602562|116100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053194|NCT01602562|116100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053195|NCT06729515||Individual Participant Data Set|https://figshare.com/s/46ea85c406ec97afc17a|
3053196|NCT00675090|H3B109689|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053197|NCT00675090|H3B109689|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053198|NCT00675090|H3B109689|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059767|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_prep/|Source code for preprocessing prostate MRI data archives.
3059768|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_baseline|Source code for training baseline diagnostic AI models.
3059769|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.
3059770|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).
3059771|NCT01387217|114070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053199|NCT00675090|H3B109689|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053200|NCT00675090|H3B109689|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055327|NCT01231620|114373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055328|NCT01231620|114373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059772|NCT01387217|114070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055329|NCT01231620|114373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059773|NCT01387217|114070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055330|NCT05814744||Individual Participant Data Set|https://drive.google.com/file/d/12gNVWYJj8dyy6Bh-6G59rFn2AQzjHycS/view?usp=share_link|
3051020|NCT00355082|LAM30055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053201|NCT00675090|H3B109689|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053202|NCT00675090|H3B109689|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053203|NCT01711723|115676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055331|NCT05814744||Informed Consent Form|https://drive.google.com/file/d/1qPpYheG63CcWJqwWAD3ma3jFmmqCPWgm/view?usp=share_link|
3055332|NCT05814744||Study Protocol|https://drive.google.com/file/d/16x_dHL6GsO6V-K3p13T9EluZi20l4WtN/view?usp=share_link|
3053204|NCT01711723|115676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055333|NCT00403962|NKP103401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055334|NCT00403962|NKP103401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053205|NCT01711723|115676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053206|NCT01711723|115676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053207|NCT01711723|115676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053208|NCT01711723|115676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053209|NCT01711723|115676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053210|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
3053211|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
3053212|NCT01055379|2009-011144-19|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2009-011144-19/results|
3053213|NCT02549014||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-001&kw=1064-001&tab=access|
3053214|NCT00704405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-009&kw=7009-009&tab=access|
3053215|NCT01395888|115247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053216|NCT01395888|115247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053217|NCT01395888|115247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053218|NCT01395888|115247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055335|NCT00403962|NKP103401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055336|NCT00403962|NKP103401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055337|NCT00403962|NKP103401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055338|NCT00403962|NKP103401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057599|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,
3057600|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
3051021|NCT00355082|LAM30055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053219|NCT01395888|115247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053220|NCT01395888|115247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053221|NCT01395888|115247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053222|NCT01498653|113714|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053223|NCT01498653|113714|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053224|NCT01498653|113714|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051022|NCT00355082|LAM30055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051023|NCT00355082|LAM30055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051024|NCT00374842|108656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051025|NCT00374842|108656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051026|NCT00374842|108656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051027|NCT00374842|108656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051028|NCT00374842|108656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051029|NCT00679939|AVD111179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053225|NCT01498653|113714|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051030|NCT00679939|AVD111179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051031|NCT00679939|AVD111179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051032|NCT00679939|AVD111179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055339|NCT00403962|NKP103401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055340|NCT06724874||Individual Participant Data Set|https://www.stat.ubc.ca/~rollin/stats/ssize/n2.html|
3055341|NCT00329225|49653/347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057601|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
3051033|NCT00679939|AVD111179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055342|NCT00329225|49653/347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055343|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
3055344|NCT00329225|49653/347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055345|NCT00329225|49653/347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057602|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
3057603|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
3057604|NCT00411073|SB 480848/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055346|NCT00329225|49653/347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055347|NCT01590810||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-001&kw=8150-001&tab=access|
3057605|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
3057606|NCT00411073|SB 480848/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057607|NCT02983916||Clinical Study Report|https://doi.org/10.1038/s41395-018-0158-9|
3057608|NCT01370616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0826-061&kw=0826-061&tab=access|
3057609|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
3059774|NCT01387217|114070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059775|NCT01387217|114070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059776|NCT01387217|114070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059777|NCT01387217|114070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059778|NCT06938126|TE-KEB/22/2023|Individual Participant Data Set|https://tf.hu/en/|For more information please email to: petridis.leonidas@tf.hu
3059779|NCT01009060|113147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055348|NCT03626337||Statistical Analysis Plan|https://osf.io/jfke3/|
3057610|NCT01648192|116681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057611|NCT01648192|116681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057612|NCT01648192|116681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057613|NCT01648192|116681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057614|NCT01648192|116681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057615|NCT01648192|116681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057616|NCT01648192|116681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059780|NCT01009060|113147|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059781|NCT01009060|113147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055349|NCT00938392|112662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055350|NCT00938392|112662|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059782|NCT01009060|113147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055351|NCT00938392|112662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055352|NCT00938392|112662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055353|NCT00938392|112662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055354|NCT00938392|112662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059783|NCT01009060|113147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059784|NCT01009060|113147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059785|NCT01009060|113147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059786|NCT00988884||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-005&kw=V503-005&tab=access|
3059787|NCT00539994|ALB110247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059788|NCT00539994|ALB110247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059789|NCT00539994|ALB110247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059790|NCT00539994|ALB110247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059791|NCT00539994|ALB110247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059792|NCT00539994|ALB110247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059793|NCT00539994|ALB110247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059794|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/22original18.pdf|
3059795|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/23original19.pdf|
3059796|NCT01342913|113107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059797|NCT01342913|113107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059798|NCT01342913|113107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059799|NCT01342913|113107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059800|NCT01342913|113107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059801|NCT01342913|113107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059802|NCT01342913|113107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059803|NCT00861705||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov|
3059804|NCT03847766|31484523|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31484523/|Data can be accessed by request from the corresponding author
3059805|NCT00938158|108370|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059806|NCT00938158|108370|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059807|NCT00938158|108370|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059808|NCT00938158|108370|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051034|NCT00679939|AVD111179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055355|NCT00938392|112662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055356|NCT01366846|LEAP-On (ITN049AD)|Individual Participant Data Set|https://www.itntrialshare.org/|
3053226|NCT01498653|113714|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053227|NCT01498653|113714|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059809|NCT00938158|108370|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059810|NCT00938158|108370|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059811|NCT00938158|108370|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059812|NCT00689390||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05063&kw=P05063&tab=access|
3059813|NCT01928927||Grading table|https://rsc.tech-res.com/clinical-research-sites/safety-reporting/daids-grading-tables|
3053228|NCT01498653|113714|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053229|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Hand Shape Representation in Parietal Reach Region. The Journal of Neuroscience."
3055357|NCT01366846|LEAP-On (ITN049AD)|Study protocol synopsis; datasets and figures from published NEJM 2016 article|https://www.itntrialshare.org/|
3055358|NCT03350880||Clinical Study Report|https://periodicos.unicesumar.edu.br/index.php/saudpesq/article/view/9938|
3055359|NCT01439308|111925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055360|NCT01439308|111925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055361|NCT01439308|111925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055362|NCT01439308|111925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055363|NCT01439308|111925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055364|NCT01439308|111925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055365|NCT01439308|111925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055366|NCT04631432||Statistical Analysis Plan|https://docs.google.com/document/d/16IlMPOgJMoh8tLIhB4JK5yeHI-0MfJVvRnQ8PdNp8-o/edit?usp=sharing|
3055367|NCT04631432||Study Protocol|https://drive.google.com/file/d/1YoXgB4ifoeu2Z8OnG6_hVWP4sBLRp9wP/view?usp=sharing|
3055368|NCT04631432||Informed Consent Form|https://drive.google.com/file/d/1WHJz01_y_b-gO4ZpZNAQsnqNf_SwdwNX/view?usp=sharing|
3055369|NCT01453296|112776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055370|NCT01453296|112776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055371|NCT01453296|112776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055372|NCT01453296|112776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055373|NCT01453296|112776|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055374|NCT01453296|112776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055375|NCT01453296|112776|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055376|NCT01867996|116073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053230|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Decoding motor imagery from the posterior parietal cortex of a tetraplegic human. Science"
3053231|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.
3053232|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.
3053233|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.
3053234|NCT01362257|112014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053235|NCT01362257|112014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053236|NCT01362257|112014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053237|NCT01362257|112014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053238|NCT01362257|112014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053239|NCT01362257|112014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053240|NCT01362257|112014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055377|NCT01867996|116073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055378|NCT01867996|116073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055379|NCT01867996|116073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055380|NCT01867996|116073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057617|NCT02095405||Published article|http://onlinelibrary.wiley.com/doi/10.1111/jce.12504/full|DOI: 10.1111/jce.12504
3055381|NCT01867996|116073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057618|NCT03449992||Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.5873190.v1|
3055382|NCT01867996|116073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055383|NCT06934421||Study Protocol|https://osf.io/8ywq6/|
3055384|NCT06934421||Statistical Analysis Plan|https://osf.io/8ywq6/|
3055385|NCT06934421||Informed Consent Form|https://osf.io/8ywq6/|
3055386|NCT06934421||Analytic Code|https://osf.io/8ywq6/|
3055387|NCT06934421||Individual Participant Data Set|https://osf.io/8ywq6/|
3055388|NCT03473821||Statistical Analysis Plan|https://lucris.lub.lu.se/admin/files/138815992/MOTIFS_Data_Management_Protocol_1.6_2023_02_24.pdf|
3055389|NCT00968539|113456|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055390|NCT00968539|113456|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051035|NCT00679939|AVD111179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051036|NCT00137930|104480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051037|NCT00137930|104480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051038|NCT00137930|104480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051039|NCT00137930|104480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051040|NCT00137930|104480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055391|NCT00968539|113456|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055392|NCT00968539|113456|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055393|NCT00968539|113456|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055394|NCT00968539|113456|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055395|NCT00968539|113456|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059814|NCT00605852|HH3110161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055396|NCT00326118|106445|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055397|NCT00326118|106445|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055398|NCT00326118|106445|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055399|NCT00326118|106445|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055400|NCT00326118|106445|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059815|NCT00605852|HH3110161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059816|NCT00605852|HH3110161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059817|NCT00605852|HH3110161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055401|NCT00326118|106445|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055402|NCT01016366|2008-003662-25|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-003662-25/results|
3057619|NCT00530790|107846|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057620|NCT00530790|107846|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059818|NCT00605852|HH3110161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055403|NCT00109278||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051041|NCT00137930|104480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051042|NCT06485817||Analytic Code|https://osf.io/3jvw8/|Project directory where study relevant documentation can be found and data will be uploaded.
3055404|NCT00005009|SDY357|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357.
3055405|NCT00005009|SDY357|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357
3055406|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
3055407|NCT06107348|10.17605/OSF.IO/2MGJK|Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
3055408|NCT01817764|114930|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055409|NCT01817764|114930|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055410|NCT01817764|114930|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055411|NCT01817764|114930|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055412|NCT01817764|114930|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055413|NCT01817764|114930|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055414|NCT01817764|114930|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055415|NCT00471237|CR9108963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055416|NCT00471237|CR9108963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055417|NCT00471237|CR9108963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055418|NCT00471237|CR9108963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055419|NCT00471237|CR9108963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055420|NCT00471237|CR9108963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055421|NCT00471237|CR9108963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055422|NCT00297063|AVD104742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055423|NCT00297063|AVD104742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057621|NCT00530790|107846|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057622|NCT00530790|107846|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057623|NCT01119846|111598|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057624|NCT01119846|111598|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051043|NCT01258608|200149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051044|NCT01258608|200149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051045|NCT01258608|200149|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053241|NCT01636960||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08556&kw=P08556&tab=access|
3057625|NCT01119846|111598|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057626|NCT01119846|111598|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057627|NCT01119846|111598|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059819|NCT00605852|HH3110161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053242|NCT00451100||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055424|NCT00297063|AVD104742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055425|NCT00297063|AVD104742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055426|NCT00297063|AVD104742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055427|NCT00297063|AVD104742|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055428|NCT00297063|AVD104742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055429|NCT02437175||Methodology paper|https://www.dovepress.com/articles.php?article_id=25534|
3055430|NCT03196960||Scoring Sheet|https://docs.google.com/document/d/1pqYbMe4S-W-vgYRHzd1d4Is7s6ZbMt_MGDlWtndRRdM/edit?usp=sharing|Mobilization Quantification Score
3055431|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/106014|
3055432|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/143046|
3055433|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889771|
3055434|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889781|
3057628|NCT01119846|111598|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057629|NCT01119846|111598|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057630|NCT00034944||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057631|NCT00482599||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057632|NCT01148459|112745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057633|NCT01148459|112745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057634|NCT01148459|112745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057635|NCT01148459|112745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051046|NCT01258608|200149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051047|NCT01258608|200149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051048|NCT01258608|200149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051049|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
3051050|NCT06182306||Study Protocol|https://www.pearbio.com/pearmet|Company website with background and information and links to protocol, etc.
3051051|NCT00428090|105640|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051052|NCT00428090|105640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051053|NCT00428090|105640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051054|NCT00428090|105640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051055|NCT00428090|105640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055435|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889773|
3055436|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
3055437|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
3055438|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
3055439|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
3055440|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
3055441|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.
3055442|NCT00539006|FFU105924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055443|NCT00539006|FFU105924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055444|NCT00539006|FFU105924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055445|NCT00539006|FFU105924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057636|NCT01148459|112745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057637|NCT01148459|112745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057638|NCT02785562||Study Protocol|http://www.g-f-p-c.org|The login can be obtained directly on gfpc site.
3057639|NCT03075332|plataforma brasil|Ethics committee project|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|all project
3055446|NCT00539006|FFU105924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055447|NCT00539006|FFU105924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057640|NCT00603382|FFA109687|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057641|NCT00603382|FFA109687|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051056|NCT00428090|105640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051057|NCT00428090|105640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055448|NCT00539006|FFU105924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055449|NCT00479739|SAM40056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055450|NCT00479739|SAM40056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055451|NCT00479739|SAM40056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055452|NCT00479739|SAM40056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055453|NCT00479739|SAM40056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055454|NCT00479739|SAM40056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055455|NCT00479739|SAM40056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055456|NCT03011385||Study Protocol|https://drive.google.com/file/d/1xGrVkCeXwUZbih7NuOujjlNJcWvQ4j6H/view?usp=sharing|The file includes the protocol for data collection and intervention sessions
3055457|NCT00538473|110223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055458|NCT00538473|110223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055459|NCT00538473|110223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055460|NCT00538473|110223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055461|NCT00538473|110223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055462|NCT00538473|110223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055463|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.
3055464|NCT00005274||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
3055465|NCT00005274||Study Forms|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
3055466|NCT00005274||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
3055467|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."
3055468|NCT01153685|110628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055469|NCT01153685|110628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055470|NCT01153685|110628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055471|NCT01153685|110628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055472|NCT01153685|110628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055473|NCT01153685|110628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055474|NCT00903409|111818|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055475|NCT00903409|111818|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055476|NCT00903409|111818|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055477|NCT00903409|111818|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055478|NCT00903409|111818|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055479|NCT00903409|111818|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055480|NCT03052374||Informed Consent Form|http://childstudies.ca/contact|
3055481|NCT03052374||Study Protocol|http://childstudies.ca/contact|
3055482|NCT03052374||Statistical Analysis Plan|http://childstudies.ca/contact|
3055483|NCT00364273|B2F104300|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053243|NCT01313637|113361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055484|NCT00364273|B2F104300|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055485|NCT00364273|B2F104300|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055486|NCT00364273|B2F104300|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057642|NCT00603382|FFA109687|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055487|NCT00364273|B2F104300|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055488|NCT00364273|B2F104300|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055489|NCT00364273|B2F104300|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057643|NCT00603382|FFA109687|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055490|NCT01563029|106855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057644|NCT00603382|FFA109687|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057645|NCT00603382|FFA109687|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057646|NCT00603382|FFA109687|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057647|NCT01039805|112571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057648|NCT01039805|112571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057649|NCT01039805|112571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055491|NCT01563029|106855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057650|NCT01039805|112571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057651|NCT01039805|112571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057652|NCT01039805|112571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057653|NCT01039805|112571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057654|NCT01088711||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-004&kw=3102-004&tab=access|
3057655|NCT03249168||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/26705527|
3057656|NCT02696174||Study Protocol|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Total protocol FILE named protocol.pdf
3059820|NCT00605852|HH3110161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059821|NCT01527123|115959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059822|NCT01527123|115959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059823|NCT01527123|115959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059824|NCT01527123|115959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059825|NCT01527123|115959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055492|NCT01563029|106855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055493|NCT01563029|106855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055494|NCT01563029|106855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055495|NCT01563029|106855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055496|NCT01563029|106855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055497|NCT00381667|B2C104604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055498|NCT00381667|B2C104604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057657|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
3057658|NCT02696174||Questionnaires|https://www.flipdrive.com/site/login|Username: HMI Password: insurance All questionnaires (English) uploaded
3057659|NCT00329745|107070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057660|NCT00329745|107070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057661|NCT00329745|107070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057662|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.
3057663|NCT00329745|107070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057664|NCT00329745|107070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057665|NCT03602833||Summary of Product Characteristics|https://www.medicines.org.uk/emc/product/8453|
3057666|NCT00657657|110071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057667|NCT00657657|110071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057668|NCT00657657|110071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057669|NCT00657657|110071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057670|NCT00657657|110071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057671|NCT00657657|110071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057672|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."
3057673|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.
3057674|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.
3057675|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.
3057676|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.
3057677|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.
3057678|NCT05880095||Study Protocol|https://ensati.wixsite.com/ensati/qu%C3%A9-es-ensati|
3057679|NCT00370591|SAM40104|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057680|NCT00370591|SAM40104|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059826|NCT01527123|115959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059827|NCT06357481|doi: 10.1111/iej.13304|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32266988/|
3059828|NCT00960063||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05883&kw=P05883&tab=access|
3059829|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.
3059830|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
3053244|NCT01313637|113361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057681|NCT00370591|SAM40104|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057682|NCT00370591|SAM40104|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057683|NCT00370591|SAM40104|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057684|NCT00370591|SAM40104|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057685|NCT00370591|SAM40104|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057686|NCT01400906|114748|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057687|NCT01400906|114748|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057688|NCT01400906|114748|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059831|NCT06555185|10.17632/2cwcz2vx4v.1|Individual Participant Data Set|https://data.mendeley.com/datasets/2cwcz2vx4v/1|
3059832|NCT00550407|SCA104779|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059833|NCT00550407|SCA104779|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059834|NCT00550407|SCA104779|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059835|NCT00550407|SCA104779|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059836|NCT02481154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3059837|NCT02481154||Study Protocol|https://clinicaltrials.servier.com/|
3059838|NCT02481154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3059839|NCT02481154||Informed Consent Form|https://clinicaltrials.servier.com/|
3059840|NCT02481154||Clinical Study Report|https://clinicaltrials.servier.com/|
3059841|NCT02481154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3059842|NCT00405080|NKV105091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059843|NCT00405080|NKV105091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057689|NCT01400906|114748|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059844|NCT00405080|NKV105091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059845|NCT00405080|NKV105091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059846|NCT00405080|NKV105091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059847|NCT00405080|NKV105091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059848|NCT01969708|PB2016-103333|Study Protocol|https://ntrl.ntis.gov/NTRL/|SCORE2 Protocol Version 3.0 (the Identifier for the appendices is PB2016-103334)
3059849|NCT00390143|108595 Mth18|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057690|NCT01400906|114748|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059850|NCT00390143|108595 Mth18|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057691|NCT01400906|114748|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057692|NCT01400906|114748|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057693|NCT05543031||Study Protocol|http://dc.etsu.edu/etd/772|
3057694|NCT05543031||Study Protocol|http://encompass.eku.edu/honors_theses|
3059851|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
3059852|NCT00390143|108595 Mth18|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059853|NCT00390143|108595 Mth18|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059854|NCT00390143|108595 Mth18|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059855|NCT00382772|107876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059856|NCT00382772|107876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059857|NCT00382772|107876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059858|NCT00382772|107876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051058|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
3053245|NCT01313637|113361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053246|NCT01313637|113361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053247|NCT01313637|113361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057695|NCT00435461|FFU109045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053248|NCT01313637|113361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057696|NCT00435461|FFU109045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059859|NCT00382772|107876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051059|NCT05154279||Study Protocol|https://www.ijrcog.org/index.php/ijrcog/article/view/3925|
3051060|NCT05154279||Study Protocol|https://ebwhj.journals.ekb.eg/article_125772.html|
3051061|NCT01627327|115805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051062|NCT01627327|115805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051063|NCT01627327|115805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051064|NCT01627327|115805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051065|NCT01627327|115805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051066|NCT01627327|115805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051067|NCT01627327|115805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051068|NCT00518115|GLP110125|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051069|NCT00518115|GLP110125|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051070|NCT00518115|GLP110125|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051071|NCT00518115|GLP110125|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057697|NCT00435461|FFU109045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057698|NCT00435461|FFU109045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057699|NCT00435461|FFU109045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057700|NCT00435461|FFU109045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051072|NCT00518115|GLP110125|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051073|NCT00518115|GLP110125|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051074|NCT00518115|GLP110125|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051075|NCT01377480||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05267&kw=P05267&tab=access|
3051076|NCT00697749|208129/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051077|NCT00697749|208129/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051078|NCT00697749|208129/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051079|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
3051080|NCT00697749|208129/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051081|NCT00697749|208129/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051082|NCT01825213|PMID: 25181365|Peer reviewed article|http://ieeexplore.ieee.org/document/6887313/?arnumber=6887313|
3051083|NCT04605978||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3051084|NCT04605978||Study Protocol|https://clinicaltrials.servier.com/|
3051085|NCT04605978||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3051086|NCT04605978||Informed Consent Form|https://clinicaltrials.servier.com/|
3051087|NCT04605978||Clinical Study Report|https://clinicaltrials.servier.com/|
3051088|NCT04605978||study-level clinical trial data|https://clinicaltrials.servier.com/|
3051089|NCT06038760||Study Protocol|https://www.pearbio.com/pearglio|
3051090|NCT00306982|106622|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057701|NCT00547248|109509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051091|NCT00306982|106622|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051092|NCT00306982|106622|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051093|NCT00306982|106622|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051094|NCT00306982|106622|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051095|NCT00306982|106622|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053249|NCT01313637|113361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051096|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"
3051097|NCT01777321|116760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057702|NCT00547248|109509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057703|NCT00547248|109509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057704|NCT00547248|109509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057705|NCT00547248|109509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057706|NCT00547248|109509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057707|NCT00547248|109509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057708|NCT01147718|111680|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057709|NCT01147718|111680|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057710|NCT01147718|111680|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057711|NCT01147718|111680|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057712|NCT01147718|111680|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057713|NCT01147718|111680|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051098|NCT01777321|116760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051099|NCT01777321|116760|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051100|NCT01777321|116760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053250|NCT01323647|114306|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053251|NCT01323647|114306|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053252|NCT01323647|114306|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051101|NCT01777321|116760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051102|NCT01777321|116760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051103|NCT01777321|116760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051104|NCT01506895|115403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051105|NCT01506895|115403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051106|NCT01506895|115403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051107|NCT01506895|115403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051108|NCT01506895|115403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051109|NCT01506895|115403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051110|NCT01506895|115403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051111|NCT06264479||Study Protocol|https://www.pearbio.com/peartree2|
3051112|NCT01337674||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4618-010&kw=4618-010&tab=access|
3051113|NCT02920697||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3051114|NCT02920697||Study Protocol|https://clinicaltrials.servier.com/|
3051115|NCT02920697||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3051116|NCT02920697||Informed Consent Form|https://clinicaltrials.servier.com/|
3051117|NCT02920697||study-level clinical trial data|https://clinicaltrials.servier.com/|
3051118|NCT02920697||Clinical Study Report|https://clinicaltrials.servier.com/|
3051119|NCT02254447|201713|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051120|NCT02254447|201713|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051121|NCT02254447|201713|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057714|NCT01147718|111680|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057715|NCT01934127|115415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057716|NCT01934127|115415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057717|NCT01934127|115415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057718|NCT01934127|115415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057719|NCT01934127|115415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057720|NCT01934127|115415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057721|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|
3057722|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.|
3057723|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.|
3057724|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|
3057725|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/15008827|
3057726|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|
3057727|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|
3057728|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|
3057729|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/20606205|
3057730|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22699609|
3059860|NCT00382772|107876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059861|NCT01673529|115246|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059862|NCT01673529|115246|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059863|NCT01673529|115246|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059864|NCT01673529|115246|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059865|NCT01673529|115246|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059866|NCT01673529|115246|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059867|NCT01673529|115246|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059868|NCT00551317|LPL110077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059869|NCT00551317|LPL110077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059870|NCT00551317|LPL110077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059871|NCT00551317|LPL110077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053253|NCT01323647|114306|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053254|NCT01323647|114306|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053255|NCT01323647|114306|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053256|NCT01808482|116702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053257|NCT01808482|116702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053258|NCT01808482|116702|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053259|NCT01808482|116702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053260|NCT01808482|116702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053261|NCT01808482|116702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053262|NCT01808482|116702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053263|NCT01138007|113351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053264|NCT01138007|113351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053265|NCT01138007|113351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053266|NCT01138007|113351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053267|NCT01138007|113351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053268|NCT01287065|114624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053269|NCT01287065|114624|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053270|NCT01287065|114624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053271|NCT01287065|114624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053272|NCT01287065|114624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053273|NCT01287065|114624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053274|NCT01287065|114624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053275|NCT01751074|115677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053276|NCT01751074|115677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053277|NCT01751074|115677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053278|NCT01751074|115677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053279|NCT01751074|115677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053280|NCT01751074|115677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053281|NCT01751074|115677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053282|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.
3053283|NCT00839657||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coag/|
3053284|NCT00839657||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coag/|
3053285|NCT00839657||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coag/|
3053286|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
3053287|NCT05981599||Clinical Study Report|https://doi.org/10.1371/journal.pone.0281544|
3053288|NCT04817761||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3053289|NCT04817761||Study Protocol|https://clinicaltrials.servier.com/|
3053290|NCT04817761||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3053291|NCT04817761||Informed Consent Form|https://clinicaltrials.servier.com/|
3053292|NCT04817761||Clinical Study Report|https://clinicaltrials.servier.com/|
3053293|NCT04817761||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3053294|NCT06727760|Survey in efficacy of probioti|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
3053295|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|
3053296|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|
3053297|NCT06727760|0-1 Yaş Arası Bebekler|rewiev|https://dergipark.org.tr/tr/pub/firattip/issue/6338/84544|
3053298|NCT06727760|kangroo care guide|Guide|https://www.who.int/publications/i/item/9241590351|
3053299|NCT06727760|The Effects of Kangaroo Mother|article|https://ijn.mums.ac.ir/article_4152.html|
3053300|NCT06727760|efficacy of probiotic|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
3053301|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|
3053302|NCT06727760|The Effect of Aromatherapy|doctora thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
3053303|NCT00710021|SDY474|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474.
3053304|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.
3053305|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.
3053306|NCT01457547|217744/094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053307|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
3053308|NCT01457547|217744/094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053309|NCT01457547|217744/094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053310|NCT01457547|217744/094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053311|NCT01457547|217744/094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055499|NCT00381667|B2C104604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055500|NCT00381667|B2C104604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055501|NCT00381667|B2C104604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055502|NCT00381667|B2C104604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055503|NCT00381667|B2C104604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055504|NCT02446496|201529|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053312|NCT00402363|OM8 Afib|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053313|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
3053314|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
3053315|NCT00402363|OM8 Afib|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053316|NCT00402363|OM8 Afib|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053317|NCT00402363|OM8 Afib|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053318|NCT00402363|OM8 Afib|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053319|NCT04140383||Clinical Study Report|http://rdcu.be/bUabz|
3053320|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)
3053321|NCT01294683||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-118&kw=0524B-118&tab=access|
3053322|NCT00398645|FFA106783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053323|NCT00398645|FFA106783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053324|NCT00398645|FFA106783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053325|NCT00398645|FFA106783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053326|NCT00398645|FFA106783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053327|NCT00398645|FFA106783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053328|NCT00398645|FFA106783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053329|NCT05905003||Individual Participant Data Set|https://nda.nih.gov/ampscz/|
3053330|NCT01128894|114179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053331|NCT01128894|114179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057731|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|
3053332|NCT01128894|114179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053333|NCT01128894|114179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053334|NCT01128894|114179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053335|NCT01128894|114179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053336|NCT01128894|114179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053337|NCT01323634|113109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053338|NCT01323634|113109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053339|NCT01323634|113109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053340|NCT01323634|113109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053341|NCT01323634|113109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053342|NCT01323634|113109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053343|NCT01323634|113109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053344|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
3053345|NCT03761511|NICOFA|Study Protocol|https://ukaachen.sharepoint.com/:b:/s/NICOFA/ESUAT8h1fTBHlTcsdu48LrQBbvvAABdsy81bvQ4Egq696g?e=8Xliis|
3053346|NCT00407069|SDY10|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
3053347|NCT00407069|SDY10|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
3053348|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.
3053349|NCT00753272|106372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057732|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|
3057733|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|
3057734|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|
3057735|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.|
3057736|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/9794114|
3057737|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|
3057738|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Zinc+as+a+potential+coadjuvant+in+therapy+for+type+2+diabetes.|
3057739|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|
3057740|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/25284151|
3057741|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/27915988|
3057742|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Insulino-mimetic+and+anti-diabetic+effects+of+zinc|
3057743|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/28615382|
3057744|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/12502486|
3057745|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22375253|
3057746|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|
3057747|NCT00519467|714703/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057748|NCT00519467|714703/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057749|NCT00519467|714703/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057750|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
3057751|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
3057752|NCT00519467|714703/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057753|NCT00519467|714703/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057754|NCT00406081|SDY2|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
3057755|NCT00406081|SDY2|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
3057756|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.
3057757|NCT03126253||Report of the survey along with sampling plan|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|
3057758|NCT00610168|110806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057759|NCT00610168|110806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057760|NCT00610168|110806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057761|NCT00610168|110806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057762|NCT00610168|110806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057763|NCT00610168|110806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057764|NCT00610168|110806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057765|NCT04842552||Informed Consent Form|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3057766|NCT04842552||Clinical Study Report|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3057767|NCT04842552||Study Protocol|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3057768|NCT04842552||Statistical Analysis Plan|http://ehsan-study.com|All requests should be submitted to the contact us/about at the study website or study.ehsan@gmail.com
3057769|NCT02588664||Full Data Package|https://www.pcori.org/about-us/governance/policy-data-management-and-data-sharing|
3057770|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
3057771|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
3057772|NCT00693615|580299/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059872|NCT00551317|LPL110077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059873|NCT00551317|LPL110077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059874|NCT00551317|LPL110077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059875|NCT00674817|MAB110123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059876|NCT00674817|MAB110123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059877|NCT00674817|MAB110123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059878|NCT00674817|MAB110123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059879|NCT00674817|MAB110123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059880|NCT00674817|MAB110123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059881|NCT00674817|MAB110123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059882|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)
3059883|NCT06644573|Virtual Consultation SOAP Note|Individual Participant Data Set|https://drive.google.com/file/d/1uAAbC0gRFOthwnUiWz3O2sDyLgkGkiKf/view?usp=sharing|Virtual Consultation SOAP Note
3059884|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
3059885|NCT06644573|PROSOMNIA Sleep Quiz|Individual Participant Data Set|https://drive.google.com/file/d/1XWzVYL0L2OR8FzFUGtd0vggjwBflBAFa/view?usp=sharing|PROSOMNIA Sleep Quiz
3059886|NCT06644573|Sleep Quiz Evaluation|Clinical Study Report|https://drive.google.com/file/d/1Hzw1OvpbAn44nCbvqbtPwC25clwCbclW/view?usp=sharing|PSHES Sleep Quiz Scoring System
3059887|NCT06644573|Mood/Emotion Quality Scale|Individual Participant Data Set|https://drive.google.com/file/d/1-UzkVbn7UG57aZMg9d1LRB9yoLkjUlWS/view?usp=sharing|Mood/Emotion Quality Scale
3059888|NCT02257398|115775|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059889|NCT02257398|115775|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059890|NCT02257398|115775|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059891|NCT02257398|115775|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059892|NCT02257398|115775|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059893|NCT02257398|115775|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059894|NCT02257398|115775|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059895|NCT00506350|109817|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059896|NCT00506350|109817|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059897|NCT00506350|109817|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059898|NCT00506350|109817|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059899|NCT00506350|109817|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059900|NCT00506350|109817|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059901|NCT00506350|109817|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059902|NCT01424384|105012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059903|NCT01424384|105012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059904|NCT01424384|105012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059905|NCT01424384|105012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059906|NCT01424384|105012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059907|NCT01424384|105012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059908|NCT01424384|105012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059909|NCT00379964||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059910|NCT01054885|112207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059911|NCT01054885|112207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059912|NCT01054885|112207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059913|NCT01054885|112207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059914|NCT01054885|112207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059915|NCT01054885|112207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059916|NCT01054885|112207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059917|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.
3059918|NCT00837434|SDY824|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|ImmPort study identifier is SDY824.
3059919|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.
3059920|NCT03435250||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3059921|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
3059922|NCT00951353|SDY951|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study identifier is SDY951.
3059923|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."
3059924|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
3059925|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
3059926|NCT00269217||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059927|NCT03941470|IRB17200056|Study Protocol|http://Email:ethics_committee12@yahoo.com|
3059928|NCT06602661||Study Protocol|https://docs.google.com/document/d/1-NMx1lP-_x1KHA0t49yEG7tNsFgepmyWPkbdFfWMPMc/edit?usp=sharing|
3059929|NCT06602661||Informed Consent Form|https://drive.google.com/file/d/1rON8VADRvws1J_I_rmqAAy2sNgL0I9c5/view?usp=sharing|
3059930|NCT00360230|106367|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059931|NCT00360230|106367|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059932|NCT00360230|106367|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059933|NCT00360230|106367|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059934|NCT00360230|106367|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059935|NCT00360230|106367|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059936|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.
3059937|NCT06999954||Informed Consent Form|https://www.sdsalliance.org/sds-gps|Available from the SDS-GPS program team at gps@sdsalliance.org
3059938|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
3059939|NCT01353898||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1972-003&kw=1972-003&tab=access|
3059940|NCT03038061||Informed Consent Form|http://ventilation.fbmi.cvut.cz/wp-content/uploads/2017/01/Informed-Consent-Form.pdf|Informed Consent
3059941|NCT06471972||Study Protocol|http://stepcare.org/biomarkers|Lab manuals and sample collection form
3059942|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/18426039|
3059943|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/19952380|
3059944|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/20922783|
3059945|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/?term=In+vitro+effects+of+detergent+sclerosants+on+coagulation%2C+platelets+and+microparticles.|
3059946|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/21725957|
3059947|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/16226898|
3059948|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/11231246|
3059949|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|
3059950|NCT01357850|112670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059951|NCT01357850|112670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059952|NCT01357850|112670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059953|NCT01357850|112670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053350|NCT00753272|106372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053351|NCT00753272|106372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059954|NCT01357850|112670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059955|NCT01357850|112670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059956|NCT01357850|112670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059957|NCT06700473|10.1097/JNR.0000000000000129.|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/28277391/|https://pubmed.ncbi.nlm.nih.gov/28277391/
3059958|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
3059959|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
3059960|NCT01656408||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-002&kw=8150-002&tab=access|
3059961|NCT06473740||Individual Participant Data Set|https://patientdatabase.ishemii.net/login|
3059962|NCT01929317|116991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059963|NCT01929317|116991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059964|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,
3059965|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)
3059966|NCT06081816|10.4314/ahs.v19i1.55|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
3059967|NCT06081816|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
3059968|NCT06591234||Study Protocol|https://www.ausl.bologna.it/|To send a request by mail
3059969|NCT00090207||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059970|NCT03584789||Study Protocol|https://www.researchprotocols.org/2021/4/e24342|
3059971|NCT00614731|SDY3|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
3059972|NCT00614731|SDY3|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
3059973|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.
3059974|NCT01416324|114985|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059975|NCT01416324|114985|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059976|NCT01416324|114985|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059977|NCT01416324|114985|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059978|NCT01416324|114985|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059979|NCT01416324|114985|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059980|NCT01416324|114985|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059981|NCT05345652||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31571625/|
3059982|NCT01128634|113950|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059983|NCT01128634|113950|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059984|NCT01128634|113950|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059985|NCT01128634|113950|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059986|NCT01128634|113950|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059987|NCT01128634|113950|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059988|NCT01128634|113950|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053352|NCT00753272|106372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053353|NCT00753272|106372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053354|NCT00753272|106372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053355|NCT00753272|106372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053356|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
3053357|NCT01177787||Individual Participant Data Set|http://dx.doi.org/10.4172/2165-7904.1000203|
3053358|NCT03434782|60622416.1.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
3053359|NCT00530868||Clinical Study Report|https://doi.org/10.1186/s13058-020-01258-x|Bevacizumab and Letrozole
3053360|NCT03992469||Individual Participant Data Set|https://vivli.org/|
3053361|NCT00992511|113809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053362|NCT00992511|113809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053363|NCT00992511|113809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053364|NCT00992511|113809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053365|NCT00992511|113809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053366|NCT00992511|113809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053367|NCT00992511|113809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053368|NCT01323621|112352|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053369|NCT01323621|112352|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053370|NCT01323621|112352|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053371|NCT01323621|112352|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053372|NCT01323621|112352|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053373|NCT01323621|112352|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053374|NCT01323621|112352|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053375|NCT00437671||FDA approved labeling information|http://www.talecris-pi.info/inserts/hypertet.pdf|
3053376|NCT05512637||Study Protocol|https://bmjopen.bmj.com/content/14/11/e084110|
3053377|NCT01372410|115321|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053378|NCT01372410|115321|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053379|NCT01372410|115321|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053380|NCT01372410|115321|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053381|NCT01372410|115321|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053382|NCT01372410|115321|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053383|NCT01372410|115321|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053384|NCT01387230|115408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053385|NCT01387230|115408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053386|NCT01387230|115408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053387|NCT01387230|115408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051122|NCT02254447|201713|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051123|NCT02254447|201713|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051124|NCT02254447|201713|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051125|NCT02254447|201713|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051126|NCT04322123||Study Protocol|https://www.medrxiv.org/content/10.1101/2020.05.19.20106997v1|Preprint of the Protocol
3051127|NCT00361959|SCO40036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051128|NCT00361959|SCO40036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051129|NCT00361959|SCO40036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051130|NCT00361959|SCO40036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051131|NCT00361959|SCO40036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051132|NCT00361959|SCO40036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051133|NCT00361959|SCO40036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051134|NCT01477853||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431E-211&kw=0431E-211&tab=access|
3051135|NCT01218126|113006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051136|NCT01218126|113006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051137|NCT01218126|113006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051138|NCT01218126|113006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051139|NCT01218126|113006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051140|NCT01218126|113006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051141|NCT01218126|113006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051142|NCT00453986|109067|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051143|NCT00453986|109067|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051144|NCT00453986|109067|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051145|NCT00453986|109067|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051146|NCT00453986|109067|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051147|NCT00453986|109067|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051148|NCT00453986|109067|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051149|NCT06670183||Individual Participant Data Set|https://www.ukbiobank.ac.uk/enable-your-research/apply-for-access|Apply for access to UK Biobank
3051150|NCT02614443|10.1186/s40814-016-0068-9|Study Protocol|https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-016-0068-9|
3051151|NCT00508261|109835|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051152|NCT00508261|109835|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051153|NCT00508261|109835|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051154|NCT00508261|109835|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051155|NCT00508261|109835|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053388|NCT01387230|115408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053389|NCT01387230|115408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053390|NCT01387230|115408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053391|NCT01405937||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-044&kw=7009-044&tab=access|
3053392|NCT04561804||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/MOH_2017-06-07_000470.aspx|Israel Ministry of Health registration number
3053393|NCT01545570|114403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053394|NCT01545570|114403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053395|NCT01545570|114403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053396|NCT01545570|114403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053397|NCT01545570|114403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053398|NCT01545570|114403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053399|NCT01545570|114403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053400|NCT00390910|107737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053401|NCT00390910|107737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053402|NCT00390910|107737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053403|NCT00390910|107737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053404|NCT00390910|107737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053405|NCT00390910|107737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053406|NCT00390910|107737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053407|NCT04024644|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
3053408|NCT04024644|10.1016/j.joms.2011.09.034|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
3053409|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.
3053410|NCT01436071|115283|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053411|NCT01436071|115283|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053412|NCT01436071|115283|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053413|NCT01436071|115283|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053414|NCT01436071|115283|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053415|NCT01436071|115283|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053416|NCT01436071|115283|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053417|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.
3053418|NCT05833087||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08079-9|
3053419|NCT05833087||Statistical Analysis Plan|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
3053420|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
3053421|NCT05833087||Analytic Code|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
3053422|NCT01313650|113373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053423|NCT01313650|113373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053424|NCT01313650|113373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053425|NCT01313650|113373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051156|NCT00508261|109835|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051157|NCT00508261|109835|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051158|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
3051159|NCT06599567|sample size|Individual Participant Data Set|https://bmjopen.bmj.com/content/10/11/e039976|reference article to see sample size with g power
3051160|NCT06599567|Nintendo Wii protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28330586/|
3051161|NCT06599567|Graded motor imagery protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32003812/|
3051162|NCT06901193||Study Protocol|https://orapps.osu.edu/buck-irb/index/view/study/64513|
3051163|NCT01879423|115207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051164|NCT01879423|115207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051165|NCT01879423|115207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051166|NCT01879423|115207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051167|NCT01879423|115207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051168|NCT01879423|115207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051169|NCT01879423|115207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051170|NCT03117725|31098|Study Protocol|https://ezdrug.mfds.go.kr|
3051171|NCT01376323|114728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051172|NCT01376323|114728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051173|NCT01376323|114728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051174|NCT01376323|114728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051175|NCT01376323|114728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051176|NCT01376323|114728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051177|NCT01376323|114728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051178|NCT00796250||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051179|NCT00118716|SFA100314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051180|NCT00118716|SFA100314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051181|NCT00118716|SFA100314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051182|NCT00118716|SFA100314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051183|NCT00118716|SFA100314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051184|NCT00118716|SFA100314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051185|NCT05435352||Study Protocol|https://www.pearbio.com/peartnbc|
3051186|NCT03681574|study protocol|Study Protocol|https://www.justbeamit.com/k7ciq|study protocol
3051187|NCT03681574|data set|Individual Participant Data Set|https://www.justbeamit.com/nwxjr|individual participant data set
3051188|NCT03681574|informed consent form|Informed Consent Form|https://www.justbeamit.com/n2c2d|consert form
3051189|NCT03681574|statistical plan|Statistical Analysis Plan|https://www.justbeamit.com/43kxq|statistical plan
3051190|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."
3051191|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."
3053426|NCT01313650|113373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053427|NCT01313650|113373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051192|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."
3053428|NCT01313650|113373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053429|NCT00863109||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05278&kw=P05278&tab=access|
3053430|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.
3053431|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.
3053432|NCT04100629||Study Protocol|https://drive.google.com/open?id=1vNjwT5j9Y32e7vdayZAMBp-3PvJWCiSK|
3053433|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.
3053434|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.
3053435|NCT01829360||Treatment & Testing Scripts|http://doi.org/10.23641/asha.9745181|See item S4 and S7.
3053436|NCT01829360||Published report of findings|http://doi.org/10.1044/2019_LSHSS-VOIA-18-0131|This article is open access
3053437|NCT01153802|112773|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053438|NCT01153802|112773|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053439|NCT01153802|112773|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053440|NCT01153802|112773|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053441|NCT01153802|112773|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053442|NCT01153802|112773|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053443|NCT01153802|112773|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053444|NCT07060235|fascial tarining|statics|https://www.anatomytrains.com/fascialfitness/fascial_fitness1.pdf|fascia and mobile app
3053445|NCT00378833||CSR synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053446|NCT01013766|111823|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053447|NCT01013766|111823|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053448|NCT01013766|111823|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053449|NCT01013766|111823|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053450|NCT01013766|111823|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053451|NCT01013766|111823|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053452|NCT01013766|111823|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053453|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
3053454|NCT00139347|444563/024|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053455|NCT00139347|444563/024|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053456|NCT00139347|444563/024|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053457|NCT00139347|444563/024|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053458|NCT00139347|444563/024|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053459|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
3053460|NCT01667107||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5592-105&kw=5592-105&tab=access|
3053461|NCT00108914|FFR30008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053462|NCT00108914|FFR30008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053463|NCT00108914|FFR30008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053464|NCT00108914|FFR30008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053465|NCT00108914|FFR30008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053466|NCT00108914|FFR30008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053467|NCT00108914|FFR30008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053468|NCT01177384||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-130&kw=0431-130&tab=access|
3053469|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
3053470|NCT02689531|VIV00008648|Individual Participant Data Set|https://doi.org/10.25934/PR00008648|
3053471|NCT01086410|106851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053472|NCT01086410|106851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053473|NCT01086410|106851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053474|NCT01086410|106851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053475|NCT01086410|106851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053476|NCT01086410|106851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053477|NCT01086410|106851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053478|NCT04160169|doi:10.15139/S3/XEXQXO|Individual Participant Data Set|https://dataverse.unc.edu/dataset.xhtml?persistentId=doi:10.15139/S3/XEXQXO|
3053479|NCT02509104|201897|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053480|NCT02509104|201897|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053481|NCT02509104|201897|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053482|NCT02509104|201897|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053483|NCT02509104|201897|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053484|NCT02509104|201897|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053485|NCT02509104|201897|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053486|NCT05689970|PubMed ID: 34763217|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/34763217/|
3053487|NCT00067951|712753/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053488|NCT00067951|712753/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053489|NCT00067951|712753/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053490|NCT00067951|712753/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053491|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
3053492|NCT00067951|712753/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053493|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
3053494|NCT00330395||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053495|NCT00766090|112202|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053496|NCT00766090|112202|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053497|NCT00766090|112202|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053498|NCT00766090|112202|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053499|NCT00766090|112202|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053500|NCT00766090|112202|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053501|NCT00766090|112202|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053502|NCT01159912|112059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051193|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.
3051194|NCT03077464||preliminary results|http://hdl.handle.net/2097/19148|Rodicheva master's thesis document with preliminary analyses
3051195|NCT00452686|108638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051196|NCT00452686|108638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051197|NCT00452686|108638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051198|NCT00452686|108638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051199|NCT00452686|108638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051200|NCT00452686|108638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051201|NCT00452686|108638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051202|NCT04699955||Individual Participant Data Set|https://osf.io/akef9/|
3051203|NCT06453655||Study Protocol|https://doi.org/10.1097/MEG.0b013e328333fca6|
3051204|NCT06579820||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|pubmed
3051205|NCT01678131||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-048&kw=7009-048&tab=access|
3051206|NCT06320626|37369395|Study Protocol|http://bmjopen.bmj.com/content/13/6/e072363.long|Published study protocol
3051207|NCT00441701||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04592&kw=7123-012&tab=access|
3051208|NCT03408275||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data available to researchers on application through the website
3051209|NCT04599686|NCT04599686|Study Protocol|http://clinicaltrials.gov/ct2/results?cond=&term=NCT04599686&cntry=&state=&city=&dist=|Please see the clinical trials NCT04599686
3051210|NCT01691521|115588|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051211|NCT01691521|115588|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051212|NCT01691521|115588|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051213|NCT01691521|115588|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051214|NCT01691521|115588|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051215|NCT01691521|115588|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051216|NCT01691521|115588|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051217|NCT02948881|BON103593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051218|NCT02948881|BON103593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051219|NCT02948881|BON103593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051220|NCT02948881|BON103593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051221|NCT02948881|BON103593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051222|NCT02948881|BON103593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051223|NCT02948881|BON103593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051224|NCT02786264||Statistical Analysis Plan|https://docs.google.com/document/d/1SUzYG_9aKT5sSkPXEmhvRTqvhXRflQLBiXJe59inDh4/edit?usp=sharing|
3051225|NCT07165613||thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp
3051226|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.
3051227|NCT05525936|University of Sydney|Individual Participant Data Set|https://redcap.sydney.edu.au/|
3051228|NCT00652938|111507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051229|NCT00652938|111507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051230|NCT00652938|111507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051231|NCT00652938|111507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051232|NCT00652938|111507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051233|NCT00652938|111507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057773|NCT00693615|580299/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057774|NCT00693615|580299/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057775|NCT00693615|580299/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057776|NCT00693615|580299/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057777|NCT00534638|106636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057778|NCT00534638|106636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057779|NCT00534638|106636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057780|NCT00534638|106636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057781|NCT00534638|106636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057782|NCT00534638|106636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057783|NCT00534638|106636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057784|NCT00481767|106069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057785|NCT00481767|106069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057786|NCT00481767|106069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057787|NCT00481767|106069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057788|NCT00481767|106069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057789|NCT00481767|106069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057790|NCT00481767|106069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057791|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.
3057792|NCT00346749|ADC105931|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053503|NCT01159912|112059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053504|NCT01159912|112059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053505|NCT01159912|112059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053506|NCT01159912|112059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053507|NCT01159912|112059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053508|NCT01159912|112059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053509|NCT01717287||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-248&kw=0518-248&tab=access|
3053510|NCT00370227|107706|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053511|NCT00370227|107706|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053512|NCT00370227|107706|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053513|NCT00370227|107706|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053514|NCT00370227|107706|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053515|NCT00370227|107706|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053516|NCT00279019|AC2103473|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053517|NCT00279019|AC2103473|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057793|NCT00346749|ADC105931|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057794|NCT00346749|ADC105931|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057795|NCT00346749|ADC105931|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051234|NCT00652938|111507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051235|NCT00979602|113480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051236|NCT00979602|113480|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051237|NCT00979602|113480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057796|NCT00346749|ADC105931|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057797|NCT00346749|ADC105931|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057798|NCT01808261|104615|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057799|NCT01808261|104615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057800|NCT01808261|104615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057801|NCT01808261|104615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057802|NCT01808261|104615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057803|NCT01808261|104615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057804|NCT01808261|104615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057805|NCT01158742|SDY291|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
3057806|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.
3057807|NCT01158742|SDY291|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
3057808|NCT00370097|FAS106533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057809|NCT00370097|FAS106533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057810|NCT00370097|FAS106533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057811|NCT00370097|FAS106533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057812|NCT00370097|FAS106533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057813|NCT00370097|FAS106533|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057814|NCT00370097|FAS106533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057815|NCT00461097|SDY218|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY218|ImmPort study identifier is SDY218
3057816|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
3057817|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.
3057818|NCT02527629||Study results|https://pubmed.ncbi.nlm.nih.gov/32386409/|
3057819|NCT00230243||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057820|NCT00268983|393229/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057821|NCT00268983|393229/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057822|NCT00268983|393229/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057823|NCT00268983|393229/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051238|NCT00979602|113480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051239|NCT00979602|113480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051240|NCT00979602|113480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059989|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.
3051241|NCT00979602|113480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051242|NCT00327184|106388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053518|NCT00279019|AC2103473|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053519|NCT00279019|AC2103473|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053520|NCT00279019|AC2103473|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053521|NCT00279019|AC2103473|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053522|NCT00279019|AC2103473|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053523|NCT01086462|114041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053524|NCT01086462|114041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053525|NCT01086462|114041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053526|NCT01086462|114041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053527|NCT01086462|114041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053528|NCT01086462|114041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053529|NCT01086462|114041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053530|NCT03662165||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/UULS6T|
3053531|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
3053532|NCT00309634|106750|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053533|NCT00309634|106750|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053534|NCT00309634|106750|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053535|NCT00309634|106750|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053536|NCT00309634|106750|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053537|NCT00309634|106750|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053538|NCT00376584||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053539|NCT06725225||Individual Participant Data Set|https://vivli.org|
3053540|NCT00169455|103477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053541|NCT00169455|103477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053542|NCT00169455|103477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053543|NCT00169455|103477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053544|NCT00169455|103477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053545|NCT00169455|103477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053546|NCT00861250||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25303369|First study article: http://www.ncbi.nlm.nih.gov/pubmed/23206270
3053547|NCT01973777||Clinical Study Report|http://www.contraceptionjournal.org/article/S0010-7824%2815%2930125-6/abstract|
3053548|NCT00768326|2006-003739-57|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2006-003739-57/results|
3053549|NCT00674583|111414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053550|NCT00674583|111414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053551|NCT00674583|111414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053552|NCT00674583|111414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053553|NCT00674583|111414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053554|NCT00674583|111414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053555|NCT00674583|111414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053556|NCT00111800|100925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053557|NCT00111800|100925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053558|NCT00111800|100925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053559|NCT00111800|100925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053560|NCT00111800|100925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053561|NCT00111800|100925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053562|NCT00111800|100925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053563|NCT00082524||CSRSynopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053564|NCT00714285|111295|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053565|NCT00714285|111295|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053566|NCT00714285|111295|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053567|NCT00714285|111295|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053568|NCT00714285|111295|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053569|NCT00714285|111295|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053570|NCT00714285|111295|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053571|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.
3053572|NCT00000551||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/act/|
3053573|NCT00000551||Study Forms|http://biolincc.nhlbi.nih.gov/studies/act/|
3053574|NCT00000551||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/act/|
3053575|NCT00282295|105753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053576|NCT00282295|105753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053577|NCT00282295|105753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053578|NCT00282295|105753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053579|NCT00282295|105753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053580|NCT00282295|105753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053581|NCT00449670|109630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053582|NCT00449670|109630|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053583|NCT00449670|109630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053584|NCT00449670|109630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053585|NCT00449670|109630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053586|NCT00449670|109630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053587|NCT00449670|109630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053588|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.
3053589|NCT00346073|106316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053590|NCT00346073|106316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053591|NCT00346073|106316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053592|NCT00346073|106316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053593|NCT00346073|106316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053594|NCT00346073|106316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053595|NCT07257666|Ethics Committee approval No.|Informed Consent Form|http://www.kcs.ac.rs/index.php/eticki-odbor|
3053596|NCT00980200|113310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059990|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.
3059991|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.
3059992|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|
3059993|NCT00345358|107058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059994|NCT00345358|107058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059995|NCT00345358|107058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059996|NCT00345358|107058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059997|NCT00345358|107058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059998|NCT00345358|107058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059999|NCT02094924|200957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060000|NCT02094924|200957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060001|NCT02094924|200957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060002|NCT02094924|200957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060003|NCT02094924|200957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060004|NCT02094924|200957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060005|NCT02094924|200957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060006|NCT00742261|MET111516|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060007|NCT00742261|MET111516|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060008|NCT00742261|MET111516|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060009|NCT00742261|MET111516|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060010|NCT00742261|MET111516|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060011|NCT00742261|MET111516|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060012|NCT00742261|MET111516|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060013|NCT02581410|201198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060014|NCT02581410|201198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060015|NCT02581410|201198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060016|NCT02581410|201198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060017|NCT02581410|201198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060018|NCT02581410|201198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060019|NCT02581410|201198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060020|NCT06595771||Study Protocol|https://haydarpasanumuneah.saglik.gov.tr/|
3060021|NCT05350397|REFERENCE|REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30982782/|
3060022|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_35_70_76_127.pdf|
3060023|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/30982782/|
3051243|NCT00327184|106388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060024|NCT05350397|REFERENCE|REFERENCE|http://dergipark.org.tr/tr/pub/ikcusbfd/issue/60165/705219|
3051244|NCT00327184|106388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051245|NCT00327184|106388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060025|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_37_60_1_10.pdf|
3051246|NCT00327184|106388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060026|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/18992625/|
3060027|NCT05350397|REFERENCE|REFERENCE|http://www.ncbi.nlm.nih.gov/books/NBK72567/|
3060028|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1016/j.ctcp.2021.101304|
3051247|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.
3051248|NCT04599738||Study Protocol|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
3051249|NCT04599738||Informed Consent Form|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
3051250|NCT07165366||Informed Consent Form|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EalUzspTf7VClbHYAyBlJg4BVp2wl1gK8uHn7MzUbZ4tbA?e=1vfYnE|
3051251|NCT07165366||Statistical Analysis Plan|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EbDir0nT8JNAlpv4-vfnOxMBCBxsvrV2UjY2_ua4APTs2g?e=zJdPmF|
3051252|NCT01590771||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-253&kw=0431-253&tab=access|
3051253|NCT00082537||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051254|NCT00682643|FFR110537|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051255|NCT00682643|FFR110537|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051256|NCT00682643|FFR110537|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051257|NCT00682643|FFR110537|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060029|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1097/HNP.0000000000000384|
3060030|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/23981400/|
3060031|NCT01745822||Individual Participant Data Set|https://dash.nichd.nih.gov/study/17511|
3060032|NCT01587924|116582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060033|NCT01587924|116582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060034|NCT01587924|116582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060035|NCT01587924|116582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060036|NCT01587924|116582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060037|NCT01587924|116582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060038|NCT01587924|116582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060039|NCT04591808||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3060040|NCT04591808||Study Protocol|https://clinicaltrials.servier.com/|
3060041|NCT04591808||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3060042|NCT04591808||Informed Consent Form|https://clinicaltrials.servier.com/|
3060043|NCT04591808||Clinical Study Report|https://clinicaltrials.servier.com/|
3060044|NCT04591808||[study-level clinical trial data]|https://clinicaltrials.servier.com/|
3060045|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.
3060046|NCT00760617|111737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060047|NCT00760617|111737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060048|NCT00760617|111737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060049|NCT00760617|111737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060050|NCT00760617|111737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060051|NCT00760617|111737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060052|NCT00760617|111737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051258|NCT00682643|FFR110537|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051259|NCT00682643|FFR110537|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060053|NCT00555061|TOC106489|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060054|NCT00555061|TOC106489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060055|NCT00555061|TOC106489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060056|NCT00555061|TOC106489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053597|NCT00980200|113310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053598|NCT00980200|113310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053599|NCT00980200|113310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053600|NCT00980200|113310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053601|NCT00980200|113310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053602|NCT00980200|113310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053603|NCT00789880|SDY14|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
3053604|NCT00789880|SDY14|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
3053605|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.
3053606|NCT05820633||Study Protocol|https://www.sealedenvelope.com/simple-randomiser/v1/lists|
3053607|NCT07171515||Study Protocol|https://data.doi.or.kr/10.22694/CANCERDATA032018070101|1\. 1. Guidelines for the Pancreatic Cancer Registry, National Cancer Center Big Data
3053608|NCT07171515||Study Protocol|https://cancerportal.kr/ncc/clinicalLibraryInfo.do|2\. CONNECT Cancer Big Data Library: Pancreatic Cancer Section
3053609|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
3053610|NCT07280962||Study Protocol|https://heyzine.com/flip-book/0d5ec370d6.html|https://heyzine.com/flip-book/0d5ec370d6.html
3053611|NCT00315744|102318|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053612|NCT00315744|102318|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053613|NCT00315744|102318|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053614|NCT00315744|102318|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053615|NCT00315744|102318|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053616|NCT00315744|102318|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053617|NCT01147744|112186|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053618|NCT01147744|112186|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053619|NCT01147744|112186|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053620|NCT01147744|112186|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053621|NCT01147744|112186|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053622|NCT01147744|112186|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053623|NCT01147744|112186|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053624|NCT06089148|Cairo unversity|Study Protocol|https://medicine.cu.edu.eg/index.php/en/postgraduate/32-research/161-research-ethics-committee|upon requirement
3055505|NCT02446496|201529|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055506|NCT02446496|201529|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055507|NCT02446496|201529|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055508|NCT02446496|201529|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055509|NCT02446496|201529|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055510|NCT02677675||Study Protocol|http://www.nmrr.gov.my|
3055511|NCT00938275|113261|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055512|NCT00938275|113261|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055513|NCT00938275|113261|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060057|NCT00555061|TOC106489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060058|NCT00555061|TOC106489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060059|NCT00555061|TOC106489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060060|NCT06947681|Not available at moment|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|Most of the informations available at This site and Google Scholar
3060061|NCT00976560|113009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060062|NCT00976560|113009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060063|NCT00976560|113009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060064|NCT00976560|113009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060065|NCT00976560|113009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060066|NCT00976560|113009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060067|NCT00976560|113009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053627|NCT01669070|115441|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053628|NCT01669070|115441|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053629|NCT01669070|115441|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053630|NCT01669070|115441|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053631|NCT01669070|115441|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060068|NCT02914301|FWA00005945|Informed Consent Form|https://files.acrobat.com/a/preview/c262292c-6de1-4f73-bae3-689555b8c77f|
3060069|NCT02914301|Post-Partum Survey|Individual Participant Data Set|https://files.acrobat.com/a/preview/5ec925dd-52ad-4b07-b6fc-2084d2f751d5|
3060070|NCT02914301|Prenatal Participant Data -22|Individual Participant Data Set|https://files.acrobat.com/a/preview/984213bb-ccef-419b-8f56-87336004ec5a|
3060071|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."
3060072|NCT01192191|114156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060073|NCT01192191|114156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060074|NCT01192191|114156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060075|NCT01192191|114156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060076|NCT01192191|114156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060077|NCT01192191|114156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060078|NCT01192191|114156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060079|NCT01175083|114056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060080|NCT01175083|114056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060081|NCT01175083|114056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060082|NCT01175083|114056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060083|NCT01175083|114056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060084|NCT01175083|114056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060085|NCT01175083|114056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060086|NCT01485172|111662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060087|NCT01485172|111662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060088|NCT01485172|111662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060089|NCT01485172|111662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060090|NCT01485172|111662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060091|NCT01485172|111662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060092|NCT00951977|SDY290|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
3060093|NCT00951977|SDY290|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
3060094|NCT00951977|SDY290|Study summary, -design, -demographics, -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
3060095|NCT00329355|TRX105852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060096|NCT00329355|TRX105852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053632|NCT01669070|115441|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060097|NCT00329355|TRX105852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060098|NCT00329355|TRX105852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060099|NCT00329355|TRX105852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060100|NCT00329355|TRX105852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057824|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
3057825|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
3057826|NCT00268983|393229/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060101|NCT00329355|TRX105852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060102|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.
3060103|NCT01318980|114604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060104|NCT01318980|114604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060105|NCT01318980|114604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060106|NCT01318980|114604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060107|NCT01318980|114604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060108|NCT01318980|114604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060109|NCT01318980|114604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060110|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
3060111|NCT01818011|116266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060112|NCT01818011|116266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060113|NCT01818011|116266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060114|NCT01818011|116266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060115|NCT01818011|116266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060116|NCT01818011|116266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060117|NCT01818011|116266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060118|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
3060119|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
3060120|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
3060121|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
3060122|NCT00265148|BRL-49653/461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060123|NCT00265148|BRL-49653/461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060124|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
3060125|NCT00389987||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3060126|NCT01049009|26285691|Publication|https://www.ncbi.nlm.nih.gov/pubmed/26285691|
3060127|NCT00535288||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06472&kw=P06472&tab=access|
3060128|NCT00368199||Individual Participant Data Set|https://peerj.com/articles/2037/|
3060129|NCT01015638|114546|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060130|NCT01015638|114546|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060131|NCT01015638|114546|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060132|NCT01015638|114546|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060133|NCT01015638|114546|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060134|NCT01702493|117041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060135|NCT01702493|117041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051260|NCT00682643|FFR110537|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051261|NCT02726776||Study Protocol|https://cloud.scientificnet.org/index.php/s/7vKbCJ1vs0UOYNN|Unfortunately available only in German
3051262|NCT02726776||Informed Consent Form|https://cloud.scientificnet.org/index.php/s/9RXyWhRxEgUgbTd|Unfortunately available only in German or Italian
3051263|NCT00144872|LAM100118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051264|NCT00144872|LAM100118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051265|NCT00144872|LAM100118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060136|NCT01702493|117041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060137|NCT01702493|117041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060138|NCT01702493|117041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060139|NCT01702493|117041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060140|NCT01702493|117041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060141|NCT01449799|113423|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060142|NCT01449799|113423|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060143|NCT01449799|113423|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060144|NCT01449799|113423|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060145|NCT01449799|113423|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060146|NCT01449799|113423|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051266|NCT00144872|LAM100118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053633|NCT01669070|115441|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060147|NCT01449799|113423|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060148|NCT07156396|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
3060149|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.
3060150|NCT01696604|116715|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060151|NCT01696604|116715|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060152|NCT01696604|116715|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060153|NCT01696604|116715|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060154|NCT01696604|116715|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060155|NCT01696604|116715|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060156|NCT01696604|116715|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060157|NCT00435045|OM9L|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060158|NCT00435045|OM9L|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060159|NCT00435045|OM9L|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060160|NCT00435045|OM9L|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060161|NCT00435045|OM9L|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060162|NCT00435045|OM9L|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060163|NCT00435045|OM9L|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060164|NCT06757920|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3060165|NCT01209104|113722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060166|NCT01209104|113722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053634|NCT02257372|201314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057827|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.
3057828|NCT01046331||Study Forms|http://biolincc.nhlbi.nih.gov/studies/h1n1/|
3057829|NCT01630135|116364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057830|NCT01630135|116364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057831|NCT01630135|116364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057832|NCT01630135|116364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057833|NCT01236040|114371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057834|NCT01236040|114371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057835|NCT01236040|114371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057836|NCT01236040|114371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057837|NCT01236040|114371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057838|NCT01236040|114371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057839|NCT03271593||Clinical Study Report|https://www.gsk-clinicalstudyregister.com/study/205369?search=study&search_terms=205369#csr|Results disclosed in the Clinical Study Report.
3057840|NCT01061541|208108/091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057841|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.
3057842|NCT01061541|208108/091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057843|NCT01061541|208108/091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057844|NCT01061541|208108/091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057845|NCT01061541|208108/091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057846|NCT00107757|FFR100010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057847|NCT00107757|FFR100010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057848|NCT00107757|FFR100010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057849|NCT00107757|FFR100010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057850|NCT00107757|FFR100010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057851|NCT00107757|FFR100010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057852|NCT00107757|FFR100010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057853|NCT01212094||Paper describing the results of interim analysis|http://onlinelibrary.wiley.com/doi/10.1002/acn3.293/full|
3057854|NCT03180203|Study Intensive Care|Study Protocol|https://www.catharinaziekenhuis.nl/contact.html|Contact can be made to request the study protocol (Dutch)
3057855|NCT00354965|AUG102821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057856|NCT00354965|AUG102821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057857|NCT00354965|AUG102821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057858|NCT00354965|AUG102821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057859|NCT00354965|AUG102821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057860|NCT00354965|AUG102821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057861|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.
3057862|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.
3057863|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
3057864|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
3057865|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.
3057866|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.
3057867|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.
3057868|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
3057869|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
3057870|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
3057871|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
3057872|NCT00371735|CDA 714703/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057873|NCT00371735|CDA 714703/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057874|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
3057875|NCT00920959|SAS30021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057876|NCT00920959|SAS30021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057877|NCT00920959|SAS30021|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057878|NCT00920959|SAS30021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057879|NCT00920959|SAS30021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057880|NCT00920959|SAS30021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057881|NCT00920959|SAS30021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057882|NCT00792909|111736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057883|NCT00792909|111736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057884|NCT00792909|111736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057885|NCT00792909|111736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057886|NCT00792909|111736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057887|NCT00792909|111736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053635|NCT02257372|201314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053636|NCT02257372|201314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053637|NCT02257372|201314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053638|NCT02257372|201314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053639|NCT02257372|201314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053640|NCT02257372|201314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053641|NCT00316680|104489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053642|NCT00316680|104489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053643|NCT00316680|104489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053644|NCT00316680|104489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053645|NCT00316680|104489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053646|NCT00316680|104489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053647|NCT02938884||Study Protocol|https://oncore.umn.edu/login/|
3053648|NCT03686436||Study Protocol|https://www.clinicaltrials.gov|
3053649|NCT05705609|Kim H, Kim S, Choe K, Kim JS|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/29579508/|web site is provided
3053650|NCT00290342|104871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053651|NCT00290342|104871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053652|NCT00290342|104871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053653|NCT00290342|104871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053654|NCT00290342|104871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053655|NCT00290342|104871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053656|NCT02134483||Article|https://www.ncbi.nlm.nih.gov/pubmed/26375142|
3053657|NCT00122681|580299/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053658|NCT00122681|580299/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053659|NCT00122681|580299/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053660|NCT00122681|580299/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053661|NCT00122681|580299/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053662|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
3053663|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
3053664|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.
3053665|NCT03715153||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3053666|NCT03715153||Study Protocol|https://clinicaltrials.servier.com/|
3053667|NCT03715153||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3053668|NCT03715153||Informed Consent Form|https://clinicaltrials.servier.com/|
3053669|NCT03715153||Clinical Study Report|https://clinicaltrials.servier.com/|
3053670|NCT03715153||study-level clinical trial data]|https://clinicaltrials.servier.com/|
3053671|NCT00695448|PIK111051|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053672|NCT00695448|PIK111051|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053673|NCT00695448|PIK111051|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053674|NCT00695448|PIK111051|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053675|NCT00695448|PIK111051|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053676|NCT00695448|PIK111051|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057888|NCT01299558|102934|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057889|NCT01299558|102934|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057890|NCT01299558|102934|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057891|NCT01299558|102934|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057892|NCT01299558|102934|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057893|NCT01299558|102934|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057894|NCT01299558|102934|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057895|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.
3057896|NCT00933595||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
3057897|NCT00933595||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
3057898|NCT00933595||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
3051267|NCT00144872|LAM100118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051268|NCT00144872|LAM100118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051269|NCT00144872|LAM100118|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051270|NCT00116844|VLX103596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051271|NCT00116844|VLX103596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051272|NCT00116844|VLX103596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051273|NCT00116844|VLX103596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051274|NCT00116844|VLX103596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051275|NCT00116844|VLX103596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051276|NCT00116844|VLX103596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051277|NCT00674635|104972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051278|NCT00674635|104972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051279|NCT00674635|104972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051280|NCT00674635|104972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051281|NCT00674635|104972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051282|NCT00674635|104972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051283|NCT00674635|104972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051284|NCT05051332|NCT03545269|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Efficacy and Safety of Treatment of Articular Cartilage Lesions With CartiLife®
3051285|NCT05051332|NCT03517046|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Safety of Treatment of Articular Cartilage Lesions With CartiLife®
3053677|NCT00695448|PIK111051|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053678|NCT04630587||Study Protocol|http://www.oulu.fi/medicine/node/52771|
3053679|NCT00490568|AVA102675|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057899|NCT02689804||Publication|http://dx.doi.org/10.1016/j.contraception.2017.01.004|Results Reference: Yes
3057900|NCT01405560||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-045&kw=7009-045&tab=access|
3057901|NCT00969228|112269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057902|NCT00969228|112269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057903|NCT00969228|112269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057904|NCT00969228|112269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057905|NCT00969228|112269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057906|NCT00969228|112269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057907|NCT00969228|112269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057908|NCT00903201|110399|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057909|NCT00903201|110399|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057910|NCT00903201|110399|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057911|NCT00903201|110399|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057912|NCT00903201|110399|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057913|NCT00903201|110399|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057914|NCT00903201|110399|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057915|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.
3057916|NCT00612820|IPR110723|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057917|NCT00612820|IPR110723|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057918|NCT00612820|IPR110723|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057919|NCT00612820|IPR110723|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057920|NCT00612820|IPR110723|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057921|NCT00612820|IPR110723|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057922|NCT00612820|IPR110723|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057923|NCT00358358|SCO104925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057924|NCT00358358|SCO104925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057925|NCT00358358|SCO104925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057926|NCT00358358|SCO104925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057927|NCT00358358|SCO104925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057928|NCT00358358|SCO104925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057929|NCT00358358|SCO104925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057930|NCT00731822|HZC111348|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057931|NCT00731822|HZC111348|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057932|NCT00731822|HZC111348|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057933|NCT00731822|HZC111348|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057934|NCT00731822|HZC111348|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057935|NCT00731822|HZC111348|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057936|NCT00731822|HZC111348|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057937|NCT00427908|108658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057938|NCT00427908|108658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057939|NCT00427908|108658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057940|NCT00427908|108658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057941|NCT00427908|108658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057942|NCT00427908|108658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057943|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
3057944|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.
3057945|NCT00097006|REDS II-CORE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/core/|
3057946|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.
3057947|NCT00097006|REDS II-LAPS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/laps/|
3057948|NCT00097006|REDS II-LAPS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/laps/|
3057949|NCT00097006|REDS II-LAPS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/laps/|
3057950|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.
3057951|NCT00097006|REDS II-MS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/redsms/|
3057952|NCT00097006|REDS II-MS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/redsms/|
3057953|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.
3057954|NCT00097006|REDS II-RISE|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rise/|
3057955|NCT00097006|REDS II-RISE|Study Forms|http://biolincc.nhlbi.nih.gov/studies/rise/|
3057956|NCT00097006|REDS II-RISE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/rise/|
3057957|NCT02855476||Study Protocol|http://hdclarity.net/study-information/|
3057958|NCT02855476||Informed Consent Form|http://hdclarity.net/study-information/|Draft informed consent form, not yet approved by an Institutional Review Board for clinical use
3057959|NCT03074695|Pro00079368|Informed Consent Form|https://eirb.mc.duke.edu/|
3057960|NCT00523913|AVD105720|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057961|NCT00523913|AVD105720|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057962|NCT00523913|AVD105720|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057963|NCT00523913|AVD105720|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057964|NCT00523913|AVD105720|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057965|NCT00523913|AVD105720|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057966|NCT00523913|AVD105720|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057967|NCT04579848||Study Protocol|https://drive.google.com/file/d/1AKuis2zJlqhUqY4OEPyVhQPpIiuPnnhr/view?usp=sharing|
3057968|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1mB2pEgRmuMhaVM_eNnnyXdqsyev4wev5/view?usp=sharing|
3057969|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1oE_9J-5uwLpboVWEsUJL6tHn4st1ea9r/view?usp=sharing|
3057970|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)
3057971|NCT00092196||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057972|NCT01702467|116698|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057973|NCT01702467|116698|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057974|NCT01702467|116698|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057975|NCT01702467|116698|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057976|NCT01702467|116698|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057977|NCT01702467|116698|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057978|NCT01702467|116698|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057979|NCT00896064|112993|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051286|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
3057980|NCT00896064|112993|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057981|NCT00896064|112993|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057982|NCT00896064|112993|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057983|NCT00896064|112993|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057984|NCT01573000|104515|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057985|NCT01573000|104515|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057986|NCT01573000|104515|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057987|NCT01573000|104515|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057988|NCT01573000|104515|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057989|NCT01573000|104515|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057990|NCT01573000|104515|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057991|NCT01545388||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-136&kw=0431A-136&tab=access|
3057992|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.
3057993|NCT04087239||Individual Participant Data Set|http://www.redcap.uzchs.ac.zw/redcap|Data being entered, now verification of enrolment case report forms
3057994|NCT01204671|114269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057995|NCT01204671|114269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057996|NCT01204671|114269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057997|NCT01204671|114269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057998|NCT01204671|114269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057999|NCT01204671|114269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058000|NCT01204671|114269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058001|NCT01725685|116524|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058002|NCT01725685|116524|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058003|NCT01725685|116524|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058004|NCT01725685|116524|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058005|NCT01725685|116524|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058006|NCT01725685|116524|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058007|NCT01725685|116524|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051287|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.
3051288|NCT00289770|100551 (EXT Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051289|NCT00289770|100551 (EXT Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051290|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
3058008|NCT00526474||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04737&kw=P04737&tab=access|
3058009|NCT02944292||Study Protocol|https://drive.google.com/open?id=0B-XpW352z4ZJMFdseHNwTWI2clU|
3058010|NCT01494636|115419|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058011|NCT01494636|115419|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058012|NCT01494636|115419|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051291|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)
3058013|NCT01494636|115419|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051292|NCT00980005|112999|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051293|NCT00980005|112999|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051294|NCT00980005|112999|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051295|NCT00980005|112999|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051296|NCT00980005|112999|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051297|NCT00980005|112999|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051298|NCT00980005|112999|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051299|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
3051300|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
3051301|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
3051302|NCT00344006|CDA 714703/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051303|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
3051304|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
3051305|NCT00344006|CDA 714703/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051306|NCT02777996||Study Protocol|http://www.ispo.it|In Italian, available under request
3051307|NCT01036022|111407|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051308|NCT01036022|111407|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051309|NCT01036022|111407|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051310|NCT01036022|111407|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051311|NCT01036022|111407|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051312|NCT01036022|111407|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051313|NCT01036022|111407|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051314|NCT00352898|105909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051315|NCT00352898|105909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051316|NCT00352898|105909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051317|NCT00352898|105909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051318|NCT00352898|105909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051319|NCT00352898|105909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051320|NCT06900699|Not available at moment|papers|https://pubmed.ncbi.nlm.nih.gov/|Most of thé informations available at This site and Google Scholar
3051321|NCT00196989|ADG20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051322|NCT00196989|ADG20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051323|NCT00196989|ADG20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051324|NCT00196989|ADG20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058014|NCT01494636|115419|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058015|NCT01494636|115419|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058016|NCT01494636|115419|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058017|NCT01218308|114541|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058018|NCT01218308|114541|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058019|NCT01218308|114541|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058020|NCT01218308|114541|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058021|NCT01218308|114541|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058022|NCT01218308|114541|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058023|NCT01218308|114541|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058024|NCT00103454|FFR30002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058025|NCT00103454|FFR30002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058026|NCT00103454|FFR30002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058027|NCT00103454|FFR30002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058028|NCT00103454|FFR30002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058029|NCT00103454|FFR30002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058030|NCT00103454|FFR30002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058031|NCT02577536||Individual Participant Data Set|https://dash.nichd.nih.gov/study/424642|Deidentified data from this study are not available in the NICHD Data and Specimen Repository.
3058032|NCT00023231|SDY131|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
3058033|NCT00023231|SDY131|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
3058034|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
3058035|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
3058036|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
3058037|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
3058038|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
3058039|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
3058040|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.
3058041|NCT00887484|114544|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058042|NCT00887484|114544|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058043|NCT00887484|114544|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058044|NCT00887484|114544|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058045|NCT00887484|114544|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058046|NCT04801251|Sarah bakry|Study Protocol|https://www.outlook.com/aun.edu.eg|All data or information will be uploaded on the website
3053680|NCT00490568|AVA102675|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058047|NCT01035749|113883|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058048|NCT01035749|113883|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053681|NCT00490568|AVA102675|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053682|NCT00490568|AVA102675|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055514|NCT00938275|113261|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055515|NCT00938275|113261|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055516|NCT00938275|113261|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055517|NCT00938275|113261|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055518|NCT00549120|MAB104954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055519|NCT00549120|MAB104954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055520|NCT00549120|MAB104954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055521|NCT00549120|MAB104954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055522|NCT00549120|MAB104954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055523|NCT00549120|MAB104954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055524|NCT00549120|MAB104954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055525|NCT01294709||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-014&kw=0974-014&tab=access|
3055526|NCT00981409|106206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055527|NCT00981409|106206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055528|NCT00981409|106206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053683|NCT00490568|AVA102675|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053684|NCT00490568|AVA102675|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053685|NCT00490568|AVA102675|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053686|NCT02699957|Data Collection Form|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|
3053687|NCT02699957|Data Dictionary|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|Element definitions and coding instructions.
3053688|NCT03177772|dtp38|Study Protocol|https://osf.io/dtp38/|Open Science Framework. we are registered
3053689|NCT00996268|113412|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053690|NCT00996268|113412|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053691|NCT00996268|113412|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053692|NCT00996268|113412|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053693|NCT00996268|113412|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053694|NCT00996268|113412|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058049|NCT01035749|113883|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058050|NCT01035749|113883|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058051|NCT01035749|113883|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058052|NCT01035749|113883|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058053|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
3053695|NCT00996268|113412|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053696|NCT00996944|113079|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053697|NCT00996944|113079|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053698|NCT00996944|113079|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053699|NCT00996944|113079|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053700|NCT00034658||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053701|NCT02467933|449|Study Protocol|https://www.socialscienceregistry.org/trials/729|Study protocol archived on American Economic Association Social Science Registry page.
3053702|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)"
3053703|NCT00382993|TRX106573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053704|NCT00382993|TRX106573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053705|NCT00382993|TRX106573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053706|NCT00382993|TRX106573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053707|NCT00382993|TRX106573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053708|NCT00382993|TRX106573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053709|NCT00382993|TRX106573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053710|NCT00385255|106323|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053711|NCT00385255|106323|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053712|NCT00385255|106323|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058054|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.
3058055|NCT00413023|NKF100096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058056|NCT00413023|NKF100096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058057|NCT00413023|NKF100096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058058|NCT00413023|NKF100096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058059|NCT00413023|NKF100096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058060|NCT00413023|NKF100096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060167|NCT01209104|113722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060168|NCT01209104|113722|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060169|NCT01209104|113722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058061|NCT00413023|NKF100096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058062|NCT00423046|108933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060170|NCT01209104|113722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060171|NCT01209104|113722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055529|NCT00443131|107731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055530|NCT00443131|107731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055531|NCT00443131|107731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055532|NCT00443131|107731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055533|NCT00443131|107731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055534|NCT00443131|107731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055535|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.
3055536|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"
3055537|NCT00607906|AXO110461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055538|NCT00607906|AXO110461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055539|NCT00607906|AXO110461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055540|NCT00607906|AXO110461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055541|NCT00607906|AXO110461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055542|NCT00607906|AXO110461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055543|NCT00607906|AXO110461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055544|NCT01480271|114450|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055545|NCT01480271|114450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055546|NCT01480271|114450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055547|NCT01480271|114450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055548|NCT01480271|114450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055549|NCT01480271|114450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055550|NCT01480271|114450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055551|NCT02691312||FDA 501(k)|https://www.accessdata.fda.gov/cdrh_docs/pdf10/K101935.pdf|
3057353|NCT01571999|114636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057354|NCT02004886||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0893-005&kw=0893-005&tab=access|
3057355|NCT02184585|117057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057356|NCT02184585|117057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057357|NCT02184585|117057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057358|NCT02184585|117057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057359|NCT02184585|117057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057360|NCT02184585|117057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057361|NCT02184585|117057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057362|NCT01154088|114248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057363|NCT01154088|114248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057364|NCT01154088|114248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057365|NCT01154088|114248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057366|NCT01154088|114248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057367|NCT01154088|114248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058063|NCT00423046|108933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058064|NCT00423046|108933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058065|NCT00423046|108933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058066|NCT00423046|108933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058067|NCT00423046|108933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058068|NCT00423046|108933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058069|NCT06523712||Informed Consent Form|https://schoolsplus.pk/schools/sharif-education-complex/|
3058070|NCT06523712||Informed Consent Form|https://apseducation123.wixsite.com/website|
3058071|NCT06523712||Informed Consent Form|https://apsaskarixi.pk/|
3058072|NCT00355641|101468/206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058073|NCT00355641|101468/206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058074|NCT00355641|101468/206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058075|NCT00355641|101468/206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058076|NCT00355641|101468/206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058077|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
3058078|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
3058079|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."
3058080|NCT00113165|LAM100034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058081|NCT00113165|LAM100034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058082|NCT00113165|LAM100034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058083|NCT00113165|LAM100034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058084|NCT00113165|LAM100034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058085|NCT00113165|LAM100034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053713|NCT00385255|106323|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053714|NCT00385255|106323|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053715|NCT00385255|106323|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053716|NCT01225731||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05495&kw=P05495&tab=access|
3053717|NCT01018628|114011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053718|NCT01018628|114011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053719|NCT01018628|114011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053720|NCT01018628|114011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053721|NCT01018628|114011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053722|NCT01018628|114011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053723|NCT01018628|114011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053724|NCT00513409|110031|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053725|NCT00513409|110031|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053726|NCT00513409|110031|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053727|NCT00513409|110031|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053728|NCT00513409|110031|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053729|NCT00513409|110031|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053730|NCT04411355|10128359|National Thesis Center|https://tez.yok.gov.tr/UlusalTezMerkezi|thesis Number: 494582
3053731|NCT00835237|111413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053732|NCT00835237|111413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055552|NCT01336608|113108|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055553|NCT01336608|113108|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055554|NCT01336608|113108|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055555|NCT01336608|113108|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055556|NCT01336608|113108|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055557|NCT01336608|113108|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055558|NCT01336608|113108|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055559|NCT00627458|111344|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055560|NCT00627458|111344|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055561|NCT00627458|111344|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053733|NCT00835237|111413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053734|NCT00835237|111413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055562|NCT00627458|111344|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055563|NCT00627458|111344|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055564|NCT00627458|111344|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055565|NCT00627458|111344|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058086|NCT00113165|LAM100034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058087|NCT00481663||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058088|NCT01027845|112640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058089|NCT01027845|112640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060172|NCT00776919|114677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060173|NCT00776919|114677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060174|NCT00776919|114677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060175|NCT00776919|114677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060176|NCT00776919|114677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060177|NCT00776919|114677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060178|NCT00776919|114677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060179|NCT00533676||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3060180|NCT02758483|63683417.1.0000.5257|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
3060181|NCT06940778|blenti|Study Protocol|https://hcor.com.br|blenti
3060182|NCT07144891||article|https://pmc.ncbi.nlm.nih.gov/articles/PMC7488296/|
3060183|NCT03673397||Individual Participant Data Set|https://doi.org/10.7910/DVN/WASN36|
3060184|NCT01128621|113132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060185|NCT01128621|113132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060186|NCT01128621|113132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060187|NCT01128621|113132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060188|NCT01128621|113132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060189|NCT01128621|113132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060190|NCT01128621|113132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060191|NCT07145281||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/TCRUW|
3060192|NCT06947330||Study Protocol|https://www.ilovepdf.com/download/6bhl069fp1wzcttl2h9kympvwcw0z348Az4p933p7tx6gm77hss9dbx3gbxjvm9ypjzwt97hdptj659jxht28ybgh1m4lyj34sth4k980tx1wzvm0A2pjghl7rs70r7pk67kblvbcfl9fn68lp5c06pjtdd07x9jqh7grqdl8b1kkp3b6271/88w|
3060193|NCT01106092|113264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060194|NCT01106092|113264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060195|NCT01106092|113264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060196|NCT01106092|113264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060197|NCT01106092|113264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060198|NCT01106092|113264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060199|NCT01106092|113264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060200|NCT00376714|AC2105333|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060201|NCT00376714|AC2105333|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060202|NCT00376714|AC2105333|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060203|NCT00376714|AC2105333|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060204|NCT00376714|AC2105333|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060205|NCT00376714|AC2105333|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060206|NCT00376714|AC2105333|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060207|NCT00470834|AVO108943|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060208|NCT00470834|AVO108943|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060209|NCT00470834|AVO108943|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060210|NCT00470834|AVO108943|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060211|NCT00470834|AVO108943|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060212|NCT00470834|AVO108943|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060213|NCT00470834|AVO108943|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060214|NCT01115322|114573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060215|NCT01115322|114573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060216|NCT01115322|114573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060217|NCT01115322|114573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060218|NCT01115322|114573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060219|NCT01115322|114573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060220|NCT01115322|114573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060221|NCT07131241||Individual Participant Data Set|https://www.fjmu.edu.cn|For more information, please contact: dajunchai@126.com
3060222|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)."
3060223|NCT03111186|HS-15-00706|Study Protocol|http://istar.usc.edu|
3060224|NCT03111186|HS-15-00706|Informed Consent Form|http://istar.usc.edu|
3060225|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
3060226|NCT04570059|Booklet of recommendation|intervention material|https://hal.archives-ouvertes.fr/|Booklet of recommendation provided to the intervention group (in French)
3060227|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.
3060228|NCT00000590||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pactg/|
3060229|NCT00000590||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/pactg/|
3060230|NCT00363545|107077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060231|NCT00363545|107077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060232|NCT00363545|107077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060233|NCT00363545|107077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060234|NCT00363545|107077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060235|NCT00363545|107077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060236|NCT00794898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3060237|NCT01328444|114417|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060238|NCT01328444|114417|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060239|NCT01328444|114417|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060240|NCT01328444|114417|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060241|NCT01328444|114417|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060242|NCT01328444|114417|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060243|NCT01328444|114417|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060244|NCT02003274||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov|
3058090|NCT01027845|112640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058091|NCT01027845|112640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058092|NCT01027845|112640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058093|NCT01027845|112640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058094|NCT01704261||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-022&kw=3102-022&tab=access|
3058095|NCT01663389|112167|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058096|NCT01663389|112167|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058097|NCT01663389|112167|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058098|NCT01663389|112167|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058099|NCT01663389|112167|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058100|NCT01663389|112167|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058101|NCT01663389|112167|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058102|NCT00545025|110674|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058103|NCT00545025|110674|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058104|NCT00545025|110674|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058105|NCT00545025|110674|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058106|NCT00545025|110674|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058107|NCT00545025|110674|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058108|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
3058109|NCT00325169|104962|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058110|NCT00325169|104962|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058111|NCT00325169|104962|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058112|NCT00325169|104962|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058113|NCT00325169|104962|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058114|NCT00325169|104962|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058115|NCT00325169|104962|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058116|NCT00478621|109836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058117|NCT00478621|109836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058118|NCT00478621|109836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058119|NCT00478621|109836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058120|NCT00478621|109836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058121|NCT00478621|109836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058122|NCT00126945|104702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058123|NCT00126945|104702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058124|NCT00126945|104702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058125|NCT00126945|104702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058126|NCT00126945|104702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058127|NCT00126945|104702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058128|NCT04434508|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
3058129|NCT03512652||scientific Article|https://ijmbs.info/index.php/ijmbs/article/view/971|
3058130|NCT00420745|106481|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058131|NCT00420745|106481|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055566|NCT00633217|111117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055567|NCT00633217|111117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055568|NCT00633217|111117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055569|NCT00633217|111117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055570|NCT00633217|111117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055571|NCT00633217|111117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055572|NCT00633217|111117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055573|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
3055574|NCT05016765|2y7fs|Study Protocol|https://osf.io/2y7fs/|
3055575|NCT02524665|114553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055576|NCT02524665|114553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055577|NCT02524665|114553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055578|NCT02524665|114553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055579|NCT02524665|114553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055580|NCT02524665|114553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055581|NCT00803673|110106|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055582|NCT00803673|110106|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055583|NCT00803673|110106|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055584|NCT00803673|110106|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055585|NCT00803673|110106|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055586|NCT00803673|110106|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055587|NCT00803673|110106|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055588|NCT00552617||CSr Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055589|NCT04688814||Study Protocol|http://www.med.alexu.edu.eg|
3055590|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|
3055591|NCT04845451|Cluster Headaches-Neuroma|Clinical Study Report|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
3055592|NCT04845451|Cluster Headaches-Neuroma|Statistical Analysis Plan|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
3055593|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."
3055594|NCT00975884|113630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055595|NCT00975884|113630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055596|NCT00975884|113630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055597|NCT00975884|113630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055598|NCT00975884|113630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055599|NCT00975884|113630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055600|NCT00289731|100382|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060245|NCT01144299|114292|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060246|NCT01144299|114292|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060247|NCT01144299|114292|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060248|NCT01144299|114292|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060249|NCT01144299|114292|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060250|NCT01144299|114292|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060251|NCT01144299|114292|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060252|NCT00406562|107924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060253|NCT00406562|107924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060254|NCT00406562|107924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060255|NCT00406562|107924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060256|NCT00406562|107924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060257|NCT00406562|107924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060258|NCT00406562|107924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060259|NCT05386628|26079868|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3060260|NCT05386628|16225693|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3060261|NCT05386628|12924842|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3060262|NCT05386628|31864435|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3060263|NCT05386628|22018755|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3060264|NCT05386628|18192154|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3060265|NCT05386628|25977305|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3060266|NCT05386628|20068255|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3060267|NCT00920803|113221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060268|NCT00920803|113221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060269|NCT00920803|113221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060270|NCT00920803|113221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060271|NCT00920803|113221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060272|NCT00920803|113221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060273|NCT02184624|200301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060274|NCT02184624|200301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060275|NCT02184624|200301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060276|NCT02184624|200301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060277|NCT02184624|200301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060278|NCT02184624|200301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060279|NCT02184624|200301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060280|NCT00456807|109801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060281|NCT00456807|109801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060282|NCT00456807|109801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060283|NCT00456807|109801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060284|NCT00456807|109801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060285|NCT00456807|109801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060286|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/34004390/|This article is from the National Library of Medicine.
3060287|NCT06078150||Systematic Review|https://pubmed.ncbi.nlm.nih.gov/32375184/|This article is from the National Library of Medicine.
3060288|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/24905451/|This article is from the National Library of Medicine.
3060289|NCT02700087|Consent form cycle 3|Informed Consent Form|https://eprotocol.stanford.edu/irb/ControlServlet?updateFlag=Y|
3060290|NCT00169442|104065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060291|NCT00169442|104065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060292|NCT00169442|104065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051325|NCT00196989|ADG20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051326|NCT00196989|ADG20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051327|NCT00196989|ADG20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051328|NCT04020003|mengxinke|Individual Participant Data Set|http://www.chictr.org.cn|
3051329|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.
3051330|NCT06925763||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/?term=nitroglycerin+in+bone+regeneration|
3051331|NCT01190215|114452|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051332|NCT01190215|114452|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051333|NCT01190215|114452|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051334|NCT01190215|114452|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051335|NCT01190215|114452|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051336|NCT01190215|114452|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051337|NCT01812382|117151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051338|NCT01812382|117151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051339|NCT01812382|117151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051340|NCT01812382|117151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051341|NCT01812382|117151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051342|NCT01812382|117151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051343|NCT01812382|117151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051344|NCT00453479|AC2108378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051345|NCT00453479|AC2108378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051346|NCT00453479|AC2108378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051347|NCT00453479|AC2108378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051348|NCT00453479|AC2108378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051349|NCT00453479|AC2108378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051350|NCT00453479|AC2108378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051351|NCT00197028|103967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051352|NCT00197028|103967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051353|NCT00197028|103967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051354|NCT00197028|103967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051355|NCT00197028|103967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051356|NCT00197028|103967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051357|NCT01017120|114576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051358|NCT01017120|114576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051359|NCT01017120|114576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051360|NCT01017120|114576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051361|NCT01017120|114576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051362|NCT01017120|114576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051363|NCT01017120|114576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058132|NCT00420745|106481|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058133|NCT00420745|106481|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058134|NCT00420745|106481|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058135|NCT00420745|106481|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058136|NCT00420745|106481|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058137|NCT00764790|111751|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058138|NCT00764790|111751|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058139|NCT00764790|111751|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058140|NCT00764790|111751|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058141|NCT00764790|111751|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058142|NCT00764790|111751|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058143|NCT00764790|111751|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058144|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."
3058145|NCT00706563|111631|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051364|NCT00451217||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051365|NCT01929330|117342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058146|NCT00706563|111631|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058147|NCT00706563|111631|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058148|NCT00706563|111631|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058149|NCT00706563|111631|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058150|NCT00706563|111631|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058151|NCT00706563|111631|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058152|NCT00849056|112755|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058153|NCT00849056|112755|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058154|NCT00849056|112755|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058155|NCT00849056|112755|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058156|NCT00849056|112755|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058157|NCT00849056|112755|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058158|NCT00849056|112755|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058159|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
3058160|NCT01524835|SDY294|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
3058161|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.
3058162|NCT01524835|SDY294|Study summary, -design, -demographics, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
3058163|NCT01416571|112691|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058164|NCT01416571|112691|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058165|NCT01416571|112691|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058166|NCT01416571|112691|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058167|NCT01416571|112691|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051366|NCT01929330|117342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051367|NCT01929330|117342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055601|NCT00289731|100382|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055602|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.
3055603|NCT00289731|100382|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055604|NCT00289731|100382|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055605|NCT00289731|100382|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055606|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.
3055607|NCT01440595||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-012&kw=5172-012&tab=access|
3055608|NCT01077531|111601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055609|NCT01077531|111601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055610|NCT01077531|111601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055611|NCT01077531|111601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055612|NCT01077531|111601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055613|NCT01077531|111601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055614|NCT01077531|111601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055615|NCT03284073|NCT01844362|Study Protocol|http://clinicaltrials.gov|
3058168|NCT01416571|112691|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058169|NCT07155863||Study Protocol|https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-024-06091-6|
3058170|NCT00358488|B2E106359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058171|NCT00358488|B2E106359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058172|NCT00358488|B2E106359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058173|NCT00358488|B2E106359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058174|NCT00358488|B2E106359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058175|NCT00358488|B2E106359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058176|NCT00358488|B2E106359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058177|NCT00034632||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058178|NCT01725672|116806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058179|NCT01725672|116806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058180|NCT01725672|116806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058181|NCT01725672|116806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058182|NCT01725672|116806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058183|NCT01725672|116806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058184|NCT01725672|116806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051368|NCT01929330|117342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058185|NCT00687700|MAB110553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058186|NCT00687700|MAB110553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058187|NCT00687700|MAB110553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051369|NCT01929330|117342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051370|NCT01929330|117342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051371|NCT01929330|117342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051372|NCT01235975|113807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051373|NCT01235975|113807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051374|NCT01235975|113807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051375|NCT01235975|113807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051376|NCT01235975|113807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051377|NCT01235975|113807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051378|NCT01678820||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-266&kw=0431D-266&tab=access|
3051379|NCT00535743||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051380|NCT00044460|49653/326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051381|NCT00044460|49653/326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051382|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
3051383|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
3051384|NCT00044460|49653/326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051385|NCT00044460|49653/326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051386|NCT00044460|49653/326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051387|NCT01868035|393229/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051388|NCT01868035|393229/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051389|NCT01868035|393229/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051390|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
3051391|NCT01868035|393229/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051392|NCT01868035|393229/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051393|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
3051394|NCT02378402|ClinicalTrials.gov/NCT02378402|Clinical Study Report|http://jcmr-online.biomedcentral.com/articles/10.1186/s12968-016-0228-3|
3051395|NCT03176446|1.941.369|Approval of the ethics committee|http://plataformabrasil.saude.gov.br|
3051396|NCT03047122|P110006|U.S. Food and Drug Administration. somo-v Automated Breast Ultrasound System|http://www.accessdata.fda.gov/cdrh_docs/pdf11/P110006b.pdf|
3051397|NCT00047983|SDY352|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
3051398|NCT00047983|SDY352|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
3051399|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.
3051400|NCT06233123||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/32021311/|
3051401|NCT06480682|RED-D|Individual Participant Data Set|https://figshare.com/account/home|All anonymised data will be published on figshare
3051402|NCT06480682|RED-D|Study Protocol|https://figshare.com/account/home|Study protocol will be published on figshare
3055616|NCT00370396|107046|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055617|NCT00370396|107046|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055618|NCT00370396|107046|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055619|NCT00370396|107046|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055620|NCT00370396|107046|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055621|NCT00370396|107046|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055622|NCT02647554||Study Protocol|http://pan.baidu.com/s/1eQJUJDK|
3055623|NCT01294605|263855/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055624|NCT01294605|263855/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055625|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
3055626|NCT01294605|263855/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055627|NCT01294605|263855/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055628|NCT01294605|263855/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055629|NCT01332513|114552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055630|NCT01332513|114552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055631|NCT01332513|114552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055632|NCT01332513|114552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055633|NCT01332513|114552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055634|NCT01332513|114552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055635|NCT01332513|114552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055636|NCT00411697|106789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055637|NCT00411697|106789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055638|NCT00411697|106789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055639|NCT00411697|106789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055640|NCT00411697|106789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055641|NCT00411697|106789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055642|NCT06565754||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563562/|
3055643|NCT03567330||Study Protocol|https://link-springer-com.udel.idm.oclc.org/article/10.1186/s12885-018-5052-8|
3055644|NCT00140738|100633|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055645|NCT00140738|100633|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055646|NCT00140738|100633|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055647|NCT00140738|100633|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055648|NCT00140738|100633|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055649|NCT00140738|100633|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055650|NCT00969059|112967|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055651|NCT00969059|112967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055652|NCT00969059|112967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055653|NCT00969059|112967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055654|NCT00969059|112967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053735|NCT00835237|111413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053736|NCT00835237|111413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053737|NCT00835237|111413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053738|NCT02692495|10.17632/8bk6h6bmkr.1|Individual Participant Data Set|https://data.mendeley.com/datasets/8bk6h6bmkr/1|
3053739|NCT02692495||Clinical Study Report|http://www.aurametrix.com/nct02692495|
3053740|NCT02692495|10.1101/139014|Preprint|http://biorxiv.org/content/early/2017/05/19/139014|Study results
3053741|NCT00790907|108888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053742|NCT00790907|108888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053743|NCT00790907|108888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053744|NCT00790907|108888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053745|NCT00790907|108888|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053746|NCT00790907|108888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053747|NCT00790907|108888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053748|NCT00092846||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053749|NCT01857869|117014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053750|NCT01857869|117014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053751|NCT01857869|117014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053752|NCT01857869|117014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053753|NCT01857869|117014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053754|NCT01857869|117014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053755|NCT01857869|117014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053756|NCT00092430||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053757|NCT02700490|10.17863/CAM.43399|Complete Data Set|https://doi.org/10.17863/CAM.43399|
3053758|NCT00976066|111848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053759|NCT00976066|111848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053760|NCT00976066|111848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053761|NCT00976066|111848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053762|NCT00976066|111848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053763|NCT00976066|111848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053764|NCT00976066|111848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053765|NCT00452699|ADA109055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053766|NCT00452699|ADA109055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053767|NCT00452699|ADA109055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053768|NCT00452699|ADA109055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053769|NCT00452699|ADA109055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053770|NCT00452699|ADA109055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053771|NCT00452699|ADA109055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053772|NCT01425203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08160&kw=P08160&tab=access|
3053773|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
3053774|NCT00548496|CR9108914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055655|NCT00969059|112967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053775|NCT00548496|CR9108914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058188|NCT00687700|MAB110553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058189|NCT00687700|MAB110553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058190|NCT00687700|MAB110553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058191|NCT00687700|MAB110553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058192|NCT06956586|Research|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37330438/|"There is no additional information."
3058193|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.
3058194|NCT07265245|MREC APPROVAL LETTER|IPD Approval letter|https://osf.io/v26ku/files/yskbz|
3058195|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."
3058196|NCT00090103|ARI40005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058197|NCT00090103|ARI40005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058198|NCT00090103|ARI40005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058199|NCT00090103|ARI40005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058200|NCT00090103|ARI40005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058201|NCT00090103|ARI40005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058202|NCT00090103|ARI40005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058203|NCT03641729||Study Protocol|http://aline.priori.fioritto@gmail.com|More information contact the principal investigator
3058204|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.
3058205|NCT00321763|107192|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058206|NCT00321763|107192|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058207|NCT00321763|107192|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058208|NCT00321763|107192|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058209|NCT00321763|107192|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058210|NCT00544271|263855/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058211|NCT00544271|263855/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058212|NCT00544271|263855/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058213|NCT00544271|263855/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058214|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
3058215|NCT00544271|263855/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058216|NCT00689741|580299/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058217|NCT00689741|580299/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058218|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
3058219|NCT00689741|580299/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058220|NCT00689741|580299/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058221|NCT00689741|580299/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058222|NCT02035540||Study results|http://pubmed.ncbi.nlm.nih.gov/30879050/|
3053776|NCT00548496|CR9108914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058223|NCT06108921||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
3060293|NCT00169442|104065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060294|NCT00169442|104065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060295|NCT00169442|104065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060296|NCT03009370||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26806685|
3060297|NCT00400608|SAS105519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060298|NCT00400608|SAS105519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060299|NCT00400608|SAS105519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060300|NCT00400608|SAS105519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060301|NCT00400608|SAS105519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060302|NCT00400608|SAS105519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060303|NCT00400608|SAS105519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060304|NCT00400478||Clinical Study Report|https://www.clinicaltrialsregister.eu/ctr-search/search;jsessionid=cJHnlkSBP30JjfQV2K-KXCK3mdjOE64o0FAsUcmzHmslzlaX5yhQ!675812678|
3060305|NCT05053373||Individual Participant Data Set|http://www.medresman.org.cn/pub/en/proj/projectshow.aspx?proj=1282|
3060306|NCT00627575|LEP108937|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060307|NCT00627575|LEP108937|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060308|NCT00627575|LEP108937|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060309|NCT00627575|LEP108937|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060310|NCT00627575|LEP108937|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060311|NCT00627575|LEP108937|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060312|NCT00627575|LEP108937|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060313|NCT02045953|201092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060314|NCT02045953|201092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060315|NCT02045953|201092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060316|NCT02045953|201092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060317|NCT02045953|201092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060318|NCT02045953|201092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060319|NCT02045953|201092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060320|NCT01451437||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=P07649&kw=P07649&tab=access|
3060321|NCT02691585||Study Protocol|http://rguhs.ac.in/|
3060322|NCT01587898|116581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060323|NCT01587898|116581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060324|NCT01587898|116581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060325|NCT01587898|116581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060326|NCT01587898|116581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060327|NCT01587898|116581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060328|NCT01587898|116581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060329|NCT00067938|SCA40917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060330|NCT00067938|SCA40917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060331|NCT00067938|SCA40917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060332|NCT00067938|SCA40917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060333|NCT00067938|SCA40917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060334|NCT00067938|SCA40917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060335|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.
3060336|NCT00000485||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hdfp/|
3060337|NCT00197158|104387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060338|NCT00197158|104387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060339|NCT00197158|104387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060340|NCT00197158|104387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051403|NCT01147692|108366|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051404|NCT01147692|108366|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051405|NCT01147692|108366|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051406|NCT01147692|108366|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051407|NCT01147692|108366|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051408|NCT01147692|108366|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051409|NCT01147692|108366|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051410|NCT00460148|ROP109087|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060341|NCT00197158|104387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060342|NCT00197158|104387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060343|NCT00541463||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3060344|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.
3060345|NCT00005132||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nghs/|
3060346|NCT00005132||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nghs/|
3060347|NCT03016676||Study Protocol|http://www.ijpbs.net/abstract.php?article=5240|
3060348|NCT00955383|112359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060349|NCT00955383|112359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060350|NCT00955383|112359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060351|NCT00955383|112359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060352|NCT00955383|112359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060353|NCT00955383|112359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060354|NCT00955383|112359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060355|NCT02393586||Link to Pubmed (Final publication)|https://www.ncbi.nlm.nih.gov/pubmed/28333342|
3060356|NCT02848443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3060357|NCT02848443||Study Protocol|https://clinicaltrials.servier.com/|
3060358|NCT02848443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3060359|NCT02848443||Informed Consent Form|https://clinicaltrials.servier.com/|
3060360|NCT02848443||Clinical Study Report|https://clinicaltrials.servier.com/|
3060361|NCT02848443||study-level clinical trial data|https://clinicaltrials.servier.com/|
3060362|NCT07239076|AssitU|Informed Consent Form|https://pmc.ncbi.nlm.nih.gov/articles/PMC10049812/|For treatment
3060363|NCT06995794||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/|
3060364|NCT06995794||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
3060365|NCT01155479||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05664&kw=P05664&tab=access|
3060366|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"
3060367|NCT01338779|ImmPort Study ID: SDY546|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
3060368|NCT01338779|ImmPort Study ID: SDY546|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
3053777|NCT00548496|CR9108914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053778|NCT00548496|CR9108914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053779|NCT00548496|CR9108914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053780|NCT00548496|CR9108914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053781|NCT00090194|SDY356|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
3053782|NCT00090194|SDY356|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
3053783|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
3053784|NCT00317109|104756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053785|NCT00317109|104756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051411|NCT00460148|ROP109087|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051412|NCT00460148|ROP109087|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051413|NCT00460148|ROP109087|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051414|NCT00460148|ROP109087|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051415|NCT00460148|ROP109087|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051416|NCT00460148|ROP109087|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051417|NCT00092170||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051418|NCT00579982|LBI108884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051419|NCT00579982|LBI108884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051420|NCT00579982|LBI108884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051421|NCT00579982|LBI108884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051422|NCT00579982|LBI108884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051423|NCT00579982|LBI108884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051424|NCT00579982|LBI108884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051425|NCT00240526|100450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051426|NCT00240526|100450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051427|NCT00240526|100450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051428|NCT00240526|100450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051429|NCT00240526|100450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051430|NCT00240526|100450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051431|NCT01607385|116511|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053786|NCT00317109|104756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053787|NCT00317109|104756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053788|NCT00317109|104756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053789|NCT00317109|104756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053790|NCT02931058||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2366-9|
3053791|NCT02931058||Clinical Study Report|https://www.clinicalkey.com/#!/content/journal/1-s2.0-S1063458422007154|
3053792|NCT01627587|115893|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053793|NCT01627587|115893|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053794|NCT01627587|115893|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053795|NCT01627587|115893|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053796|NCT01627587|115893|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053797|NCT01627587|115893|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053798|NCT01627587|115893|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053799|NCT00731250|111611|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053800|NCT00731250|111611|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053801|NCT00731250|111611|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060369|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|
3051432|NCT01607385|116511|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051433|NCT01607385|116511|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051434|NCT01607385|116511|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051435|NCT01607385|116511|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051436|NCT01607385|116511|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051437|NCT01607385|116511|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051438|NCT01424436|113043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051439|NCT01424436|113043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051440|NCT01424436|113043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051441|NCT01424436|113043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051442|NCT01424436|113043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051443|NCT01424436|113043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051444|NCT01424436|113043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051445|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.
3051446|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
3051447|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
3051448|NCT00034645||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051449|NCT01751113|116572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051450|NCT01751113|116572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051451|NCT01751113|116572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051452|NCT01751113|116572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051453|NCT01751113|116572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051454|NCT00224523|FFR104503|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051455|NCT00224523|FFR104503|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051456|NCT00224523|FFR104503|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051457|NCT00224523|FFR104503|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051458|NCT00224523|FFR104503|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051459|NCT00224523|FFR104503|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051460|NCT00224523|FFR104503|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051461|NCT00517309||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051462|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
3051463|NCT00742885|111756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051464|NCT00742885|111756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051465|NCT00742885|111756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051466|NCT00742885|111756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051467|NCT00742885|111756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051468|NCT00742885|111756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058224|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.
3058225|NCT01431976|115377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058226|NCT01431976|115377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058227|NCT01431976|115377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058228|NCT01431976|115377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058229|NCT01431976|115377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058230|NCT01134042|106829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058231|NCT01134042|106829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058232|NCT01134042|106829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058233|NCT01134042|106829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058234|NCT01134042|106829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058235|NCT01134042|106829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058236|NCT01134042|106829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058237|NCT00453687|AC2108380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058238|NCT00453687|AC2108380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058239|NCT00453687|AC2108380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058240|NCT00453687|AC2108380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058241|NCT00453687|AC2108380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058242|NCT00453687|AC2108380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058243|NCT00453687|AC2108380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058244|NCT04744181||Individual Participant Data Set|https://redcap-irccs.policlinicogemelli.it/|
3058245|NCT01192178|113872|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058246|NCT01192178|113872|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058247|NCT01192178|113872|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058248|NCT01192178|113872|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058249|NCT01192178|113872|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058250|NCT01192178|113872|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058251|NCT01192178|113872|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058252|NCT01706328|116974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051469|NCT00742885|111756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051470|NCT03877705|Pubmed|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/m/pubmed/30455769/?i=6&from=xylitol%20review|
3053802|NCT00731250|111611|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053803|NCT00731250|111611|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053804|NCT00731250|111611|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053805|NCT00731250|111611|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053806|NCT04106648||Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/|
3053807|NCT00972673|112018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051471|NCT01648179|116595|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051472|NCT01648179|116595|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051473|NCT01648179|116595|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051474|NCT01648179|116595|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051475|NCT01648179|116595|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051476|NCT01648179|116595|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051477|NCT01648179|116595|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051478|NCT00318149|104886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051479|NCT00318149|104886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051480|NCT00318149|104886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051481|NCT00318149|104886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051482|NCT00318149|104886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058253|NCT01706328|116974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058254|NCT01706328|116974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058255|NCT01706328|116974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058256|NCT01706328|116974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058257|NCT01706328|116974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058258|NCT01706328|116974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058259|NCT01014091|113810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058260|NCT01014091|113810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058261|NCT01014091|113810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058262|NCT01014091|113810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058263|NCT01014091|113810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058264|NCT01014091|113810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058265|NCT01014091|113810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058266|NCT01405859||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983677/|Final Study Results, Published in Tremor and Other Hyperkinetic Disorders
3058267|NCT07258888||Individual Participant Data Set|https://dishekimligi.ksu.edu.tr/|Data sharing will follow institutional policies and ethical guidelines to ensure participant confidentiality.
3058268|NCT00000935|SDY355|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
3058269|NCT00000935|SDY355|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
3058270|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.
3058271|NCT07130370|fabatool@numl.edu.pk|Informed Consent Form|https://pakjmcr.com/index.php/1/article/view/67|It is not applicable at this time.
3058272|NCT00765076|112147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058273|NCT00765076|112147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058274|NCT00765076|112147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058275|NCT00765076|112147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058276|NCT00765076|112147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058277|NCT00765076|112147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058278|NCT05704309|DPPOS|Individual Participant Data Set|https://repository.niddk.nih.gov/studies/dppos/|
3058279|NCT05704309||Individual Participant Data Set|https://naccdata.org/requesting-data/data-request-process|will be available in 2025
3058280|NCT07011264||Study Protocol|https://reporter.nih.gov/search/xHobiVLiPU68u-6wSogmsA/project-details/11052906|
3058281|NCT00386698|104887|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058282|NCT00386698|104887|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058283|NCT00386698|104887|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058284|NCT00386698|104887|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058285|NCT00386698|104887|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058286|NCT00386698|104887|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058287|NCT07121348|END-7-25-3400|Study Protocol|http://www.tanta.edu.eg|
3058288|NCT06855810|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
3058289|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
3058290|NCT01610388|113376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058291|NCT01610388|113376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058292|NCT01610388|113376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058293|NCT01610388|113376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058294|NCT01610388|113376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058295|NCT01610388|113376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058296|NCT01610388|113376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058297|NCT05104346|COVID and acute appendicitis|Study Protocol|http://www.mans.edu.eg/|
3058298|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.
3058299|NCT00005123||Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/hhp/|
3058300|NCT00536835|PLK107427|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058301|NCT00536835|PLK107427|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058302|NCT00536835|PLK107427|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058303|NCT00536835|PLK107427|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3060370|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.
3060371|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.
3060372|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.
3060373|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
3060374|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
3060375|NCT00829985|SDY223|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
3060376|NCT00829985|SDY223|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
3060377|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.
3060378|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.
3060379|NCT04335422||references|https://www.ncbi.nlm.nih.gov/pubmed/28540536|
3060380|NCT04488107|ICH topic S9|ICH topic S9 - nonclinical evaluation for anticancer pharmaceuticals. 2009|https://database.ich.org/sites/default/files/S9_Guideline.pdf|
3060381|NCT04488107|IBRANCE® (palbociclib) capsule|label for IBRANCE® (palbociclib) capsules|https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/207103s000lbl.pdf|
3060382|NCT04488107|IBRANCE® (palbociclib) tablets|label for IBRANCE® (palbociclib) tablets,|https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf|
3060383|NCT04488107|KISQALI® (ribociclib) tablets|Label for KISQALI® (ribociclib) tablets|https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209092s005lbl.pdf|
3060384|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|
3060385|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|
3060386|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.
3060387|NCT07304921||Individual Participant Data Set|https://zenodo.org/records/16900133|
3060388|NCT07309094||Statistical Analysis Plan|http://osf.io/|
3060389|NCT07309094||Analytic Code|http://osf.io|
3058304|NCT00536835|PLK107427|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058305|NCT00536835|PLK107427|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053808|NCT00972673|112018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053809|NCT00972673|112018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053810|NCT00972673|112018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053811|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
3058306|NCT00536835|PLK107427|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058307|NCT00385840|108708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058308|NCT00385840|108708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058309|NCT00385840|108708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058310|NCT00385840|108708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058311|NCT00385840|108708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058312|NCT00385840|108708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058313|NCT07080528||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2024-515545-41-00|
3058314|NCT01245933||general information|http://www.asconet.net|
3058315|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.
3058316|NCT01248975|114387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058317|NCT01248975|114387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058318|NCT01248975|114387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058319|NCT01248975|114387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058320|NCT01248975|114387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058321|NCT01248975|114387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058322|NCT01248975|114387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058323|NCT02836769||Study Protocol|http://www.implementationscience.com/content/10/1/6|Publication of the initial project protocol
3058324|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
3058325|NCT00127010|103388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058326|NCT00127010|103388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058327|NCT00127010|103388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058328|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.
3058329|NCT00127010|103388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058330|NCT00127010|103388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058331|NCT01899703|117213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058332|NCT01899703|117213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058333|NCT01899703|117213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055656|NCT00969059|112967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055657|NCT00386100|AVT105913|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055658|NCT00386100|AVT105913|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055659|NCT00386100|AVT105913|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055660|NCT00386100|AVT105913|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055661|NCT00386100|AVT105913|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055662|NCT00386100|AVT105913|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055663|NCT00386100|AVT105913|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055664|NCT00879970|111960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055665|NCT00879970|111960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055666|NCT00879970|111960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055667|NCT00879970|111960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055668|NCT00879970|111960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055669|NCT00879970|111960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055670|NCT00879970|111960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055671|NCT04355767||Individual Participant Data Set|https://biodatacatalyst.nhlbi.nih.gov/|
3055672|NCT00524576|108988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058334|NCT01899703|117213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058335|NCT01899703|117213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058336|NCT01899703|117213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058337|NCT01899703|117213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058338|NCT01371682|112771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058339|NCT01371682|112771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058340|NCT01371682|112771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058341|NCT01371682|112771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058342|NCT01371682|112771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058343|NCT01371682|112771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058344|NCT01371682|112771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058345|NCT00335075||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058346|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.
3058347|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.
3058348|NCT00729001|444563/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058349|NCT00729001|444563/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058350|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
3058351|NCT00729001|444563/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058352|NCT00729001|444563/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058353|NCT00729001|444563/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058354|NCT01059851||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-023&kw=4305-023&tab=access|
3058355|NCT06882057|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
3058356|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
3058357|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
3058358|NCT00134719|102370 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058359|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.
3058360|NCT00134719|102370 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058361|NCT01996995||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/s13063-015-0622-4|
3058362|NCT07301775||Individual Participant Data Set|http://www.eyecon.pk|
3058363|NCT07301047|No individual participant data|No individual participant data (IPD) or supporting documents will be shared. Only aggregated study results may be published in journals or presented at conferences.|https://www.cgmh.org.tw/|No individual participant data (IPD) or supporting documents will be shared. Only aggregated study results may be published in journals or presented at conferences.
3058364|NCT00496327||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058365|NCT07233525||Study Protocol|https://osf.io/ryq6k/overview?view_only=82691366adfe4dd3999bfba95ce6466d|The full study protocol
3058366|NCT01039675|113120|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058367|NCT01039675|113120|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058368|NCT01039675|113120|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058369|NCT01039675|113120|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058370|NCT01039675|113120|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058371|NCT01039675|113120|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058372|NCT01039675|113120|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058373|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
3058374|NCT03496675||Individual Participant Data Set|https://osf.io/tpdhu/|
3058375|NCT04976725||Statistical Analysis Plan|https://doi.org/10.1016/J.JCM.2019.12.001|
3058376|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"
3058377|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."
3058378|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"
3058379|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.
3058380|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.
3058381|NCT00976391|108486|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058382|NCT00976391|108486|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058383|NCT00976391|108486|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058384|NCT00976391|108486|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058385|NCT00976391|108486|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058386|NCT00976391|108486|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058387|NCT00976391|108486|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058388|NCT04967703||Full Paper|http://www.europeanreview.org/article/32287|
3051483|NCT00318149|104886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051484|NCT01340911|115444|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051485|NCT01340911|115444|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051486|NCT01340911|115444|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051487|NCT01340911|115444|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051488|NCT01340911|115444|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051489|NCT01340911|115444|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051490|NCT00551213||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04721&kw=P04721&tab=access|
3051491|NCT00432679|AVD105248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051492|NCT00432679|AVD105248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051493|NCT00432679|AVD105248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053812|NCT01110200|113874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053813|NCT01110200|113874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053814|NCT01110200|113874|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053815|NCT01110200|113874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053816|NCT01110200|113874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053817|NCT01110200|113874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053818|NCT01110200|113874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053819|NCT00861744|111870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053820|NCT00861744|111870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053821|NCT00861744|111870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053822|NCT00861744|111870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053823|NCT00861744|111870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053824|NCT00861744|111870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053825|NCT00861744|111870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053826|NCT01014117|114009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053827|NCT01014117|114009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053828|NCT01014117|114009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053829|NCT01014117|114009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053830|NCT01014117|114009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053831|NCT01014117|114009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053832|NCT00505453|110502|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053833|NCT00505453|110502|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053834|NCT00505453|110502|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053835|NCT00505453|110502|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053836|NCT00505453|110502|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053837|NCT00505453|110502|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053838|NCT00505453|110502|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053839|NCT07273786|merve özkul/author|Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/|
3058389|NCT00705965||treatment manual and supplemental content|http://links.lww.com/PSYMED/A275|
3051494|NCT00432679|AVD105248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051495|NCT00432679|AVD105248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051496|NCT00432679|AVD105248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058390|NCT00985790|113237|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058391|NCT00985790|113237|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058392|NCT00985790|113237|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058393|NCT00985790|113237|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058394|NCT00985790|113237|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058395|NCT00985790|113237|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058396|NCT00120848|580299/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058397|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
3058398|NCT00120848|580299/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058399|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
3058400|NCT00120848|580299/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055673|NCT00524576|108988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055674|NCT00524576|108988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055675|NCT00524576|108988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055676|NCT00524576|108988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055677|NCT00550420|AVA102677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055678|NCT00550420|AVA102677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055679|NCT00550420|AVA102677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055680|NCT00550420|AVA102677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055681|NCT00550420|AVA102677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055682|NCT00550420|AVA102677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055683|NCT00550420|AVA102677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055684|NCT01663714|104514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055685|NCT01663714|104514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055686|NCT01663714|104514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055687|NCT01663714|104514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055688|NCT01663714|104514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055689|NCT01663714|104514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055690|NCT01663714|104514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055691|NCT05163379||Study Protocol|https://khgmekodemedb.saglik.gov.tr/Eklenti/23273/0/fizik-tedavi-ve-rehabilitasyon-islemleri-degerlendirme-olcekleripdf.pdf|
3055692|NCT01416376|115830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058401|NCT00120848|580299/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058402|NCT00120848|580299/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058403|NCT00676052|AC2110664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058404|NCT00676052|AC2110664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055693|NCT01416376|115830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055694|NCT01416376|115830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055695|NCT01416376|115830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051497|NCT00432679|AVD105248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051498|NCT00317174|759346/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051499|NCT00317174|759346/002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051500|NCT00317174|759346/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051501|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
3051502|NCT00317174|759346/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051503|NCT00317174|759346/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051504|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.
3051505|NCT00000556||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/affirm/|
3051506|NCT00000556||Study Forms|http://biolincc.nhlbi.nih.gov/studies/affirm/|
3051507|NCT07257237|10.5281/zenodo.16529837|Individual Participant Data Set|https://doi.org/10.5281/zenodo.16529837|Deidentified individual participant data set including sociodemographic variables, baseline and 8-week PSQI scores, and systolic and diastolic blood pressure measurements for all randomized participants. Data are shared together with a data dictionary under the license specified on the Zenodo record.
3051508|NCT06138236||Study Protocol|https://www.sanita.puglia.it/web/policlinico-di-bari-ospedale-giovanni-xxiii/comitato-etico|
3051509|NCT00605371|LEP111102|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051510|NCT00605371|LEP111102|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051511|NCT00605371|LEP111102|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051512|NCT00605371|LEP111102|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051513|NCT00605371|LEP111102|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051514|NCT00605371|LEP111102|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051515|NCT00605371|LEP111102|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058405|NCT00676052|AC2110664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058406|NCT00676052|AC2110664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058407|NCT00676052|AC2110664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058408|NCT00676052|AC2110664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058409|NCT00676052|AC2110664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058410|NCT01894360|117100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058411|NCT01894360|117100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051516|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.
3051517|NCT04731714|mtbzf|Individual Participant Data Set|https://osf.io/mtbzf/|IPD, study protocol, SAP, and ICF will all be posted at this location.
3051518|NCT00090272||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051519|NCT00992160|111364|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051520|NCT00992160|111364|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051521|NCT00992160|111364|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051522|NCT00992160|111364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051523|NCT00992160|111364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058412|NCT01894360|117100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058413|NCT01894360|117100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058414|NCT01894360|117100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058415|NCT01894360|117100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058416|NCT01894360|117100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058417|NCT01064284|NEJM2016;374:2054-206|Article|http://www.nejm.org/doi/full/10.1056/NEJMoa1516437?af=R&rss=currentIssue&|
3058418|NCT07055932||Study Protocol|https://theses.gla.ac.uk/1017/|
3058419|NCT00552279|109179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058420|NCT00552279|109179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058421|NCT00552279|109179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058422|NCT00552279|109179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058423|NCT00552279|109179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058424|NCT00552279|109179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058425|NCT00552279|109179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058426|NCT01379937|115115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058427|NCT01379937|115115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058428|NCT01379937|115115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058429|NCT01379937|115115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058430|NCT01379937|115115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058431|NCT01379937|115115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058432|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.
3058433|NCT00000544||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dash/|
3058434|NCT00000544||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/dash/|
3058435|NCT05872945||Individual Participant Data Set|https://github.com/dradolfomunoz/PF12RED|
3058436|NCT01691482|114956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051524|NCT00992160|111364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058437|NCT01691482|114956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058438|NCT01691482|114956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058439|NCT01691482|114956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058440|NCT01691482|114956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058441|NCT01691482|114956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058442|NCT01691482|114956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058443|NCT01370642||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-043&kw=7009-043&tab=access|
3058444|NCT03755154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3058445|NCT03755154||Study Protocol|https://clinicaltrials.servier.com/|
3058446|NCT03755154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3058447|NCT03755154||Informed Consent Form|https://clinicaltrials.servier.com/|
3058448|NCT03755154||Clinical Study Report|https://clinicaltrials.servier.com/|
3058449|NCT03755154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3058450|NCT01266980|113970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058451|NCT01266980|113970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058452|NCT01266980|113970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058453|NCT01266980|113970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058454|NCT01266980|113970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058455|NCT01266980|113970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058456|NCT01266980|113970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058457|NCT01313676|113782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058458|NCT01313676|113782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058459|NCT01313676|113782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058460|NCT01313676|113782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058461|NCT01313676|113782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058462|NCT01313676|113782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058463|NCT01313676|113782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058464|NCT01934231|117150|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058465|NCT01934231|117150|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058466|NCT01934231|117150|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058467|NCT01934231|117150|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058468|NCT01934231|117150|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058469|NCT01934231|117150|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058470|NCT01934231|117150|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058471|NCT00871000|111815|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058472|NCT00871000|111815|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058473|NCT00871000|111815|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058474|NCT00871000|111815|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058475|NCT00871000|111815|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058476|NCT00871000|111815|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055696|NCT01416376|115830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055697|NCT01416376|115830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055698|NCT03189797||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed|
3055699|NCT02879747||Study Protocol|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
3055700|NCT02879747||Statistical Analysis Plan|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
3055701|NCT02094937|201135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055702|NCT02094937|201135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055703|NCT02094937|201135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055704|NCT02094937|201135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055705|NCT02094937|201135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055706|NCT00297206|HS210914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055707|NCT00297206|HS210914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055708|NCT00297206|HS210914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055709|NCT00297206|HS210914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055710|NCT00297206|HS210914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055711|NCT00297206|HS210914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055712|NCT00297206|HS210914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055713|NCT02496221|201834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055714|NCT02496221|201834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055715|NCT02496221|201834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055716|NCT02496221|201834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055717|NCT02496221|201834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055718|NCT02496221|201834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055719|NCT02496221|201834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055720|NCT01165242|114249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055721|NCT01165242|114249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055722|NCT01165242|114249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055723|NCT01165242|114249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055724|NCT01165242|114249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055725|NCT01165242|114249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055726|NCT01162590|113545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055727|NCT01162590|113545|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055728|NCT01162590|113545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055729|NCT01162590|113545|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055730|NCT01162590|113545|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055731|NCT01162590|113545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055732|NCT00950833|112801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055733|NCT00950833|112801|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055734|NCT00950833|112801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055735|NCT00950833|112801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055736|NCT00950833|112801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055737|NCT00950833|112801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055738|NCT00950833|112801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055739|NCT00964223|114547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055740|NCT00964223|114547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055741|NCT00964223|114547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055742|NCT00964223|114547|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055743|NCT00964223|114547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055744|NCT00964223|114547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055745|NCT00964223|114547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055746|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.
3055747|NCT00000531||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/avid/|
3055748|NCT00000531||Study Forms|http://biolincc.nhlbi.nih.gov/studies/avid/|
3055749|NCT00000531||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/avid/|
3055750|NCT05709054||Clinical Study Report|https://doi.org/10.1016/j.ijosm.2018.07.006|
3055751|NCT06538168||Informed Consent Form|https://www.facebook.com/gghgmabadfsd/?paipv=0&eav=AfbwgEmoehvAkH8F8E-KZ9WClHEgcLyNQwBOij0PYLNHpvrJZ1KZbTJdZYuWB21J8rA&_rdr|
3055752|NCT00345683|105988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055753|NCT00345683|105988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055754|NCT00345683|105988|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055755|NCT00345683|105988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055756|NCT00345683|105988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055757|NCT00345683|105988|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055758|NCT00345683|105988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055759|NCT00606684|B2C111045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055760|NCT00606684|B2C111045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055761|NCT00606684|B2C111045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055762|NCT00606684|B2C111045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055763|NCT00606684|B2C111045|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055764|NCT00606684|B2C111045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055765|NCT00606684|B2C111045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055766|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.
3055767|NCT00000606||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nett/|
3055768|NCT00000606||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nett/|
3055769|NCT02169583|201022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055770|NCT02169583|201022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055771|NCT02169583|201022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055772|NCT02169583|201022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055773|NCT02169583|201022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055774|NCT02169583|201022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055775|NCT02169583|201022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055776|NCT02224521|112071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055777|NCT02224521|112071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055778|NCT02224521|112071|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055779|NCT02224521|112071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055780|NCT02224521|112071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055781|NCT02224521|112071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055782|NCT02224521|112071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055783|NCT00551564|DIX110434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055784|NCT00551564|DIX110434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055785|NCT00551564|DIX110434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055786|NCT00551564|DIX110434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055787|NCT00551564|DIX110434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055788|NCT00551564|DIX110434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055789|NCT00551564|DIX110434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055790|NCT04716673||Individual Participant Data Set|https://info.swissubase.ch|
3055791|NCT00229112||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055792|NCT01001169|113847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055793|NCT01001169|113847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055794|NCT01001169|113847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055795|NCT01001169|113847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055796|NCT01001169|113847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055797|NCT01001169|113847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055798|NCT01001169|113847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058477|NCT00871000|111815|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058478|NCT00132912||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058479|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.
3058480|NCT00000603||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coblt/|
3058481|NCT00000603||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coblt/|
3058482|NCT00000603||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coblt/|
3058483|NCT00480025|109493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058484|NCT00480025|109493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058485|NCT00480025|109493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058486|NCT00480025|109493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058487|NCT00480025|109493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055799|NCT02058628|200398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058488|NCT00480025|109493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053840|NCT00808444|111654|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053841|NCT00808444|111654|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053842|NCT00808444|111654|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053843|NCT00808444|111654|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053844|NCT00808444|111654|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053845|NCT00808444|111654|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053846|NCT00808444|111654|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053847|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
3053848|NCT02889458|BrCA.risk.001|Study Protocol|http://www.hkuctr.com/Study/Show/b122235f3995420a97d570a85d03b542|
3055800|NCT02058628|200398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055801|NCT02058628|200398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055802|NCT02058628|200398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055803|NCT02058628|200398|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055804|NCT02058628|200398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055805|NCT02058628|200398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055806|NCT00616928|110464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055807|NCT00616928|110464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055808|NCT00616928|110464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055809|NCT00616928|110464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051525|NCT00992160|111364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051526|NCT00920374|113018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055810|NCT00616928|110464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055811|NCT00616928|110464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055812|NCT00616928|110464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055813|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
3055814|NCT01626820|116664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055815|NCT01626820|116664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055816|NCT01626820|116664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055817|NCT01626820|116664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055818|NCT01626820|116664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055819|NCT01626820|116664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055820|NCT01626820|116664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055821|NCT00274703|MEE103226|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055822|NCT00274703|MEE103226|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055823|NCT00274703|MEE103226|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055824|NCT00274703|MEE103226|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055825|NCT00274703|MEE103226|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055826|NCT01209052|112483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055827|NCT01209052|112483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055828|NCT01209052|112483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055829|NCT01209052|112483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055830|NCT01209052|112483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055831|NCT01209052|112483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055832|NCT01209052|112483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055833|NCT00743067|MET111648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055834|NCT00743067|MET111648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055835|NCT00743067|MET111648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055836|NCT00743067|MET111648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055837|NCT00743067|MET111648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055838|NCT00743067|MET111648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055839|NCT00743067|MET111648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055840|NCT01000857|112812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058489|NCT00480025|109493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058490|NCT02477046||Statistical Analysis Plan|https://idmod.sharepoint.com/projects/_layouts/15/guestaccess.aspx?guestaccesstoken=3%2bxJO%2bcBwXx6PfMuzCQmu8ESB0X7mhLPtowTTLaYTmY%3d&docid=02ab39752ccb14c10bdfd61c0a731e6ff&rev=1|
3058491|NCT03142451||Study Protocol|http://foamix.co.il/|
3058492|NCT02100644|200776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058493|NCT02100644|200776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058494|NCT02100644|200776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055841|NCT01000857|112812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053849|NCT01353703|111157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053850|NCT01353703|111157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053851|NCT01353703|111157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053852|NCT01353703|111157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053853|NCT01353703|111157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053854|NCT01353703|111157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053855|NCT01471665|115134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053856|NCT01471665|115134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053857|NCT01471665|115134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053858|NCT01471665|115134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053859|NCT01471665|115134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053860|NCT01471665|115134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053861|NCT01471665|115134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053862|NCT00039988|Study identifier is SDY471|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
3053863|NCT00039988|Study identifier is SDY471|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
3053864|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|
3053865|NCT00814957|110269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053866|NCT00814957|110269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053867|NCT00814957|110269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053868|NCT00814957|110269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053869|NCT00814957|110269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053870|NCT00814957|110269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053871|NCT00814957|110269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053872|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
3053873|NCT01209026|102936|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053874|NCT01209026|102936|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053875|NCT01209026|102936|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053876|NCT01209026|102936|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053877|NCT01209026|102936|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053878|NCT01209026|102936|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053879|NCT01209026|102936|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055842|NCT01000857|112812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055843|NCT01000857|112812|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055844|NCT04413747|guest_1|Study Protocol|http://giardinostlucia.it|
3055845|NCT04413747|guest_2|Informed Consent Form|http://giardinostlucia.it|
3055846|NCT04413747|guest_3|Individual Participant Data Set|http://giardinostlucia.it|
3055847|NCT00035009||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055848|NCT04956666||Individual Participant Data Set|https://clinicaltrials.servier.com|
3055849|NCT04956666||Study Protocol|https://clinicaltrials.servier.com|
3055850|NCT04956666||Statistical Analysis Plan|https://clinicaltrials.servier.com|
3055851|NCT04956666||Informed Consent Form|https://clinicaltrials.servier.com|
3055852|NCT04956666||Clinical Study Report|https://clinicaltrials.servier.com|
3055853|NCT04956666||Study-level clinical trial data|https://clinicaltrials.servier.com|
3051527|NCT00920374|113018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051528|NCT00920374|113018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051529|NCT00920374|113018|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051530|NCT00920374|113018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055854|NCT00946257|112438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055855|NCT00946257|112438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051531|NCT00920374|113018|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051532|NCT00920374|113018|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051533|NCT05776030||Statistical Analysis Plan|https://osf.io/87wfq/files/osfstorage|
3051534|NCT00519636|FFU105927|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051535|NCT00519636|FFU105927|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051536|NCT00519636|FFU105927|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051537|NCT00519636|FFU105927|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051538|NCT00519636|FFU105927|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051539|NCT00519636|FFU105927|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051540|NCT00519636|FFU105927|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051541|NCT01161160|114495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051542|NCT01161160|114495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051543|NCT01161160|114495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051544|NCT01161160|114495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051545|NCT01161160|114495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051546|NCT01161160|114495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051547|NCT01161160|114495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051548|NCT04610203||Study Protocol|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3051549|NCT04610203||Informed Consent Form|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3051550|NCT04610203||Clinical Study Report|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3051551|NCT04610203||Individual Participant Data Set|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
3051552|NCT04610203||Statistical Analysis Plan|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|Included in the Study Protocol and Clinical Study report
3051553|NCT01323660|114418|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051554|NCT01323660|114418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051555|NCT01323660|114418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051556|NCT01323660|114418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051557|NCT01323660|114418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051558|NCT01323660|114418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051559|NCT01323660|114418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051560|NCT00933062|113140|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051561|NCT00933062|113140|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051562|NCT00933062|113140|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051563|NCT00933062|113140|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051564|NCT00933062|113140|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051565|NCT00933062|113140|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051566|NCT00933062|113140|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051567|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.
3051568|NCT03904082||Clinical Study Report|http://doi.org/10.1016/j.jclinane.2018.06.033|
3051569|NCT02985697|DEXProtocol|Study Protocol|https://drive.google.com/open?id=0BwBFaEmsvS0PYnlzVDUyMGREWFk|Protocol for the study; includes introduction, design, and references/citations.
3053880|NCT00684515||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05005&kw=P05005&tab=access|
3055856|NCT00946257|112438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055857|NCT00946257|112438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055858|NCT00946257|112438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055859|NCT00946257|112438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055860|NCT00946257|112438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055861|NCT04517006||Individual Participant Data Set|https://osf.io/63yg9/|Not yet available, but will be posted once study is complete.
3055862|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.
3055863|NCT04517006||Informed Consent Form|https://osf.io/63yg9/|
3055864|NCT04517006||Analytic Code|https://osf.io/63yg9/|Will be posted after study is complete.
3055865|NCT01691508|115575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055866|NCT01691508|115575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055867|NCT01691508|115575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055868|NCT01691508|115575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055869|NCT01691508|115575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055870|NCT01691508|115575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055871|NCT01691508|115575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055872|NCT00197275|104733|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055873|NCT00197275|104733|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055874|NCT00197275|104733|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051570|NCT01627340|115918|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053881|NCT00132730||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-005&kw=0873-005&tab=access|
3053882|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.
3053883|NCT01353742|114957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053884|NCT01353742|114957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053885|NCT01353742|114957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053886|NCT01353742|114957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053887|NCT01353742|114957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053888|NCT01353742|114957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053889|NCT01353742|114957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055875|NCT00197275|104733|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055876|NCT00197275|104733|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055877|NCT00197275|104733|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055878|NCT00684671|111572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055879|NCT00684671|111572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055880|NCT00684671|111572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055881|NCT00684671|111572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055882|NCT00684671|111572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055883|NCT00684671|111572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055884|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
3055885|NCT00425737|444563/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055886|NCT00425737|444563/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055887|NCT00425737|444563/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055888|NCT00425737|444563/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055889|NCT00425737|444563/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055890|NCT03974633||Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1dEjSUmhIkqAOvh30WaJ0svs6jrdEGDyU5FXHeBuTOF8/edit?usp=sharing|
3055891|NCT00996671|113581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055892|NCT00996671|113581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055893|NCT00996671|113581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055894|NCT00996671|113581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055895|NCT00996671|113581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055896|NCT00996671|113581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055897|NCT00996671|113581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055898|NCT00317161|100480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055899|NCT00317161|100480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055900|NCT00317161|100480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055901|NCT00317161|100480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055902|NCT00317161|100480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055903|NCT00317161|100480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055904|NCT07296640|BPIT-GFFI-2024-001|Individual Participant Data Set|https://mmsxauthority.com/BPIT-2024doc.html|"De-identified individual participant data (strength, HRV, knee valgus, injury logs) available upon reasonable request to Principal Investigator: Dr. Neeraj Mehta, PhD (info@mmsxauthority.com). All supporting documents (Protocol, Ethics, Consent, Observation Logs, AE Forms, Final Report) uploaded under Study Documents tab."
3055905|NCT06705400||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/40866846/|
3055906|NCT06705400||Statistical Analysis Plan|https://findresearcher.sdu.dk/ws/portalfiles/portal/298847036/Statistical_Analysis_Plan_for_the_Bloom_Study_14112025_FINAL.pdf|
3055907|NCT03869892||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3055908|NCT03869892||Study Protocol|https://clinicaltrials.servier.com/|
3055909|NCT03869892||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3055910|NCT03869892||Informed Consent Form|https://clinicaltrials.servier.com/|
3055911|NCT03869892||Clinical Study Report|https://clinicaltrials.servier.com/|
3055912|NCT03869892||study-level clinical trial data|https://clinicaltrials.servier.com/|
3055913|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)
3055914|NCT06935656||Study Protocol|https://osf.io/9mp83|
3055915|NCT01928914|114582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055916|NCT01928914|114582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055917|NCT01928914|114582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055918|NCT01928914|114582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055919|NCT01928914|114582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055920|NCT01928914|114582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055921|NCT01928914|114582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055922|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/33036555/|
3055923|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/32247709/|
3055924|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/34252034/|
3055925|NCT01974895|200806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055926|NCT01974895|200806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055927|NCT01974895|200806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055928|NCT01974895|200806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055929|NCT01974895|200806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055930|NCT01974895|200806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055931|NCT01974895|200806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055932|NCT00376779|106786|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055933|NCT00376779|106786|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055934|NCT00376779|106786|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055935|NCT00376779|106786|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055936|NCT00376779|106786|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055937|NCT00376779|106786|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055938|NCT00329602|ROR104836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055939|NCT00329602|ROR104836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055940|NCT00329602|ROR104836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055941|NCT00329602|ROR104836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055942|NCT00329602|ROR104836|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055943|NCT00329602|ROR104836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055944|NCT00329602|ROR104836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055945|NCT00569062|PKI108574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055946|NCT00569062|PKI108574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055947|NCT00569062|PKI108574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055948|NCT00569062|PKI108574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055949|NCT00569062|PKI108574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055950|NCT00404274|NKV105097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055951|NCT00404274|NKV105097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055952|NCT00404274|NKV105097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055953|NCT00404274|NKV105097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055954|NCT00404274|NKV105097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055955|NCT00404274|NKV105097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055956|NCT00404274|NKV105097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055957|NCT00502775|FFU109047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055958|NCT00502775|FFU109047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055959|NCT00502775|FFU109047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055960|NCT00502775|FFU109047|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055961|NCT00502775|FFU109047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055962|NCT00502775|FFU109047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055963|NCT00502775|FFU109047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055964|NCT01047345||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-006&kw=V503-006&tab=access|
3055965|NCT00394056|NKP106254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055966|NCT00394056|NKP106254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055967|NCT00394056|NKP106254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055968|NCT00394056|NKP106254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055969|NCT00394056|NKP106254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055970|NCT00394056|NKP106254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055971|NCT00109109||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055972|NCT00861809|111809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055973|NCT00861809|111809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055974|NCT00861809|111809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055975|NCT00861809|111809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055976|NCT00861809|111809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055977|NCT00861809|111809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055978|NCT00861809|111809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055979|NCT01385033||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3328-002&kw=3328-002&tab=access|
3055980|NCT00950807|113073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055981|NCT00950807|113073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055982|NCT00950807|113073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055983|NCT00950807|113073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055984|NCT00950807|113073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055985|NCT00950807|113073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055986|NCT00950807|113073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055987|NCT04025034||Informed Consent Form|http://microsoftwindows.com|Navigator
3055988|NCT00269048|LPL104884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055989|NCT00269048|LPL104884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055990|NCT00269048|LPL104884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055991|NCT00269048|LPL104884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055992|NCT00269048|LPL104884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055993|NCT00269048|LPL104884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055994|NCT00269048|LPL104884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055995|NCT00436007|106369|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055996|NCT00436007|106369|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055997|NCT00436007|106369|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055998|NCT00436007|106369|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055999|NCT00436007|106369|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058495|NCT02100644|200776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058496|NCT02100644|200776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058497|NCT00202852||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058498|NCT02592655||Primary Outcome Ultrasound Images|https://doi.org/10.5281/zenodo.236263|NCT02592655 Primary Outcome Tourniquet Study
3058499|NCT02592655||Individual Participant Data Set|https://doi.org/10.5281/zenodo.237773|NCT02592655 Individual level data set
3058500|NCT02592655||Informed Consent Form|https://doi.org/10.5281/zenodo.245150|Informed consent form containing description of study and procedures.
3058501|NCT01316900|113360|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058502|NCT01316900|113360|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058503|NCT01316900|113360|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058504|NCT01316900|113360|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058505|NCT01316900|113360|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058506|NCT01316900|113360|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058507|NCT01316900|113360|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058508|NCT00289900||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-024&kw=0524B-024&tab=access|
3058509|NCT01703221||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-020&kw=3102-020&tab=access|
3058510|NCT01362530||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-208&kw=0869-208&tab=access|
3058511|NCT00970710||Study Protocol|http://bmcpediatr.biomedcentral.com/articles/10.1186/1471-2431-12-93|
3058512|NCT00970710||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=mustila+taina+vacopp|
3058513|NCT02074839||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3058514|NCT02074839||Study Protocol|https://clinicaltrials.servier.com/|
3058515|NCT02074839||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3058516|NCT02074839||Informed Consent Form|https://clinicaltrials.servier.com/|
3058517|NCT02074839||Clinical Study Report|https://clinicaltrials.servier.com/|
3058518|NCT02074839||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3058519|NCT00911157|111436|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058520|NCT00911157|111436|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058521|NCT00911157|111436|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058522|NCT00298155||Paper with attached protocol and outcomes|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887479/|
3058523|NCT06791044||Study Protocol|https://eka-hosp.gr/|
3058524|NCT00459550|106006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058525|NCT00459550|106006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058526|NCT00459550|106006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058527|NCT00459550|106006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058528|NCT00459550|106006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058529|NCT00459550|106006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058530|NCT02988076|CNSR012 Protocol|Study Protocol|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of the protocol
3058531|NCT02988076|CNSR012 ICD|Informed Consent Form|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of ICD
3058532|NCT00434811|SDY1178|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study ID is SDY1178.
3058533|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.
3058534|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.
3058535|NCT00078195|SDY1|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
3058536|NCT00078195|SDY1|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
3058537|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
3058538|NCT00078195|CASALE ITN019AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
3051571|NCT01627340|115918|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051572|NCT01627340|115918|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051573|NCT01627340|115918|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051574|NCT01627340|115918|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051575|NCT01627340|115918|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051576|NCT03173248||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3051577|NCT03173248||Study Protocol|https://clinicaltrials.servier.com/|
3051578|NCT03173248||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3051579|NCT03173248||Informed Consent Form|https://clinicaltrials.servier.com/|
3051580|NCT03173248||Clinical Study Report|https://clinicaltrials.servier.com/|
3051581|NCT03173248||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3051582|NCT03205020||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25118503|
3051583|NCT00410384|HGS1006-C1056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051584|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
3051585|NCT00410384|HGS1006-C1056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051586|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
3051587|NCT00410384|HGS1006-C1056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051588|NCT00410384|HGS1006-C1056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051589|NCT00410384|HGS1006-C1056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051590|NCT01577732|115389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051591|NCT01577732|115389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051592|NCT01577732|115389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051593|NCT01577732|115389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051594|NCT01577732|115389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051595|NCT01577732|115389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056000|NCT00436007|106369|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051596|NCT01125774||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-065&kw=0974-065&tab=access|
3051597|NCT00097370|100901|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051598|NCT00097370|100901|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051599|NCT00097370|100901|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051600|NCT00097370|100901|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051601|NCT00097370|100901|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051602|NCT00097370|100901|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056001|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.
3056002|NCT00000619||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/escape/|
3051603|NCT00097370|100901|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051604|NCT00697554|208129/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051605|NCT00697554|208129/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051606|NCT00697554|208129/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051607|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
3051608|NCT00697554|208129/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056003|NCT00000619||Study Forms|http://biolincc.nhlbi.nih.gov/studies/escape/|
3056004|NCT02197468||Clinical Study Report|https://www.frontiersin.org/articles/10.3389/fped.2018.00347/full|Publication from this study
3056005|NCT02746952||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3056006|NCT02746952||Study Protocol|https://clinicaltrials.servier.com/|
3056007|NCT02746952||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3056008|NCT02746952||Informed Consent Form|https://clinicaltrials.servier.com/|
3056009|NCT02746952||Clinical Study Report|https://clinicaltrials.servier.com/|
3056010|NCT02746952||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3056011|NCT06000280|Repositorio|Informed Consent Form|http://repositorio.bc.ufg.br|Repositorio da Biblioteca Central da Universidade Federal de Goias
3056012|NCT00622609|MAG103114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056013|NCT00622609|MAG103114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056014|NCT00622609|MAG103114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056015|NCT00622609|MAG103114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056016|NCT00622609|MAG103114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056017|NCT00622609|MAG103114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056018|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.
3056019|NCT00000566||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pioped/|
3056020|NCT00000566||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pioped/|
3056021|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.
3056022|NCT01295372|2010-022181-28|EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2010-022181-28/result|
3056023|NCT00442936||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-011&kw=0974-011&tab=access|
3056024|NCT01019603|114565|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056025|NCT01019603|114565|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056026|NCT01019603|114565|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056027|NCT01019603|114565|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056028|NCT01019603|114565|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056029|NCT01019603|114565|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056030|NCT01019603|114565|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056031|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."
3056032|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
3056033|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.
3051609|NCT06919211||Study Protocol|https://eyewiki.org/Retinal_Detachment|
3056034|NCT01974999|SDY1094|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|ImmPort study identifier is SDY1094.
3056035|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.
3056036|NCT04437693||Clinical Study Report|https://www.worldometers.info/coronavirus/|https://www.worldometers.info/coronavirus/
3056037|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
3056038|NCT01866319||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3475-006&kw=3475-006&tab=access|
3056039|NCT03167671|ISBN-10: 1886039224|Book|https://www.amazon.com/Prescription-Drug-Abuse-Epidemic-Understanding/dp/1886039224|
3056040|NCT07217353|IRB 2025-158|Study Protocol|https://www.axiommentor.com/pages/irb/sectionsOfProtocol.cfm?id=977&b=MP|
3056041|NCT00062790|ARI40014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056042|NCT00062790|ARI40014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056043|NCT00062790|ARI40014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056044|NCT00062790|ARI40014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056045|NCT00062790|ARI40014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056046|NCT00062790|ARI40014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056047|NCT00062790|ARI40014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056048|NCT01030965|113589|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056049|NCT01030965|113589|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056050|NCT01030965|113589|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056051|NCT01030965|113589|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056052|NCT01030965|113589|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056053|NCT01030965|113589|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056054|NCT01030965|113589|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056055|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, \[osf.io/d5t4m/\].
3056056|NCT00993187||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-202&kw=NCT00993187&tab=access|
3056057|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
3056058|NCT03222765||Study Protocol|http://www.epredice.eu|Study Protocol Version 5.0
3056059|NCT00076934|SDY661|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661|ImmPort study identifier is SDY661
3056060|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
3056061|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.
3056062|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.
3056063|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
3056064|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
3056065|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
3056066|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.
3056067|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
3056068|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
3057368|NCT00325156|100917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051610|NCT00578227|110886|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053890|NCT00368576|LPL107629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053891|NCT00368576|LPL107629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053892|NCT00368576|LPL107629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053893|NCT00368576|LPL107629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053894|NCT00368576|LPL107629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053895|NCT00368576|LPL107629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053896|NCT00368576|LPL107629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053897|NCT02480933|https://doi.org/10.3892/mco.20|Study Protocol|http://www.spandidos-publications.com/mco|feasibility of the protocol paper
3053898|NCT01017952|102970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053899|NCT01017952|102970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053900|NCT01017952|102970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053901|NCT01017952|102970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053902|NCT01017952|102970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053903|NCT01017952|102970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053904|NCT01017952|102970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053905|NCT03276611||Statistical Analysis Plan|http://www.ncbi.nlm.nih.gov/|
3053906|NCT00982904||Publication of results|http://www.dndi.org/wp-content/uploads/2009/06/ClinicalPK_Tarral_FexinidazoleHAT_2014.pdf|Publication of results
3053907|NCT01462266||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-260&kw=0431-260&tab=access|
3053908|NCT03194984|27045285|Metanalysis, systematic review|https://www.ncbi.nlm.nih.gov/pubmed/?term=27045285|
3053909|NCT03194984|21740236|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21740236|
3053910|NCT03194984|21488723|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21488723|
3053911|NCT03194984|27007348|Informed Consent Form|https://www.ncbi.nlm.nih.gov/pubmed/?term=27007348|
3053912|NCT02000804|117326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053913|NCT02000804|117326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053914|NCT02000804|117326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056069|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).
3056070|NCT03044171|57655916.3.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
3056071|NCT03579303|123|Individual Participant Data Set|http://bethesda.org?data-id=123|De-identified data for primary and secondary outcome measures
3056072|NCT00358449|MEE103219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056073|NCT00358449|MEE103219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056074|NCT00358449|MEE103219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056075|NCT00358449|MEE103219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056076|NCT00358449|MEE103219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056077|NCT00358449|MEE103219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056078|NCT00358449|MEE103219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056079|NCT00693966|580299/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056080|NCT00693966|580299/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056081|NCT00693966|580299/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056082|NCT00693966|580299/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056083|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
3056084|NCT00693966|580299/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056085|NCT00454909|109377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056086|NCT00454909|109377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056087|NCT00454909|109377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056088|NCT00454909|109377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056089|NCT00454909|109377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056090|NCT00454909|109377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056091|NCT00454909|109377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056092|NCT01954264|200187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056093|NCT01954264|200187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056094|NCT01954264|200187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056095|NCT01954264|200187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056096|NCT01954264|200187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056097|NCT01954264|200187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056098|NCT01376167|112582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056099|NCT01376167|112582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056100|NCT01376167|112582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056101|NCT01376167|112582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056102|NCT01376167|112582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056103|NCT01376167|112582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056104|NCT07025395|28 May 2025|Study Protocol|https://youtu.be/ql8SD07abnI|Core Training Protocol by Ioannis Tsartsapakis Ph.D.
3056105|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
3056106|NCT01171989|113978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056107|NCT01171989|113978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056108|NCT01171989|113978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056109|NCT01171989|113978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056110|NCT01171989|113978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056111|NCT01171989|113978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056112|NCT01171989|113978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056113|NCT02605395|201528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056114|NCT02605395|201528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056115|NCT02605395|201528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056116|NCT02605395|201528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056117|NCT01472341||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-113&kw=0000-113&tab=access|
3056118|NCT00379600|ARA102198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056119|NCT00379600|ARA102198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056120|NCT00379600|ARA102198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056121|NCT00379600|ARA102198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051611|NCT00578227|110886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051612|NCT00578227|110886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051613|NCT00578227|110886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051614|NCT00578227|110886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051615|NCT00578227|110886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051616|NCT00578227|110886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051617|NCT01114620|114270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051618|NCT01114620|114270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056122|NCT00379600|ARA102198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056123|NCT00379600|ARA102198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056124|NCT00379600|ARA102198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056125|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"
3056126|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"
3057369|NCT00325156|100917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057370|NCT00325156|100917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057371|NCT00325156|100917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057372|NCT00325156|100917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057373|NCT00325156|100917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057374|NCT01424514|114974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057375|NCT01424514|114974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057376|NCT01424514|114974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057377|NCT01424514|114974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051619|NCT01114620|114270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051620|NCT01114620|114270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053915|NCT02000804|117326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053916|NCT02000804|117326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053917|NCT02000804|117326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053918|NCT02000804|117326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053919|NCT05506397||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/|
3053920|NCT00920660|113161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053921|NCT00920660|113161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053922|NCT00920660|113161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053923|NCT00920660|113161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053924|NCT00920660|113161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053925|NCT00920660|113161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053926|NCT00920660|113161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053927|NCT01475734|108372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056127|NCT04391933|CPR|Informed Consent Form|https://komite.regionsyddanmark.dk/wm258128|
3053928|NCT01475734|108372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053929|NCT01475734|108372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053930|NCT01475734|108372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053931|NCT01475734|108372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053932|NCT01475734|108372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053933|NCT01475734|108372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053934|NCT01552681|SDY823|Study Protocol|http://www.immport.org/immport-open/public/home/home|ImmPort study identifier is SDY823.
3053935|NCT01552681|SDY823|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/home|ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public.
3053936|NCT00379951||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053937|NCT04887493|Misoprostol|Study Protocol|https://www.researchgate.net/publication/351331713_Efficacy_and_Safety_of_Sublingual_versus_Vaginal_Misoprostol_for_Induction_of_Labor_at_Term_and_Post_Term_Pregnancies_A_Randomized_Clinical_Trial_Efficacy_and_Safety_of_Sublingual_versus_Vaginal_Misop|
3053938|NCT01097629||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-029&kw=4305-029&tab=access|
3053939|NCT00783393||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3053940|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
3053941|NCT00137917|710158/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053942|NCT00137917|710158/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053943|NCT00137917|710158/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053944|NCT00137917|710158/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053945|NCT01827631|116416|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053946|NCT01827631|116416|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053947|NCT01827631|116416|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053948|NCT01827631|116416|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053949|NCT01827631|116416|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051621|NCT01114620|114270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051622|NCT01114620|114270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051623|NCT01114620|114270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053950|NCT01827631|116416|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058539|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
3058540|NCT03495635|osf.io/8ukfv|Individual Participant Data Set|https://osf.io/|
3058541|NCT01101555|113299|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058542|NCT01101555|113299|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058543|NCT01101555|113299|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058544|NCT01101555|113299|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058545|NCT01101555|113299|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058546|NCT01101555|113299|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058547|NCT01101555|113299|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058548|NCT06694064||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/36464977/|
3058549|NCT01817777|116086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058550|NCT01817777|116086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058551|NCT01817777|116086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058552|NCT01817777|116086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058553|NCT01817777|116086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058554|NCT01817777|116086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058555|NCT01817777|116086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058556|NCT05600517|10.1016/j.ebiom.2017.11.019|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832611/|
3058557|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."
3058558|NCT04292496||Study Protocol|https://doi.org/10.1007/s00464-023-10025-w|
3058559|NCT02233088|PMC6589338|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/30234352|A manuscript summarizing the development of the intervention.
3058560|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.
3058561|NCT01353729|114346|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058562|NCT01353729|114346|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058563|NCT01353729|114346|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058564|NCT01353729|114346|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058565|NCT01353729|114346|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058566|NCT01353729|114346|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058567|NCT01353729|114346|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058568|NCT01916226|200165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058569|NCT01916226|200165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058570|NCT01916226|200165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058571|NCT01916226|200165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058572|NCT01916226|200165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058573|NCT01916226|200165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058574|NCT01916226|200165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058575|NCT00979407|113535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058576|NCT00979407|113535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058577|NCT00979407|113535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058578|NCT00979407|113535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051624|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
3058579|NCT00979407|113535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058580|NCT00979407|113535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058581|NCT02842671||Study Protocol|http://irb.psu.edu|
3058582|NCT02842671||Informed Consent Form|http://irb.psu.edu|for participants
3058583|NCT02842671||Accommodation Survey|http://irb.psu.edu|
3058584|NCT02842671||Patient Satisfaction Survey|http://irb.psu.edu|
3058585|NCT02842671||Medical Student Survey|http://irb.psu.edu|
3058586|NCT02842671||Summary Explanation of Research|http://irb.psu.edu|for medical students
3058587|NCT01051661|114000|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058588|NCT01051661|114000|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058589|NCT01051661|114000|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058590|NCT01051661|114000|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058591|NCT01051661|114000|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058592|NCT01051661|114000|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058593|NCT00005479||NCBI website|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724776/|
3058594|NCT00492544|110168|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058595|NCT00492544|110168|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058596|NCT00492544|110168|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058597|NCT00492544|110168|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058598|NCT00492544|110168|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058599|NCT00492544|110168|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058600|NCT00492544|110168|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058601|NCT00680914|110808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058602|NCT00680914|110808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058603|NCT00680914|110808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058604|NCT00680914|110808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058605|NCT00680914|110808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058606|NCT00680914|110808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058607|NCT00680914|110808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051625|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
3058608|NCT04164186|NSCLC Radiomics Interobserver|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics-Interobserver1|
3058609|NCT04164186|NSCLC Radiomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics|
3058610|NCT04164186|NSCLC Radiogenomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC+Radiogenomics|
3058611|NCT00734032|LPL110118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058612|NCT00734032|LPL110118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058613|NCT00734032|LPL110118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058614|NCT00734032|LPL110118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058615|NCT00734032|LPL110118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056128|NCT00624065|COR111096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056129|NCT00624065|COR111096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056130|NCT00624065|COR111096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056131|NCT00624065|COR111096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056132|NCT00624065|COR111096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056133|NCT00624065|COR111096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056134|NCT00624065|COR111096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056135|NCT01171963|113808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056136|NCT01171963|113808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056137|NCT01171963|113808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056138|NCT01171963|113808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056139|NCT01171963|113808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056140|NCT01171963|113808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056141|NCT01171963|113808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056142|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.
3056143|NCT00302952|SDY473|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473
3056144|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
3056145|NCT02841488||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
3056146|NCT01536405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V221-027&kw=V221-027&tab=access|
3056147|NCT02578953|204646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056148|NCT02578953|204646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056149|NCT02578953|204646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056150|NCT03306394||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3056151|NCT03306394||Study Protocol|https://clinicaltrials.servier.com/|
3056152|NCT03306394||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3056153|NCT03306394||Informed Consent Form|https://clinicaltrials.servier.com/|
3056154|NCT03306394||Clinical Study Report|https://clinicaltrials.servier.com/|
3056155|NCT03306394||study-level clinical trial data|https://clinicaltrials.servier.com/|
3056156|NCT04752592||Study Protocol|https://www.seroselecttb.org/resources|
3056157|NCT01037114|112266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056158|NCT01037114|112266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056159|NCT01037114|112266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056160|NCT01037114|112266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056161|NCT01037114|112266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056162|NCT01037114|112266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056163|NCT01037114|112266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056164|NCT01639092|25596179|Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25596179|Publication for the primary study results
3056165|NCT01421277||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-076&kw=0974-076&tab=access|
3056166|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
3056167|NCT00609674|FFU111439|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056168|NCT00609674|FFU111439|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056169|NCT00609674|FFU111439|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058616|NCT00734032|LPL110118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053951|NCT01827631|116416|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053952|NCT00600171|B2C109575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053953|NCT00600171|B2C109575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053954|NCT00600171|B2C109575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053955|NCT00600171|B2C109575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053956|NCT00600171|B2C109575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053957|NCT00600171|B2C109575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053958|NCT00600171|B2C109575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053959|NCT05521737||Protocol reapproval report|https://drive.google.com/file/d/1P3sbgleW3murWJq_FIaerBlFU12aga9z/view?usp=sharing|
3053960|NCT02698098||Study Protocol|http://dx.doi.org/10.7910/DVN/RO34OK|
3053961|NCT02698098||Individual Participant Data Set|http://dx.doi.org/10.7910/DVN/RO34OK|
3053962|NCT02698098||Analytic Code|http://dx.doi.org/10.7910/DVN/RO34OK|
3053963|NCT04719351||Individual Participant Data Set|https://osf.io/uz3b7/?view_only=ba37189d0b594529b159ba27564dfb81|
3053964|NCT01879410|114951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053965|NCT01879410|114951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053966|NCT01879410|114951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053967|NCT01879410|114951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053968|NCT01879410|114951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053969|NCT01879410|114951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053970|NCT01879410|114951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053971|NCT02899858|140503|Study Protocol|https://www4.vanderbilt.edu/irb/|
3053972|NCT04106622||Pubmed|https://www.ncbi.nlm.nih.gov/pubmed/|
3053973|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.
3053974|NCT00849017|112756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053975|NCT00849017|112756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053976|NCT00849017|112756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053977|NCT00849017|112756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053978|NCT00849017|112756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053979|NCT00849017|112756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053980|NCT00849017|112756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053981|NCT00609596|ARI111402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053982|NCT00609596|ARI111402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053983|NCT00609596|ARI111402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053984|NCT00609596|ARI111402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053985|NCT00609596|ARI111402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053986|NCT00609596|ARI111402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053987|NCT00609596|ARI111402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053988|NCT03311048|Sistema Nacional de Informação|Informed Consent Form|http://portal2.saude.gov.br/sisnep/pesquisador|
3053989|NCT00976144|113208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053990|NCT00976144|113208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053991|NCT00976144|113208|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053992|NCT00976144|113208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053993|NCT00976144|113208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053994|NCT00976144|113208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053995|NCT00976144|113208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053996|NCT01428466|114849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053997|NCT01428466|114849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053998|NCT01428466|114849|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3053999|NCT01428466|114849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054000|NCT04067518||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3049718|NCT00042029||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054001|NCT04067518||Study Protocol|https://clinicaltrials.servier.com/|
3054002|NCT04067518||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3054003|NCT04067518||Informed Consent Form|https://clinicaltrials.servier.com/|
3054004|NCT04067518||Clinical Study Report|https://clinicaltrials.servier.com/|
3054005|NCT04067518||study-level clinical trial data|https://clinicaltrials.servier.com/|
3054006|NCT01648231|116797|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054007|NCT01648231|116797|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054008|NCT01648231|116797|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054009|NCT01648231|116797|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054010|NCT01648231|116797|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054011|NCT01648231|116797|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054012|NCT01648231|116797|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054013|NCT04523532||Study Protocol|http://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s13148-017-0407-6|
3054014|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
3054015|NCT01086436|113552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054016|NCT01086436|113552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054017|NCT01086436|113552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054018|NCT01086436|113552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054019|NCT01086436|113552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054020|NCT01086436|113552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054021|NCT00348140|AVA102670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054022|NCT00348140|AVA102670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054023|NCT00348140|AVA102670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054024|NCT00348140|AVA102670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054025|NCT00348140|AVA102670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054026|NCT00348140|AVA102670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054027|NCT00348140|AVA102670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054028|NCT00868790||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3577-009&kw=3577-009&tab=access|
3054029|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.
3054030|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.
3054031|NCT00537719|GLP107030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054032|NCT00537719|GLP107030|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054033|NCT00537719|GLP107030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058617|NCT00332566|106602|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058618|NCT00332566|106602|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051626|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
3058619|NCT00332566|106602|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058620|NCT00332566|106602|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058621|NCT00332566|106602|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058622|NCT00332566|106602|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058623|NCT01706315|116778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058624|NCT01706315|116778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058625|NCT01706315|116778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058626|NCT01706315|116778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058627|NCT01706315|116778|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058628|NCT01706315|116778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058629|NCT01706315|116778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058630|NCT00086515||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058631|NCT00323622|104297|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058632|NCT00323622|104297|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058633|NCT00323622|104297|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058634|NCT00323622|104297|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058635|NCT00323622|104297|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058636|NCT00323622|104297|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058637|NCT02743221||Individual Participant Data Set|http://clinicaltrials.servier.com/|
3058638|NCT02743221||Study Protocol|https://clinicaltrials.servier.com/|
3058639|NCT02743221||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3058640|NCT02743221||Informed Consent Form|https://clinicaltrials.servier.com/|
3058641|NCT02743221||Clinical Study Report|https://clinicaltrials.servier.com/|
3058642|NCT02743221||study-level clinical trial data|https://clinicaltrials.servier.com/|
3058643|NCT03044899||Study Protocol|http://www.asos.org.za/|ASOS Protocol version 1.0
3051627|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
3051628|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
3051629|NCT00119743|347414/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051630|NCT00119743|347414/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051631|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
3051632|NCT00119743|347414/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051633|NCT00119743|347414/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051634|NCT00119743|347414/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051635|NCT04553302||Clinical Study Report|http://ard.bmj.com/content/79/Suppl_1/555.2|
3051636|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
3051637|NCT03668067||Individual Participant Data Set|http://www.abcd-vision.org/references/2WIN%20Bus%20de-identified%209-6-18.pdf|Public de-identified ongoing
3051638|NCT01244984|113989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051639|NCT01244984|113989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051640|NCT01244984|113989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054034|NCT00537719|GLP107030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054035|NCT00537719|GLP107030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054036|NCT00537719|GLP107030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054037|NCT00537719|GLP107030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054038|NCT01154101|114296|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054039|NCT01154101|114296|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054040|NCT01154101|114296|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054041|NCT01154101|114296|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054042|NCT01154101|114296|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054043|NCT01154101|114296|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054044|NCT03289130||Individual Participant Data Set|https://pcap.bioinf.unc.edu/|
3054045|NCT00792298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-006&kw=4305-006&tab=access|
3054046|NCT02706938|Clinical Trial Protocol|Study Protocol|https://drive.google.com/open?id=0B6Uam9x9PtiiV2xUcDBKU3RHYU0|
3054047|NCT00707798|111651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054048|NCT00707798|111651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054049|NCT00707798|111651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054050|NCT00707798|111651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054051|NCT00707798|111651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054052|NCT02069002||Study Protocol|http://bmjopen.bmj.com/content/6/6/e011003.full.pdf+html|
3054053|NCT04091347|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
3054054|NCT04091347|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
3054055|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)
3058644|NCT00140920||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058645|NCT02989857||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3058646|NCT02989857||Study Protocol|https://clinicaltrials.servier.com/|
3058647|NCT02989857||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3058648|NCT02989857||Informed Consent Form|https://clinicaltrials.servier.com/|
3058649|NCT02989857||Clinical Study Report|https://clinicaltrials.servier.com/|
3058650|NCT02989857||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3058651|NCT06250257||Individual Participant Data Set|https://kf.kobotoolbox.org/#/forms/aSWyWhEb2TmCqshx54qTW7|
3058652|NCT00157872||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058653|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
3058654|NCT00140686|102247/036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058655|NCT00140686|102247/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058656|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
3058657|NCT00140686|102247/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058658|NCT00140686|102247/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058659|NCT00140686|102247/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051641|NCT01244984|113989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051642|NCT01244984|113989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051643|NCT01244984|113989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054056|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)
3054057|NCT07199218||Informed Consent Form|https://osf.io/f69ds/files/osf|
3054058|NCT07236723||Data Monitoring Committee Charter|https://pmc.ncbi.nlm.nih.gov/articles/PMC7571449/|https://pmc.ncbi.nlm.nih.gov/articles/PMC7571449/
3054059|NCT00358813|NKT102783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054060|NCT00358813|NKT102783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054061|NCT00358813|NKT102783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054062|NCT00358813|NKT102783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054063|NCT00358813|NKT102783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054064|NCT00358813|NKT102783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054065|NCT00358813|NKT102783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054066|NCT06896929|permethrin|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/21860157/|Comparison of permethrin and ivermectin in scabies was done
3054067|NCT01495026|115708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054068|NCT01495026|115708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054069|NCT01495026|115708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054070|NCT01495026|115708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054071|NCT01495026|115708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054072|NCT01495026|115708|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054073|NCT01495026|115708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054074|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
3054075|NCT00996840|111592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054076|NCT00996840|111592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054077|NCT00996840|111592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054078|NCT00996840|111592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054079|NCT00996840|111592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056170|NCT00609674|FFU111439|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056171|NCT00609674|FFU111439|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056172|NCT00609674|FFU111439|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056173|NCT00609674|FFU111439|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056174|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|
3056175|NCT00385320|444563/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056176|NCT00385320|444563/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056177|NCT00385320|444563/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056178|NCT00385320|444563/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051644|NCT01244984|113989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051645|NCT01096056|114182|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058660|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.
3058661|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
3051646|NCT01096056|114182|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058662|NCT02738463||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/pubmed|
3058663|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
3058664|NCT01999530||Publication|https://www.ncbi.nlm.nih.gov/pubmed/28233334|
3058665|NCT04831229|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
3058666|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
3058667|NCT06835959|Informed consent form|Informed Consent Form|https://drive.google.com/file/d/1q09u34SVFOO2TXC7vXuDAE0MAjJfgVyA/view?usp=drive_link|
3051647|NCT01096056|114182|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051648|NCT01096056|114182|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051649|NCT01096056|114182|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051650|NCT01096056|114182|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051651|NCT00364442|SAS10019|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051652|NCT00364442|SAS10019|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051653|NCT00364442|SAS10019|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051654|NCT00364442|SAS10019|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051655|NCT00364442|SAS10019|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051656|NCT00364442|SAS10019|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051657|NCT00364442|SAS10019|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051658|NCT00263679|100406/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051659|NCT00263679|100406/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051660|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
3051661|NCT00263679|100406/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058668|NCT07004348|PROM link|Statistical Analysis Plan|https://livenorthumbriaac-my.sharepoint.com/:w:/g/personal/frank_lai_northumbria_ac_uk/EbKJJ3cbnk5Ikr-NpppTxHoBmGuJLYpePT6qQ1ZnXA4P-w?e=ZZuX7U|
3058669|NCT00373542|RRL103660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058670|NCT00373542|RRL103660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058671|NCT00373542|RRL103660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058672|NCT00373542|RRL103660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058673|NCT00373542|RRL103660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058674|NCT00373542|RRL103660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058675|NCT00373542|RRL103660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058676|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.
3058677|NCT00005121|FHS-Cohort|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
3058678|NCT00005121|FHS-Cohort|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
3058679|NCT00005121|FHS-Cohort|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
3058680|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.
3058681|NCT00005121|FHS-OS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
3058682|NCT00005121|FHS-OS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
3049719|NCT01286831|106181|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058683|NCT00005121|FHS-OS|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
3058684|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.
3058685|NCT00005121|FHS-Gen III|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/gen3/|
3058686|NCT00005121|FHS-Gen III|Study Forms|http://biolincc.nhlbi.nih.gov/studies/gen3/|
3058687|NCT00005121|FHS-Gen III|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/gen3/|
3058688|NCT01702298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-312&kw=0431D-312&tab=access|
3058689|NCT05162755||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3058690|NCT05162755||Study Protocol|https://clinicaltrials.servier.com/|
3058691|NCT05162755||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3058692|NCT05162755||Informed Consent Form|https://clinicaltrials.servier.com/|
3058693|NCT05162755||Clinical Study Report|https://clinicaltrials.servier.com/|
3049720|NCT01286831|106181|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049721|NCT01286831|106181|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049722|NCT01286831|106181|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051662|NCT00263679|100406/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051663|NCT00263679|100406/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051664|NCT06103422||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/26935213/|
3051665|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/26935213/|
3051666|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/11078134/|
3051667|NCT04401722|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|through elnakeebayman@yahoo.com
3051668|NCT01738867|116753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051669|NCT01738867|116753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051670|NCT01738867|116753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051671|NCT01738867|116753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051672|NCT01738867|116753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051673|NCT01738867|116753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051674|NCT01738867|116753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051675|NCT00197236|208109/232|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051676|NCT00197236|208109/232|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051677|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
3051678|NCT00197236|208109/232|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051679|NCT00197236|208109/232|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051680|NCT00197236|208109/232|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051681|NCT00140673|444563/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051682|NCT00140673|444563/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051683|NCT00140673|444563/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051684|NCT00140673|444563/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051685|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
3058694|NCT05162755||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3058695|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
3058696|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
3051686|NCT00140673|444563/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051687|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
3051688|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.
3051689|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.
3051690|NCT00004560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pad/|
3051691|NCT04405713|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
3051692|NCT01984086|200921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051693|NCT01984086|200921|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051694|NCT01984086|200921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051695|NCT01984086|200921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051696|NCT01984086|200921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051697|NCT01984086|200921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051698|NCT01984086|200921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051699|NCT01457560|217744/060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051700|NCT01457560|217744/060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051701|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
3051702|NCT01457560|217744/060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051703|NCT01457560|217744/060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051704|NCT01196988|113275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051705|NCT01196988|113275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051706|NCT01196988|113275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051707|NCT01196988|113275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051708|NCT01196988|113275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051709|NCT01196988|113275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051710|NCT01196988|113275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051711|NCT01078233||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-058&kw=0518-058&tab=access|
3051712|NCT00502593|107066|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051713|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.
3051714|NCT00502593|107066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051715|NCT00502593|107066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051716|NCT00502593|107066|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051717|NCT00502593|107066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051718|NCT00502593|107066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051719|NCT00586339|107863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051720|NCT00586339|107863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051721|NCT00586339|107863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051722|NCT00586339|107863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056179|NCT00385320|444563/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056180|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
3049723|NCT01286831|106181|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049724|NCT01286831|106181|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049725|NCT01286831|106181|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049726|NCT03121027||Individual Participant Data Set|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|Detail about sampling and BDHS 2011 report
3049727|NCT01277042|114590|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049728|NCT01277042|114590|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049729|NCT01277042|114590|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049730|NCT01277042|114590|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049731|NCT01277042|114590|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049732|NCT01277042|114590|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049733|NCT00510874|110028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049734|NCT00510874|110028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056181|NCT03192163||Survey|http://j.mp/2qdz7P2|This is the RedCap survey that subjects will take.
3056182|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
3056183|NCT02197481|PMID:25925431|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25925431|
3056184|NCT01899755|116987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056185|NCT01899755|116987|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056186|NCT01899755|116987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049735|NCT00510874|110028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049736|NCT00510874|110028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049737|NCT00510874|110028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049738|NCT00510874|110028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049739|NCT00510874|110028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049740|NCT02777736||Study Protocol|http://www.lymphoma.cz/docs/studies/dlbcl/CLSG-CNS-01_en.pdf|
3049741|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."
3049742|NCT01067443||Study Protocol|http://journals.plos.org/plosntds/article/file?type=supplementary&id=info:doi/10.1371/journal.pntd.0004880.s002|Final Study Protocol
3049743|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 \[there-on other citations are referenced 1 citation later\]
3049744|NCT00688207|AVA109941|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049745|NCT00688207|AVA109941|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049746|NCT00688207|AVA109941|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049747|NCT00688207|AVA109941|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049748|NCT00688207|AVA109941|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049749|NCT00688207|AVA109941|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049750|NCT00688207|AVA109941|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049751|NCT01266941|111789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049752|NCT01266941|111789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056187|NCT01899755|116987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058697|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.
3058698|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.
3058699|NCT00317122|759346/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058700|NCT00317122|759346/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054080|NCT00996840|111592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054081|NCT00996840|111592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054082|NCT01164878||Individual Participant Data Set|https://dfzljdn9uc3pi.cloudfront.net/2016/2483/1/SPSS_repa_et_al.sav|SPSS Data Set for Analysis
3054083|NCT00818259||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=0869-134&kw=0869-134&tab=access|
3054084|NCT00684177|TOC110977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054085|NCT00684177|TOC110977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054086|NCT00684177|TOC110977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054087|NCT00684177|TOC110977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054088|NCT00684177|TOC110977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054089|NCT00684177|TOC110977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054090|NCT00684177|TOC110977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054091|NCT01471327|115705|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054092|NCT01471327|115705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054093|NCT01471327|115705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054094|NCT01471327|115705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054095|NCT01471327|115705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054096|NCT01471327|115705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054097|NCT01471327|115705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054098|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.
3054099|NCT00312013|FRX106365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054100|NCT00312013|FRX106365|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054101|NCT00312013|FRX106365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054102|NCT00312013|FRX106365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054103|NCT00312013|FRX106365|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054104|NCT00312013|FRX106365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054105|NCT00312013|FRX106365|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054106|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.
3054107|NCT02740309|Sala Institute|Sala Institute for Child & Family Centered Care|http://nyulangone.org/locations/hassenfeld-childrens-hospital/sala-institute-for-child-family-centered-care|
3054108|NCT00291343|105239 (mth24-30)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054109|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
3054110|NCT00291343|105239 (mth24-30)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051723|NCT00586339|107863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051724|NCT00586339|107863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051725|NCT00538213|110263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051726|NCT00538213|110263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051727|NCT00538213|110263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051728|NCT00538213|110263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051729|NCT00538213|110263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051730|NCT00538213|110263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051731|NCT00538213|110263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051732|NCT02281318|200862|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051733|NCT02281318|200862|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051734|NCT02281318|200862|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051735|NCT02281318|200862|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051736|NCT02281318|200862|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051737|NCT02281318|200862|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051738|NCT02281318|200862|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051739|NCT04727489||Study Protocol|http://www.inserm.fr|
3051740|NCT04727489||Informed Consent Form|http://www.inserm.fr|
3051741|NCT07299383|AYÇA ÇALBAY|Study Protocol|https://atauni.edu.tr/|online access is not available, accessible via e-mail
3051742|NCT07300137|comparison of 2 dressings|comparison between two types of dressings|https://pjmhsonline.com/index.php/pjmhs/article/view/3992|Mean duration of healing with sodium Carboxylic methyl-cellulose silver dressing was less than petroleum gauze dressing for management of second-degree burns.
3051743|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.
3051744|NCT02683811||Study Protocol|http://www.diariodellasalute.it|Study protocol (Italian version) can be requested by contacting the project manager (lmarinaro@aslcn2.it)
3051745|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.
3051746|NCT00501020|49653/284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051747|NCT00501020|49653/284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051748|NCT00501020|49653/284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051749|NCT00501020|49653/284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051750|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
3051751|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
3051752|NCT00501020|49653/284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051753|NCT01013974|113377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051754|NCT01013974|113377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051755|NCT01013974|113377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051756|NCT01013974|113377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051757|NCT01013974|113377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051758|NCT01013974|113377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051759|NCT01013974|113377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051760|NCT01025843||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5478-001&kw=5478-001&tab=access|
3051761|NCT02808442||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3051762|NCT02808442||Study Protocol|https://clinicaltrials.servier.com/|
3051763|NCT02808442||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3051764|NCT02808442||Informed Consent Form|https://clinicaltrials.servier.com/|
3051765|NCT02808442||Clinical Study Report|https://clinicaltrials.servier.com/|
3056188|NCT01899755|116987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056189|NCT01899755|116987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056190|NCT01899755|116987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056191|NCT01929863|200185|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056192|NCT01929863|200185|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056193|NCT01929863|200185|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056194|NCT01929863|200185|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056195|NCT01929863|200185|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056196|NCT01929863|200185|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056197|NCT01929863|200185|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056198|NCT01818024|116343|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056199|NCT01818024|116343|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056200|NCT01818024|116343|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051766|NCT02808442||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3051767|NCT00420316|109810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051768|NCT00420316|109810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051769|NCT00420316|109810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051770|NCT00420316|109810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051771|NCT00420316|109810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051772|NCT00420316|109810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051773|NCT00420316|109810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051774|NCT01651949||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-003&kw=V503-003&tab=access|
3051775|NCT06615128||Study Protocol|https://doi.org/10.4049/jimmunol.182.3.1541|
3051776|NCT06615128||Study Protocol|https://doi.org/10.1371/journal.pone.0047748|
3051777|NCT00843193|106870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051778|NCT00843193|106870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051779|NCT00843193|106870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051780|NCT00843193|106870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056201|NCT01818024|116343|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056202|NCT01818024|116343|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056203|NCT01818024|116343|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056204|NCT01818024|116343|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056205|NCT00268203|BEX104545|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056206|NCT00268203|BEX104545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056207|NCT00268203|BEX104545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051781|NCT00843193|106870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051782|NCT00843193|106870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051783|NCT00843193|106870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056208|NCT00268203|BEX104545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056209|NCT07289971|PMID: 35852013|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35852013/|https://pubmed.ncbi.nlm.nih.gov/
3056210|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
3056211|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.
3056212|NCT00005292||Study Forms|https://biolincc.nhlbi.nih.gov/studies/aadr/Forms/|
3056213|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.
3051784|NCT00197015|208109/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051785|NCT00197015|208109/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051786|NCT00197015|208109/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051787|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
3051788|NCT00197015|208109/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051789|NCT00197015|208109/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051790|NCT00961142||Results|https://www.clinicaltrialsregister.eu/ctr-search/search?query=2007-006016-33|
3051791|NCT06706882||INFORMATION SHEET|https://drive.google.com/file/d/1Y90Fr8O30tFqNL_OjAjMfrayrK8-KKxt/view?usp=sharing|
3051792|NCT06706882|Informed Consent Form|Informed Consent Form|https://drive.google.com/file/d/1eQLHRV80sIPlZNoHR5HFS4uauF8RWoDI/view?usp=sharing|
3051793|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.
3051794|NCT00937846|110771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051795|NCT00937846|110771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056214|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).
3056215|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).
3056216|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).
3056217|NCT02045849|117349|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056218|NCT02045849|117349|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056219|NCT02045849|117349|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056220|NCT02045849|117349|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056221|NCT02045849|117349|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056222|NCT02045849|117349|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056223|NCT02045849|117349|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056224|NCT00363077|107975|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056225|NCT00363077|107975|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056226|NCT00363077|107975|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056227|NCT00363077|107975|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056228|NCT00363077|107975|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056229|NCT01039961|113022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056230|NCT01039961|113022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056231|NCT01039961|113022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056232|NCT01039961|113022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051796|NCT00937846|110771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051797|NCT00937846|110771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051798|NCT00937846|110771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056233|NCT01039961|113022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056234|NCT01039961|113022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051799|NCT00937846|110771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051800|NCT00937846|110771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049753|NCT01266941|111789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049754|NCT01266941|111789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049755|NCT01266941|111789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049756|NCT01266941|111789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049757|NCT01266941|111789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049758|NCT00887406|104865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049759|NCT00887406|104865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049760|NCT00887406|104865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049761|NCT00887406|104865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049762|NCT00887406|104865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049763|NCT00887406|104865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049764|NCT03272230||Study Protocol|https://data.mendeley.com/datasets/mv8hndcd95/2|The ECOCAPTURE ethograms: apathy ethogram and disinhibition ethogram
3049765|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
3049766|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
3049767|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
3049768|NCT01323946|109825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049769|NCT01323946|109825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049770|NCT01323946|109825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049771|NCT01323946|109825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049772|NCT01323946|109825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049773|NCT01323946|109825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049774|NCT01323946|109825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049775|NCT00371007||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3049776|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
3049777|NCT02826850||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
3049778|NCT02826850||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
3049779|NCT05648071|[ PMID ]31560378|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31560378/|
3049780|NCT05648071|PMID:30285222|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30285222/|
3049781|NCT05648071|PMID:31378236|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31378236/|
3049782|NCT05648071|PMID:32997907|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32997907/|
3049783|NCT05648071|PMID:30955977|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30955977/|
3049784|NCT05648071|PMID:31402780|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31402780/|
3049785|NCT05648071|PMID:32781263|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32781263/|
3049786|NCT05648071|PMID: 34358724|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34358724/|
3049787|NCT05648071|PMID: 29229461|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29229461/|
3049788|NCT05648071|PMID: 30119083|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30119083/|
3049789|NCT05749770||Individual Participant Data Set|https://zenodo.org/records/5913009|
3049790|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
3049791|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
3049792|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
3049793|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
3049794|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
3049795|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
3049796|NCT00101829|SDY961|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
3049797|NCT00101829|SDY961|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
3049798|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
3049799|NCT01036061|108414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049800|NCT01036061|108414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049801|NCT01036061|108414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049802|NCT01036061|108414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049803|NCT01036061|108414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049804|NCT01036061|108414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049805|NCT06933992||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|
3049806|NCT01039974|112648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049807|NCT01039974|112648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049808|NCT01039974|112648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049809|NCT01039974|112648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054111|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
3054112|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.
3054113|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
3054114|NCT03094247||Individual Participant Data Set|https://openscholarship.wustl.edu/data/101/|
3054115|NCT02184637|200951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054116|NCT02184637|200951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054117|NCT02184637|200951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054118|NCT02184637|200951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054119|NCT02184637|200951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054120|NCT02184637|200951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051801|NCT01235949|112921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051802|NCT01235949|112921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051803|NCT01235949|112921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051804|NCT01235949|112921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051805|NCT01235949|112921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051806|NCT01235949|112921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051807|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
3051808|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25939657|Report of vascular function testing
3051809|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/24548114|Report of platelet function and physiology
3051810|NCT03912948||Web site for patient information on studies bases on patients data (RGPD)|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|
3051811|NCT06210334||Clinical Study Report|https://www.researchdata.org.cn/|
3051812|NCT00970307|112157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051813|NCT00970307|112157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051814|NCT00970307|112157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051815|NCT00970307|112157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051816|NCT00970307|112157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051817|NCT00970307|112157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051818|NCT00970307|112157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051819|NCT01370694||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=8808-001&kw=8808-001&tab=access|
3051820|NCT02289560||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
3051821|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.
3051822|NCT00711126|B2C106180|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051823|NCT00711126|B2C106180|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051824|NCT00711126|B2C106180|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051825|NCT00711126|B2C106180|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051826|NCT00711126|B2C106180|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051827|NCT00711126|B2C106180|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051828|NCT00711126|B2C106180|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051829|NCT01930045||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-295&kw=0518-295&tab=access|
3051830|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.
3051831|NCT00241644|102248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051832|NCT00241644|102248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051833|NCT00241644|102248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051834|NCT00241644|102248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051835|NCT00241644|102248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051836|NCT00241644|102248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051837|NCT05888155|01095697530|Clinical Study Report|http://Shaimaa4796@gmail.com|
3051838|NCT00972504|112864|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051839|NCT00972504|112864|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051840|NCT00972504|112864|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051841|NCT00972504|112864|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051842|NCT00972504|112864|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051843|NCT00972504|112864|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051844|NCT00972504|112864|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051845|NCT05171218||Individual Participant Data Set|https://osf.io/efya2/|
3051846|NCT05171218||Study Protocol|https://doi.org/10.17605/OSF.IO/VHCA5|
3051847|NCT05171218||Statistical Analysis Plan|https://doi.org/10.17605/OSF.IO/VHCA5|
3051848|NCT05171218||Informed Consent Form|https://osf.io/efya2/|
3051849|NCT00622830|LPL110736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051850|NCT00622830|LPL110736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051851|NCT00622830|LPL110736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051852|NCT00622830|LPL110736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051853|NCT00622830|LPL110736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051854|NCT00622830|LPL110736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051855|NCT00622830|LPL110736|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051856|NCT01406262|107085|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051857|NCT01406262|107085|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051858|NCT01406262|107085|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051859|NCT01406262|107085|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051860|NCT01406262|107085|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051861|NCT01406262|107085|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051862|NCT01406262|107085|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054121|NCT02184637|200951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054122|NCT00473694||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054123|NCT01772134|116135|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054124|NCT01772134|116135|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054125|NCT01772134|116135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054126|NCT01772134|116135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054127|NCT01772134|116135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054128|NCT01772134|116135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054129|NCT01772134|116135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054130|NCT03322358||Individual Participant Data Set|https://www.sleepdata.org/datasets/urbanpoor|
3054131|NCT03184948||Statistical Analysis Plan|http://ketkisheth.weebly.com/|
3058701|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
3058702|NCT00317122|759346/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058703|NCT00317122|759346/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058704|NCT00317122|759346/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058705|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
3058706|NCT07161297||Study Protocol|https://www.humanitas-research.com/|Requests should be submitted to: ibd@humanitas.it Subject: REMI-IBD
3058707|NCT06379828||Study Protocol|https://newborn-health-standards.org/about/project-overview/|
3058708|NCT01697085||Clinical Study Report|http://www.maturitas.org/article/S0378-5122%2814%2900239-4/abstract?cc=y=|
3058709|NCT00730756|FFR111158|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058710|NCT00730756|FFR111158|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058711|NCT00730756|FFR111158|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058712|NCT00730756|FFR111158|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058713|NCT00730756|FFR111158|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058714|NCT00730756|FFR111158|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054132|NCT06935851||Study Protocol|https://osf.io|signing a data agreement
3054133|NCT00463437|109507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058715|NCT00730756|FFR111158|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051863|NCT01405924||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-030&kw=0517-030&tab=access|
3054134|NCT00463437|109507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054135|NCT00463437|109507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058716|NCT01495013|115317|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054136|NCT00463437|109507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054137|NCT00463437|109507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049810|NCT01039974|112648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049811|NCT01039974|112648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054138|NCT00463437|109507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054139|NCT00463437|109507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054140|NCT04457921|Mary Colleen Simonelli|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/30102886/|web site is provided
3054141|NCT01583036|116216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054142|NCT01583036|116216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054143|NCT01583036|116216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054144|NCT01583036|116216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054145|NCT01583036|116216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054146|NCT01583036|116216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054147|NCT01583036|116216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054148|NCT00942162|111476|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054149|NCT00942162|111476|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054150|NCT00942162|111476|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054151|NCT00942162|111476|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054152|NCT00942162|111476|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054153|NCT00942162|111476|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054154|NCT00942162|111476|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054155|NCT05446675|EC/EH/220608-SK|Individual Participant Data Set|https://ehs-hernia-registry.com|
3054156|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.
3054157|NCT00499707|712753/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054158|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
3054159|NCT00499707|712753/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054160|NCT00499707|712753/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054161|NCT00499707|712753/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054162|NCT00499707|712753/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054163|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
3054164|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.
3054165|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.
3054166|NCT00814710|111188|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054167|NCT00814710|111188|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054168|NCT00814710|111188|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054169|NCT00814710|111188|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054170|NCT00814710|111188|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049812|NCT01039974|112648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049813|NCT00290277|104951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054171|NCT00814710|111188|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054172|NCT00814710|111188|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056235|NCT01039961|113022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056236|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/31353554/|
3056237|NCT07067515||PMC article.|https://pubmed.ncbi.nlm.nih.gov/30734608/|
3056238|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/35508275/|
3051864|NCT02918916||Tables. Training program, Phototherapy parameters, Time point of outcomes|https://pt.scribd.com/document/325401697/Documents-ClinicalTrials-ID-2015-25219-0|
3051865|NCT01648140|115879|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051866|NCT01648140|115879|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051867|NCT01648140|115879|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051868|NCT01648140|115879|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051869|NCT01648140|115879|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051870|NCT01648140|115879|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051871|NCT01123083|115494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051872|NCT01123083|115494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051873|NCT01123083|115494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051874|NCT01123083|115494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051875|NCT01123083|115494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051876|NCT01123083|115494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051877|NCT01123083|115494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051878|NCT00688519|114741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051879|NCT00688519|114741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051880|NCT00688519|114741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051881|NCT00688519|114741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051882|NCT00688519|114741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056239|NCT00197249|270362/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056240|NCT00197249|270362/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051883|NCT00688519|114741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051884|NCT00688519|114741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051885|NCT04893213||Study Protocol|https://osf.io/yku5q/|Protocol on the Open Science Framework (OSF)
3051886|NCT04893213||Statistical Analysis Plan|https://osf.io/yku5q/|
3051887|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.
3056241|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
3056242|NCT00197249|270362/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049814|NCT00290277|104951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054173|NCT01009463|102871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054174|NCT01009463|102871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054175|NCT01009463|102871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054176|NCT01009463|102871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054177|NCT01009463|102871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054178|NCT01009463|102871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054179|NCT01009463|102871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054180|NCT00920543|SAM40086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054181|NCT00920543|SAM40086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054182|NCT00920543|SAM40086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054183|NCT00920543|SAM40086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054184|NCT00920543|SAM40086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054185|NCT00920543|SAM40086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054186|NCT00920543|SAM40086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054187|NCT00693706|110127|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054188|NCT00693706|110127|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054189|NCT00693706|110127|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054190|NCT00693706|110127|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054191|NCT00693706|110127|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054192|NCT00693706|110127|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054193|NCT00693706|110127|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054194|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
3054195|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
3049815|NCT00290277|104951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049816|NCT00290277|104951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049817|NCT00290277|104951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049818|NCT00290277|104951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049819|NCT00290277|104951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049820|NCT03075046||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
3049821|NCT00023244|SDY133|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
3049822|NCT00023244|SDY133|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
3049823|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
3049824|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.
3049825|NCT00135564|711202/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049826|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
3049827|NCT00135564|711202/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049828|NCT00135564|711202/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058717|NCT01495013|115317|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058718|NCT01495013|115317|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058719|NCT01495013|115317|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058720|NCT01495013|115317|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058721|NCT01495013|115317|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058722|NCT00445094||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058723|NCT01110057|113049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058724|NCT01110057|113049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051888|NCT00723450|SCA102833|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051889|NCT00723450|SCA102833|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051890|NCT00723450|SCA102833|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051891|NCT00723450|SCA102833|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051892|NCT00723450|SCA102833|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051893|NCT00723450|SCA102833|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051894|NCT00723450|SCA102833|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051895|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.
3051896|NCT07293052||Study Protocol|https://pdf.ac/0wrnmMTIc3|
3051897|NCT06729164|Open Science Framework|The study's relevant instructional context measures. Supporting materials include the assessment instrument, protocols, etc.|https://osf.io/eq5s8/overview|
3051898|NCT00465816|109063|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051899|NCT00465816|109063|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051900|NCT00465816|109063|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051901|NCT00465816|109063|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051902|NCT00465816|109063|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051903|NCT00465816|109063|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051904|NCT00465816|109063|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051905|NCT01831791|114264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051906|NCT01831791|114264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051907|NCT01831791|114264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051908|NCT01831791|114264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051909|NCT01831791|114264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051910|NCT01831791|114264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051911|NCT01831791|114264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051912|NCT02744521|Study protocol|Study Protocol|https://sites.google.com/site/relevantdocuments2016|I shared this protocol on Google Plus.
3051913|NCT00478738|MAB104958|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051914|NCT00478738|MAB104958|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051915|NCT00478738|MAB104958|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051916|NCT00478738|MAB104958|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051917|NCT00478738|MAB104958|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051918|NCT00478738|MAB104958|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056243|NCT00197249|270362/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056244|NCT01934205|116666|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056245|NCT01934205|116666|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049829|NCT00135564|711202/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056246|NCT01934205|116666|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056247|NCT01934205|116666|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056248|NCT01934205|116666|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056249|NCT01934205|116666|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056250|NCT01934205|116666|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049830|NCT00135564|711202/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056251|NCT05866263||Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/23405164/|
3056252|NCT05866263||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/23405164/|
3056253|NCT00294047|104820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056254|NCT00294047|104820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056255|NCT00294047|104820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056256|NCT00294047|104820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056257|NCT00294047|104820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056258|NCT00294047|104820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056259|NCT01494532|111569|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056260|NCT01494532|111569|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056261|NCT01494532|111569|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056262|NCT01494532|111569|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056263|NCT01494532|111569|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056264|NCT01494532|111569|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056265|NCT00196963|103532|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056266|NCT00196963|103532|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056267|NCT00196963|103532|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056268|NCT00196963|103532|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056269|NCT00196963|103532|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056270|NCT00429481|444563/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056271|NCT00429481|444563/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056272|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
3056273|NCT00429481|444563/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056274|NCT00429481|444563/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056275|NCT00429481|444563/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056276|NCT01717950||Clinical Study Report|https://smhs.gwu.edu/mitm-crg/|
3056277|NCT04748991||Product monograph - Vernakalant|https://pdf.hres.ca/dpd_pm/00038441.PDF|
3056278|NCT04748991||Product monograph - Amiodarone|https://pdf.hres.ca/dpd_pm/00035425.PDF|
3056279|NCT00985751|113171|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056280|NCT00985751|113171|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058725|NCT01110057|113049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058726|NCT01110057|113049|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058727|NCT01110057|113049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058728|NCT01110057|113049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058729|NCT01110057|113049|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051919|NCT00478738|MAB104958|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051920|NCT00202865||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051921|NCT00891176|112830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051922|NCT00891176|112830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051923|NCT00891176|112830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051924|NCT00891176|112830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051925|NCT00891176|112830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051926|NCT00891176|112830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058730|NCT07003204|msabry776@yahoo.com|Clinical Study Report|https://pmc.ncbi.nlm.nih.gov/articles/PMC8075197/|very good
3058731|NCT00652743|111443|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058732|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.
3058733|NCT00652743|111443|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058734|NCT00652743|111443|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058735|NCT00652743|111443|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058736|NCT00652743|111443|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058737|NCT01128569|113090|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058738|NCT01128569|113090|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051927|NCT00346151|SDY674|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674
3051928|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.
3051929|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
3051930|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.
3051931|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.
3051932|NCT00880477|217744/069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058739|NCT01128569|113090|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058740|NCT01128569|113090|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058741|NCT01128569|113090|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058742|NCT01128569|113090|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051933|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
3051934|NCT00880477|217744/069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051935|NCT00880477|217744/069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058743|NCT01128569|113090|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056281|NCT00985751|113171|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049831|NCT05377203|PMID: 37276913|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/37276913|
3049832|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.
3049833|NCT00679055||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0736-006&kw=0736-006&tab=access|
3049834|NCT00543543||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-001&kw=V503-001&tab=access|
3049835|NCT06934850||Clinical Study Report|https://etik.inonu.edu.tr/panel/index|
3056282|NCT00985751|113171|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056283|NCT00985751|113171|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056284|NCT00268216|SCO30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056285|NCT00268216|SCO30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056286|NCT00268216|SCO30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056287|NCT00268216|SCO30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049836|NCT01926015||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-060&kw=V260-060&tab=access|
3049837|NCT00857883|111314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049838|NCT00857883|111314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049839|NCT00857883|111314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049840|NCT00857883|111314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049841|NCT00857883|111314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049842|NCT00857883|111314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049843|NCT00857883|111314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049844|NCT07278141|Study Protocol ACTIVAM|Study Protocol|https://alumnossantotomas-my.sharepoint.com/:b:/g/personal/ivonnejorquera_santotomas_cl/EeBXjIa_2FBMivQW63r3zkQBXK4j0X4-TiOdpAqmw_w2sg?e=Fh6PcR|The study protocol is accessible to anyone with the link
3049845|NCT07278141|Ethics Committee Approval|Data Monitoring Committee Charter|https://alumnossantotomas-my.sharepoint.com/:b:/g/personal/ivonnejorquera_santotomas_cl/EfT4D7DeqWJKg0G9BoL0JEIBgmCcMobhIPrQMe2MeCZu0g?e=QlrDDK|The file is publicly available via link
3056288|NCT00268216|SCO30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056289|NCT00268216|SCO30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056290|NCT00268216|SCO30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056291|NCT01573819|115719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056292|NCT01573819|115719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056293|NCT01573819|115719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056294|NCT01573819|115719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056295|NCT01573819|115719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056296|NCT01573819|115719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056297|NCT01573819|115719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056298|NCT01989884||Clinical Study Report|https://doi.org/10.1007/s11060-019-03116-z|
3056299|NCT05341453||Study Protocol|https://www.chmirakl.cz/aktuality/study-protokol|
3056300|NCT05341453||Statistical Analysis Plan|https://www.chmirakl.cz/aktuality/statistical-analysis-plan|
3056301|NCT05341453||Informed Consent Form|https://www.chmirakl.cz/aktuality/type-informed-consent-form|
3056302|NCT03045458||Clinical Study Report|http://mc.manuscriptcentral.com/jperio|
3056303|NCT07138755||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/39489090/|
3056304|NCT00452348|ADA109057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056305|NCT00452348|ADA109057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051936|NCT00880477|217744/069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051937|NCT02916758||Individual Participant Data Set|http://grad.kean.edu/ot/faculty|Please contact cmulry@kean.edu to request the data set
3051938|NCT00327665|106068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051939|NCT00327665|106068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051940|NCT00327665|106068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051941|NCT00327665|106068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051942|NCT00327665|106068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051943|NCT00327665|106068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051944|NCT06783530||Study Protocol|https://dentfac.mans.edu.eg|Faculty of Dentistry, Mansoura University - Ethical Committee Information.
3051945|NCT01780298||Individual Participant Data Set|https://doi.org/10.12688/f1000research.11698.2|
3051946|NCT03343197||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3051947|NCT03343197||Study Protocol|https://clinicaltrials.servier.com/|
3051948|NCT03343197||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3051949|NCT03343197||Informed Consent Form|https://clinicaltrials.servier.com/|
3051950|NCT03343197||Clinical Study Report|https://clinicaltrials.servier.com/|
3051951|NCT03343197||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3051952|NCT01424397|111924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051953|NCT01424397|111924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051954|NCT01424397|111924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051955|NCT01424397|111924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051956|NCT01424397|111924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051957|NCT01424397|111924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051958|NCT01424397|111924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051959|NCT01607372|116392|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051960|NCT01607372|116392|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051961|NCT01607372|116392|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051962|NCT01607372|116392|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051963|NCT01607372|116392|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051964|NCT01607372|116392|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051965|NCT01607372|116392|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051966|NCT00687011||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3051967|NCT00126997|104020|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051968|NCT00126997|104020|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051969|NCT00126997|104020|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051970|NCT00126997|104020|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051971|NCT00126997|104020|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051972|NCT00126997|104020|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051973|NCT06972433||Study Protocol|http://www.scd.edu.pk|
3051974|NCT06973135||Statistical Analysis Plan|https://dent.alexu.edu.eg/index.php/ar/|
3051975|NCT00529516|109821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051976|NCT00529516|109821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051977|NCT00529516|109821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051978|NCT00529516|109821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054196|NCT07030387||Study Protocol|https://www.precis-2.org/Help/Documentation/Help|
3056306|NCT00452348|ADA109057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056307|NCT00452348|ADA109057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056308|NCT00452348|ADA109057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056309|NCT00452348|ADA109057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056310|NCT00452348|ADA109057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056311|NCT00533507|109861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056312|NCT00533507|109861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056313|NCT00533507|109861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056314|NCT00533507|109861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051979|NCT00529516|109821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051980|NCT00529516|109821|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051981|NCT00529516|109821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051982|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.
3051983|NCT01000597|113477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049846|NCT07278141|INFORMED CONSENT|Informed Consent Form|https://alumnossantotomas-my.sharepoint.com/:b:/g/personal/ivonnejorquera_santotomas_cl/ETTRNyC4tIpKgXo3bKwcG-EBWanx328fkqIPiudt0LoMvA?e=m8mMB6|
3049847|NCT06667661||NIH Reporter Information|https://reporter.nih.gov/search/w2y2LWuI50aTEgDfuqR7lg/project-details/11017278|Final Data set will be deposited into NICHD DASH database.
3049848|NCT00699764|208141/017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049849|NCT00699764|208141/017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049850|NCT00699764|208141/017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049851|NCT00699764|208141/017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049852|NCT00699764|208141/017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049853|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
3049854|NCT00289718|100556 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049855|NCT00289718|100556 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051984|NCT01000597|113477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051985|NCT01000597|113477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056315|NCT00533507|109861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056316|NCT00533507|109861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056317|NCT00533507|109861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056318|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)"
3056319|NCT05895435||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/12841881/|
3056320|NCT07254182||Individual Participant Data Set|https://zenodo.org/records/17255092|
3056321|NCT07254182||Study Protocol|https://zenodo.org/records/17255092|
3056322|NCT07254182||Statistical Analysis Plan|https://zenodo.org/records/17255092|
3056323|NCT06793592||More information on IPD sharing|https://osf.io/preprints/osf/6pwxe|
3056324|NCT00279045|49653/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056325|NCT00279045|49653/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056326|NCT00279045|49653/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056327|NCT00279045|49653/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056328|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
3056329|NCT00279045|49653/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056330|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
3056331|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"
3056332|NCT01119625|113266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051986|NCT01000597|113477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056333|NCT01119625|113266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056334|NCT01119625|113266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056335|NCT01119625|113266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056336|NCT01119625|113266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056337|NCT01119625|113266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056338|NCT01119625|113266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056339|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
3056340|NCT03221972||Study Protocol|http://www.chinanutri.cn/gzrw_132/zgjmyyyjkzkjcxm/201412/t20141229_108493.html|
3056341|NCT00377572|SDY211|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
3056342|NCT00377572|SDY211|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
3056343|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.
3056344|NCT00307541|105554|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056345|NCT00307541|105554|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056346|NCT00307541|105554|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056347|NCT00307541|105554|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056348|NCT00307541|105554|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056349|NCT00307541|105554|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056350|NCT00139815|103420|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056351|NCT00139815|103420|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056352|NCT00139815|103420|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051987|NCT01000597|113477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051988|NCT01000597|113477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051989|NCT01000597|113477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051990|NCT00704184||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-007&kw=7009-007&tab=access|
3051991|NCT05489250||Informed Consent Form|https://platon-network.de/contact|
3051992|NCT05489250||See Use & Access Regulation|https://platon-network.de/contact|
3051993|NCT00802464|112077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051994|NCT00802464|112077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051995|NCT00802464|112077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051996|NCT00802464|112077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051997|NCT00802464|112077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051998|NCT00802464|112077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3051999|NCT00802464|112077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052000|NCT04641741|FGBMEP202001|Study Protocol|https://www.idisantiago.es/|The study protocol was added to clinicaltrials.gov
3052001|NCT02439827||Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-015-2543-2|Study design paper
3052002|NCT02439827||Individual Participant Data Set|http://www.scielo.br/scielo.php?pid=S1980-00372016000200207&script=sci_arttext|Instrument validation study
3052003|NCT02439827||Individual Participant Data Set|http://journals.humankinetics.com/doi/abs/10.1123/jpah.2016-0113|Intervention results
3052004|NCT03181711||Study Protocol|http://mah.se|can be requested by mail Karin.Ridell@mah.se
3052005|NCT00000936|SDY354|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
3052006|NCT00000936|SDY354|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
3052007|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.
3052008|NCT04649008||Individual Participant Data Set|https://www.ieeg.org/|
3052009|NCT01808339|117156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052010|NCT01808339|117156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052011|NCT01808339|117156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052012|NCT01808339|117156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052013|NCT01808339|117156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052014|NCT01808339|117156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052015|NCT01808339|117156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052016|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.
3052017|NCT05179200||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08035-7|
3052018|NCT03997916||Individual Participant Data Set|http://redcap.uhhospitals.org/redcap|
3052019|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"
3054197|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.
3054198|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.
3054199|NCT01362322|114778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054200|NCT01362322|114778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054201|NCT01362322|114778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054202|NCT01362322|114778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054203|NCT01362322|114778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054204|NCT01362322|114778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054205|NCT06961422|0009-0009-61|Individual Participant Data Set|https://orcid.org/0009-0009-6142-6201|
3054206|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.
3054207|NCT01857895|200016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054208|NCT01857895|200016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054209|NCT01857895|200016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054210|NCT01857895|200016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054211|NCT01857895|200016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052020|NCT00123903|COR103560|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052021|NCT00123903|COR103560|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054212|NCT01857895|200016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054213|NCT01857895|200016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054214|NCT07228520|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
3054215|NCT07228520|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
3054216|NCT04406038|ID|Individual Participant Data Set|http://github.com/eusporg/spb_covid_study20|Please consult with the README.md for the repository.
3054217|NCT01972425||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1442-x|
3054218|NCT05957562|orcid.org/0000-0003-0558-6402|Study Protocol|http://orcid.org/0000-0003-0558-6402|
3054219|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.
3054220|NCT00971321|113462|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054221|NCT00971321|113462|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054222|NCT00971321|113462|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049856|NCT00289718|100556 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049857|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.
3054223|NCT00971321|113462|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054224|NCT00971321|113462|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056353|NCT00139815|103420|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056354|NCT00139815|103420|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056355|NCT00139815|103420|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056356|NCT00139815|103420|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056357|NCT01873339|115678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056358|NCT01873339|115678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056359|NCT01873339|115678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056360|NCT01873339|115678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056361|NCT01873339|115678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056362|NCT01873339|115678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056363|NCT01873339|115678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056364|NCT00224484|208141/040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056365|NCT00224484|208141/040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056366|NCT00224484|208141/040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056367|NCT00224484|208141/040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056368|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
3056369|NCT00224484|208141/040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056370|NCT00346892|444563/014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056371|NCT00346892|444563/014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056372|NCT00346892|444563/014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056373|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
3056374|NCT00346892|444563/014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056375|NCT00346892|444563/014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056376|NCT00633022|PM1111138|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054225|NCT00971321|113462|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054226|NCT00971321|113462|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054227|NCT04160403||Study Protocol|https://www.ncbi.nlm.nih.gov/|
3054228|NCT04936672||Study Protocol|https://doi.org/10.1249/MSS.0b013e318213fefb|The protocol setting and data collection process is based on this reference
3054229|NCT00474253||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054230|NCT03407391||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data is available for use by researchers on application through the website
3054231|NCT04752787||Study Protocol|http://files.eric.ed.gov/fulltext/EJ1086361.pdf|
3054232|NCT04752787||Study Protocol|https://mhealth.jmir.org/2018/4/e109/|
3054233|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.
3054234|NCT00196937|103514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054235|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.
3054236|NCT00196937|103514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054237|NCT00196937|103514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054238|NCT00196937|103514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054239|NCT00196937|103514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054240|NCT00196937|103514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054241|NCT00410371|LBI108614|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054242|NCT00410371|LBI108614|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054243|NCT00410371|LBI108614|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054244|NCT00410371|LBI108614|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054245|NCT00410371|LBI108614|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054246|NCT00410371|LBI108614|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054247|NCT00410371|LBI108614|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054248|NCT00984659|112989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054249|NCT00984659|112989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054250|NCT00984659|112989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054251|NCT00984659|112989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054252|NCT00984659|112989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054253|NCT00984659|112989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054254|NCT00984659|112989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054255|NCT02525224|DOI: 10.1111/jocd.12295|Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1111/jocd.12295/full|
3054256|NCT05700344||Summary of Product Characteristics|https://www.ema.europa.eu/en/documents/product-information/bavencio-epar-product-information_en.pdf|Summary of Product Characteristics
3054257|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
3054258|NCT01516450|116119|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054259|NCT01516450|116119|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054260|NCT01516450|116119|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054261|NCT01516450|116119|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054262|NCT01516450|116119|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054263|NCT01516450|116119|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056377|NCT00633022|PM1111138|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056378|NCT00633022|PM1111138|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056379|NCT00633022|PM1111138|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056380|NCT00633022|PM1111138|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056381|NCT00633022|PM1111138|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056382|NCT00633022|PM1111138|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056383|NCT05583097||Study Protocol|https://www.gu.se/forskning/tyreoideacancer|
3052022|NCT00123903|COR103560|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052023|NCT00123903|COR103560|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052024|NCT00123903|COR103560|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052025|NCT00123903|COR103560|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052026|NCT00123903|COR103560|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052027|NCT01673555|116008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052028|NCT01673555|116008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052029|NCT01673555|116008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056384|NCT01192776||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25536254|
3056385|NCT01706263|114551|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056386|NCT01706263|114551|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056387|NCT01706263|114551|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056388|NCT01706263|114551|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056389|NCT01706263|114551|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056390|NCT01706263|114551|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056391|NCT02416180|201909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052030|NCT01673555|116008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052031|NCT01673555|116008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052032|NCT01673555|116008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052033|NCT01673555|116008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052034|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|
3052035|NCT05782231|VIV0001019|Individual Participant Data Set|https://doi.org/10.25934/PR00010109|
3052036|NCT05909618||Nature Communications manuscript|https://www.nature.com/articles/s41467-021-22186-0|
3052037|NCT00314860|101468/204|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052038|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
3052039|NCT00314860|101468/204|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056392|NCT02416180|201909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052040|NCT00314860|101468/204|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052041|NCT00314860|101468/204|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052042|NCT00314860|101468/204|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052043|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
3052044|NCT07048717||General information about the study plus information about application for data|https://www.umu.se/en/research/groups/the-mauritius-study/|
3052045|NCT07065084|dilek.cecen@cbu.edu.tr|Clinical Study Report|https://cdn.clinicaltrials.gov/large-docs/02/NCT04069702/ICF_000.pdf|
3052046|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
3052047|NCT03172468||Informed Consent Form|https://box.medunigraz.at/s/QuTYym3xsqXybWI|
3052048|NCT03172468||Study Protocol|https://box.medunigraz.at/s/YbufqAn3DBI1f4Q|
3056393|NCT02416180|201909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056394|NCT02416180|201909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056395|NCT02416180|201909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056396|NCT02416180|201909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056397|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.
3056398|NCT00296530|ADA103578|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056399|NCT00296530|ADA103578|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056400|NCT00296530|ADA103578|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056401|NCT00296530|ADA103578|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056402|NCT00296530|ADA103578|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056403|NCT00296530|ADA103578|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056404|NCT00296530|ADA103578|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056405|NCT00333450|106623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052049|NCT07217600||Study Protocol|https://www.chictr.org.cn/showproj.html?proj=253510|
3052050|NCT01017146|114575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052051|NCT01017146|114575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052052|NCT01017146|114575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052053|NCT01017146|114575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052054|NCT01017146|114575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054264|NCT01516450|116119|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054265|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.
3054266|NCT00000530||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rts/|
3054267|NCT00000530||Study Forms|http://biolincc.nhlbi.nih.gov/studies/rts/|
3054268|NCT00945750||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0208-144&kw=0208-144&tab=access|
3054269|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.
3054270|NCT00283712|SDY655|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|ImmPort study identifier is SDY655
3054271|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
3054272|NCT01367743||Statistical Analysis Plan|http://cic-p-nancy.fr/wp-content/uploads/2019/01/revUS_SAP_OPTIMA_CC_KD_NG.pdf|
3054273|NCT00440128|NKV100781|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054274|NCT00440128|NKV100781|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054275|NCT00440128|NKV100781|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054276|NCT00440128|NKV100781|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054277|NCT00440128|NKV100781|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054278|NCT00440128|NKV100781|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054279|NCT00440128|NKV100781|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054280|NCT03136705|STU00089165|Study Protocol|https://irb.northwestern.edu/contact|
3054281|NCT03136705|STU00089165|Informed Consent Form|https://irb.northwestern.edu/contact|
3054282|NCT01097616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-028&kw=4305-028&tab=access|
3054283|NCT02345161|116853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054284|NCT02345161|116853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054285|NCT02345161|116853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054286|NCT02345161|116853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054287|NCT02345161|116853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054288|NCT02345161|116853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054289|NCT02345161|116853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054290|NCT00126451||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054291|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
3054292|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/22607780/|Dysfunctional movement patterns are directly related to the mechanism of injury
3054293|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
3054294|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.
3052055|NCT01017146|114575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052056|NCT01017146|114575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052057|NCT00976105|111849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052058|NCT00976105|111849|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052059|NCT00976105|111849|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052060|NCT00976105|111849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052061|NCT00976105|111849|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052062|NCT00976105|111849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052063|NCT04119284||Informed Consent Form|http://irbnet.org|The Informed consent form can be obtained while the patient is seen for scoliosis at Nemours-AIDHC.
3052064|NCT07214896|De-identified biometric audit|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
3052065|NCT07214896|ESG compliance logs|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
3052066|NCT07214896|Wage token minting and transfe|Individual Participant Data Set|https://truwayhealth.com|truwayhealth.com
3052067|NCT07214896|SHA-256 notarized study protoc|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3052068|NCT07214896|Statistical analysis plan (SAP|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3052069|NCT07214896|Informed consent form (ICF)|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3052070|NCT07214896|Clinical study report (CSR)|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3052071|NCT07214896|Analytic code for biometric sc|Individual Participant Data Set|https://www.truwayhealth.com|truwayhealth.com
3052072|NCT00792636|110948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052073|NCT00792636|110948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052074|NCT00792636|110948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052075|NCT00792636|110948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052076|NCT00792636|110948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052077|NCT00792636|110948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052078|NCT00792636|110948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052079|NCT00611559|110478|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052080|NCT00611559|110478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052081|NCT00611559|110478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052082|NCT00611559|110478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052083|NCT00611559|110478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052084|NCT00611559|110478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052085|NCT00611559|110478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052086|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)
3052087|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)
3052088|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)
3052089|NCT03739450|602d|Individual Participant Data Set|https://www.tbindsc.org/StaticFiles/SOP/602d%20-%20External%20Use%20TBIMS%20National%20Database%20Notification.pdf|
3052090|NCT03111290||Summary Data Set|http://dx.doi.org/10.5281/zenodo.45811|Dataset supporting Alagapan et al. 2016 PLoS Biology
3052091|NCT02073994||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3052092|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
3052093|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
3056406|NCT00333450|106623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056407|NCT00333450|106623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052094|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
3052095|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
3056408|NCT00333450|106623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056409|NCT00333450|106623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056410|NCT00333450|106623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056411|NCT03211039|37114|Individual Participant Data Set|http://view.ncbi.nlm.nih.gov/dbgap-controlled|
3056412|NCT03211039|37114|Summary level phenotype data|http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs002094.v1.p1|
3056413|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|
3056414|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.
3056415|NCT00000516||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/solvd/|
3056416|NCT00000516||Study Forms|http://biolincc.nhlbi.nih.gov/studies/solvd/|
3056417|NCT00000516||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/solvd/|
3052096|NCT03423303||Statistical Analysis Plan|https://bmjopen.bmj.com/content/bmjopen/14/1/e075595.full.pdf|
3052097|NCT06795880||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/33062451/|
3052098|NCT06791993||Individual Participant Data Set|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op
3052099|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
3052100|NCT05147155|10.1183/23120541.00939-2024|Clinical Study Report|https://publications.ersnet.org/content/erjor/early/2024/11/21/2312054100939-2024|Kotsiou Ourania S., Kirgou Paraskevi, Siachpazidou Dimitra, Bartziokas Konstantinos, Tourlakopoulos Konstantinos, Malli Foteini, Pinaka Maria, Daniil Zoe, Gourgoulianis Konstantinos I. Early benefit of mepolizumab on small airways in severe asthma: insights from IMPOSE study. ERJ Open Research 2024 00939-2024; DOI: https://doi.org/10.1183/23120541.00939-2024
3052101|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.
3052102|NCT02240472||Study Protocol|http://senomac.se/Home/study%20protocol.html|Study protocol and patient information (English)
3056418|NCT07254273|The individual participant dat|Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1ZN1TbLb_kPid_fZNsQVWYNu02qO5s-mv/edit?usp=sharing&ouid=107542558214893941575&rtpof=true&sd=true|https://docs.google.com/spreadsheets/d/1ZN1TbLb\_kPid\_fZNsQVWYNu02qO5s-mv/edit?usp=sharing\&ouid=107542558214893941575\&rtpof=true\&sd=true
3057378|NCT01424514|114974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052103|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
3052104|NCT06447519||Study Protocol|https://ikee.lib.auth.gr|https://ikee.lib.auth.gr
3056419|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.
3056420|NCT00000555||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/wave/|
3056421|NCT00000555||Study Forms|http://biolincc.nhlbi.nih.gov/studies/wave/|
3056422|NCT00000555||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/wave/|
3056423|NCT00363857|101468/249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056424|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
3056425|NCT00363857|101468/249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056426|NCT00363857|101468/249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056427|NCT00363857|101468/249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056428|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
3056429|NCT00363857|101468/249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056430|NCT00396630|106260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052105|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
3056431|NCT00396630|106260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056432|NCT00396630|106260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056433|NCT00396630|106260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056434|NCT00396630|106260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056435|NCT00396630|106260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056436|NCT00396630|106260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054295|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
3056437|NCT00139932||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3056438|NCT00108082|COR100216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056439|NCT00108082|COR100216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056440|NCT00108082|COR100216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056441|NCT00108082|COR100216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056442|NCT00108082|COR100216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056443|NCT00108082|COR100216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056444|NCT00108082|COR100216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056445|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
3056446|NCT06899438||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/tezDetay.jsp?id=ojJkM_gxQRaH4Sn9fMdQWw&no=8WIZbpBlZOGWvkUUwksxFg|
3056447|NCT00743860|LPL112498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056448|NCT00743860|LPL112498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056449|NCT00743860|LPL112498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056450|NCT00743860|LPL112498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056451|NCT00743860|LPL112498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056452|NCT00743860|LPL112498|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056453|NCT00743860|LPL112498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056454|NCT02724826||Clinical Study Report|http://resolver.ebscohost.com/openurl?sid=Entrez%3aPubMed&id=pmid%3a18090079&site=ftf-live|
3056455|NCT00129116|792014/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056456|NCT00129116|792014/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056457|NCT00129116|792014/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052106|NCT04522375||Study Protocol|http://clinicaltrials.gov|clinicaltrials.gov
3052107|NCT04522375||Statistical Analysis Plan|http://clinicaltrials.gov|clinicaltrials.gov
3052108|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
3052109|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.
3052110|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.
3052111|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.
3052112|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.
3052113|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.
3054296|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
3054297|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
3054298|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
3056458|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
3056459|NCT00129116|792014/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056460|NCT01039454|109710|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056461|NCT01039454|109710|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056462|NCT01039454|109710|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056463|NCT01039454|109710|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056464|NCT01039454|109710|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056465|NCT01039454|109710|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056466|NCT01077505|107032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056467|NCT01077505|107032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056468|NCT01077505|107032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056469|NCT01077505|107032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056470|NCT01077505|107032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052114|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.
3052115|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.
3052116|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.
3052117|NCT02132936||Clinical Study Report|https://www.leopharmatrials.com/en|Clinical Trials at LEO Pharma
3052118|NCT06830330||ethics committee approval|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
3052119|NCT03060421||Study Protocol|http://www.parkerinst.dk|
3052120|NCT06786429||Clinical Study Report|https://www.nust.ac.zw|
3052121|NCT06786429|tba|Clinical Study Report|https://www.nust.ac.zw|
3052122|NCT06188754||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/38762486/|
3052123|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
3052124|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
3052125|NCT05459688||Trial Results Summary|https://www.trialsummaries.com/Study/StudyDetails?id=25790&tenant=MT_MED_9011|Trial Results Summary
3052126|NCT04979351||Review|https://dergipark.org.tr/tr/download/article-file/117117|
3052127|NCT04979351||Clinical Study Report|https://dergipark.org.tr/tr/download/article-file/29524|
3052128|NCT06852430|042025201171|Study Protocol|https://docs.google.com/document/d/18-WWwL8l_EB2nHv4wr1-Q1cslJ1VUYUf/edit?usp=drivesdk&ouid=111849282554145262325&rtpof=true&sd=true|
3052129|NCT06272903|MBRU IRB-2023-228|Study Protocol|http://www.mbru.ac.ae|
3052130|NCT02733159||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/PePS2/index.aspx|
3052131|NCT06836102|drmostafanasr1988@gmail.com|Study Protocol|https://doi.org/10.1016/j.hermed.2021.100468|
3052132|NCT07063940||Study Protocol|http://www.birmingham.ac.uk/ExaLT|
3052133|NCT07063940||Informed Consent Form|http://www.birmingham.ac.uk/ExaLT|
3052134|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
3056471|NCT01077505|107032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056472|NCT01077505|107032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056473|NCT01098539|114130|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056474|NCT01098539|114130|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052135|NCT06821919|2022-09-22_012059|Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
3052136|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"
3052137|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"
3052138|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"
3052139|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"
3052140|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"
3052141|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"
3052142|NCT01385189||Clinical Study Report|http://smhs.gwu.edu/mitm-crg/clinical-trials|
3052143|NCT05989685||Statistical Analysis Plan|https://osf.io/dmyuq/files/osfstorage/67cb0a2098ee14b2b7fd7157|Statistical Analysis Plan available in OSF.
3052144|NCT06814223||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
3052145|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).
3056475|NCT01098539|114130|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056476|NCT01098539|114130|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056477|NCT01098539|114130|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056478|NCT01098539|114130|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056479|NCT01098539|114130|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056480|NCT00725764|MET111646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056481|NCT00725764|MET111646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056482|NCT00725764|MET111646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056483|NCT00725764|MET111646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056484|NCT00725764|MET111646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056485|NCT00725764|MET111646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056486|NCT00725764|MET111646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056487|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.
3056488|NCT00489099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3056489|NCT00197080|101468/205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056490|NCT00197080|101468/205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056491|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
3056492|NCT00197080|101468/205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056493|NCT00197080|101468/205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056494|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
3056495|NCT00197080|101468/205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056496|NCT00476307|110221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056497|NCT00476307|110221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056498|NCT00476307|110221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056499|NCT00476307|110221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056500|NCT00476307|110221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056501|NCT00476307|110221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056502|NCT00476307|110221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056503|NCT01956487|116371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056504|NCT01956487|116371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056505|NCT01956487|116371|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056506|NCT01956487|116371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056507|NCT01956487|116371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056508|NCT01956487|116371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052146|NCT06817746||Study Protocol|https://www.fsm.unipi.it|
3052147|NCT06805448|2024-516715-25-00|Study Protocol|https://euclinicaltrials.eu/|
3052148|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"
3052149|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
3052150|NCT05591924||C3RP Laboratory Website|https://c3rp.org/leligdowiczlab|
3052151|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
3056509|NCT01956487|116371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056510|NCT00784134|Data repository-VISTA|Data repository-VISTA|http://vista.gla.ac.uk|when available
3056511|NCT00784134||Study Protocol|http://vista.gla.ac.uk|when available
3056512|NCT00784134||Statistical Analysis Plan|http://vista.gla.ac.uk|when available
3056513|NCT00480324|107625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056514|NCT00480324|107625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056515|NCT00480324|107625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056516|NCT00480324|107625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056517|NCT00480324|107625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056518|NCT00480324|107625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056519|NCT00480324|107625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056520|NCT02940678|10.6084/m9.figshare.4042572.v1|Study Protocol|https://dx.doi.org/10.6084/m9.figshare.4042572.v1|
3056521|NCT00792623|208133/178|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056522|NCT00792623|208133/178|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056523|NCT00792623|208133/178|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056524|NCT00792623|208133/178|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056525|NCT00792623|208133/178|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056526|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
3056527|NCT02369120||Study Protocol|http://www.biomedcentral.com/1472-6947/15/97|
3056528|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
3056529|NCT00749411|DB1111581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056530|NCT00749411|DB1111581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056531|NCT00749411|DB1111581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056532|NCT00749411|DB1111581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056533|NCT00749411|DB1111581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056534|NCT00749411|DB1111581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056535|NCT00749411|DB1111581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052152|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
3056536|NCT04828434||International Cognitive Stimulation Therapy Centre Website|http://www.ucl.ac.uk/international-cognitive-stimulation-therapy|
3056537|NCT02502734|107112|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056538|NCT02502734|107112|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056539|NCT02502734|107112|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056540|NCT02502734|107112|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056541|NCT02502734|107112|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056542|NCT02502734|107112|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056543|NCT02502734|107112|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056544|NCT00964106|112684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056545|NCT00964106|112684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056546|NCT00964106|112684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056547|NCT00964106|112684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056548|NCT00964106|112684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056549|NCT00964106|112684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056550|NCT00964106|112684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056551|NCT06290219||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
3056552|NCT01043926||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-017&kw=4305-017&tab=access|
3056553|NCT00240617|TRX103635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056554|NCT00240617|TRX103635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056555|NCT00240617|TRX103635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056556|NCT00240617|TRX103635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056557|NCT00240617|TRX103635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056558|NCT00240617|TRX103635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056559|NCT00240617|TRX103635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056560|NCT00109486|FFR101747|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056561|NCT00109486|FFR101747|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056562|NCT00109486|FFR101747|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056563|NCT00109486|FFR101747|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056564|NCT00109486|FFR101747|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056565|NCT00109486|FFR101747|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056566|NCT00109486|FFR101747|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056567|NCT02682147|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
3056568|NCT00296491|ADA103575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056569|NCT00296491|ADA103575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056570|NCT00296491|ADA103575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056571|NCT00296491|ADA103575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056572|NCT00296491|ADA103575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056573|NCT00296491|ADA103575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056574|NCT00296491|ADA103575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056575|NCT01577693|115148|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056576|NCT01577693|115148|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056577|NCT01577693|115148|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056578|NCT01577693|115148|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056579|NCT01577693|115148|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056580|NCT01577693|115148|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056581|NCT01577693|115148|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056582|NCT01294566|114422|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052153|NCT06824558|Fear of Childbirth Scale|Individual Participant Data Set|https://gcris.pau.edu.tr/bitstream/11499/6124/1/7ba3f584-23f9-4af0-9a4a-56f72570f94d.pdf|
3052154|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.
3056583|NCT01294566|114422|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056584|NCT01294566|114422|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056585|NCT01294566|114422|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056586|NCT01294566|114422|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056587|NCT01294566|114422|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056588|NCT01294566|114422|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056589|NCT07280546||Study Protocol|https://www.vghtpe.gov.tw/Index.action|The study protocol describing the methodology of electronic auscultation of breath sounds during anesthesia will be available. De-identified respiratory sound data and related analysis scripts may be shared upon reasonable request to the principal investigator.
3056590|NCT07279909||Main reference|https://diabetes.org/|it is the main reference used to identify definitions of the Diabetes \& its complications
3056591|NCT01797926|116799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056592|NCT01797926|116799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056593|NCT01797926|116799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056594|NCT01797926|116799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056595|NCT01797926|116799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056596|NCT01797926|116799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056597|NCT01797926|116799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056598|NCT01267006|114922|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052155|NCT06883916|Ethics Committee Approval|Informed Consent Form|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
3052156|NCT06824922|Protocolo_ECA_piloto|Study Protocol|https://drive.google.com/file/d/1PhNe1G9PVs2FkOmKeyXazMLW3l-sxRR7/view?usp=sharing|
3052157|NCT06863207||Individual Participant Data Set|https://vivli.org/|
3052158|NCT06744946|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3052159|NCT06997874|COMBAT trial|Study Protocol|https://nictu.hscni.net/service/combat/|
3052160|NCT02415933||Study Protocol|https://knowledge.uchicago.edu/handle/11417/69|
3052161|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
3056599|NCT01267006|114922|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052162|NCT06886594||Study Protocol|https://bap.ksu.edu.tr/|
3052163|NCT06881381||Study Protocol|https://docs.google.com/document/d/19ZwAv6y0UUaSa_Hjb3jlzuhMfTro0Y6p/edit?usp=drive_link&ouid=101334879348395838064&rtpof=true&sd=true|STUDY PROTOKOL DIAGRAM
3056600|NCT01267006|114922|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056601|NCT01267006|114922|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056602|NCT01267006|114922|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056603|NCT01267006|114922|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056604|NCT01267006|114922|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056605|NCT01466322|114919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056606|NCT01466322|114919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056607|NCT01466322|114919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056608|NCT01466322|114919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056609|NCT01466322|114919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056610|NCT01466322|114919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056611|NCT01466322|114919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056612|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
3056613|NCT02662231||Study Protocol|http://globalsurg.org/globalsurg-2-protocol/|GlobalSurg-II Study Protocol: available in multiple languages
3056614|NCT05917691||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
3056615|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
3056616|NCT00333723|49653/143|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056617|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
3056618|NCT00333723|49653/143|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056619|NCT00333723|49653/143|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056620|NCT00333723|49653/143|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056621|NCT00333723|49653/143|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056622|NCT02119286|200110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056623|NCT02119286|200110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056624|NCT02119286|200110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056625|NCT02119286|200110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056626|NCT02119286|200110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056627|NCT02119286|200110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056628|NCT02119286|200110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056629|NCT00289757|100576 (Y11)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056630|NCT00289757|100576 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056631|NCT00289757|100576 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056632|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
3056633|NCT00289757|100576 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056634|NCT00289757|100576 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056635|NCT00158756|104021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056636|NCT00158756|104021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056637|NCT00158756|104021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056638|NCT00158756|104021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056639|NCT00158756|104021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056640|NCT00158756|104021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056641|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
3056642|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|
3056643|NCT02006537|117023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052165|NCT04098276|10.1186/s12889-021-11930-2|Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-021-11930-2|
3052166|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
3052167|NCT06692621|Yöktez|Individual Participant Data Set|https://tez.yok.gov.tr/UlusalTezMerkezi/tezlerim.jsp?sira=0|You can reach us at harunzengin71@gmail.com
3054299|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
3056644|NCT02006537|117023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056645|NCT02006537|117023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056646|NCT02006537|117023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056647|NCT02006537|117023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056648|NCT02006537|117023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056649|NCT02006537|117023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056650|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
3056651|NCT00316147|104005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056652|NCT00316147|104005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056653|NCT00316147|104005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056654|NCT00316147|104005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056655|NCT00316147|104005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056656|NCT00316147|104005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056657|NCT01849016|Version 7.0 - 5/31/2016|Statistical Analysis Plan|http://www2.hematologie-amc.nl/nac_studie|
3056658|NCT00306943|104745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056659|NCT00306943|104745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056660|NCT00306943|104745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056661|NCT00306943|104745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056662|NCT00306943|104745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056663|NCT03182582||Study Protocol|https://eprotocol.stanford.edu/|
3054300|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
3056664|NCT01195792|111850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056665|NCT01195792|111850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056666|NCT01195792|111850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056667|NCT01195792|111850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056668|NCT01195792|111850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054301|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.
3056669|NCT01195792|111850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056670|NCT01195792|111850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056671|NCT00929331|110586|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056672|NCT00929331|110586|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056673|NCT00929331|110586|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056674|NCT00929331|110586|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056675|NCT00929331|110586|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056676|NCT00929331|110586|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056677|NCT00929331|110586|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056678|NCT00048204|NKD20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056679|NCT00048204|NKD20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056680|NCT00048204|NKD20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056681|NCT00048204|NKD20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056682|NCT00048204|NKD20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056683|NCT00048204|NKD20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056684|NCT00048204|NKD20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056685|NCT00144911|SCO40043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056686|NCT00144911|SCO40043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056687|NCT00144911|SCO40043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056688|NCT00144911|SCO40043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056689|NCT00144911|SCO40043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056690|NCT00144911|SCO40043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056691|NCT00144911|SCO40043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057379|NCT01424514|114974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057380|NCT01424514|114974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057381|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.
3057382|NCT00005276||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/access|
3057383|NCT00005276||Study Forms|http://biolincc.nhlbi.nih.gov/studies/access|
3057384|NCT00005276||Procedures Manual|http://biolincc.nhlbi.nih.gov/studies/access|
3057385|NCT03228316||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/27208713|
3057386|NCT00035295||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057387|NCT01899742|116960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057388|NCT01899742|116960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057389|NCT01899742|116960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057390|NCT01899742|116960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057391|NCT01899742|116960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058744|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).
3058745|NCT07150442||Study Protocol|https://bit.ly/45NuVGB|https://bit.ly/45NuVGB
3057392|NCT01899742|116960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056692|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.
3056693|NCT00169481|103488|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056694|NCT00169481|103488|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056695|NCT00169481|103488|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056696|NCT00169481|103488|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056697|NCT00169481|103488|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056698|NCT00307034|105539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056699|NCT00307034|105539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056700|NCT00307034|105539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056701|NCT00307034|105539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056702|NCT00307034|105539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056703|NCT00307034|105539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056704|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"
3056705|NCT03324321||Funder|http://dunhillmedical.org.uk/|Dunhill RTF Grant (RTF97/0117)
3056706|NCT00763438|2007-002160-10|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-002160-10/results|
3056707|NCT00069836|712753/009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056708|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
3056709|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
3056710|NCT00069836|712753/009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056711|NCT00069836|712753/009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056712|NCT00069836|712753/009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056713|NCT00069836|712753/009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056714|NCT00197288|104437|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056715|NCT00197288|104437|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056716|NCT00197288|104437|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056717|NCT00197288|104437|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056718|NCT00197288|104437|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056719|NCT00197288|104437|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056720|NCT00197288|104437|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056721|NCT00117325|FFR30006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056722|NCT00117325|FFR30006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056723|NCT00117325|FFR30006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056724|NCT00117325|FFR30006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056725|NCT00117325|FFR30006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056726|NCT00117325|FFR30006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056727|NCT00117325|FFR30006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056728|NCT00548171|110804|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056729|NCT00548171|110804|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056730|NCT00548171|110804|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056731|NCT00548171|110804|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056732|NCT00548171|110804|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056733|NCT00548171|110804|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056734|NCT00548171|110804|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056735|NCT00541970|110659|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056736|NCT00541970|110659|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056737|NCT00541970|110659|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056738|NCT00541970|110659|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056739|NCT00541970|110659|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056740|NCT00541970|110659|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056741|NCT00541970|110659|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056742|NCT00273039|NKF100110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056743|NCT00273039|NKF100110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056744|NCT00273039|NKF100110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056745|NCT00273039|NKF100110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056746|NCT00273039|NKF100110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056747|NCT00273039|NKF100110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056748|NCT00273039|NKF100110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056749|NCT03274882||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3056750|NCT03274882||Study Protocol|https://clinicaltrials.servier.com/|
3056751|NCT03274882||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3056752|NCT03274882||Informed Consent Form|https://clinicaltrials.servier.com/|
3056753|NCT03274882||Clinical Study Report|https://clinicaltrials.servier.com/|
3056754|NCT03274882||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3056755|NCT03762486||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/citmatch|
3056756|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.
3056757|NCT00000476||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dig/|
3056758|NCT00000476||Study Forms|http://biolincc.nhlbi.nih.gov/studies/dig/|
3056759|NCT01335997||CSR Synsopsi Link|http://www.merck.com/clinical-trials/study.html?id=0524B-143&kw=0524B-143&tab=access|
3056760|NCT00811356|111319|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056761|NCT00811356|111319|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056762|NCT00811356|111319|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056763|NCT00811356|111319|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056764|NCT00811356|111319|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056765|NCT00811356|111319|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056766|NCT00811356|111319|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056767|NCT01711463|115199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056768|NCT01711463|115199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056769|NCT01711463|115199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056770|NCT01711463|115199|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056771|NCT01711463|115199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056772|NCT01711463|115199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056773|NCT01711463|115199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056774|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.
3056775|NCT02904824||Clinical Study Report|http://www.dynasolutions.com|CRO data base
3056776|NCT00196924|580299/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056777|NCT00196924|580299/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056778|NCT00196924|580299/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056779|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.
3056780|NCT00196924|580299/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056781|NCT00196924|580299/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056782|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
3052168|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.
3052169|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.
3056783|NCT04838522||Breast Milk At the Dawn of New Discoveries|https://betterbeginnings.org/what-we-do/research/breast-milk/|
3056784|NCT02664935||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/lung-matrix/index.aspx|
3056785|NCT00883909|103094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056786|NCT00883909|103094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052170|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.
3056787|NCT00883909|103094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056788|NCT00883909|103094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056789|NCT00883909|103094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056790|NCT00883909|103094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056791|NCT00883909|103094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056792|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"
3056793|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
3056794|NCT00258700|103974 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056795|NCT00258700|103974 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056796|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
3056797|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
3056798|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
3056799|NCT06613204||data set|http://www.ohsu.edu/alzheimers-disease-research-center/data-resources|
3056800|NCT00678886|115495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056801|NCT00678886|115495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056802|NCT00678886|115495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056803|NCT00678886|115495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056804|NCT00678886|115495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056805|NCT00678886|115495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056806|NCT00678886|115495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056807|NCT00474266|109670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056808|NCT00474266|109670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056809|NCT00474266|109670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056810|NCT00474266|109670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056811|NCT00474266|109670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056812|NCT00474266|109670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056813|NCT00474266|109670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056814|NCT06982014|lecturer|Individual Participant Data Set|https://kocaelisaglik.edu.tr/|
3056815|NCT00426361|108464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056816|NCT00426361|108464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056817|NCT00426361|108464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056818|NCT00426361|108464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056819|NCT00426361|108464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052171|NCT06762756||Analytic Code|https://osf.io/v5deq/?view_only=d5dd1f5903a0480d94402c7c6528c6a4|Scripts are available on Open Science Framework
3052172|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
3052173|NCT06744270|Inonu University Clinical Rese|Clinical Study Report|https://www.inonu.edu.tr/klinik.etik|https://www.inonu.edu.tr/klinik.etik
3056820|NCT00426361|108464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056821|NCT00426361|108464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058746|NCT00325143|217744/100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058747|NCT00325143|217744/100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058748|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
3058749|NCT00325143|217744/100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058750|NCT00325143|217744/100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058751|NCT00325143|217744/100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058752|NCT00421148||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058753|NCT03150264||Study Protocol|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161575/|
3058754|NCT01978145|115646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058755|NCT01978145|115646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058756|NCT01978145|115646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058757|NCT01978145|115646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058758|NCT01978145|115646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058759|NCT01978145|115646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058760|NCT01978145|115646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058761|NCT03750019|10.5255/UKDA-SN-853370|Individual Participant Data Set|http://dx.doi.org/10.5255/UKDA-SN-853370|
3058762|NCT03750019|10.17605/OSF.IO/WYCKJ|Study Protocol|https://doi.org/10.17605/OSF.IO/WYCKJ|
3058763|NCT00335881|106745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058764|NCT00335881|106745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058765|NCT00335881|106745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058766|NCT00335881|106745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058767|NCT00335881|106745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058768|NCT00335881|106745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058769|NCT00688467||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05363&kw=P05363&tab=access|
3058770|NCT01436110|115285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058771|NCT01436110|115285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058772|NCT01436110|115285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058773|NCT01436110|115285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058774|NCT01436110|115285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058775|NCT01436110|115285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058776|NCT01436110|115285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058777|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
3058778|NCT00538057|HZA105871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058779|NCT00538057|HZA105871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058780|NCT00538057|HZA105871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058781|NCT00538057|HZA105871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058782|NCT00538057|HZA105871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058783|NCT00538057|HZA105871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058784|NCT00538057|HZA105871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056822|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
3056823|NCT04815889||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35704376/|
3056824|NCT00871741|111761|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056825|NCT00871741|111761|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056826|NCT00871741|111761|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056827|NCT00871741|111761|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056828|NCT00871741|111761|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056829|NCT00871741|111761|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056830|NCT00871741|111761|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056831|NCT01371812|114660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056832|NCT01371812|114660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056833|NCT01371812|114660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058785|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
3058786|NCT01073293||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-007&kw=V503-007&tab=access|
3058787|NCT01000506|112997|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058788|NCT01000506|112997|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058789|NCT01000506|112997|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058790|NCT01000506|112997|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058791|NCT01000506|112997|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058792|NCT01000506|112997|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058793|NCT01000506|112997|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058794|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"
3058795|NCT01030822|112909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058796|NCT01030822|112909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058797|NCT01030822|112909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058798|NCT01030822|112909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058799|NCT01030822|112909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058800|NCT01030822|112909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058801|NCT01030822|112909|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058802|NCT00363311|AVO105948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058803|NCT00363311|AVO105948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058804|NCT00363311|AVO105948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058805|NCT00363311|AVO105948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058806|NCT00363311|AVO105948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058807|NCT00363311|AVO105948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058808|NCT00363311|AVO105948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058809|NCT00225862|100310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052174|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.
3052175|NCT06764238|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
3052176|NCT06950970|tetinstitute.rn@gmail.com|Informed Consent Form|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
3052177|NCT06950970|tetinstitute.rn@gmail.com|Statistical Analysis Plan|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
3052178|NCT06828367|not necessary|Study Protocol|https://docs.google.com/document/d/1hvjyp_RfCDDpHWkrTv_s7qhztM4Pqw9T/edit|is a public document
3054302|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
3054303|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
3054304|NCT01101568|113506|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054305|NCT01101568|113506|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054306|NCT01101568|113506|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054307|NCT01101568|113506|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054308|NCT01101568|113506|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054309|NCT01101568|113506|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054310|NCT01101568|113506|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054311|NCT00169494|580299/012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054312|NCT00169494|580299/012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054313|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
3054314|NCT00169494|580299/012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054315|NCT00169494|580299/012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054316|NCT00169494|580299/012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056834|NCT01371812|114660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056835|NCT01371812|114660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056836|NCT01371812|114660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056837|NCT01371812|114660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056838|NCT06989255|doi: 10.5281/zenodo.11371924|Study Protocol|https://zenodo.org/records/11371924|Study protocol including ICF
3056839|NCT02152605|201211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056840|NCT02152605|201211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056841|NCT02152605|201211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056842|NCT02152605|201211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056843|NCT02152605|201211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056844|NCT02152605|201211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056845|NCT02152605|201211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056846|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.
3056847|NCT00609180||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/omega/|
3056848|NCT00609180||Study Forms|http://biolincc.nhlbi.nih.gov/studies/omega/|
3058810|NCT00225862|100310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058811|NCT00225862|100310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058812|NCT00225862|100310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058813|NCT00225862|100310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058814|NCT00225862|100310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058815|NCT00225862|100310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058816|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
3058817|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
3058818|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
3058819|NCT05173376||Study Protocol|https://osf.io/scjn6/|Protocol on the Open Science Framework (OSF)
3058820|NCT05173376||Statistical Analysis Plan|https://osf.io/scjn6/|
3058821|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.
3058822|NCT00400855|SIG103337|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058823|NCT00400855|SIG103337|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058824|NCT00400855|SIG103337|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058825|NCT00400855|SIG103337|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058826|NCT00400855|SIG103337|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058827|NCT00400855|SIG103337|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058828|NCT00400855|SIG103337|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058829|NCT06187857||Study Protocol|https://osf.io/cavkf/?view_only=cc219af15f614756b43742875b6b0b39|
3058830|NCT05711875|Sridhar A, Shiliang Z, Woodson|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/33140989/|web site is provided
3058831|NCT00488514|TXA107977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058832|NCT00488514|TXA107977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058833|NCT00488514|TXA107977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058834|NCT00488514|TXA107977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058835|NCT00488514|TXA107977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058836|NCT00488514|TXA107977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058837|NCT00488514|TXA107977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058838|NCT01475721|115359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058839|NCT01475721|115359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058840|NCT01475721|115359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058841|NCT01475721|115359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058842|NCT01475721|115359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058843|NCT01475721|115359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058844|NCT01475721|115359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058845|NCT01453491|115951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058846|NCT01453491|115951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058847|NCT01453491|115951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056849|NCT01160003|113209|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056850|NCT01160003|113209|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056851|NCT01160003|113209|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056852|NCT01160003|113209|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056853|NCT01160003|113209|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056854|NCT01160003|113209|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056855|NCT01160003|113209|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052179|NCT01128595|113126|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052180|NCT01128595|113126|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052181|NCT01128595|113126|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052182|NCT01128595|113126|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052183|NCT01128595|113126|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052184|NCT01128595|113126|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052185|NCT01128595|113126|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052186|NCT00857766|112355|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052187|NCT00857766|112355|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052188|NCT00857766|112355|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052189|NCT00857766|112355|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052190|NCT00857766|112355|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052191|NCT00857766|112355|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052192|NCT00857766|112355|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052193|NCT07038772|EAT-40|Study Protocol|https://www.eat-26.com/|
3052194|NCT05018143|GUID|Individual Participant Data Set|https://nda.nih.gov/|
3052195|NCT06762743||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|registered clinical trial about Brivaracetam oral solution on Chinese website
3058848|NCT01453491|115951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058849|NCT01453491|115951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058850|NCT01453491|115951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052196|NCT06776536||institutional review board|https://camsakurasehir.saglik.gov.tr/|
3052197|NCT01702376|113789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052198|NCT01702376|113789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052199|NCT01702376|113789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052200|NCT01702376|113789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052201|NCT01702376|113789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052202|NCT01702376|113789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052203|NCT01702376|113789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052204|NCT00756067|111652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052205|NCT00756067|111652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052206|NCT00756067|111652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052207|NCT00756067|111652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052208|NCT00756067|111652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052209|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.
3052210|NCT00979121||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/sails/|
3052211|NCT00979121||Study Forms|http://biolincc.nhlbi.nih.gov/studies/sails/|
3052212|NCT00309166|580299/011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052213|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
3052214|NCT00309166|580299/011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058851|NCT01453491|115951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058852|NCT01366573|115256|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058853|NCT01366573|115256|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058854|NCT01366573|115256|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058855|NCT01366573|115256|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058856|NCT01366573|115256|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058857|NCT01366573|115256|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058858|NCT01366573|115256|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058859|NCT01999842|201072|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058860|NCT01999842|201072|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058861|NCT01999842|201072|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058862|NCT01999842|201072|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058863|NCT01999842|201072|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058864|NCT01999842|201072|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058865|NCT01999842|201072|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058866|NCT00920556|113222|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058867|NCT00920556|113222|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058868|NCT00920556|113222|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058869|NCT00920556|113222|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058870|NCT00920556|113222|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058871|NCT00920556|113222|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058872|NCT05223673||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3058873|NCT05223673||Study Protocol|https://clinicaltrials.servier.com/|
3058874|NCT05223673||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3058875|NCT05223673||Informed Consent Form|https://clinicaltrials.servier.com/|
3058876|NCT05223673||Clinical Study Report|https://clinicaltrials.servier.com/|
3058877|NCT05223673||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3058878|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.
3058879|NCT00292071||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3058880|NCT00289172|103792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058881|NCT00289172|103792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058882|NCT00289172|103792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058883|NCT00289172|103792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058884|NCT00289172|103792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058885|NCT00289172|103792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058886|NCT00005739||Abstract|http://ajph.aphapublications.org/doi/pdf/10.2105/AJPH.86.8_Pt_1.1146|
3058887|NCT02771405||Informed Consent Form|http://www.megafileupload.com/f3sT/Attachments_201656.zip|
3058888|NCT00412191|LAM105379|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058889|NCT00412191|LAM105379|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058890|NCT00412191|LAM105379|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058891|NCT00412191|LAM105379|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058892|NCT00412191|LAM105379|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058893|NCT00412191|LAM105379|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058894|NCT00412191|LAM105379|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058895|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.
3058896|NCT00127855|792014/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058897|NCT00127855|792014/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058898|NCT00127855|792014/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058899|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
3058900|NCT00127855|792014/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058901|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.
3058902|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.
3058903|NCT03910075||Study Protocol|http://www.nihstrokenet.org/i-acquire/resources|
3058904|NCT01484496|112341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058905|NCT01484496|112341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058906|NCT01484496|112341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058907|NCT01484496|112341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058908|NCT01484496|112341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058909|NCT01484496|112341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058910|NCT01484496|112341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058911|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
3049858|NCT00289718|100556 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049859|NCT01254032|114169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049860|NCT01254032|114169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049861|NCT01254032|114169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049862|NCT01254032|114169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049863|NCT01254032|114169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049864|NCT01453725||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07642&kw=8259-006&tab=access|
3049865|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)."
3049866|NCT00968890|113525|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049867|NCT00968890|113525|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049868|NCT00968890|113525|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049869|NCT00968890|113525|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056856|NCT02549027||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-003&kw=1064-003&tab=access|
3056857|NCT02105974|200820|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056858|NCT02105974|200820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056859|NCT02105974|200820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056860|NCT02105974|200820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056861|NCT02105974|200820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058912|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|
3058913|NCT03202433|ISSN 0124-8146|Study Protocol|http://scielo.org.co/scielo.php?script=sci_arttext&pid=S0124-81462013000200010|
3058914|NCT03202433||Clinical Practice Guide|http://www.criscancer.org|
3058915|NCT00540592|110847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058916|NCT00540592|110847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058917|NCT00540592|110847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058918|NCT00540592|110847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058919|NCT00540592|110847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058920|NCT00540592|110847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058921|NCT00540592|110847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058922|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
3058923|NCT02833129||Study Protocol|http://arxiv.org/abs/1607.01756|
3058924|NCT00943761||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-028&kw=7009-028&tab=access|
3058925|NCT06085235||Individual Participant Data Set|https://osf.io/y8e2r/|
3058926|NCT00742131|MET111647|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058927|NCT00742131|MET111647|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058928|NCT00742131|MET111647|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058929|NCT00742131|MET111647|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058930|NCT00742131|MET111647|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058931|NCT00742131|MET111647|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058932|NCT00742131|MET111647|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058933|NCT00906178||Intervention website|http://www.cybersenga.com|
3058934|NCT01018017|114010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052215|NCT00309166|580299/011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052216|NCT00309166|580299/011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052217|NCT00309166|580299/011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052218|NCT06662136||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3052219|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"
3052220|NCT00449774|LBI108617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058935|NCT01018017|114010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058936|NCT01018017|114010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058937|NCT01018017|114010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058938|NCT01018017|114010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058939|NCT01018017|114010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058940|NCT01018017|114010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058941|NCT02052661|106793|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058942|NCT02052661|106793|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058943|NCT02052661|106793|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058944|NCT02052661|106793|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058945|NCT02052661|106793|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058946|NCT02052661|106793|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058947|NCT02052661|106793|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049870|NCT00968890|113525|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056862|NCT02105974|200820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056863|NCT02105974|200820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056864|NCT02000765|115774|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056865|NCT02000765|115774|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056866|NCT02000765|115774|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056867|NCT02000765|115774|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056868|NCT02000765|115774|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056869|NCT02000765|115774|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056870|NCT02000765|115774|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056871|NCT01590797||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-254&kw=0431-254&tab=access|
3056872|NCT00224471|208141/042|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056873|NCT00224471|208141/042|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056874|NCT00224471|208141/042|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056875|NCT00224471|208141/042|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056876|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
3056877|NCT00224471|208141/042|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056878|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.
3056879|NCT00000620||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/accord|
3056880|NCT00000620||Study Forms|http://biolincc.nhlbi.nih.gov/studies/accord|
3056881|NCT00000620||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/accord|
3056882|NCT00385008|TRX105848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056883|NCT00385008|TRX105848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056884|NCT00385008|TRX105848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056885|NCT00385008|TRX105848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056886|NCT00385008|TRX105848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056887|NCT00385008|TRX105848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056888|NCT00385008|TRX105848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056889|NCT00323050|102547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056890|NCT00323050|102547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056891|NCT00323050|102547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056892|NCT00323050|102547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056893|NCT00323050|102547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056894|NCT00323050|102547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056895|NCT00315731|393229/027|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056896|NCT00315731|393229/027|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056897|NCT00315731|393229/027|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056898|NCT00315731|393229/027|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056899|NCT00315731|393229/027|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049871|NCT00968890|113525|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049872|NCT00968890|113525|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049873|NCT00334607|107531|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049874|NCT00334607|107531|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049875|NCT00334607|107531|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054317|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.
3054318|NCT00404768||Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054319|NCT00404768||Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054320|NCT00404768||Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054321|NCT00404768||Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054322|NCT00404768||Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054323|NCT00404768||Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054324|NCT00404768||Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054325|NCT03246035|CODIM-MBM-17-052|Study Protocol|http://www.ladydavis.ca/en/jonathanafilalo|Pilot study protocol
3054326|NCT03246035|CODIM-MBM-17-052|Informed Consent Form|http://www.ladydavis.ca/en/jonathanafilalo|Patient consent Caregiver consent French and English available
3054327|NCT02124798|200339|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054328|NCT02124798|200339|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054329|NCT02124798|200339|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054330|NCT02124798|200339|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054331|NCT02124798|200339|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054332|NCT02124798|200339|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054333|NCT02124798|200339|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054334|NCT00866294|112810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054335|NCT00866294|112810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054336|NCT00866294|112810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054337|NCT00866294|112810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056900|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
3056901|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
3056902|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.
3056903|NCT00000474||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/paths/|
3056904|NCT00000474||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/paths/|
3056905|NCT05063708||Analytic Code|http://zenodo.org|
3056906|NCT05063708||Statistical Analysis Plan|http://zenodo.org|
3056907|NCT01890863|200260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056908|NCT01890863|200260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056909|NCT01890863|200260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056910|NCT01890863|200260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056911|NCT01890863|200260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056912|NCT01890863|200260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056913|NCT01890863|200260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058948|NCT01277705|711866/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058949|NCT01277705|711866/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058950|NCT01277705|711866/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058951|NCT01277705|711866/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058952|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
3058953|NCT01277705|711866/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058954|NCT02397915|201474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058955|NCT02397915|201474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058956|NCT02397915|201474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058957|NCT02397915|201474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058958|NCT02397915|201474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058959|NCT02397915|201474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058960|NCT02397915|201474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058961|NCT02726464||Patient Brochure|http://www.lightintegra.com/prism-study|
3058962|NCT02993627|18039384|Clinical Study Report|http://lipidworld.biomedcentral.com/articles/10.1186/1476-511X-6-33/|
3049876|NCT00334607|107531|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049877|NCT00334607|107531|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049878|NCT00334607|107531|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049879|NCT00397215|108251|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049880|NCT00397215|108251|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049881|NCT00397215|108251|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049882|NCT00397215|108251|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058963|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
3058964|NCT00140712|101468/253|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058965|NCT00140712|101468/253|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058966|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
3058967|NCT00140712|101468/253|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058968|NCT00140712|101468/253|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058969|NCT00140712|101468/253|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058970|NCT03160456|IPG598|"NICE guidance Hypoglossal Nerve Stimulation"|https://www.nice.org.uk/guidance/ipg598|National Institute for Health and Care Excellence
3058971|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.
3058972|NCT00883948||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/eden/|
3058973|NCT00883948||Study Forms|http://biolincc.nhlbi.nih.gov/studies/eden/|
3058974|NCT00097929||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3049883|NCT00397215|108251|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049884|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.
3049885|NCT00851344|110163|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049886|NCT00851344|110163|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049887|NCT00851344|110163|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052221|NCT00449774|LBI108617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052222|NCT00449774|LBI108617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058975|NCT00456625|108984|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058976|NCT00456625|108984|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058977|NCT00456625|108984|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058978|NCT00456625|108984|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058979|NCT00456625|108984|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058980|NCT00456625|108984|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058981|NCT00456625|108984|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058982|NCT01165125|105548|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058983|NCT01165125|105548|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058984|NCT01165125|105548|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058985|NCT01165125|105548|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058986|NCT01165125|105548|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058987|NCT01165125|105548|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058988|NCT01165125|105548|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058989|NCT00972517|113638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058990|NCT00972517|113638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058991|NCT00972517|113638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058992|NCT00972517|113638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058993|NCT00972517|113638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058994|NCT00972517|113638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058995|NCT00972517|113638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058996|NCT01536561|104728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058997|NCT01536561|104728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058998|NCT01536561|104728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3058999|NCT01536561|104728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059000|NCT01536561|104728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052223|NCT00449774|LBI108617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052224|NCT00449774|LBI108617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052225|NCT00449774|LBI108617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052226|NCT00449774|LBI108617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052227|NCT05201599|zxt4|Study Protocol|https://pan.baidu.com/s/1PNKfPWrpeJtodX1RwH8k-w|
3052228|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.
3059001|NCT01536561|104728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059002|NCT01536561|104728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052229|NCT06861205||Study Protocol|https://doi.org/10.3389/fnut.2024.1438740|
3052230|NCT01119651|114574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052231|NCT01119651|114574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059003|NCT02218697|117276|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059004|NCT02218697|117276|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059005|NCT02218697|117276|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059006|NCT02218697|117276|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059007|NCT02218697|117276|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059008|NCT02218697|117276|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059009|NCT02218697|117276|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059010|NCT01534351||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0906A-149&kw=0906A-149&tab=access|
3059011|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.
3059012|NCT00434993||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/alta/|
3059013|NCT00434993||Study Forms|http://biolincc.nhlbi.nih.gov/studies/alta/|
3059014|NCT01899638|115380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059015|NCT01899638|115380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059016|NCT01899638|115380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059017|NCT01899638|115380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059018|NCT01899638|115380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059019|NCT01899638|115380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059020|NCT01899638|115380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059021|NCT00329576|106640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059022|NCT00329576|106640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059023|NCT00329576|106640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059024|NCT00329576|106640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059025|NCT00329576|106640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059026|NCT00703846|114568|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059027|NCT00703846|114568|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059028|NCT00703846|114568|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059029|NCT00703846|114568|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059030|NCT00703846|114568|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059031|NCT00703846|114568|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059032|NCT00703846|114568|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059033|NCT02947802||Study Instrument (Online Survey)|https://hbs.qualtrics.com/SE/?SID=SV_1LdkKR5P4DyCevH|This is the online survey participants will complete.
3059034|NCT03511508||Study Protocol|http://doi.org/10.1186/s13063-019-3405-5|Study Protocol
3059035|NCT00104416|LAM100036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059036|NCT00104416|LAM100036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059037|NCT00104416|LAM100036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059038|NCT00104416|LAM100036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059039|NCT00104416|LAM100036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059040|NCT00104416|LAM100036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059041|NCT00104416|LAM100036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059042|NCT00758069||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052232|NCT01119651|114574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052233|NCT01119651|114574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052234|NCT01119651|114574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052235|NCT01119651|114574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052236|NCT01119651|114574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052237|NCT06753526|ahmed-mahmoud@sohag.med.edu.eg|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/9008325/|
3052238|NCT03019835||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/7880668|
3052239|NCT06750744|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
3052240|NCT06952582|doi.org/10.17605/OSF.IO/SE8M7|Individual Participant Data Set|https://osf.io/puxgw/|
3052241|NCT01491815||Study Protocol|http://www.biomedcentral.com/search?query=glinatsi&searchType=publisherSearch|Publication of the protocol. Glinatsi et al. Trials (2017) 18:161
3052242|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|
3052243|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|
3059043|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.
3059044|NCT00875485|110699|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059045|NCT00875485|110699|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059046|NCT00875485|110699|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059047|NCT00875485|110699|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059048|NCT00875485|110699|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059049|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.
3059050|NCT02060344||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
3059051|NCT02060344||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
3059052|NCT00466947|109563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059053|NCT00466947|109563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059054|NCT00466947|109563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059055|NCT00466947|109563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059056|NCT00466947|109563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059057|NCT00466947|109563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059058|NCT00306293|VLX105832|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059059|NCT00306293|VLX105832|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059060|NCT00306293|VLX105832|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059061|NCT00306293|VLX105832|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059062|NCT00306293|VLX105832|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052244|NCT01332552|115040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052245|NCT01332552|115040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059063|NCT00306293|VLX105832|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059064|NCT00306293|VLX105832|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059065|NCT00633074|111454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059066|NCT00633074|111454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059067|NCT00633074|111454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059068|NCT00633074|111454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059069|NCT00633074|111454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059070|NCT00633074|111454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059071|NCT00633074|111454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059072|NCT01822899|116134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052246|NCT01332552|115040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052247|NCT01332552|115040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052248|NCT01332552|115040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059073|NCT01822899|116134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059074|NCT01822899|116134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052249|NCT01332552|115040|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052250|NCT01332552|115040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059075|NCT01822899|116134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059076|NCT01822899|116134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059077|NCT01822899|116134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059078|NCT01822899|116134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059079|NCT03030352||Pilot Study of the How-to trial|http://link.springer.com/article/10.1007/s10826-013-9751-0|
3059080|NCT00500461|AC2106213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059081|NCT00500461|AC2106213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059082|NCT00500461|AC2106213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059083|NCT00500461|AC2106213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059084|NCT00500461|AC2106213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059085|NCT00500461|AC2106213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059086|NCT00500461|AC2106213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059087|NCT00404378|NKV105093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059088|NCT00404378|NKV105093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059089|NCT00404378|NKV105093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059090|NCT00404378|NKV105093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059091|NCT00404378|NKV105093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059092|NCT00404378|NKV105093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059093|NCT00404378|NKV105093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059094|NCT05896098||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/14616599/|
3052251|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
3052252|NCT00489554|109661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052253|NCT00489554|109661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059095|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
3059096|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
3059097|NCT03257202|HS-17-00319|Study Protocol|http://istar.usc.edu|
3059098|NCT03257202|HS-17-00319|Informed Consent Form|http://istar.usc.edu|
3059099|NCT00344318|107007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059100|NCT00344318|107007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059101|NCT00344318|107007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059102|NCT00344318|107007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059103|NCT00344318|107007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059104|NCT00344318|107007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059105|NCT04569136|DOI：10.6315/2009.37(4)06|Clinical Study Report|http://www.airitilibrary.com/Publication/alDetailedMesh?DocID=10253009-200912-201002050027-201002050027-261-268|
3059106|NCT01762774|114068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059107|NCT01762774|114068|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059108|NCT01762774|114068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059109|NCT01762774|114068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059110|NCT01762774|114068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059111|NCT01762774|114068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059112|NCT01762774|114068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059113|NCT01431937|114347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059114|NCT01431937|114347|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059115|NCT01431937|114347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059116|NCT01431937|114347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059117|NCT01431937|114347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059118|NCT01431937|114347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059119|NCT01431937|114347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059120|NCT00473668|104977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059121|NCT00473668|104977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059122|NCT00473668|104977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059123|NCT00473668|104977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059124|NCT00473668|104977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059125|NCT00473668|104977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059126|NCT00625196|HZA102940|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059127|NCT00625196|HZA102940|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059128|NCT00625196|HZA102940|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059129|NCT00625196|HZA102940|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059130|NCT00625196|HZA102940|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059131|NCT00625196|HZA102940|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059132|NCT00625196|HZA102940|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059133|NCT00758264|111393|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059134|NCT00758264|111393|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052254|NCT00489554|109661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052255|NCT00489554|109661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059135|NCT00758264|111393|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059136|NCT00758264|111393|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059137|NCT00758264|111393|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059138|NCT00758264|111393|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059139|NCT00758264|111393|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059140|NCT02998203||Manuscript and supplementary files|https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0219420|
3059141|NCT00697866|208129/037|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059142|NCT00697866|208129/037|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059143|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
3059144|NCT00697866|208129/037|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059145|NCT00697866|208129/037|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059146|NCT00697866|208129/037|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059147|NCT00519376|B2C110165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059148|NCT00519376|B2C110165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059149|NCT00519376|B2C110165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059150|NCT00519376|B2C110165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059151|NCT00519376|B2C110165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059152|NCT00519376|B2C110165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059153|NCT00519376|B2C110165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052256|NCT00489554|109661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052257|NCT00489554|109661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052258|NCT01767688||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-031&kw=3102-031&tab=access|
3059154|NCT01245738||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-204&kw=0000-204&tab=access|
3059155|NCT01792817||Publication|http://onlinelibrary.wiley.com/doi/10.1111/head.12896/full|Non-Invasive Vagus Nerve Stimulation for the ACute Treatment of Cluster Headache: Findings From the Randomized, Double-Blind, Sham-Controlled ACT1 Study Stephen D. Silberstein, MD; Laszlo L. Mechtler, MD; David B. Kudrow, MD; Anne H. Calhoun, MD; Candace McClure, PhD; Joel R. Saper, MD; Eric J. Liebler; Emily Rubenstein Engel, MD; Stewart J. Tepper, MD; on Behalf of the ACT1 Study Group
3059156|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.
3059157|NCT00000593||Study Forms|http://biolincc.nhlbi.nih.gov/studies/vats/|
3052259|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.
3052260|NCT00057499|SDY568|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY568|ImmPort study identifier is SDY568.
3052261|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.
3052262|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.
3054338|NCT00866294|112810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059158|NCT01155466||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04938&kw=P04938&tab=access|
3059159|NCT05446792||Approval of the Ethics Committee for Research with Human Beings in Brazil|https://plataformabrasil.saude.gov.br/login.jsf|
3054339|NCT01614769||CSR Snyposis Link|http://www.merck.com/clinical-trials/study.html?id=0000-253&kw=0000-253&tab=access|
3059160|NCT00964340|113312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059161|NCT00964340|113312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059162|NCT00964340|113312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059163|NCT00964340|113312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059164|NCT00964340|113312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059165|NCT00964340|113312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059166|NCT03192020||Study Protocol|http://bmjopen.bmj.com/content/8/3/e019054|Protocol in BMJ Open access
3059167|NCT00500058|ILI105618|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059168|NCT00500058|ILI105618|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059169|NCT00500058|ILI105618|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059170|NCT00500058|ILI105618|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059171|NCT00500058|ILI105618|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059172|NCT00500058|ILI105618|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059173|NCT00500058|ILI105618|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059174|NCT00908115|208355/128|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059175|NCT00908115|208355/128|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059176|NCT00908115|208355/128|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059177|NCT00908115|208355/128|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059178|NCT00908115|208355/128|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059179|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
3059180|NCT01165320||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0991-074&kw=0991-074&tab=access|
3049888|NCT00851344|110163|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059181|NCT06660953||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37971133/|
3059182|NCT00316693|104798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059183|NCT00316693|104798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059184|NCT00316693|104798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059185|NCT00316693|104798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059186|NCT00316693|104798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059187|NCT00316693|104798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059188|NCT01691885|116601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059189|NCT01691885|116601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059190|NCT01691885|116601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059191|NCT01691885|116601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059192|NCT01691885|116601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059193|NCT01691885|116601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059194|NCT01691885|116601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049889|NCT00851344|110163|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049890|NCT00851344|110163|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049891|NCT00851344|110163|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059195|NCT06896500|Ethics Committee Application|Clinical Study Report|https://drive.google.com/file/d/19dj7wMiq4mPOobklxuHQObULyObAOvgc/view?usp=sharing|
3059196|NCT06896500|informed consent form|Informed Consent Form|https://docs.google.com/document/d/1PuTtTRr_LxSuZvbzWyvw3EQZYQ0VyA7b/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
3059197|NCT06896500|Vaginal flatus status form|Forms|https://docs.google.com/document/d/1kFejPnvwa_N52yM8A2UKoAgZ3s1uPYuw/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
3054340|NCT06253286||Study Protocol|https://drive.google.com/file/d/1edivKccFOAyt3_A6aNnNROe7JQnRmp4C/view?usp=sharing|
3056914|NCT02006602|201011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056915|NCT02006602|201011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056916|NCT02006602|201011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056917|NCT02006602|201011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056918|NCT02006602|201011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056919|NCT02006602|201011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056920|NCT02006602|201011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056921|NCT00979641||Clinical Study Report|http://www.anticancerresearch.com|
3059198|NCT06896500|study main data|Study Protocol|https://drive.google.com/file/d/1yPsrrEh2E2eVLPD-_QtWy8F0rgT0dM9g/view?usp=sharing|
3059199|NCT03207321||Individual Participant Data Set|http://apcaps.lshtm.ac.uk/|
3059200|NCT00559468||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059201|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
3059202|NCT00871117|111852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059203|NCT00871117|111852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059204|NCT00871117|111852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059205|NCT00871117|111852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059206|NCT00871117|111852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059207|NCT00871117|111852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059208|NCT00871117|111852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059209|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.
3059210|NCT00896363|109035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059211|NCT00896363|109035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059212|NCT00896363|109035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059213|NCT00896363|109035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059214|NCT00896363|109035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059215|NCT00896363|109035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059216|NCT00896363|109035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059217|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27179664|
3059218|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27629371|
3059219|NCT06891469|https://doi.org/10.6084/m9.fig|Individual Participant Data Set|https://figshare.com|figshare
3059220|NCT00549900|107336|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059221|NCT00549900|107336|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059222|NCT00549900|107336|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059223|NCT00549900|107336|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059224|NCT00549900|107336|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059225|NCT00549900|107336|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052263|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.
3052264|NCT01772199|116477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052265|NCT01772199|116477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052266|NCT01772199|116477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052267|NCT01772199|116477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052268|NCT01772199|116477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052269|NCT01772199|116477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056922|NCT02872376||Study Protocol|https://sites.google.com/site/ridartstudy/|
3056923|NCT02872376||Informed Consent Form|https://sites.google.com/site/ridartstudy/|
3056924|NCT02257385|116961|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056925|NCT02257385|116961|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056926|NCT02257385|116961|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056927|NCT02257385|116961|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056928|NCT02257385|116961|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056929|NCT02257385|116961|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056930|NCT02257385|116961|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056931|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
3056932|NCT00086593|101464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056933|NCT00086593|101464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056934|NCT00086593|101464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056935|NCT00086593|101464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056936|NCT00086593|101464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056937|NCT00086593|101464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056938|NCT01499446|FFA20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056939|NCT01499446|FFA20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056940|NCT01499446|FFA20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056941|NCT01499446|FFA20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056942|NCT01499446|FFA20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056943|NCT01499446|FFA20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056944|NCT01499446|FFA20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052270|NCT01772199|116477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054341|NCT06253286||Informed Consent Form|https://drive.google.com/file/d/1gA2nThyz6di3bSZKJQ7aQ_Usy1_wpOrR/view?usp=sharing|
3056945|NCT00366366|217744/075|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056946|NCT00366366|217744/075|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056947|NCT00366366|217744/075|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056948|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
3056949|NCT00366366|217744/075|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056950|NCT00366366|217744/075|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052271|NCT00910962|111810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052272|NCT00910962|111810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056951|NCT05088135||Clinical Study Report|https://doi.org/10.3389/fphys.2023.1215757|
3052273|NCT00910962|111810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052274|NCT00910962|111810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052275|NCT00910962|111810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052276|NCT00910962|111810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052277|NCT00910962|111810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052278|NCT00985088|113440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052279|NCT00985088|113440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056952|NCT00533312||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3056953|NCT01295320|114825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056954|NCT01295320|114825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056955|NCT01295320|114825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056956|NCT01295320|114825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056957|NCT01295320|114825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056958|NCT01295320|114825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056959|NCT01295320|114825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056960|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.
3056961|NCT00000591||Study Forms|http://biolincc.nhlbi.nih.gov/studies/tcd/|
3056962|NCT01887171|10.15825/1995-1191-2015-3-24|Clinical Study Report|http://journal.transpl.ru/vtio/article/view/561/488|
3056963|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|
3056964|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
3056965|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.
3056966|NCT00463697|B2C106996|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056967|NCT00463697|B2C106996|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056968|NCT00463697|B2C106996|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056969|NCT00463697|B2C106996|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056970|NCT00463697|B2C106996|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056971|NCT00463697|B2C106996|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056972|NCT00463697|B2C106996|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056973|NCT01332292|102942|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056974|NCT01332292|102942|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056975|NCT01332292|102942|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056976|NCT01332292|102942|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056977|NCT01332292|102942|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056978|NCT01332292|102942|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056979|NCT01332292|102942|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056980|NCT00306995|102499|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056981|NCT00306995|102499|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056982|NCT00306995|102499|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056983|NCT00306995|102499|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056984|NCT00306995|102499|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056985|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
3056986|NCT00307021|105874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056987|NCT00307021|105874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056988|NCT00307021|105874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056989|NCT00307021|105874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056990|NCT00307021|105874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056991|NCT00307021|105874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056992|NCT00562848|MOT107043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056993|NCT00562848|MOT107043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056994|NCT00562848|MOT107043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056995|NCT00562848|MOT107043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056996|NCT00562848|MOT107043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056997|NCT00562848|MOT107043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056998|NCT00562848|MOT107043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3056999|NCT03718832|doi:10.7910/DVN/LZUTU0|Individual Participant Data Set|https://doi.org/10.7910/DVN/LZUTU0|
3057000|NCT03718832|doi:10.7910/DVN/LZUTU0|Analytic Code|https://doi.org/10.7910/DVN/LZUTU0|
3057001|NCT01198769|114351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057002|NCT01198769|114351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057003|NCT01198769|114351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057004|NCT01198769|114351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057005|NCT01198769|114351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057006|NCT01198769|114351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057007|NCT01198769|114351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057008|NCT00511823|NKV110483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057009|NCT00511823|NKV110483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057010|NCT00511823|NKV110483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057011|NCT00511823|NKV110483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057012|NCT00511823|NKV110483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057013|NCT00511823|NKV110483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057014|NCT00511823|NKV110483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057015|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.
3057016|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.
3057017|NCT00696423|111535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057018|NCT00696423|111535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057019|NCT00696423|111535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057020|NCT00696423|111535|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057021|NCT00696423|111535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057022|NCT00696423|111535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057023|NCT00696423|111535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057024|NCT07192640||Study Protocol|https://doi.org/10.1590/acb370702|https://doi.org/10.1590/acb370702
3057025|NCT01557504||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-296&kw=0431A-296&tab=access|
3057026|NCT00810667|2008-001441-26|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-001441-26/results|
3052280|NCT00985088|113440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052281|NCT00985088|113440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052282|NCT00985088|113440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052283|NCT00985088|113440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052284|NCT00985088|113440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052285|NCT01827839|116796|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052286|NCT01827839|116796|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052287|NCT01827839|116796|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052288|NCT01827839|116796|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052289|NCT01827839|116796|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052290|NCT01827839|116796|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052291|NCT01827839|116796|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052292|NCT00614614|110870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052293|NCT00614614|110870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052294|NCT00614614|110870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052295|NCT00614614|110870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052296|NCT00614614|110870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052297|NCT00614614|110870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052298|NCT00614614|110870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052299|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
3052300|NCT00273052|COR103561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052301|NCT00273052|COR103561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052302|NCT00273052|COR103561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052303|NCT00273052|COR103561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052304|NCT00273052|COR103561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052305|NCT00273052|COR103561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052306|NCT00273052|COR103561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052307|NCT01074242||CSR Synopsis|http://www.merck.com/clinical-trials/search.html?kw=V260-037|
3052308|NCT01957163|200109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052309|NCT01957163|200109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052310|NCT01957163|200109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052311|NCT01957163|200109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052312|NCT01957163|200109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052313|NCT01957163|200109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052314|NCT01957163|200109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052315|NCT00907933|111610|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057027|NCT01110018|112008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057028|NCT01110018|112008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057029|NCT01110018|112008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057030|NCT01110018|112008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057031|NCT01110018|112008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057032|NCT01110018|112008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057033|NCT01110018|112008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057034|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.
3057035|NCT03173209|Calm Moments Cards program|intervention materials|http://www.everymomentcounts.org|Calm Moments Cards program
3057036|NCT01847404|116480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057037|NCT01847404|116480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057038|NCT01847404|116480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057039|NCT01847404|116480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057040|NCT01847404|116480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057041|NCT01847404|116480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057042|NCT02836002||Individual Participant Data Set|https://datadryad.org//resource/doi:10.5061/dryad.60h41|
3057043|NCT00695305|LP2105521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057044|NCT00695305|LP2105521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057045|NCT00695305|LP2105521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057046|NCT00695305|LP2105521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057047|NCT00695305|LP2105521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057048|NCT00695305|LP2105521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057049|NCT00695305|LP2105521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057050|NCT03494712||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3057051|NCT03494712||Study Protocol|https://clinicaltrials.servier.com/|
3057052|NCT03494712||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3057053|NCT03494712||Informed Consent Form|https://clinicaltrials.servier.com/|
3057054|NCT03494712||Clinical Study Report|https://clinicaltrials.servier.com/|
3057055|NCT03494712||study-level clinical trial data|https://clinicaltrials.servier.com/|
3057056|NCT07192172|No. 1611-124-811|Study Protocol|http://cris.snuh.org|http://cris.snuh.org
3057057|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.
3057058|NCT01563042|114594|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057059|NCT01563042|114594|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057060|NCT01563042|114594|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057061|NCT01563042|114594|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057062|NCT01563042|114594|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057063|NCT01563042|114594|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057064|NCT01563042|114594|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057065|NCT00005235||NCBI website|http://www.ncbi.nlm.nih.gov/pubmed/8353919|
3057066|NCT00197171|100386 (EXT Y5)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057067|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
3059226|NCT01224821|104731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059227|NCT01224821|104731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059228|NCT01224821|104731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059229|NCT01224821|104731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059230|NCT01224821|104731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059231|NCT01224821|104731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059232|NCT01224821|104731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059233|NCT00937404|112581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059234|NCT00937404|112581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059235|NCT00937404|112581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059236|NCT00937404|112581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059237|NCT00937404|112581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059238|NCT00937404|112581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059239|NCT02014480|116132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059240|NCT02014480|116132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059241|NCT02014480|116132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059242|NCT02014480|116132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059243|NCT02014480|116132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059244|NCT02014480|116132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059245|NCT02014480|116132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059246|NCT03760016|424597|Individual Participant Data Set|https://dash.nichd.nih.gov/study/424597|
3059247|NCT00624819|111345 (Mth 12)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059248|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
3059249|NCT00624819|111345 (Mth 12)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052316|NCT00907933|111610|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052317|NCT00907933|111610|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052318|NCT00907933|111610|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052319|NCT00907933|111610|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059250|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
3059251|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
3059252|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
3059253|NCT01357135||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-201&kw=0431-201&tab=access|
3059254|NCT00642148|MKI102428|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059255|NCT00642148|MKI102428|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059256|NCT00642148|MKI102428|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059257|NCT00642148|MKI102428|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059258|NCT00642148|MKI102428|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059259|NCT00642148|MKI102428|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059260|NCT00642148|MKI102428|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059261|NCT00035360||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059262|NCT05455008||Individual Participant Data Set|https://iro.uiowa.edu/esploro/outputs/dataset/9984236057502771|
3059263|NCT03630744||web page|http://fluidday.com|
3059264|NCT03029078||Study Protocol|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003048-11/FR|
3059265|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
3059266|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
3059267|NCT00343915|101695 Ext. Mth30|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059268|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
3059269|NCT00343915|101695 Ext. Mth30|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059270|NCT00355342|SCO40041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059271|NCT00355342|SCO40041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059272|NCT00355342|SCO40041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059273|NCT00355342|SCO40041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059274|NCT00355342|SCO40041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059275|NCT00355342|SCO40041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059276|NCT00355342|SCO40041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059277|NCT01480609|115214|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059278|NCT01480609|115214|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059279|NCT01480609|115214|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059280|NCT01480609|115214|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059281|NCT01480609|115214|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059282|NCT01480609|115214|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059283|NCT01480609|115214|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059284|NCT06357091||results can be obtained from principal investigator|https://www.kh-schwaz.at/|results can be obtained from the principle investigator
3059285|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.
3059286|NCT00474617||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059287|NCT00379977|106345|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059288|NCT00379977|106345|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059289|NCT00379977|106345|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059290|NCT00379977|106345|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059291|NCT00379977|106345|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059292|NCT00379977|106345|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059293|NCT00307567|105555|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059294|NCT00307567|105555|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059295|NCT00307567|105555|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059296|NCT00307567|105555|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059297|NCT00307567|105555|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059298|NCT00307567|105555|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059299|NCT00289198|FFR106080|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059300|NCT00289198|FFR106080|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059301|NCT00289198|FFR106080|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059302|NCT00289198|FFR106080|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059303|NCT00289198|FFR106080|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059304|NCT00289198|FFR106080|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059305|NCT00289198|FFR106080|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059306|NCT04786418||Study Protocol|http://www.directclinicaltrial.org.uk|
3059307|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.
3059308|NCT00000558||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/peace/|
3059309|NCT00000558||Study Forms|http://biolincc.nhlbi.nih.gov/studies/peace/|
3059310|NCT01360398|114378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059311|NCT01360398|114378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059312|NCT01360398|114378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059313|NCT01360398|114378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054342|NCT01254604||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=2452-002&kw=2452-002&tab=access|
3059314|NCT01360398|114378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059315|NCT01360398|114378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059316|NCT01360398|114378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059317|NCT03745183||Study Protocol|https://drive.google.com/open?id=1ial1puH4ar075LyGcoWIrU1AXclt3FO-|
3059318|NCT03745183||Tables 1-5|https://drive.google.com/open?id=1pmZyUhTfoOPWRDJgEFjMsa_K9bvQ_Lon|
3059319|NCT03745183||Figure 1. Flow chart of the study procedure|https://drive.google.com/open?id=1MpUGMeNkzeOlThYZ_Zur4xTgt5cOvQNN|
3059320|NCT03745183||Informed Consent Form|https://drive.google.com/open?id=1kV91jvmtUDi_BA2paf-iszXb7bCnKHZO|
3059321|NCT03745183||Individual Participant Data Set|https://drive.google.com/open?id=1n3y-FDFc63KGyGfbkNBlpLJ-6HE9BBUZ|
3059322|NCT03745183||Appendix E. Illustrated checklist for the T'boli|https://drive.google.com/open?id=1t2b-wyQsJaTEy6qqJCiL4Opg-Hdvdxzj|
3059323|NCT03745183||Appendix F. Illustrated instruction on Senna alata decoction preparation|https://drive.google.com/open?id=17hMRr2-GhROnq7Gdw0Skd1KFApCpCgzy|
3059324|NCT06367907|SM 68/6-1|Study Protocol|https://gepris.dfg.de/gepris/projekt/424869737|
3059325|NCT00134732|103478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059326|NCT00134732|103478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059327|NCT00134732|103478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059328|NCT00134732|103478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059329|NCT00134732|103478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059330|NCT00134732|103478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059331|NCT00354666|B2E101312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059332|NCT00354666|B2E101312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059333|NCT00354666|B2E101312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059334|NCT00354666|B2E101312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059335|NCT00354666|B2E101312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059336|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
3059337|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
3059338|NCT00126984|104703 (Primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059339|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
3052320|NCT00907933|111610|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052321|NCT00907933|111610|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052322|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32532623/|Study scientific background
3052323|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.
3052324|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32727835/|Study scientific background.
3052325|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32769063/|Study scientific background.
3052326|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/25636714/|Study scientific background.
3052327|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/24444048/|Alemtuzumab medication
3052328|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/27766281/|Alemtuzumab medication
3052329|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31898276/|Alemtuzumab medication
3052330|NCT05075499|PMID|Study Protocol|http://products.sanofi.us/aubagio/aubagio.html|Aubagio (teriflunomide) \[prescribing information\]. Cambridge (MA): Genzyme Corporation; September 2012.
3052331|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/31898276/|Aubagio (teriflunomide) medication
3052332|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/29275977/|Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria.
3052333|NCT00240994|SDY134|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
3059340|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.
3059341|NCT00126984|104703 (Primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059342|NCT07041424||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28955539/|
3057068|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.
3057069|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
3057070|NCT00197171|100386 (EXT Y5)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057071|NCT01254643||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-008&kw=V503-008&tab=access|
3057072|NCT00779935||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057073|NCT01551771|115802|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057074|NCT01551771|115802|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057075|NCT01551771|115802|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057076|NCT01551771|115802|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057077|NCT01551771|115802|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057078|NCT01551771|115802|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057079|NCT01551771|115802|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057080|NCT06968286||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/39758269/|
3057081|NCT06676878||Study Protocol|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
3057082|NCT06676878||Informed Consent Form|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
3057083|NCT03411161||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3057084|NCT03411161||Study Protocol|https://clinicaltrials.servier.com/|
3057085|NCT03411161||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3057086|NCT03411161||Informed Consent Form|https://clinicaltrials.servier.com/|
3057087|NCT03411161||Clinical Study Report|https://clinicaltrials.servier.com/|
3057088|NCT03411161||study-level clinical trial data|https://clinicaltrials.servier.com/|
3057089|NCT07097649||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/33946001/|
3057090|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.
3057091|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.
3057092|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.
3057093|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.
3057094|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.
3057095|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.
3057096|NCT06881329|GSE290201|Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE290201|Gene Expression Omnibus repository
3057097|NCT00471081|109375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057098|NCT00471081|109375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057099|NCT00471081|109375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057100|NCT00471081|109375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057101|NCT00471081|109375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057102|NCT00471081|109375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057103|NCT00471081|109375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057104|NCT01822639|116798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057105|NCT01822639|116798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057106|NCT01822639|116798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052334|NCT00240994|SDY134|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
3052335|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
3057107|NCT01822639|116798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057108|NCT01822639|116798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057109|NCT01822639|116798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057110|NCT01822639|116798|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057111|NCT00485732|107291|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057112|NCT00485732|107291|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057113|NCT00485732|107291|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057114|NCT00485732|107291|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057115|NCT00485732|107291|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057116|NCT00485732|107291|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057117|NCT00485732|107291|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052336|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.
3052337|NCT00718120|110584|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052338|NCT00718120|110584|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057118|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
3057119|NCT00811967||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3057120|NCT00422604|AC2106956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057121|NCT00422604|AC2106956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049892|NCT00118690|SFA100316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049893|NCT00118690|SFA100316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049894|NCT00118690|SFA100316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049895|NCT00118690|SFA100316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049896|NCT00118690|SFA100316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049897|NCT02714907||Study Protocol|http://cortrium.com|In Danish language
3049898|NCT00318058|104540|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052339|NCT00718120|110584|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049899|NCT00318058|104540|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049900|NCT00318058|104540|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049901|NCT00318058|104540|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049902|NCT00318058|104540|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049903|NCT00318058|104540|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049904|NCT01893203|25109244|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/|
3052340|NCT00718120|110584|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052341|NCT00718120|110584|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052342|NCT00718120|110584|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052343|NCT00718120|110584|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052344|NCT00972686|112826|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057122|NCT00422604|AC2106956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049905|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
3052345|NCT00972686|112826|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052346|NCT00972686|112826|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059343|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
3059344|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
3059345|NCT00363727|101468/228|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059346|NCT00363727|101468/228|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059347|NCT00363727|101468/228|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059348|NCT00363727|101468/228|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059349|NCT00363727|101468/228|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059350|NCT00320463|105910|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059351|NCT00320463|105910|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059352|NCT00320463|105910|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059353|NCT00320463|105910|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059354|NCT00320463|105910|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049906|NCT06652529||Study Protocol|https://www.aromics.es/en/|
3052347|NCT00972686|112826|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052348|NCT00972686|112826|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052349|NCT00972686|112826|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052350|NCT00972686|112826|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052351|NCT02236611|201315|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052352|NCT02236611|201315|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052353|NCT02236611|201315|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052354|NCT02236611|201315|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052355|NCT02236611|201315|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052356|NCT02236611|201315|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052357|NCT02236611|201315|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052358|NCT03928665||DDLS - reference|https://www.sign.ac.uk/assets/sign144_disc_chart_colour.pdf|
3054343|NCT01702363|115361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054344|NCT01702363|115361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054345|NCT01702363|115361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054346|NCT01702363|115361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052359|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
3052360|NCT07044193||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521375-31-00|
3052361|NCT00929526|112949|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052362|NCT00929526|112949|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052363|NCT00929526|112949|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052364|NCT00929526|112949|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052365|NCT00929526|112949|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052366|NCT00929526|112949|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054347|NCT01702363|115361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057123|NCT00422604|AC2106956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052367|NCT01072149|110946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052368|NCT01072149|110946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052369|NCT01072149|110946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052370|NCT01072149|110946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052371|NCT01072149|110946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052372|NCT01072149|110946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052373|NCT01072149|110946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052374|NCT01602900|116038|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052375|NCT01602900|116038|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052376|NCT01602900|116038|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052377|NCT01602900|116038|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052378|NCT01602900|116038|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052379|NCT01602900|116038|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052380|NCT01602900|116038|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052381|NCT07013123|2025-521258-41-00|Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en|avalable after authorization of competent authorities
3052382|NCT04526171||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/Q3P4WX|
3052383|NCT04205669||Individual Participant Data Set|https://www.kaggle.com/julianmatthewman/grattigratta-data|
3052384|NCT04338568||Clinical Study Report|https://www.castoredc.com/|
3052385|NCT01316913|113374|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057124|NCT00422604|AC2106956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052386|NCT01316913|113374|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052387|NCT01316913|113374|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052388|NCT01316913|113374|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052389|NCT01316913|113374|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052390|NCT01316913|113374|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052391|NCT01316913|113374|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052392|NCT05400525||Study Protocol|https://discoverthesecretofgoodhealth.weebly.com|
3059355|NCT00320463|105910|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059356|NCT01636713|114634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059357|NCT01636713|114634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059358|NCT01636713|114634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059359|NCT01636713|114634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059360|NCT01636713|114634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059361|NCT01636713|114634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059362|NCT01636713|114634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059363|NCT06979739||Informed Consent Form|https://www.hku.edu.tr/iletisim/|
3059364|NCT00353873|SAM104926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059365|NCT00353873|SAM104926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059366|NCT00353873|SAM104926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059367|NCT00353873|SAM104926|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059368|NCT00353873|SAM104926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059369|NCT00353873|SAM104926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059370|NCT00353873|SAM104926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059371|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
3059372|NCT02011490||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-105&kw=8616-105&tab=access|
3059373|NCT01669083|116741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059374|NCT01669083|116741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059375|NCT01669083|116741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059376|NCT01669083|116741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059377|NCT01669083|116741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059378|NCT01669083|116741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059379|NCT01669083|116741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059380|NCT05936528||Individual Participant Data Set|https://drive.google.com/drive/folders/1CBAPVtAVYsi2x1iLQdWl48b9OowGSxw9|
3059381|NCT01762813||Study Protocol|http://translational-medicine.biomedcentral.com/articles/10.1186/s12967-016-0951-4|
3059382|NCT00306644|49653/334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059383|NCT00306644|49653/334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059384|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
3052393|NCT06477549|Protocol version 1.0|Study Protocol|https://cloud.mail.ru/public/wQ1q/8amGwZdMb|Study protocol signed
3052394|NCT00346398|SDY545|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY545|ImmPort study identifier is SDY545.
3052395|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.
3054348|NCT01702363|115361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054349|NCT01702363|115361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054350|NCT00875784|103629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059385|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
3059386|NCT00306644|49653/334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059387|NCT00306644|49653/334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059388|NCT00306644|49653/334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059389|NCT00969436|109995|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059390|NCT00969436|109995|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059391|NCT00969436|109995|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059392|NCT00969436|109995|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059393|NCT00969436|109995|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059394|NCT00969436|109995|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059395|NCT00969436|109995|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059396|NCT00422994|RRL103628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059397|NCT00422994|RRL103628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059398|NCT00422994|RRL103628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059399|NCT00422994|RRL103628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059400|NCT00422994|RRL103628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059401|NCT00422994|RRL103628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054351|NCT00875784|103629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057125|NCT00422604|AC2106956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057126|NCT00422604|AC2106956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057127|NCT07089667||Study Protocol|https://drive.google.com/drive/folders/1QpzE6ACGieVNCGQ1nsLJHxUWtB-fUfLV?usp=sharing|
3057128|NCT01894386|200587|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057129|NCT01894386|200587|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057130|NCT01894386|200587|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057131|NCT01894386|200587|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057132|NCT01894386|200587|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057133|NCT01894386|200587|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057134|NCT01894386|200587|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057135|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
3057136|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
3057137|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
3057138|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
3057139|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
3057140|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
3057141|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
3057142|NCT00226499|100388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057143|NCT00226499|100388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057144|NCT00226499|100388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057145|NCT00226499|100388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057146|NCT00226499|100388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057147|NCT00226499|100388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057148|NCT07111780|example study protokol|Study Protocol|https://www.nature.com/articles/s41598-024-79811-3|
3057149|NCT07111143||Health-Damaging Climate Events Highlight the Need for Interdisciplinary, Engaged Research|https://pubmed.ncbi.nlm.nih.gov/38371354/|
3057150|NCT06941233||Study Protocol|https://hjpwd.ahs.uic.edu|study protocol may be accessed by contacting the research team
3057151|NCT00661557|107408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057152|NCT00661557|107408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057153|NCT00661557|107408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057154|NCT00661557|107408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057155|NCT00661557|107408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057156|NCT00661557|107408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057157|NCT00661557|107408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057158|NCT00838903|112753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057159|NCT00838903|112753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057160|NCT00838903|112753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057161|NCT00838903|112753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057162|NCT00838903|112753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049907|NCT00354536|GLP106073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059402|NCT00422994|RRL103628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059403|NCT06103929||Individual Participant Data Set|https://le.ac.uk/people/sam-tromans|
3059404|NCT06103929||Study Protocol|https://le.ac.uk/people/sam-tromans|
3059405|NCT06103929||Statistical Analysis Plan|https://le.ac.uk/people/sam-tromans|
3059406|NCT06103929||Informed Consent Form|https://le.ac.uk/people/sam-tromans|
3059407|NCT00475215||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059408|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/0310250742582348|
3059409|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/1823080587913061|
3059410|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
3059411|NCT00652951|110142|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059412|NCT00652951|110142|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059413|NCT00652951|110142|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059414|NCT00652951|110142|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059415|NCT00652951|110142|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059416|NCT00652951|110142|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059417|NCT01462617|115117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059418|NCT01462617|115117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059419|NCT01462617|115117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059420|NCT01462617|115117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059421|NCT01462617|115117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059422|NCT01462617|115117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059423|NCT01462617|115117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059424|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
3059425|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.
3059426|NCT00771615|111729|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059427|NCT00771615|111729|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059428|NCT00771615|111729|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059429|NCT00771615|111729|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059430|NCT00771615|111729|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059431|NCT00771615|111729|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059432|NCT00771615|111729|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059433|NCT00945932|112851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059434|NCT00945932|112851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049908|NCT00354536|GLP106073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049909|NCT00354536|GLP106073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049910|NCT00354536|GLP106073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049911|NCT00354536|GLP106073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059435|NCT00945932|112851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059436|NCT00945932|112851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059437|NCT00945932|112851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059438|NCT00945932|112851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059439|NCT00945932|112851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059440|NCT01209078|113414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059441|NCT01209078|113414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059442|NCT01209078|113414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059443|NCT01209078|113414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059444|NCT01209078|113414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059445|NCT01209078|113414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059446|NCT01209078|113414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059447|NCT00307554|105553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059448|NCT00307554|105553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059449|NCT00307554|105553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059450|NCT00307554|105553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059451|NCT00307554|105553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059452|NCT00307554|105553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059453|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
3059454|NCT00231413|102115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059455|NCT00231413|102115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059456|NCT00231413|102115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059457|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.
3059458|NCT00231413|102115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059459|NCT00231413|102115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059460|NCT01147900|113055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059461|NCT01147900|113055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059462|NCT01147900|113055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059463|NCT01147900|113055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059464|NCT01147900|113055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059465|NCT01147900|113055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059466|NCT01600092||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-035&kw=V260-035&tab=access|
3059467|NCT04303299|Thai government data|Data references|https://ddc.moph.go.th|
3059468|NCT04303299||News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
3059469|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)
3059470|NCT04303299||Reference News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
3059471|NCT01381536|114243|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059472|NCT01381536|114243|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059473|NCT01381536|114243|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059474|NCT01381536|114243|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059475|NCT01381536|114243|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054352|NCT00875784|103629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052396|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.
3052397|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.
3052398|NCT00470483|TMT106386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052399|NCT00470483|TMT106386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052400|NCT00470483|TMT106386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052401|NCT00470483|TMT106386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052402|NCT00470483|TMT106386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052403|NCT00470483|TMT106386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052404|NCT00035048||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052405|NCT06699511||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34847915/|
3052406|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
3052407|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"
3052408|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
3052409|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
3052410|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
3052411|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
3052412|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
3052413|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
3057163|NCT00838903|112753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052414|NCT05214248||Study Protocol|https://doi.org/10.1016/S0377-1237(10)80131-5|Article Title: Meconium Aspiration Syndrome: An Insight
3049912|NCT00354536|GLP106073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049913|NCT00354536|GLP106073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049914|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.
3049915|NCT00000488||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|
3049916|NCT01622231|116365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049917|NCT01622231|116365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049918|NCT01622231|116365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049919|NCT01622231|116365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049920|NCT06462885||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
3049921|NCT00347360|CFD105453|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049922|NCT00347360|CFD105453|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049923|NCT00347360|CFD105453|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049924|NCT00347360|CFD105453|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049925|NCT00347360|CFD105453|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049926|NCT00347360|CFD105453|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049927|NCT00347360|CFD105453|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049928|NCT01148472|2004-005069-39|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2004-005069-39/results|
3049929|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.
3049930|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
3049931|NCT00094172|ITN020AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN020AI
3049932|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.
3049933|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
3049934|NCT01471678|115707|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049935|NCT01471678|115707|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049936|NCT01471678|115707|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049937|NCT01471678|115707|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049938|NCT01471678|115707|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049939|NCT01471678|115707|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049940|NCT01471678|115707|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049941|NCT00369824|107682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049942|NCT00369824|107682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049943|NCT00369824|107682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049944|NCT00369824|107682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049945|NCT00369824|107682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049946|NCT00369824|107682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052415|NCT03884478||Study Protocol|https://www.researchprotocols.org/2021/4/e24647|available open access at URL provided
3049947|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
3049948|NCT01254071|114694|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049949|NCT01254071|114694|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049950|NCT01254071|114694|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049951|NCT01254071|114694|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049952|NCT01254071|114694|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049953|NCT01254071|114694|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049954|NCT01254071|114694|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049955|NCT02809612||Study Protocol|http://www.kbh.uu.se|
3049956|NCT00043901|LAM40097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049957|NCT00043901|LAM40097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049958|NCT00043901|LAM40097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049959|NCT00043901|LAM40097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054353|NCT00875784|103629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052416|NCT01381445|113435|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052417|NCT01381445|113435|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052418|NCT01381445|113435|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052419|NCT01381445|113435|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052420|NCT01381445|113435|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052421|NCT01381445|113435|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052422|NCT01381445|113435|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052423|NCT00424476|HGS1006-C1057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052424|NCT00424476|HGS1006-C1057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052425|NCT00424476|HGS1006-C1057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052426|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
3052427|NCT00424476|HGS1006-C1057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052428|NCT00424476|HGS1006-C1057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052429|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
3052430|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.
3052431|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
3052432|NCT00632736|101468/248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052433|NCT00632736|101468/248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052434|NCT00632736|101468/248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052435|NCT00632736|101468/248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052436|NCT00632736|101468/248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052437|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
3052438|NCT00879827|217744/049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049960|NCT00043901|LAM40097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049961|NCT00043901|LAM40097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049962|NCT00043901|LAM40097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049963|NCT00289783|103813|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049964|NCT00289783|103813|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049965|NCT00289783|103813|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049966|NCT00289783|103813|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049967|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.
3049968|NCT03733470|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
3049969|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.
3049970|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.
3049971|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.
3049972|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.
3049973|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.
3049974|NCT00043914|LAM40013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049975|NCT00043914|LAM40013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049976|NCT00043914|LAM40013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049977|NCT00043914|LAM40013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049978|NCT00043914|LAM40013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049979|NCT00043914|LAM40013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049980|NCT00043914|LAM40013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049981|NCT00109122||CSR Synopsiis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3049982|NCT00508365|CFD109701|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049983|NCT00508365|CFD109701|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049984|NCT00508365|CFD109701|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049985|NCT00508365|CFD109701|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049986|NCT00508365|CFD109701|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049987|NCT00508365|CFD109701|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049988|NCT00508365|CFD109701|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049989|NCT00758836||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-046&kw=0974-046&tab=access|
3049990|NCT05930912||Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
3049991|NCT05930912|zenodo.7382529|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7382529|
3049992|NCT05930912|zenodo.6942208|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6942208|
3049993|NCT05930912|zenodo.7188211|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7188211|
3049994|NCT05930912|zenodo.6941906|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6941906|
3049995|NCT05930912|zenodo.6952516|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6952516|
3049996|NCT05930912|zenodo.7022873|Analytic Code|http://doi.org/10.5281/zenodo.7022873|The technological-psychoanalytic mass psychological observation and analysis schemes.
3049997|NCT00963937|111035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049998|NCT00963937|111035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052439|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
3052440|NCT00879827|217744/049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052441|NCT00879827|217744/049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052442|NCT00879827|217744/049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052443|NCT03151694||Peer-Reviewed Article|http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12646/full|
3052444|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529982|
3052445|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529983|
3052446|NCT00787371||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052447|NCT00103857||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052448|NCT00866619|110021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052449|NCT00866619|110021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059476|NCT01381536|114243|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059477|NCT01521377|114635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059478|NCT01521377|114635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059479|NCT01521377|114635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3049999|NCT00963937|111035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050000|NCT00963937|111035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050001|NCT01762878|116617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059480|NCT01521377|114635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059481|NCT01521377|114635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059482|NCT01521377|114635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059483|NCT01521377|114635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059484|NCT01300455||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-036&kw=4305-036&tab=access|
3059485|NCT03696901|Xydalba|Study Protocol|https://awbdb.bfarm.de/ords/f?p=101:STARTSEITE::::::|BfArM AWB Datenbank
3059486|NCT00778895|111635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059487|NCT00778895|111635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050002|NCT01762878|116617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052450|NCT00866619|110021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052451|NCT00866619|110021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052452|NCT00866619|110021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052453|NCT00866619|110021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052454|NCT00092378||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052455|NCT00197262|FFR104861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052456|NCT00197262|FFR104861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052457|NCT00197262|FFR104861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052458|NCT00197262|FFR104861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052459|NCT00197262|FFR104861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052460|NCT00197262|FFR104861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052461|NCT00197262|FFR104861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052462|NCT04883541||PhD thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
3052463|NCT02404012||Website|https://ngletsum.wixsite.com/nito|
3052464|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.
3052465|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
3052466|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.
3059488|NCT00778895|111635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059489|NCT00778895|111635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059490|NCT00778895|111635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059491|NCT00778895|111635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059492|NCT04892108||Study Protocol|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
3052467|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.
3052468|NCT00227422|102394|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059493|NCT04892108||Statistical Analysis Plan|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
3059494|NCT04892108||Informed Consent Form|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
3059495|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.
3059496|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
3059497|NCT04657783||Study Protocol|https://drive.google.com/drive/my-drive|
3059498|NCT06583694||Clinical Study Report|https://www.bangkoknoimodel.com/stat.|
3059499|NCT00343707|NKP102280|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059500|NCT00343707|NKP102280|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059501|NCT00343707|NKP102280|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059502|NCT00343707|NKP102280|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059503|NCT00343707|NKP102280|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059504|NCT00343707|NKP102280|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059505|NCT01147848|113091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059506|NCT01147848|113091|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052469|NCT00227422|102394|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052470|NCT00227422|102394|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052471|NCT00227422|102394|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052472|NCT00227422|102394|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052473|NCT00227422|102394|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052474|NCT04419571|285260|Individual Participant Data Set|https://www.myresearchproject.org.uk/|Data collection template available on IRAS (Integrated Research Application System) registration
3052475|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
3052476|NCT04419571|285260|Study Protocol|https://www.myresearchproject.org.uk/|Protocol available on IRAS (Integrated Research Application System) registration
3052477|NCT02907489||Study Protocol|https://www.scribd.com/document/328018560/Protocol-Omaia-Repaired-Autosaved|
3052478|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.
3052479|NCT00000492||Study Forms|http://biolincc.nhlbi.nih.gov/studies/bhat/|
3052480|NCT04503434||Informed Consent Form|https://enquesta.clinic.cat/index.php/admin/survey/sa/view/surveyid/818692|
3052481|NCT02384122|27619827|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27619827|
3052482|NCT06700161|Study Protocol|Study Protocol|https://tipfakultesi.ksu.edu.tr/Default.aspx?SId=24451|
3052483|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.
3059507|NCT01147848|113091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059508|NCT01147848|113091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059509|NCT01147848|113091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059510|NCT01147848|113091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059511|NCT01147848|113091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050003|NCT01762878|116617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050004|NCT01762878|116617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050005|NCT01762878|116617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050006|NCT01762878|116617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050007|NCT01762878|116617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050008|NCT05695209|VIV00009027|Individual Participant Data Set|https://vivli.org|https://doi.org/10.25934/PR00009027
3050009|NCT01606800||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8908B-059&kw=8908B-059&tab=access|
3050010|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/auad/issue/60075/826745|
3050011|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/411491|
3050012|NCT06253572||Review|http://journalofomepturkey.org/index.php/eccd/article/view/78|
3050013|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.
3050014|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/199140|
3050015|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/rep/issue/63330/827844|
3050016|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
3050017|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
3050018|NCT01648101|114855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050019|NCT01648101|114855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050020|NCT01648101|114855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050021|NCT01648101|114855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050022|NCT01648101|114855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050023|NCT01648101|114855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050024|NCT01648101|114855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050025|NCT01168167|01168167|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT01168167|
3050026|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.
3050027|NCT00000557||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
3050028|NCT00000557||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
3050029|NCT01323959|113060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050030|NCT01323959|113060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050031|NCT01323959|113060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050032|NCT01323959|113060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050033|NCT01323959|113060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050034|NCT01323959|113060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050035|NCT00169546|SAM40100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050036|NCT00169546|SAM40100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050037|NCT00169546|SAM40100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050038|NCT00169546|SAM40100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054354|NCT00875784|103629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054355|NCT00875784|103629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050039|NCT00169546|SAM40100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059512|NCT02891382||Individual Participant Data Set|https://figshare.com/articles/REDEEM_Study_Feasibility_pilot_study/7180802|
3050040|NCT00169546|SAM40100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050041|NCT00169546|SAM40100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050042|NCT01262911|115083|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050043|NCT01262911|115083|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050044|NCT01262911|115083|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050045|NCT01262911|115083|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050046|NCT01262911|115083|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050047|NCT01262911|115083|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050048|NCT01262911|115083|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050049|NCT01577680|114637|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050050|NCT01577680|114637|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050051|NCT01577680|114637|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050052|NCT01577680|114637|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050053|NCT01577680|114637|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050054|NCT01577680|114637|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050055|NCT01577680|114637|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050056|NCT05792709||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788277/|
3050057|NCT00907777|112807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050058|NCT00907777|112807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050059|NCT00907777|112807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050060|NCT00907777|112807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050061|NCT00907777|112807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050062|NCT00907777|112807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050063|NCT00684593||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04481&kw=7123-009&tab=access|
3050064|NCT04329871||Individual Participant Data Set|http://Metabolic-institute.com|
3050065|NCT04213079||Study Protocol|http://mdds.nyc/|
3050066|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.
3050067|NCT01916720|480848/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050068|NCT01916720|480848/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050069|NCT01916720|480848/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050070|NCT01916720|480848/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050071|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
3050072|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
3050073|NCT01916720|480848/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059513|NCT00148941|213503/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059514|NCT00148941|213503/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050074|NCT00617123||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05183&kw=P05183&tab=access|
3050075|NCT00783003|112146|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050076|NCT00783003|112146|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050077|NCT00783003|112146|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050078|NCT00783003|112146|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050079|NCT00783003|112146|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050080|NCT00783003|112146|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050081|NCT00783003|112146|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050082|NCT02446483|201527|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050083|NCT02446483|201527|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050084|NCT02446483|201527|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050085|NCT02446483|201527|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050086|NCT02446483|201527|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050087|NCT01802931|117016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050088|NCT01802931|117016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050089|NCT01802931|117016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050090|NCT01802931|117016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050091|NCT01802931|117016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050092|NCT01802931|117016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050093|NCT01802931|117016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050094|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.
3050095|NCT00318630|104385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050096|NCT00318630|104385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050097|NCT00318630|104385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050098|NCT00318630|104385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050099|NCT00318630|104385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050100|NCT00318630|104385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050101|NCT00318630|104385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050102|NCT07001969||Individual Participant Data Set|https://t.me/drmassoud77/24301|Book of author about technique
3050103|NCT00530309|GLP107865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050104|NCT00530309|GLP107865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050105|NCT00530309|GLP107865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050106|NCT00530309|GLP107865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050107|NCT00530309|GLP107865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050108|NCT00530309|GLP107865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050109|NCT00530309|GLP107865|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050110|NCT00197132|49653/375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050111|NCT00197132|49653/375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050112|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
3050113|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
3050114|NCT00197132|49653/375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050115|NCT00197132|49653/375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050116|NCT00197132|49653/375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050117|NCT01366521|114092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050118|NCT01366521|114092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050119|NCT01366521|114092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050120|NCT01366521|114092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050121|NCT01366521|114092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050122|NCT01366521|114092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050123|NCT01366521|114092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050124|NCT00843024|107979|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050125|NCT00843024|107979|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050126|NCT00843024|107979|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050127|NCT00843024|107979|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050128|NCT00843024|107979|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050129|NCT00843024|107979|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050130|NCT00843024|107979|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050131|NCT01372137|doi: 10.1111/bph.13433|Manuscript|http://onlinelibrary.wiley.com/doi/10.1111/bph.13433/abstract;jsessionid=E657A6C9667BB70DE92E5B69B86B1D3F.f01t01|
3050132|NCT02877615||Study Protocol|https://clinicaltrials.servier.com/|
3050133|NCT02877615||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050134|NCT02877615||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3050135|NCT02877615||Informed Consent Form|https://clinicaltrials.servier.com/|
3050136|NCT02877615||Clinical Study Report|https://clinicaltrials.servier.com/|
3050137|NCT02877615||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3050138|NCT00694993|HHI110157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050139|NCT00694993|HHI110157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050140|NCT00694993|HHI110157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050141|NCT00694993|HHI110157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050142|NCT00694993|HHI110157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050143|NCT00694993|HHI110157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050144|NCT00694993|HHI110157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050145|NCT01411111|112362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050146|NCT01411111|112362|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050147|NCT01411111|112362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054356|NCT00875784|103629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054357|NCT00828867|111341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054358|NCT00828867|111341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050148|NCT01411111|112362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050149|NCT01411111|112362|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050150|NCT01411111|112362|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050151|NCT01411111|112362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050152|NCT01366560|114639|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050153|NCT01366560|114639|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050154|NCT01366560|114639|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050155|NCT01366560|114639|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050156|NCT01366560|114639|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050157|NCT01366560|114639|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050158|NCT01366560|114639|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050159|NCT00811798|111712|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050160|NCT00811798|111712|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050161|NCT00811798|111712|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050162|NCT00811798|111712|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050163|NCT00811798|111712|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050164|NCT00811798|111712|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050165|NCT00811798|111712|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050166|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)."
3050167|NCT04221009||Informed Consent Form|https://arc.research.usf.edu/Prod/sd/Doc/0/DDRU7K2KMHLK9ECT12FPTMA60B/3S78A88933BKN7869JO1NSMT62.pdf|
3050168|NCT04221009||Study Protocol|https://arc.research.usf.edu/Prod/sd/Doc/0/06USV5NTK2VKJ06CUK3TQJR578/Protocol%20v01%202019-10-24.docx|
3050169|NCT01018186|106839|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050170|NCT01018186|106839|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050171|NCT01018186|106839|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050172|NCT01018186|106839|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050173|NCT01018186|106839|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050174|NCT01018186|106839|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050175|NCT01018186|106839|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050176|NCT00609492|109621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050177|NCT00609492|109621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050178|NCT00609492|109621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054359|NCT00828867|111341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050179|NCT00609492|109621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050180|NCT00609492|109621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050181|NCT00609492|109621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050182|NCT00609492|109621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050183|NCT00372112|B2C108562|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050184|NCT00372112|B2C108562|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050185|NCT00372112|B2C108562|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050186|NCT00372112|B2C108562|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050187|NCT00372112|B2C108562|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050188|NCT00372112|B2C108562|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050189|NCT00372112|B2C108562|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050190|NCT01428453|114458|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050191|NCT01428453|114458|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050192|NCT01428453|114458|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050193|NCT01428453|114458|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050194|NCT01428453|114458|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050195|NCT01428453|114458|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050196|NCT01428453|114458|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050197|NCT01077856||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-033&kw=V501-033&tab=access|
3050198|NCT03134287||Textbook|http://onlinelibrary.wiley.com/doi/10.1111/j.1742-6723.2004.00655.x/full|Samuels LE, Roberts JR, Hedges JR. Nasogastric and Feeding Tube Placement, In: Clinical Procedures in Emergency Medicine. 4th ed. WB Saunders; 2004. p784-804.
3050199|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.
3050200|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.
3050201|NCT00356369|107386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050202|NCT00356369|107386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050203|NCT00356369|107386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050204|NCT00356369|107386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050205|NCT00356369|107386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050206|NCT00356369|107386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050207|NCT00044278|LAM20007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050208|NCT00044278|LAM20007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050209|NCT00044278|LAM20007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050210|NCT00044278|LAM20007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050211|NCT00044278|LAM20007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050212|NCT00044278|LAM20007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050213|NCT00044278|LAM20007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050214|NCT01124422|113877|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050215|NCT01124422|113877|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050216|NCT01124422|113877|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050217|NCT01124422|113877|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050218|NCT01124422|113877|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050219|NCT01124422|113877|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050220|NCT01124422|113877|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050221|NCT01607086|111649|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050222|NCT01607086|111649|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050223|NCT01607086|111649|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050224|NCT01607086|111649|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050225|NCT01607086|111649|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050226|NCT01607086|111649|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050227|NCT01607086|111649|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050228|NCT03012802||Study Protocol|http://www.grupogerm.es/power|
3050229|NCT03012802||Statistical Analysis Plan|http://www.grupogerm.es/power|
3050230|NCT03012802||Clinical Study Report|http://www.grupogerm.es/power|
3050231|NCT01702454|116023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050232|NCT01702454|116023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050233|NCT01702454|116023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050234|NCT01702454|116023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050235|NCT01702454|116023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050236|NCT01702454|116023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052484|NCT00733577|111829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052485|NCT00733577|111829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052486|NCT00733577|111829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052487|NCT00733577|111829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052488|NCT00733577|111829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052489|NCT00733577|111829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052490|NCT00733577|111829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052491|NCT00352963|217744/097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052492|NCT00352963|217744/097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052493|NCT00352963|217744/097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052494|NCT00352963|217744/097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052495|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
3052496|NCT00352963|217744/097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050237|NCT01702454|116023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052497|NCT00475436|AC4106889|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052498|NCT00475436|AC4106889|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052499|NCT00475436|AC4106889|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052500|NCT00475436|AC4106889|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050238|NCT01030939|112861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050239|NCT01030939|112861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050240|NCT01030939|112861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050241|NCT01030939|112861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050242|NCT01030939|112861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050243|NCT01030939|112861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050244|NCT01030939|112861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050245|NCT00256893|ROF102100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050246|NCT00256893|ROF102100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050247|NCT00256893|ROF102100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050248|NCT00256893|ROF102100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050249|NCT00256893|ROF102100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050250|NCT00256893|ROF102100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050251|NCT00256893|ROF102100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050252|NCT00496093||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050253|NCT00412854|104567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050254|NCT00412854|104567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050255|NCT00412854|104567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050256|NCT00412854|104567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050257|NCT00412854|104567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050258|NCT00412854|104567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050259|NCT00412854|104567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050260|NCT00369993|SAS104449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050261|NCT00369993|SAS104449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050262|NCT00369993|SAS104449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050263|NCT00369993|SAS104449|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054360|NCT00828867|111341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054361|NCT00828867|111341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054362|NCT00828867|111341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050264|NCT00369993|SAS104449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050265|NCT00369993|SAS104449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050266|NCT00369993|SAS104449|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050267|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)
3050268|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf|CDC/NHSN Surveillance Definitions for Specific Types of Infections
3050269|NCT00877877|111375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050270|NCT00877877|111375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050271|NCT00877877|111375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050272|NCT00877877|111375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050273|NCT00877877|111375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050274|NCT00877877|111375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050275|NCT00877877|111375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050276|NCT03715166||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050277|NCT03715166||Study Protocol|https://clinicaltrials.servier.com/|
3050278|NCT03715166||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3050279|NCT03715166||Informed Consent Form|https://clinicaltrials.servier.com/|
3050280|NCT03715166||Clinical Study Report|https://clinicaltrials.servier.com/|
3050281|NCT03715166||study-level clinical trial data|https://clinicaltrials.servier.com/|
3050282|NCT03577743|BMTN|Study Protocol|http://clinicaltrials.gov/NCT03577743|Phase 2 study to evaluate the effect of bevacizumab in metastatic triple negative breast cancer patients
3050283|NCT01949051|200285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050284|NCT01949051|200285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050285|NCT01949051|200285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050286|NCT01949051|200285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050287|NCT01949051|200285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050288|NCT01949051|200285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050289|NCT01949051|200285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050290|NCT04464369|LPDSItopride study|Study Protocol|http://www.targid.eu|
3050291|NCT01777256|115919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050292|NCT01777256|115919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050293|NCT01777256|115919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050294|NCT01777256|115919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050295|NCT01777256|115919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050296|NCT01777256|115919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050297|NCT01777256|115919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050298|NCT00102882|SFA100062|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050299|NCT00102882|SFA100062|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050300|NCT00102882|SFA100062|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050301|NCT00102882|SFA100062|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050302|NCT00102882|SFA100062|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050303|NCT00102882|SFA100062|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050304|NCT00102882|SFA100062|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050305|NCT03019133|201609843|Informed Consent Form|http://hawkirb.research.uiowa.edu|
3050306|NCT04631081||Individual Participant Data Set|https://www.project-redcap.org/|
3050307|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
3050308|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
3050309|NCT00503009|HZA109895|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050310|NCT00503009|HZA109895|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050311|NCT00503009|HZA109895|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050312|NCT00503009|HZA109895|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050313|NCT00503009|HZA109895|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050314|NCT00503009|HZA109895|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050315|NCT00268996|SB-480848/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050316|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
3050317|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
3050318|NCT00268996|SB-480848/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050319|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
3050320|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
3050321|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
3050322|NCT02028065||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-101&kw=8616-101&tab=access|
3050323|NCT01847417|116498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050324|NCT01847417|116498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050325|NCT01847417|116498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050326|NCT01847417|116498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050327|NCT01847417|116498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050328|NCT01847417|116498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050329|NCT02045797|116704|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050330|NCT02045797|116704|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050331|NCT02045797|116704|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050332|NCT02045797|116704|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050333|NCT02045797|116704|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050334|NCT02045797|116704|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050335|NCT02045797|116704|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050336|NCT05069454||Study Protocol|http://www.isim.az|
3050337|NCT02982967||Individual Participant Data Set|https://figshare.com/s/8f238bd02ca631cfe5fd|
3050338|NCT00451321|115493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050339|NCT00451321|115493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050340|NCT00451321|115493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050341|NCT00451321|115493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050342|NCT00451321|115493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050343|NCT00451321|115493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050344|NCT00451321|115493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050345|NCT01686633|116863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050346|NCT01686633|116863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050347|NCT01686633|116863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050348|NCT01686633|116863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050349|NCT01686633|116863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050350|NCT01686633|116863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050351|NCT01686633|116863|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050352|NCT00056407|ARI40006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050353|NCT00056407|ARI40006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050354|NCT00056407|ARI40006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050355|NCT00056407|ARI40006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050356|NCT00056407|ARI40006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050357|NCT00056407|ARI40006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050358|NCT00056407|ARI40006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050359|NCT04742101||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050360|NCT04742101||Study Protocol|https://clinicaltrials.servier.com/|
3050361|NCT04742101||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3050362|NCT04742101||Informed Consent Form|https://clinicaltrials.servier.com/|
3050363|NCT04742101||Clinical Study Report|https://clinicaltrials.servier.com/|
3050364|NCT04742101||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3050365|NCT02369341|201959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050366|NCT02369341|201959|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050367|NCT02369341|201959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050368|NCT02369341|201959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050369|NCT02369341|201959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050370|NCT02369341|201959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050371|NCT02369341|201959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050372|NCT02626520||Study Protocol|https://docs.google.com/viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxyZWFsd29ybGRvbmNvbG9neXxneDo2OGI0ZDgxMzdkZDIxYWJh|
3050373|NCT00608283|SDY289|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
3050374|NCT00608283|SDY289|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
3050375|NCT00608283|SDY289|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
3050376|NCT00873509||Individual Participant Data Set|https://ndar.nih.gov|
3050377|NCT00527943||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04736&kw=P04736&tab=access|
3050378|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
3050379|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
3050380|NCT00197041|257049/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050381|NCT00197041|257049/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050382|NCT00197041|257049/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050383|NCT00197041|257049/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050384|NCT00197041|257049/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050385|NCT01641692|116402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059515|NCT00148941|213503/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059516|NCT00148941|213503/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050386|NCT01641692|116402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050387|NCT01641692|116402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050388|NCT01641692|116402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050389|NCT01641692|116402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050390|NCT01641692|116402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050391|NCT01641692|116402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050392|NCT01107587|113518|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050393|NCT01107587|113518|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050394|NCT01107587|113518|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050395|NCT01107587|113518|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050396|NCT01107587|113518|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050397|NCT01107587|113518|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050398|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.
3050399|NCT00060476||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050400|NCT03141281|https://osf.io/dp8n5/|Statistical Analysis Plan|https://osf.io/kq8yz/register/565fb3678c5e4a66b5582f67|Open Science Foundation registration of Data Analysis Plan
3050401|NCT01756495|116628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050402|NCT01756495|116628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050403|NCT01756495|116628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050404|NCT01756495|116628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050405|NCT01756495|116628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050406|NCT01756495|116628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050407|NCT01756495|116628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050408|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.
3050409|NCT00000586||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/MSH/|
3050410|NCT00000586||Study Forms|http://biolincc.nhlbi.nih.gov/studies/MSH/|
3050411|NCT03578081||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|
3050412|NCT01948739||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25570900|
3050413|NCT04999150|B0710118|Study Protocol|https://irbrcm.rcm.upr.edu/|
3050414|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.
3050415|NCT04608500||Study Protocol|http://foamix.co.il/|
3050416|NCT01010906||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-005&kw=7009-005&tab=access|
3050417|NCT00454987|109664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050418|NCT00454987|109664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050419|NCT00454987|109664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050420|NCT00454987|109664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050421|NCT00454987|109664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050422|NCT04187560||Clinical Study Report|http://lbpharma.us/wp-content/uploads/2020/12/lb-102-001-clinical-study-report-final.pdf|
3050423|NCT01984775|117191|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050424|NCT01984775|117191|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050425|NCT01984775|117191|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050426|NCT01984775|117191|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050427|NCT01984775|117191|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050428|NCT01984775|117191|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050429|NCT04644614||Study Protocol|https://doi.org/10.1016/j.urols.2015.06.286|
3050430|NCT01782664|116679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050431|NCT01782664|116679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059517|NCT00148941|213503/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059518|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
3059519|NCT02747017||Study Protocol|http://insight.ccbr.umn.edu/official_documents/CDIFF/protocol_documents/I7-Protocol.pdf|
3059520|NCT05502510||Analytic Code|https://osf.io/bty8n/?view_only=f8bb6e5a7698443494d4c3788a45cc0f|The analytic code will be uploaded to OSF upon publishing the manuscript.
3059521|NCT01000324|112267|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059522|NCT01000324|112267|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059523|NCT01000324|112267|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059524|NCT01000324|112267|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059525|NCT01000324|112267|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059526|NCT01000324|112267|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059527|NCT01000324|112267|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059528|NCT00871338|111709|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059529|NCT00871338|111709|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059530|NCT00871338|111709|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059531|NCT00871338|111709|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059532|NCT00871338|111709|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059533|NCT00871338|111709|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059534|NCT00871338|111709|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059535|NCT01431963|115376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059536|NCT01431963|115376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059537|NCT01431963|115376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059538|NCT01431963|115376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059539|NCT01431963|115376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059540|NCT04904848||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/25437107/|
3059541|NCT00348309|AVA102672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059542|NCT00348309|AVA102672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059543|NCT00348309|AVA102672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059544|NCT00348309|AVA102672|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059545|NCT00348309|AVA102672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059546|NCT00348309|AVA102672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059547|NCT00348309|AVA102672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059548|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
3059549|NCT00532298|110620|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059550|NCT00532298|110620|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059551|NCT00532298|110620|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059552|NCT00532298|110620|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059553|NCT00532298|110620|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059554|NCT00532298|110620|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050432|NCT01782664|116679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050433|NCT01782664|116679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050434|NCT01782664|116679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050435|NCT01782664|116679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050436|NCT01782664|116679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050437|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.
3050438|NCT00000560||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/best/|
3050439|NCT00000560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/best/|
3050440|NCT00779012||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050441|NCT01462669|115860|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050442|NCT01462669|115860|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050443|NCT01462669|115860|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050444|NCT01462669|115860|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050445|NCT01462669|115860|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050446|NCT01462669|115860|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050447|NCT01462669|115860|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050448|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.
3050449|NCT07171762||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/18166260/|
3050450|NCT07180485|t780927t@yahoo.com.tw|Study Protocol|https://orcid.org/0000-0002-8823-6901|t780927t@yahoo.com.tw
3050451|NCT01147861|114187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050452|NCT01147861|114187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050453|NCT01147861|114187|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050454|NCT01147861|114187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050455|NCT01147861|114187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050456|NCT01147861|114187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050457|NCT01147861|114187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050458|NCT00048607||CSR Synospis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050459|NCT00751348|110876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050460|NCT00751348|110876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050461|NCT00751348|110876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050462|NCT00751348|110876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050463|NCT00751348|110876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050464|NCT00751348|110876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050465|NCT01330485||Individual Participant Data Set|https://osf.io/426pd|
3050466|NCT01330485||All study files|https://osf.io/uhwnb|
3050467|NCT00451386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050468|NCT06906133||Information site for participants (in Icelandic)|https://www.unak.is/is/rannsoknir/rannsoknir-vid-ha/svefn|
3050469|NCT00380393|106464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050470|NCT00380393|106464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050471|NCT00380393|106464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050472|NCT00380393|106464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052501|NCT00475436|AC4106889|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052502|NCT00475436|AC4106889|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052503|NCT00475436|AC4106889|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052504|NCT00733551|MOT109681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052505|NCT00733551|MOT109681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052506|NCT00733551|MOT109681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052507|NCT00733551|MOT109681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052508|NCT00733551|MOT109681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052509|NCT00733551|MOT109681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052510|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.
3052511|NCT00197119|100566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052512|NCT00197119|100566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052513|NCT00197119|100566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052514|NCT00197119|100566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052515|NCT00197119|100566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052516|NCT06200480|NorHead|Study Protocol|https://www.ntnu.no/norhead/om|English Study protocol available by request to the Norwegian Centre of Headache Research (NorHead)
3052517|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)
3052518|NCT02214017|doi: 10.1177/1357633X15608984|publication|https://www.ncbi.nlm.nih.gov/pubmed/26468213|
3052519|NCT00092365||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052520|NCT00434577|108494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052521|NCT00434577|108494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052522|NCT00434577|108494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052523|NCT00434577|108494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052524|NCT00434577|108494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052525|NCT00434577|108494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052526|NCT00434577|108494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052527|NCT00356564|106744|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052528|NCT00356564|106744|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052529|NCT00356564|106744|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052530|NCT00356564|106744|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052531|NCT00356564|106744|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052532|NCT00356564|106744|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052533|NCT00938041|393229/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050473|NCT00380393|106464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050474|NCT00380393|106464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050475|NCT01075698||Study Protocol|https://prsinfo.clinicaltrials.gov/definitions.html|
3050476|NCT01391065||Published article|https://doi.org/10.1016/j.ijrobp.2019.10.037|
3050477|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
3050478|NCT00129129|101858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050479|NCT00129129|101858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050480|NCT00129129|101858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050481|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.
3050482|NCT00129129|101858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050483|NCT00907985|112676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050484|NCT00907985|112676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050485|NCT00907985|112676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050486|NCT00907985|112676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050487|NCT00907985|112676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050488|NCT00907985|112676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050489|NCT00907985|112676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050490|NCT00322335|106672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050491|NCT00322335|106672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050492|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.
3050493|NCT00322335|106672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050494|NCT00322335|106672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050495|NCT00322335|106672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050496|NCT00228917|103812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050497|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.
3050498|NCT00228917|103812|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050499|NCT00228917|103812|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050500|NCT00228917|103812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050501|NCT00228917|103812|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050502|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
3050503|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
3050504|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
3050505|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.
3050506|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.
3050507|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.
3052534|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
3052535|NCT00938041|393229/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052536|NCT00938041|393229/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052537|NCT00938041|393229/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052538|NCT00938041|393229/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052539|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
3052540|NCT01031186|113324|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052541|NCT01031186|113324|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052542|NCT01031186|113324|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050508|NCT00896558|112668|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050509|NCT00896558|112668|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050510|NCT00896558|112668|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050511|NCT00896558|112668|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050512|NCT00896558|112668|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050513|NCT00896558|112668|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050514|NCT00896558|112668|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050515|NCT00133874|TOC100224|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050516|NCT00133874|TOC100224|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050517|NCT00133874|TOC100224|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050518|NCT00133874|TOC100224|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050519|NCT00133874|TOC100224|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050520|NCT00133874|TOC100224|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050521|NCT00133874|TOC100224|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050522|NCT00116831|AVD100521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050523|NCT00116831|AVD100521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050524|NCT00116831|AVD100521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050525|NCT00116831|AVD100521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050526|NCT00116831|AVD100521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050527|NCT00116831|AVD100521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050528|NCT00116831|AVD100521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050529|NCT03672435||Individual Participant Data Set|http://www.abcd-vision.org/OCR/OCR%20proparacaine%20de-identified.pdf|deidentified OCR topical anesthetic recovery outcomes
3050530|NCT02319031|PMID: 26822022|Primary Publication|http://www.ncbi.nlm.nih.gov/pubmed/26822022|
3050531|NCT02735083||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050532|NCT02735083||Study Protocol|https://clinicaltrials.servier.com/|
3050533|NCT02735083||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3050534|NCT02735083||Informed Consent Form|https://clinicaltrials.servier.com/|
3050535|NCT02735083||Clinical Study Report|https://clinicaltrials.servier.com/|
3050536|NCT02735083||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3050537|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.
3050538|NCT00578175|110058|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050539|NCT00578175|110058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050540|NCT00578175|110058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050541|NCT00578175|110058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050542|NCT00578175|110058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050543|NCT00578175|110058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050544|NCT00578175|110058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050545|NCT01165138|106827|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050546|NCT01165138|106827|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050547|NCT01165138|106827|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050548|NCT01165138|106827|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050549|NCT01165138|106827|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050550|NCT01165138|106827|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050551|NCT01165138|106827|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050552|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.
3050553|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.
3050554|NCT00000514||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/shep/|
3050555|NCT00000514||Study Forms|http://biolincc.nhlbi.nih.gov/studies/shep/|
3050556|NCT00000514||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/shep/|
3054363|NCT00828867|111341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050557|NCT00603746|FFA109684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050558|NCT00603746|FFA109684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050559|NCT00603746|FFA109684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050560|NCT00603746|FFA109684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050561|NCT00603746|FFA109684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050562|NCT00603746|FFA109684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050563|NCT00603746|FFA109684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050564|NCT00196950|134612/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050565|NCT00196950|134612/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050566|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.
3050567|NCT00196950|134612/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050568|NCT00196950|134612/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050569|NCT00196950|134612/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050570|NCT00394030|GLP107724|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050571|NCT00394030|GLP107724|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050572|NCT00394030|GLP107724|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050573|NCT00394030|GLP107724|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050574|NCT00394030|GLP107724|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050575|NCT00394030|GLP107724|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050576|NCT00394030|GLP107724|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050577|NCT04164901||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050578|NCT07044180||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521373-13-00|
3050579|NCT01934153|117157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050580|NCT01934153|117157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050581|NCT01934153|117157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050582|NCT01934153|117157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050583|NCT01934153|117157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050584|NCT01934153|117157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050585|NCT01934153|117157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050586|NCT07110077|vanesssatob@gmail.com|Study Protocol|https://drive.google.com/drive/folders/1oaz8ewLKW--cX5Nm7Y0I_j0jPhJzwzVS?usp=sharing|
3050587|NCT01494610|114334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050588|NCT01494610|114334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050589|NCT01494610|114334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050590|NCT01494610|114334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050591|NCT01494610|114334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050592|NCT01494610|114334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050593|NCT01494610|114334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050594|NCT00519649|110474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050595|NCT00519649|110474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050596|NCT00519649|110474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050597|NCT00519649|110474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050598|NCT00519649|110474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050599|NCT00519649|110474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050600|NCT00519649|110474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050601|NCT04126785|CAAE 96882818.3.0000.5398|Brazil Research Ethics Committees|http://plataformabrasil.saude.gov.br/|
3050602|NCT02016963|HGS1021-C1069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050603|NCT02016963|HGS1021-C1069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050604|NCT02016963|HGS1021-C1069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050605|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
3050606|NCT02016963|HGS1021-C1069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050607|NCT02016963|HGS1021-C1069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050608|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
3050609|NCT01573624|115938|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050610|NCT01573624|115938|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050611|NCT01573624|115938|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050612|NCT01573624|115938|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050613|NCT01573624|115938|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050614|NCT01573624|115938|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050615|NCT01573624|115938|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050616|NCT00924911|112034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050617|NCT00924911|112034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050618|NCT00924911|112034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050619|NCT00924911|112034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050620|NCT00924911|112034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050621|NCT00924911|112034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050622|NCT00924911|112034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050623|NCT03672695||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050624|NCT03672695||Study Protocol|https://clinicaltrials.servier.com/|
3050625|NCT03672695||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3050626|NCT03672695||Informed Consent Form|https://clinicaltrials.servier.com/|
3050627|NCT03672695||Clinical Study Report|https://clinicaltrials.servier.com/|
3050628|NCT00945503|109731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050629|NCT00945503|109731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050630|NCT00945503|109731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050631|NCT00945503|109731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050632|NCT00945503|109731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050633|NCT00945503|109731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050634|NCT00945503|109731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050635|NCT06876779||Study Protocol|https://www.ugc.edu.hk/eng/rgc/funding_opport/fds/funded%20research/fds2425.html|
3050636|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.
3050637|NCT03900299||Study Protocol|http://www.med.alexu.edu.eg/ethics-committee/|
3050638|NCT00812929|112025|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050639|NCT00812929|112025|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050640|NCT00812929|112025|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050641|NCT00812929|112025|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050642|NCT00812929|112025|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050643|NCT00812929|112025|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050644|NCT00812929|112025|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050645|NCT02632708||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3050646|NCT02632708||Study Protocol|https://clinicaltrials.servier.com/|
3050647|NCT02632708||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3050648|NCT02632708||Informed Consent Form|https://clinicaltrials.servier.com/|
3050649|NCT02632708||Clinical Study Report|https://clinicaltrials.servier.com/|
3050650|NCT02632708||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3050651|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.
3050652|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).
3057164|NCT00838903|112753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057165|NCT06575504||Study Protocol|https://guides.lib.umich.edu/datamanagement/clinicaltrials|
3057166|NCT00133848|TOC103469|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057167|NCT00133848|TOC103469|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057168|NCT00133848|TOC103469|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057169|NCT00133848|TOC103469|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052543|NCT01031186|113324|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052544|NCT01031186|113324|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052545|NCT01031186|113324|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052546|NCT01031186|113324|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052547|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
3052548|NCT00603278|FFA109685|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052549|NCT00603278|FFA109685|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052550|NCT00603278|FFA109685|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052551|NCT00603278|FFA109685|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052552|NCT00603278|FFA109685|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052553|NCT00603278|FFA109685|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052554|NCT00603278|FFA109685|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052555|NCT02033668|116891|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052556|NCT02033668|116891|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052557|NCT02033668|116891|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052558|NCT02033668|116891|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052559|NCT02033668|116891|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052560|NCT02033668|116891|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052561|NCT02033668|116891|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052562|NCT00383903|444563/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052563|NCT00383903|444563/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052564|NCT00383903|444563/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052565|NCT00383903|444563/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052566|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
3057170|NCT00133848|TOC103469|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052567|NCT00383903|444563/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052568|NCT01697592||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=3102-015&kw=3102-015&tab=access|
3052569|NCT00591409||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052570|NCT01772147|116136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052571|NCT01772147|116136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052572|NCT01772147|116136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052573|NCT01772147|116136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052574|NCT01772147|116136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052575|NCT01772147|116136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052576|NCT01772147|116136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052577|NCT02071680||Published article|http://www.heartrhythmjournal.com/article/S1547-5271(16)30735-4/fulltext|DOI: http://dx.doi.org/10.1016/j.hrthm.2016.08.038
3052578|NCT00684203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04772&kw=P04772&tab=access|
3052579|NCT04018547||Individual Participant Data Set|http://www.oxitone.com|De-identified data for primary and secondary outcome measures
3052580|NCT03013725||Study Protocol|http://husk.b.uib.no/prototest/|Protocol
3052581|NCT01742234|SDY292|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292|ImmPort study identifier is SDY292
3052582|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.
3052583|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."
3052584|NCT00522678|HZA102928|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052585|NCT00522678|HZA102928|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052586|NCT00522678|HZA102928|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052587|NCT00522678|HZA102928|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052588|NCT00522678|HZA102928|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052589|NCT00522678|HZA102928|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052590|NCT00522678|HZA102928|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052591|NCT03116672|UABC|Clinical Study Report|http://www.uabc.mx|Clinical trial that evaluate drug and placebo
3052592|NCT03116672|protocol guide|Individual Participant Data Set|http://www.uabc.mx|Clinical Guide
3052593|NCT00721812|111406|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052594|NCT00721812|111406|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052595|NCT00721812|111406|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052596|NCT00721812|111406|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052597|NCT00721812|111406|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052598|NCT00721812|111406|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052599|NCT00721812|111406|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052600|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
3052601|NCT03037814|26161601|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/26161601|
3052602|NCT03037814|19953810|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/19953810|
3052603|NCT03037814|12542617|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/12542617|
3052604|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 \[CIP\_PhD Rampidis Georgios\_1.1\]"
3052605|NCT00144846|SB030002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052606|NCT00144846|SB030002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052607|NCT00144846|SB030002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052608|NCT00144846|SB030002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052609|NCT00144846|SB030002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052610|NCT00144846|SB030002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052611|NCT00144846|SB030002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052612|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.
3052613|NCT01274559||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0524A-133&kw=0524A-133&tab=access|
3052614|NCT00064428|103413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052615|NCT00064428|103413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052616|NCT00064428|103413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052617|NCT00064428|103413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052618|NCT00064428|103413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052619|NCT00064428|103413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052620|NCT00064428|103413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052621|NCT00372255|106252|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052622|NCT00372255|106252|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052623|NCT00372255|106252|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052624|NCT00372255|106252|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052625|NCT00372255|106252|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052626|NCT00372255|106252|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052627|NCT02991781|neurofeedback-auth|Individual Participant Data Set|http://ckan.smokefreebrain.eu/|
3052628|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.
3052629|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.
3052630|NCT00005278|REDS-HTLV|Study Forms|http://biolincc.nhlbi.nih.gov/studies/reds/|
3052631|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.
3052632|NCT06244693|aparral|Individual Participant Data Set|http://www.redcap.med.uchile.cl|Data registry online system provided by sponsor
3052633|NCT00118703|FFR30007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052634|NCT00118703|FFR30007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052635|NCT00118703|FFR30007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052636|NCT00118703|FFR30007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052637|NCT00118703|FFR30007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052638|NCT00118703|FFR30007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052639|NCT00118703|FFR30007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052640|NCT04882748||Individual Participant Data Set|https://www.frontiersin.org/articles/10.3389/fnbot.2021.715632/full#supplementary-material|
3052641|NCT00038961|103414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052642|NCT00038961|103414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054364|NCT01323673|115054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054365|NCT01323673|115054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054366|NCT01323673|115054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054367|NCT01323673|115054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054368|NCT01323673|115054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054369|NCT01323673|115054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054370|NCT01323673|115054|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054371|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.
3054372|NCT00000567||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/hifi/|
3054373|NCT00000567||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hifi/|
3054374|NCT00000567||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hifi/|
3054375|NCT00726323|MET111644|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054376|NCT00726323|MET111644|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054377|NCT00726323|MET111644|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054378|NCT00726323|MET111644|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054379|NCT00726323|MET111644|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057171|NCT00133848|TOC103469|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057172|NCT00133848|TOC103469|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057173|NCT01262872|114174|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057174|NCT01262872|114174|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057175|NCT01262872|114174|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057176|NCT01262872|114174|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057177|NCT01262872|114174|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057178|NCT01262872|114174|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057179|NCT00920439|112683|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057180|NCT00920439|112683|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057181|NCT00920439|112683|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054380|NCT00726323|MET111644|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054381|NCT04552236||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
3054382|NCT03102775||final report (Norwegian)|https://skriftserien.hioa.no/index.php/skriftserien/article/view/649|
3057182|NCT00920439|112683|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052643|NCT00038961|103414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052644|NCT00038961|103414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052645|NCT00038961|103414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052646|NCT00038961|103414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052647|NCT05907317||Study Protocol|https://www.rigshospitalet.dk/english/departments/juliane-marie-centre/department-of-neonatology/research/safeboosc-iiiv/Pages/protocol.aspx|
3052648|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.
3052649|NCT00005541||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/heirs/|
3052650|NCT00005541||Study Forms|http://biolincc.nhlbi.nih.gov/studies/heirs/|
3052651|NCT00005541||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/heirs/|
3052652|NCT01138098|113954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052653|NCT01138098|113954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052654|NCT01138098|113954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052655|NCT01138098|113954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052656|NCT01138098|113954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052657|NCT01138098|113954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052658|NCT04629443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3052659|NCT04629443||Study Protocol|https://clinicaltrials.servier.com/|
3052660|NCT04629443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3052661|NCT04629443||Informed Consent Form|https://clinicaltrials.servier.com/|
3052662|NCT04629443||Clinical Study Report|https://clinicaltrials.servier.com/|
3052663|NCT04629443||study-level clinical trial data|https://clinicaltrials.servier.com/|
3052664|NCT01086384|106837|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052665|NCT01086384|106837|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052666|NCT01086384|106837|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052667|NCT01086384|106837|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052668|NCT01086384|106837|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052669|NCT01086384|106837|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052670|NCT01086384|106837|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052671|NCT02348372|115385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052672|NCT02348372|115385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052673|NCT02348372|115385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052674|NCT02348372|115385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052675|NCT02348372|115385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052676|NCT02348372|115385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052677|NCT02348372|115385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052678|NCT00197223|104438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052679|NCT00197223|104438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052680|NCT00197223|104438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052681|NCT00197223|104438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052682|NCT00197223|104438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052683|NCT00197223|104438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052684|NCT00197223|104438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052685|NCT04498988||Official study group website|https://tu-dresden.de/bereichsuebergreifendes/sfb940/|
3052686|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).
3052687|NCT01316887|113359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052688|NCT01316887|113359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052689|NCT01316887|113359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052690|NCT01316887|113359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052691|NCT01316887|113359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052692|NCT01316887|113359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052693|NCT01316887|113359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052694|NCT00157898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052695|NCT02075619|200561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052696|NCT02075619|200561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052697|NCT02075619|200561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052698|NCT02075619|200561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052699|NCT02075619|200561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052700|NCT02075619|200561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052701|NCT02075619|200561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052702|NCT01015677||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6913-004&kw=6913-004&tab=access|
3052703|NCT06254755||Individual Participant Data Set|http://competetrials@gmail.com|
3052704|NCT00749359|PCR111656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052705|NCT00749359|PCR111656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052706|NCT00749359|PCR111656|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052707|NCT00749359|PCR111656|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052708|NCT00749359|PCR111656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052709|NCT00749359|PCR111656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052710|NCT00749359|PCR111656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052711|NCT00516139|LEP105972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052712|NCT00516139|LEP105972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052713|NCT00516139|LEP105972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052714|NCT00516139|LEP105972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052715|NCT00516139|LEP105972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052716|NCT00516139|LEP105972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052717|NCT00516139|LEP105972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052718|NCT03034850||Study Protocol|https://drive.google.com/open?id=0B0qo2hDQpXhncWZFZkNfZXhZMjVuUGcxc0IzZll5TEtjaXdn|
3052719|NCT03034850|eudract/B-nr B37120154199|Advice Ethical Committee|https://drive.google.com/open?id=0B0qo2hDQpXhnU3AzRHY0d1NtVmlsSmx1cFhKOGtKLTVscno0|
3052720|NCT01648153|116378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052721|NCT01648153|116378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052722|NCT01648153|116378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052723|NCT01648153|116378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052724|NCT01648153|116378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052725|NCT01648153|116378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052726|NCT01648153|116378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052727|NCT01841697||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-026&kw=3102-026&tab=access|
3052728|NCT00719043|110624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052729|NCT00719043|110624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052730|NCT00719043|110624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052731|NCT00719043|110624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052732|NCT00719043|110624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052733|NCT00719043|110624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052734|NCT01006616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05575&kw=7123-019&tab=access|
3052735|NCT00823836|106066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052736|NCT00823836|106066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052737|NCT00823836|106066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052738|NCT00823836|106066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052739|NCT00823836|106066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052740|NCT02446613|204509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052741|NCT02446613|204509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052742|NCT02446613|204509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052743|NCT02446613|204509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052744|NCT02446613|204509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052745|NCT02446613|204509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052746|NCT02446613|204509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052747|NCT01691547|116415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052748|NCT01691547|116415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052749|NCT01691547|116415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052750|NCT01691547|116415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052751|NCT01691547|116415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052752|NCT01691547|116415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052753|NCT01691547|116415|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054383|NCT01165203|112673|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054384|NCT01165203|112673|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054385|NCT01165203|112673|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054386|NCT01165203|112673|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054387|NCT01165203|112673|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054388|NCT01165203|112673|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054389|NCT01165203|112673|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054390|NCT01147731|111681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054391|NCT01147731|111681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050653|NCT00637195|111567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050654|NCT00637195|111567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050655|NCT00637195|111567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050656|NCT00637195|111567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050657|NCT00637195|111567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050658|NCT00637195|111567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050659|NCT00637195|111567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050660|NCT00689481|114742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050661|NCT00689481|114742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050662|NCT00689481|114742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050663|NCT00689481|114742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050664|NCT00689481|114742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050665|NCT00689481|114742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050666|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).
3050667|NCT01462357|115411|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050668|NCT01462357|115411|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050669|NCT01462357|115411|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050670|NCT01462357|115411|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050671|NCT01462357|115411|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050672|NCT01462357|115411|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050673|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)
3050674|NCT01930058||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8876-003&kw=8876-003|
3050675|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|
3050676|NCT01310413|114464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050677|NCT01310413|114464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050678|NCT01310413|114464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050679|NCT01310413|114464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050680|NCT01310413|114464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050681|NCT01310413|114464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050682|NCT05007457|Benedetta Isani|Study Protocol|http://aosp.bo.it|
3050683|NCT03125265||Study Protocol|http://bmjopen.bmj.com/content/5/3/e006897.long|
3050684|NCT01114841|114572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050685|NCT01114841|114572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050686|NCT01114841|114572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050687|NCT01114841|114572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050688|NCT01114841|114572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050689|NCT01114841|114572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050690|NCT01114841|114572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050691|NCT00263692|213503/047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050692|NCT00263692|213503/047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050693|NCT00263692|213503/047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050694|NCT00263692|213503/047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050695|NCT00263692|213503/047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050696|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
3050697|NCT01957189|200254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050698|NCT01957189|200254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050699|NCT01957189|200254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050700|NCT01957189|200254|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050701|NCT01957189|200254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050702|NCT01957189|200254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050703|NCT01957189|200254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050704|NCT00779766|107638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050705|NCT00779766|107638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050706|NCT00779766|107638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050707|NCT00779766|107638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050708|NCT00779766|107638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050709|NCT00779766|107638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050710|NCT00779766|107638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050711|NCT06919185|2025-01028-01|Study Protocol|https://slmf.se/forskning/lungmedicinsk-forskning/sparc/|
3050712|NCT00094380|SDY798|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY798|ImmPort study identifier is SDY798.
3050713|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.
3050714|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.
3050715|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.
3050716|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.
3050717|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.
3050718|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.
3050719|NCT00075829|BMT CTN-0102|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
3050720|NCT00075829|BMT CTN-0102|Study Forms|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
3050721|NCT01706250|114550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050722|NCT01706250|114550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050723|NCT01706250|114550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050724|NCT01706250|114550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050725|NCT01706250|114550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050726|NCT00482079||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050727|NCT05262205||Study Protocol|http://irb.mans.edu.eg|
3050728|NCT00586469|111258|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050729|NCT00586469|111258|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050730|NCT00586469|111258|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050731|NCT00586469|111258|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050732|NCT00586469|111258|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050733|NCT00586469|111258|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050734|NCT00586469|111258|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050735|NCT04891679|PATIENT INFORMATION SHEET|Informed Consent Form|https://figshare.com/s/a6c10a2a4be65f30144b|
3050736|NCT04891679|STUDY PROTOCOL|Study Protocol|https://figshare.com/s/3f978a10eee4e90173bb|
3050737|NCT01181895|112060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050738|NCT01181895|112060|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050739|NCT01181895|112060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050740|NCT01181895|112060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050741|NCT01181895|112060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050742|NCT01181895|112060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050743|NCT01181895|112060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050744|NCT01003418|113629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050745|NCT01003418|113629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050746|NCT01003418|113629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050747|NCT01003418|113629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050748|NCT01003418|113629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050749|NCT01003418|113629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050750|NCT01837316|116592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050751|NCT01837316|116592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050752|NCT01837316|116592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050753|NCT01837316|116592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050754|NCT01837316|116592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050755|NCT01837316|116592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050756|NCT01837316|116592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050757|NCT00338351|106208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050758|NCT00338351|106208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050759|NCT00338351|106208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050760|NCT00338351|106208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050761|NCT00338351|106208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050762|NCT00338351|106208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050763|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.
3050764|NCT07086287|rhBNP|Study Protocol|https://www.chictr.org.cn/|China Clinical Trial Registration Center
3050765|NCT00298831||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3050766|NCT00432380|109216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050767|NCT00432380|109216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052754|NCT02242643|201234|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052755|NCT02242643|201234|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052756|NCT02242643|201234|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052757|NCT02242643|201234|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052758|NCT02242643|201234|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052759|NCT02242643|201234|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052760|NCT02242643|201234|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052761|NCT01777334|117115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052762|NCT01777334|117115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052763|NCT01777334|117115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052764|NCT01777334|117115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052765|NCT01777334|117115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052766|NCT01777334|117115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052767|NCT01777334|117115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052768|NCT05394090||Individual Participant Data Set|http://www.pum.edu.pl|
3052769|NCT07267637|https://doi.org/10.1111/clr.14|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/39132806/|This data includes radiographic changes from the clinical trial involving alveolar ridge preservation using autogenous tooth particles and xenograft materials.
3052770|NCT07267637|https://doi.org/10.1186/s40729|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/28361377/|"This study explores the use of autologous particulated dentin as a novel approach for alveolar ridge preservation. The intervention involves the patient's own extracted tooth, which is processed into dentin particles and used as a bone graft material. The study demonstrates successful outcomes in terms of bone regeneration and subsequent implant placement, suggesting that autologous dentin may be a promising alternative to traditional grafting materials."
3052771|NCT07267559||Study Protocol|https://osf.io/8mvn6|
3052772|NCT07267559||Informed Consent Form|https://osf.io/5kuyn|
3052773|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFNnVaQWlTakh5dEU|
3052774|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFazRhT1hZVm41RzA|05.01.2017 updated because of an amendment of ethnic proposal.
3052775|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
3052776|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
3052777|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
3052778|NCT00379769|BRL-049653/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052779|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
3052780|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
3052781|NCT00379769|BRL-049653/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052782|NCT01245140|117221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052783|NCT01245140|117221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052784|NCT01245140|117221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052785|NCT01245140|117221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052786|NCT01245140|117221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052787|NCT01245140|117221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052788|NCT01245140|117221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052789|NCT07267000||Individual Participant Data Set|https://project-redcap.org/|IPD will be collected in the REDCap database. Since enrolment of patients has not started yet, no data has yet been entered. We are undecided on whether to share IPD with other researchers in future.
3052790|NCT00443209||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-012&kw=0974-012&tab=access|
3054392|NCT01147731|111681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054393|NCT01147731|111681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054394|NCT01147731|111681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050768|NCT00432380|109216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050769|NCT00432380|109216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050770|NCT00432380|109216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050771|NCT00432380|109216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050772|NCT00432380|109216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050773|NCT02696850|CGI scale|Questionnaire|https://www.psywellness.com.sg/docs/CGI.pdf|
3054395|NCT01147731|111681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054396|NCT01147731|111681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054397|NCT06011005|MBRU IRB-2022-174|Study Protocol|http://www.mbru.ac.ae|
3054398|NCT00861484|111155|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054399|NCT00861484|111155|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054400|NCT00861484|111155|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054401|NCT00861484|111155|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054402|NCT00861484|111155|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054403|NCT00861484|111155|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054404|NCT00861484|111155|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054405|NCT01299597|109652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054406|NCT01299597|109652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054407|NCT01299597|109652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054408|NCT01299597|109652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054409|NCT01299597|109652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054410|NCT01299597|109652|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054411|NCT01299597|109652|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054412|NCT03731416||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27283920|
3054413|NCT00933335|393229/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050774|NCT01978119|115645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050775|NCT01978119|115645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050776|NCT01978119|115645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050777|NCT01978119|115645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050778|NCT01978119|115645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050779|NCT01978119|115645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050780|NCT00812812|112487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050781|NCT00812812|112487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050782|NCT00812812|112487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050783|NCT00812812|112487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050784|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.
3052791|NCT00725712|MET111643|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052792|NCT00725712|MET111643|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052793|NCT00725712|MET111643|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052794|NCT00725712|MET111643|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052795|NCT00725712|MET111643|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052796|NCT00725712|MET111643|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052797|NCT00725712|MET111643|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052798|NCT02224469|k9f10|Individual Participant Data Set|http://datadryad.org/resource/doi:10.5061/dryad.k9f10|
3052799|NCT00092183||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052800|NCT01381575|114700|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052801|NCT01381575|114700|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052802|NCT01381575|114700|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052803|NCT01381575|114700|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052804|NCT01381575|114700|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052805|NCT01381575|114700|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052806|NCT01453023|112777|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052807|NCT01453023|112777|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052808|NCT01453023|112777|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052809|NCT01453023|112777|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052810|NCT01453023|112777|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052811|NCT01453023|112777|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052812|NCT01453023|112777|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052813|NCT07260201|no identifier available|Individual participant data will not be shared because the study is retrospective and based on anonymized medical records.|https://www.hisarhospital.com|This publication provides background evidence supporting the evaluation of triglyceride-glucose-based indices as markers of insulin resistance.
3052814|NCT01407276||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-009&kw=3102-009&tab=access|
3052815|NCT01431950|114496|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052816|NCT01431950|114496|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052817|NCT01431950|114496|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052818|NCT01431950|114496|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052819|NCT01431950|114496|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052820|NCT01431950|114496|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052821|NCT01431950|114496|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052822|NCT04240249||Individual Participant Data Set|https://github.com/hmep/r2fu/|
3052823|NCT04240249||Analytic Code|https://github.com/hmep/r2fu/|
3052824|NCT00546078|109628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052825|NCT00546078|109628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052826|NCT00546078|109628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052827|NCT00546078|109628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052828|NCT00546078|109628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052829|NCT00546078|109628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052830|NCT00546078|109628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052831|NCT00383123|104858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052832|NCT00383123|104858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052833|NCT00383123|104858|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052834|NCT00383123|104858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052835|NCT00383123|104858|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052836|NCT00383123|104858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052837|NCT00383123|104858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052838|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.
3052839|NCT05688618||Study Protocol|https://drive.google.com/drive/u/0/folders/1JG22lkEchQULxW79ktlsVcM5uGNB4iVh|
3052840|NCT00390260||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052841|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.
3052842|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.
3052843|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.
3052844|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.
3052845|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.
3052846|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.
3052847|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.
3052848|NCT00968526|113459|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052849|NCT00968526|113459|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052850|NCT00968526|113459|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052851|NCT00968526|113459|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052852|NCT00968526|113459|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052853|NCT00968526|113459|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052854|NCT00968526|113459|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052855|NCT00479882||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-063&kw=0524B-063&tab=access|
3052856|NCT00334334|107005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052857|NCT00334334|107005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052858|NCT00334334|107005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052859|NCT00334334|107005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052860|NCT00334334|107005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052861|NCT00334334|107005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052862|NCT00344032|104479|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052863|NCT00344032|104479|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052864|NCT00344032|104479|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052865|NCT00344032|104479|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052866|NCT00344032|104479|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052867|NCT00344032|104479|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052868|NCT06509360||Individual Participant Data Set|https://www.castoredc.com/|Individual participant data is collected anonymously in Castor EDC.
3052869|NCT00263653|103954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052870|NCT00263653|103954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052871|NCT00263653|103954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052872|NCT00263653|103954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052873|NCT00263653|103954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052874|NCT00263653|103954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052875|NCT01160237|114454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052876|NCT01160237|114454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052877|NCT01160237|114454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052878|NCT01160237|114454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052879|NCT01160237|114454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052880|NCT01160237|114454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052881|NCT01160237|114454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052882|NCT05555745||Statistical Analysis Plan|https://osf.io/zw5cq|
3052883|NCT00090155||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052884|NCT03260478||Study Protocol|https://bmjopen.bmj.com/content/12/10/e067117.info|
3052885|NCT03266926||Study Protocol|https://www.scribd.com/document/344597619/Study-Protocol|
3052886|NCT03266926||Informed Consent Form|https://www.scribd.com/document/344597523/Consent-Form|
3052887|NCT03266926||Individual Participant Data Set|https://www.scribd.com/document/344597573/Data-Collection-Spreadsheet|
3052888|NCT03266926||Participant Documents|https://www.scribd.com/document/344597424/Participant-Documents|
3052889|NCT02718261|NCT02467621|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT02467621?term=SUP-ICU&rank=1|SUP-ICU Website
3052890|NCT00770744|2008-000479-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-000479-11/results|
3054414|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
3054415|NCT00933335|393229/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054416|NCT00933335|393229/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054417|NCT00933335|393229/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054418|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
3054419|NCT00933335|393229/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052891|NCT03567629||Individual Participant Data Set|https://en.wikipedia.org/wiki/United_States_National_Library_of_Medicine|
3052892|NCT00388440|209762/147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052893|NCT00388440|209762/147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052894|NCT00388440|209762/147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052895|NCT00388440|209762/147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052896|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
3052897|NCT00632502||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05365&kw=7123-017&tab=access|
3054420|NCT00139334|103992|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054421|NCT00139334|103992|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054422|NCT00139334|103992|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054423|NCT00139334|103992|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054424|NCT00139334|103992|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054425|NCT00139334|103992|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054426|NCT06527274||Study Protocol|https://nagano.umontreal.ca/login|Protocol and other documentation available upon request to the principal investigator email
3054427|NCT03167580||Study Protocol|https://sites.google.com/view/relaxtrial/study-details-and-documents/protocol|
3054428|NCT01425190||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07614&kw=P07614&tab=access|
3057183|NCT00920439|112683|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057184|NCT00920439|112683|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057185|NCT06456775||Individual Participant Data Set|https://bit.ly/49RBPuQ|
3057186|NCT07152041|CAMS-Ph+B-ALL|Individual Participant Data Set|https://login.imedidata.com|CAMS-Ph+ALL-2025 DATASET
3057187|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.
3057188|NCT00617890||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04720&kw=P04720&tab=access|
3057189|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.
3057190|NCT00288626||Study summary, -design, -demographics, and -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY549|ImmPort study identifier is SDY549
3057191|NCT00996125|112022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057192|NCT00996125|112022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057193|NCT00996125|112022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057194|NCT00996125|112022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057195|NCT00996125|112022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057196|NCT00996125|112022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057197|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/22118062/|
3057198|NCT00095420||Clinical Study Report|http://www.researchgate.net/publication/10751612_General_Education_Teacher|
3057199|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/20673234/|
3057200|NCT00095420||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076578/|
3057201|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/27620949/|
3057202|NCT02006589|200956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057203|NCT02006589|200956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057204|NCT02006589|200956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057205|NCT02006589|200956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057206|NCT02006589|200956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057207|NCT02006589|200956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057208|NCT02006589|200956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057209|NCT02637206|200920|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057210|NCT02637206|200920|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057211|NCT02637206|200920|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057212|NCT02637206|200920|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057213|NCT02637206|200920|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057214|NCT02637206|200920|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057215|NCT02637206|200920|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050785|NCT00129259|SDY524|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY524|ImmPort study identifier is SDY524.
3050786|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.
3050787|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.
3050788|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.
3050789|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.
3050790|NCT00264615|LEP103944|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050791|NCT00264615|LEP103944|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050792|NCT00264615|LEP103944|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050793|NCT00264615|LEP103944|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050794|NCT00264615|LEP103944|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050795|NCT00264615|LEP103944|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050796|NCT00264615|LEP103944|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050797|NCT00701389||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-026&kw=0974-026&tab=access|
3050798|NCT01267071|114136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050799|NCT01267071|114136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050800|NCT01267071|114136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050801|NCT01267071|114136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050802|NCT01267071|114136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050803|NCT01267071|114136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050804|NCT01267071|114136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3050805|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
3050806|NCT02143518||Clinical Study Report|https://gwvru.smhs.gwu.edu/clinical|
3050807|NCT01814722||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-266&kw=0518-266&tab=access|
3050808|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
3052898|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
3052899|NCT00678301|110521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052900|NCT00678301|110521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052901|NCT00678301|110521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052902|NCT00678301|110521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052903|NCT00678301|110521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052904|NCT00678301|110521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052905|NCT00678301|110521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052906|NCT01939353||Poster Abstracts|https://apsard.org/wp-content/uploads/2016/11/Poster-Abstracts-Compiled1.pdf|Poster number 25
3052907|NCT01132443|115902|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052908|NCT01132443|115902|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052909|NCT01132443|115902|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052910|NCT01132443|115902|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052911|NCT01132443|115902|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052912|NCT01132443|115902|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052913|NCT01132443|115902|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052914|NCT04954326||Individual Participant Data Set|https://clinicaltrials.servier.com|
3052915|NCT04954326||Study Protocol|https://clinicaltrials.servier.com|
3052916|NCT04954326||Statistical Analysis Plan|https://clinicaltrials.servier.com|
3052917|NCT04954326||Informed Consent Form|https://clinicaltrials.servier.com|
3052918|NCT04954326||Clinical Study Report|https://clinicaltrials.servier.com|
3052919|NCT04954326||Study-level clinical trial data|https://clinicaltrials.servier.com|
3052920|NCT04110704|IRAS 261294|Study Protocol|http://preview-kcl.cloud.contensis.com/Preview/1/research/project?id=478a6e61-4446-4a12-945e-c41a3879371d|
3052921|NCT01333813|112688|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052922|NCT01333813|112688|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052923|NCT01333813|112688|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052924|NCT01333813|112688|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052925|NCT01333813|112688|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052926|NCT01333813|112688|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052927|NCT04728139||Study Protocol|http://rehamhany809@gmail.com|
3052928|NCT00972322||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8245-012&kw=8245-012&tab=access|
3052929|NCT07124052|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
3052930|NCT01734239||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V110-018&kw=V110-018&tab=access|
3052931|NCT00635128|110947|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052932|NCT00635128|110947|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052933|NCT00635128|110947|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052934|NCT00635128|110947|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052935|NCT00635128|110947|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052936|NCT00635128|110947|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052937|NCT00635128|110947|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052938|NCT01376232|113634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052939|NCT01376232|113634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052940|NCT01376232|113634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052941|NCT01376232|113634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052942|NCT01376232|113634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052943|NCT01376232|113634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052944|NCT01376232|113634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052945|NCT02145468|116197|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052946|NCT02145468|116197|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052947|NCT02145468|116197|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054429|NCT00441441|SFA106484|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054430|NCT00441441|SFA106484|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054431|NCT00441441|SFA106484|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054432|NCT00441441|SFA106484|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054433|NCT00441441|SFA106484|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054434|NCT00441441|SFA106484|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054435|NCT00441441|SFA106484|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054436|NCT01245426|114749|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054437|NCT01245426|114749|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054438|NCT01245426|114749|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054439|NCT01245426|114749|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054440|NCT01245426|114749|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054441|NCT01245426|114749|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054442|NCT01245426|114749|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054443|NCT00606697|NKI110334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054444|NCT00606697|NKI110334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054445|NCT00606697|NKI110334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054446|NCT00606697|NKI110334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054447|NCT00606697|NKI110334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054448|NCT00606697|NKI110334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054449|NCT00606697|NKI110334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054450|NCT01640990|115387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054451|NCT01640990|115387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054452|NCT01640990|115387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054453|NCT01640990|115387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054454|NCT01640990|115387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054455|NCT01640990|115387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054456|NCT01640990|115387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054457|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.
3054458|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
3054459|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Forms|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
3054460|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.
3054461|NCT00000579|ARDSNet-LASRS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
3054462|NCT00000579|ARDSNet-LASRS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
3054463|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.
3054464|NCT00000579|ARDSNet-ALVEOLI|Study Forms|http://biolincc.nhlbi.nih.gov/studies/alveoli/|
3054465|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.
3054466|NCT00000579|ARDSNet-FACTT|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/factt/|
3054467|NCT00000579|ARDSNet-FACTT|Study Forms|http://biolincc.nhlbi.nih.gov/studies/factt/|
3054468|NCT00256867|AVS101946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054469|NCT00256867|AVS101946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054470|NCT00256867|AVS101946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054471|NCT00256867|AVS101946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054472|NCT00256867|AVS101946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054473|NCT00256867|AVS101946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054474|NCT00256867|AVS101946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054475|NCT01258530|115096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054476|NCT01258530|115096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054477|NCT01258530|115096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054478|NCT01258530|115096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054479|NCT01258530|115096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054480|NCT01258530|115096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054481|NCT01258530|115096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054482|NCT00444509|HZA108799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054483|NCT00444509|HZA108799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054484|NCT00444509|HZA108799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054485|NCT00444509|HZA108799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054486|NCT00444509|HZA108799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054487|NCT00444509|HZA108799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054488|NCT00444509|HZA108799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054489|NCT00048594||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054490|NCT01842620|117219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054491|NCT01842620|117219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054492|NCT01842620|117219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054493|NCT01842620|117219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054494|NCT01842620|117219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054495|NCT01842620|117219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054496|NCT01842620|117219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054497|NCT01000727|480848/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054498|NCT01000727|480848/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054499|NCT01000727|480848/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054500|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
3054501|NCT01000727|480848/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054502|NCT01000727|480848/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054503|NCT06459622||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29337030/|
3054504|NCT00377611|107564|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054505|NCT00377611|107564|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054506|NCT00377611|107564|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054507|NCT00377611|107564|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054508|NCT00377611|107564|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054509|NCT00377611|107564|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054510|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
3054511|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
3054512|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
3054513|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
3054514|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
3054515|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
3054516|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
3054517|NCT01954251|117036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054518|NCT01954251|117036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054519|NCT01954251|117036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054520|NCT01954251|117036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054521|NCT01954251|117036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054522|NCT01954251|117036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054523|NCT01954251|117036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054524|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.
3054525|NCT00120289|AIM-HIGH|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
3054526|NCT00120289|AIM-HIGH|Study forms|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
3054527|NCT04987853|BR10965164|Study Protocol|https://is.ncste.kz/login|
3054528|NCT04987853|BR10965164|Informed Consent Form|https://is.ncste.kz/login|
3054529|NCT04987853|BR10965164|Clinical Study Report|https://is.ncste.kz/login|
3054530|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
3054531|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
3054532|NCT00380211|IDB-200-001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054533|NCT00380211|IDB-200-001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054534|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
3054535|NCT01098461|110932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054536|NCT01098461|110932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054537|NCT01098461|110932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054538|NCT01098461|110932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054539|NCT01098461|110932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054540|NCT01098461|110932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054541|NCT01098461|110932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054542|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
3054543|NCT00757770|444563/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054544|NCT00757770|444563/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054545|NCT00757770|444563/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054546|NCT00757770|444563/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054547|NCT00757770|444563/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054548|NCT00992784|113094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054549|NCT00992784|113094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054550|NCT00992784|113094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054551|NCT00992784|113094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054552|NCT00992784|113094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054553|NCT00992784|113094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054554|NCT00992784|113094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054555|NCT00718666|112021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054556|NCT00718666|112021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054557|NCT00718666|112021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054558|NCT00718666|112021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054559|NCT00718666|112021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054560|NCT00718666|112021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054561|NCT01062074||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-059&kw=V501-059&tab=access|
3054562|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
3054563|NCT00430521|107495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054564|NCT00430521|107495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054565|NCT00430521|107495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054566|NCT00430521|107495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054567|NCT00430521|107495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054568|NCT00430521|107495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054569|NCT00430521|107495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054570|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.
3054571|NCT05532995||Informed Consent Form|https://drive.google.com/file/d/1qiU0UgEzvPBntfA0lLWFe_AzOGngacl9/view?usp=sharing|
3054572|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.
3054573|NCT00377585|104888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054574|NCT00377585|104888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054575|NCT00377585|104888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054576|NCT00377585|104888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054577|NCT00377585|104888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054578|NCT00289185|104298|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054579|NCT00289185|104298|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054580|NCT00289185|104298|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054581|NCT00289185|104298|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054582|NCT00289185|104298|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054583|NCT00289185|104298|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054584|NCT00135486|711202/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054585|NCT00135486|711202/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057216|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
3057217|NCT00566020|SCA106052|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057218|NCT00566020|SCA106052|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057219|NCT00566020|SCA106052|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057220|NCT00566020|SCA106052|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057221|NCT01154114|480848/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057222|NCT01154114|480848/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057223|NCT01154114|480848/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057224|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
3057225|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
3057226|NCT01154114|480848/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057227|NCT01154114|480848/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057228|NCT00812981|111954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057229|NCT00812981|111954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057230|NCT00812981|111954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057231|NCT00812981|111954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057232|NCT00812981|111954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057233|NCT00812981|111954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057234|NCT00812981|111954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057235|NCT01777282|116170|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057236|NCT01777282|116170|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057237|NCT01777282|116170|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057238|NCT01777282|116170|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057239|NCT01777282|116170|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057240|NCT01777282|116170|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057241|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.
3057242|NCT00116818|FFR20002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057243|NCT00116818|FFR20002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057244|NCT00116818|FFR20002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057245|NCT00116818|FFR20002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057246|NCT00116818|FFR20002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054586|NCT00135486|711202/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054587|NCT00135486|711202/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054588|NCT00135486|711202/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054589|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
3054590|NCT00838916|112754|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054591|NCT00838916|112754|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054592|NCT00838916|112754|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054593|NCT00838916|112754|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054594|NCT00838916|112754|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054595|NCT00838916|112754|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054596|NCT00838916|112754|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054597|NCT01021852||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6096-011&kw=6096-011&tab=access|
3054598|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."
3054599|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."
3054600|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."
3054601|NCT00043875|LAM20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054602|NCT00043875|LAM20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054603|NCT00043875|LAM20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054604|NCT00043875|LAM20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054605|NCT00043875|LAM20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054606|NCT00043875|LAM20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054607|NCT00043875|LAM20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054608|NCT01153893|113199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054609|NCT01153893|113199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054610|NCT01153893|113199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054611|NCT01153893|113199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054612|NCT01153893|113199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054613|NCT01153893|113199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054614|NCT01615796|115198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054615|NCT01615796|115198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054616|NCT01615796|115198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054617|NCT01615796|115198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054618|NCT01615796|115198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054619|NCT01615796|115198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054620|NCT01615796|115198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057247|NCT00116818|FFR20002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054621|NCT00880763||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-016&kw=7009-016&tab=access|
3054622|NCT01293006||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-032&kw=4305-032&tab=access|
3054623|NCT01551758|115151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054624|NCT01551758|115151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054625|NCT01551758|115151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054626|NCT01551758|115151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054627|NCT01551758|115151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054628|NCT01551758|115151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054629|NCT01551758|115151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054630|NCT01842607|115661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057248|NCT00116818|FFR20002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057249|NCT02476578||Study Protocol|https://goo.gl/B6j1oF|LIMIT HEBREW PROTOCOL Version 3 (Final)
3057250|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
3057251|NCT00291876|100571 (M138)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057252|NCT00291876|100571 (M138)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057253|NCT00291876|100571 (M138)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057254|NCT00291876|100571 (M138)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057255|NCT00291876|100571 (M138)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057256|NCT04132323||Study Protocol|https://www.venousregistry.org/index.php?f=1&id=97|
3057257|NCT01521390|115487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057258|NCT01521390|115487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057259|NCT01521390|115487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057260|NCT01521390|115487|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057261|NCT01521390|115487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057262|NCT01521390|115487|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057263|NCT01521390|115487|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057264|NCT01863667||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3102-027&kw=3102-027&tab=access|
3052948|NCT02145468|116197|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052949|NCT02145468|116197|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052950|NCT02145468|116197|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052951|NCT02145468|116197|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052952|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.
3052953|NCT00586612|110215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052954|NCT00586612|110215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052955|NCT00586612|110215|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052956|NCT00586612|110215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052957|NCT00586612|110215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052958|NCT00586612|110215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052959|NCT04340791||Study Protocol|https://osf.io/kq9c8/|
3052960|NCT04340791||Statistical Analysis Plan|https://osf.io/kq9c8/|
3052961|NCT04340791||Informed Consent Form|https://osf.io/kq9c8/|
3052962|NCT04340791||Individual Participant Data Set|https://osf.io/kq9c8/|When results will be published
3052963|NCT00989625|108504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052964|NCT00989625|108504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052965|NCT00989625|108504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052966|NCT00989625|108504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052967|NCT00989625|108504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052968|NCT00989625|108504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052969|NCT00989625|108504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052970|NCT01725126|116623|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052971|NCT01725126|116623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057265|NCT00839527|112757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057266|NCT00839527|112757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057267|NCT00839527|112757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057268|NCT00839527|112757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057269|NCT00839527|112757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057270|NCT00839527|112757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057271|NCT00839527|112757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052972|NCT01725126|116623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054631|NCT01842607|115661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054632|NCT01842607|115661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054633|NCT01842607|115661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054634|NCT01842607|115661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054635|NCT01842607|115661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054636|NCT01842607|115661|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054637|NCT01299610|113434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054638|NCT01299610|113434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054639|NCT01299610|113434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054640|NCT01299610|113434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054641|NCT01299610|113434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054642|NCT01299610|113434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054643|NCT01299610|113434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054644|NCT00671216|DB1111509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054645|NCT00671216|DB1111509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054646|NCT00671216|DB1111509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054647|NCT00671216|DB1111509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054648|NCT00671216|DB1111509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054649|NCT00671216|DB1111509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054650|NCT00671216|DB1111509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052973|NCT01725126|116623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052974|NCT01725126|116623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052975|NCT01725126|116623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052976|NCT01725126|116623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052977|NCT00091559||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3052978|NCT00109330|776423/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052979|NCT00109330|776423/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052980|NCT00109330|776423/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052981|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
3052982|NCT00109330|776423/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052983|NCT00109330|776423/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052984|NCT02963025||Study Protocol|http://prothor.info|
3052985|NCT00056277|SCA30924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052986|NCT00056277|SCA30924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052987|NCT00056277|SCA30924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052988|NCT00056277|SCA30924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052989|NCT00056277|SCA30924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052990|NCT00056277|SCA30924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052991|NCT00056277|SCA30924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054651|NCT00989612|113519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054652|NCT00989612|113519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054653|NCT00989612|113519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054654|NCT00989612|113519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054655|NCT00989612|113519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054656|NCT00989612|113519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054657|NCT00989612|113519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054658|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)
3054659|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)
3054660|NCT00989404|113625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054661|NCT00989404|113625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054662|NCT00989404|113625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054663|NCT00989404|113625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054664|NCT00989404|113625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054665|NCT00989404|113625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054666|NCT00989404|113625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054667|NCT01245764||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-046&kw=V501-046&tab=access|
3057272|NCT04068129||Individual Participant Data Set|http://www.abcd-vision.org/references/index.html|
3057273|NCT02064504|201010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057274|NCT02064504|201010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057275|NCT02064504|201010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057276|NCT02064504|201010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057277|NCT02064504|201010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3052992|NCT04445727|vitamin c|Clinical Study Report|http://www.bonusan.es/vademecum/vitamina_c1000_complejo_de_ascorbatos.html|
3057278|NCT02064504|201010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057279|NCT02064504|201010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054668|NCT01231607|114263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054669|NCT01231607|114263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054670|NCT01231607|114263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054671|NCT01231607|114263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054672|NCT01231607|114263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054673|NCT01231607|114263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054674|NCT01231607|114263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054675|NCT04744636||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3054676|NCT04744636||Study Protocol|https://clinicaltrials.servier.com/|
3054677|NCT04744636||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3054678|NCT04744636||Informed Consent Form|https://clinicaltrials.servier.com/|
3054679|NCT04744636||Clinical Study Report|https://clinicaltrials.servier.com/|
3057280|NCT06575127||Informed Consent Form|https://drive.google.com/file/d/1_CG_0wzCH_ZUxWXsfARsyWlcx37fOcRq/view?usp=drive_link|
3057281|NCT06968169||Study Protocol|https://doi.org/10.17605/OSF.IO/AJDZS|
3057282|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
3057283|NCT05497518||Study Protocol|https://tuftsmedicalcenter.box.com/s/bplcm9clgjsnnq23zcwwwuze6up368q4|
3057284|NCT05664360||Individual Participant Data Set|https://www.doi.org/10.17605/OSF.IO/TRU4N|
3057285|NCT00347139|B2C106093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057286|NCT00347139|B2C106093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057287|NCT00347139|B2C106093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057288|NCT00347139|B2C106093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057289|NCT00347139|B2C106093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057290|NCT00347139|B2C106093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057291|NCT00347139|B2C106093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057292|NCT01014988|113678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057293|NCT01014988|113678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057294|NCT01014988|113678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057295|NCT01014988|113678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057296|NCT01014988|113678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057297|NCT01014988|113678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057298|NCT01014988|113678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057299|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
3057300|NCT00381238|AVA104617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057301|NCT00381238|AVA104617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054680|NCT04744636||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3057302|NCT00381238|AVA104617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057303|NCT00381238|AVA104617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057304|NCT00381238|AVA104617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057305|NCT00381238|AVA104617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057306|NCT00381238|AVA104617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054681|NCT00823940|111497|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054682|NCT00823940|111497|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054683|NCT00823940|111497|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054684|NCT00823940|111497|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054685|NCT00823940|111497|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054686|NCT00823940|111497|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054687|NCT00823940|111497|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054688|NCT00731393|100351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054689|NCT00731393|100351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054690|NCT00731393|100351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054691|NCT00731393|100351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054692|NCT00731393|100351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054693|NCT00731393|100351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054694|NCT00731393|100351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054695|NCT00083343||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054696|NCT00971425|113572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054697|NCT00971425|113572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054698|NCT00971425|113572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054699|NCT00971425|113572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054700|NCT00971425|113572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054701|NCT00971425|113572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054702|NCT00971425|113572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054703|NCT00044486||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054704|NCT02979366||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3054705|NCT02979366||Study Protocol|https://clinicaltrials.servier.com/|
3054706|NCT02979366||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3054707|NCT02979366||Informed Consent Form|https://clinicaltrials.servier.com/|
3054708|NCT02979366||Clinical Study Report|https://clinicaltrials.servier.com/|
3054709|NCT02979366||Study-level clinical trial data|https://clinicaltrials.servier.com/|
3054710|NCT00240539|100449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054711|NCT00240539|100449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054712|NCT00240539|100449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054713|NCT00240539|100449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054714|NCT00240539|100449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054715|NCT01153841|113151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054716|NCT01153841|113151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054717|NCT01153841|113151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054718|NCT01153841|113151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054719|NCT01153841|113151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054720|NCT01153841|113151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054721|NCT00406211|208136/039|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054722|NCT00406211|208136/039|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054723|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
3054724|NCT00406211|208136/039|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054725|NCT00406211|208136/039|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054726|NCT00406211|208136/039|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054727|NCT00533611||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054728|NCT00118729|FFR101816|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054729|NCT00118729|FFR101816|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054730|NCT00118729|FFR101816|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054731|NCT00118729|FFR101816|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054732|NCT00118729|FFR101816|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054733|NCT00118729|FFR101816|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054734|NCT00118729|FFR101816|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054735|NCT00438022|Study ID is SDY4|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
3054736|NCT00438022|Study ID is SDY4|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
3054737|NCT00438022|Study ID is SDY4|Study details, -download packages, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
3054738|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.
3054739|NCT01376245|113684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054740|NCT01376245|113684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054741|NCT01376245|113684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054742|NCT01376245|113684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054743|NCT01376245|113684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054744|NCT01376245|113684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054745|NCT01376245|113684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054746|NCT01315847||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-067&kw=0974-067&tab=access|
3054747|NCT00546286||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054748|NCT02141217|117044|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054749|NCT02141217|117044|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054750|NCT02141217|117044|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054751|NCT02141217|117044|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054752|NCT02141217|117044|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054753|NCT02141217|117044|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054754|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.
3054755|NCT04392869|clinicaltrialsCRAFT|Human Subjects Review|https://drive.ugr.es/index.php/s/DGKxnBhZfm058DA|Human Subjects Review approval and its translation into English
3054756|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.
3054757|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.
3054758|NCT00866515|112205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054759|NCT00866515|112205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054760|NCT00866515|112205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054761|NCT00866515|112205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054762|NCT00866515|112205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054763|NCT00866515|112205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054764|NCT00866515|112205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054765|NCT01357889|114856|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054766|NCT01357889|114856|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054767|NCT01357889|114856|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054768|NCT01357889|114856|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054769|NCT01357889|114856|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054770|NCT01357889|114856|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054771|NCT01357889|114856|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054772|NCT00964158|113528|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054773|NCT00964158|113528|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054774|NCT00964158|113528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054775|NCT00964158|113528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054776|NCT00964158|113528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054777|NCT00964158|113528|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054778|NCT00964158|113528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054779|NCT01527110|115215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054780|NCT01527110|115215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054781|NCT01527110|115215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054782|NCT01527110|115215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054783|NCT01527110|115215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054784|NCT01527110|115215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054785|NCT00092482||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054786|NCT05184309|Principle investigator|Statistical Analysis Plan|https://pubmed.ncbi.nlm.nih.gov/28446376/|
3054787|NCT07091838||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28179436/|
3054788|NCT01021813||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-009&kw=4305-009&tab=access|
3054789|NCT03336827||Study design|http://pdf.lu/YtWd|
3054790|NCT03336827||List of questionnaires|http://pdf.lu/TJ4c|
3054791|NCT03336827||Informed Consent Form|http://pdf.lu/dN2P|
3054792|NCT03336827||Informed Consent Form|http://pdf.lu/07Xz|
3054793|NCT02800720||Embedded Qualitative Study|http://link.springer.com/article/10.1007/s12671-015-0458-8|
3054794|NCT01319019|115032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054795|NCT01319019|115032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054796|NCT01319019|115032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054797|NCT01319019|115032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054798|NCT01319019|115032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054799|NCT01319019|115032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054800|NCT01319019|115032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054801|NCT00334152|NKT102552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054802|NCT00334152|NKT102552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054803|NCT00334152|NKT102552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054804|NCT00334152|NKT102552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054805|NCT00334152|NKT102552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054806|NCT00334152|NKT102552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054807|NCT00334152|NKT102552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057307|NCT00115492|SCO100250|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057308|NCT00115492|SCO100250|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057309|NCT00115492|SCO100250|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057310|NCT00115492|SCO100250|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057311|NCT00115492|SCO100250|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057312|NCT00115492|SCO100250|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057313|NCT00115492|SCO100250|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057314|NCT00256854|ROX104805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057315|NCT00256854|ROX104805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057316|NCT00256854|ROX104805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057317|NCT00256854|ROX104805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057318|NCT00256854|ROX104805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057319|NCT00256854|ROX104805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057320|NCT00256854|ROX104805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057321|NCT00268177|SCO30005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057322|NCT00268177|SCO30005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057323|NCT00268177|SCO30005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057324|NCT00268177|SCO30005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057325|NCT00268177|SCO30005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057326|NCT00268177|SCO30005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057327|NCT00268177|SCO30005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057328|NCT00976820|113482|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057329|NCT00976820|113482|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057330|NCT00976820|113482|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057331|NCT00976820|113482|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057332|NCT00976820|113482|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057333|NCT00976820|113482|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057334|NCT00370318|107017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057335|NCT00370318|107017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057336|NCT00370318|107017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057337|NCT00370318|107017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057338|NCT00370318|107017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057339|NCT00370318|107017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057340|NCT00784550|111114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054808|NCT00141037|SDY132|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
3054809|NCT00141037|SDY132|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
3054810|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
3054811|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
3054812|NCT03909672||Study Protocol|http://facisa.ufrn.br|
3054813|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.
3054814|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.
3054815|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.
3054816|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.
3054817|NCT02542813|201558|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054818|NCT02542813|201558|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054819|NCT02542813|201558|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054820|NCT02542813|201558|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054821|NCT02542813|201558|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054822|NCT02542813|201558|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054823|NCT02542813|201558|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054824|NCT05885048||Study Protocol|https://www.researchprotocols.org/2024/1/e51145|
3054825|NCT00704431|LPL111814|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054826|NCT00704431|LPL111814|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054827|NCT00704431|LPL111814|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054828|NCT00704431|LPL111814|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054829|NCT00704431|LPL111814|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054830|NCT00704431|LPL111814|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054831|NCT00996593|104507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054832|NCT00996593|104507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054833|NCT00996593|104507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054834|NCT00996593|104507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054835|NCT00996593|104507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054836|NCT00996593|104507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054837|NCT00996593|104507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054838|NCT02697058||Individual Participant Data Set|https://clinicaltrials.servier.com/|
3054839|NCT02697058||Study Protocol|https://clinicaltrials.servier.com/|
3054840|NCT02697058||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
3054841|NCT02697058||Informed Consent Form|https://clinicaltrials.servier.com/|
3054842|NCT02697058||Clinical Study Report|https://clinicaltrials.servier.com/|
3054843|NCT02697058||study-level clinical trial data|https://clinicaltrials.servier.com/|
3054844|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.
3054845|NCT00290303|100478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054846|NCT00290303|100478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054847|NCT00290303|100478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054848|NCT00290303|100478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054849|NCT00290303|100478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054850|NCT00290303|100478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054851|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
3054852|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.
3054853|NCT00005306||Study Forms|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|
3054854|NCT01376388|115362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054855|NCT01376388|115362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054856|NCT01376388|115362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054857|NCT01376388|115362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054858|NCT01235728||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-022&kw=0873-022&tab=access|
3054859|NCT05752786||Study Protocol|https://osf.io/3gts8/|
3054860|NCT05752786||Statistical Analysis Plan|https://osf.io/3gts8/|
3054861|NCT05752786||Individual Participant Data Set|https://osf.io/3gts8/|
3054862|NCT00702910|B2C111401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054863|NCT00702910|B2C111401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054864|NCT00702910|B2C111401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054865|NCT00702910|B2C111401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054866|NCT00702910|B2C111401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054867|NCT00702910|B2C111401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054868|NCT00702910|B2C111401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054869|NCT00306241|106001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054870|NCT00306241|106001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054871|NCT00306241|106001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054872|NCT00306241|106001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054873|NCT00306241|106001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054874|NCT00306241|106001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054875|NCT05464472||BECK DEPRESSION INVENTORY|https://www.ismanet.org/doctoryourspirit/pdfs/Beck-Depression-Inventory-BDI.pdf|
3054876|NCT05464472||SF-36 QUESTIONNAIRE|https://clinmedjournals.org/articles/jmdt/jmdt-2-023-figure-1.pdf|
3054877|NCT00383227|208129/032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054878|NCT00383227|208129/032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054879|NCT00383227|208129/032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054880|NCT00383227|208129/032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054881|NCT00383227|208129/032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054882|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
3054883|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.
3054884|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.
3054885|NCT02197598|2014-000413-31|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-000413-31/results|
3054886|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
3054887|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
3054888|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
3054889|NCT00937326|113160|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054890|NCT00937326|113160|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054891|NCT00937326|113160|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054892|NCT00937326|113160|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054893|NCT00937326|113160|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054894|NCT00937326|113160|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054895|NCT00937326|113160|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054896|NCT06120192|10.6084/m9.figshare.23994768|Informed Consent Form|https://doi.org/10.6084/m9.figshare.23994768|
3054897|NCT06120192|10.6084/m9.figshare.23994768|Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.23994768|
3054898|NCT01031108|114089|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054899|NCT01031108|114089|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054900|NCT01031108|114089|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054901|NCT01031108|114089|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054902|NCT01031108|114089|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054903|NCT01031108|114089|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054904|NCT01031108|114089|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054905|NCT03427138|C2495|Individual Participant Data Set|http://ndar.nih.gov|
3054906|NCT01594749||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-031&kw=0517-031&tab=access|
3054907|NCT00092404||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054908|NCT00654420||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0646-007&kw=0646-007&tab=access|
3054909|NCT00264667|ADG103440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054910|NCT00264667|ADG103440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054911|NCT00264667|ADG103440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054912|NCT00264667|ADG103440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054913|NCT00264667|ADG103440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054914|NCT00264667|ADG103440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054915|NCT00264667|ADG103440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054916|NCT01366534|114460|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054917|NCT01366534|114460|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054918|NCT01366534|114460|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054919|NCT01366534|114460|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054920|NCT01366534|114460|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054921|NCT01366534|114460|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054922|NCT00750178||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054923|NCT01177826|111426|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054924|NCT01177826|111426|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054925|NCT01177826|111426|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054926|NCT01177826|111426|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054927|NCT01177826|111426|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054928|NCT01177826|111426|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054929|NCT02798640||Informed Consent Form|https://mega.nz/#!C5U1HZwI!7XB2jar-JDElrnYOZTbwg0RD5T1WPQEv3HkzT0XPXz8|
3054930|NCT02798640||Clinical Investigation plan|https://mega.nz/#!3gEnFCDK!DK911mpjGBw_bAKdfsR4F2RgzCQG7mYR3oBqrVkRtpA|
3054931|NCT02798640||Clinical Study Report|https://mega.nz/#!S1tThKrL!gaWPII28P3I0BLBrLD9iZJYRqb2R1x-uZT5djgV4ML8|
3054932|NCT00076856||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054933|NCT05837000|MKSU 51- 2 _ 16|Study Protocol|http://kfs.edu.eg/engkfs/|
3054934|NCT00911144|112933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054935|NCT00911144|112933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054936|NCT00911144|112933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054937|NCT00911144|112933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054938|NCT00911144|112933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054939|NCT00911144|112933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054940|NCT00911144|112933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054941|NCT00329784|SDY660|Individual Participant Data Set|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
3054942|NCT00329784|SDY660|Study summary, -design, -adverse event(s), -demographics, -study files|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
3054943|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)
3054944|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)
3054945|NCT03612674||Analytic Code|http://www.epiclin.it|
3054946|NCT00684463||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054947|NCT01431521||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4074-008&kw=4074-008&tab=access|
3054948|NCT00111891||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3054949|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
3054950|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
3054951|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).
3054952|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.
3054953|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.
3054954|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.
3054955|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/|
3054956|NCT05394363||Current GenV collaborations|https://www.genv.org.au/for-researchers/current-genv-collaborations/|
3054957|NCT05394363||Working Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/working-papers/|
3054958|NCT05394363||Published Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/published-papers/|
3054959|NCT00783549|111596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054960|NCT00783549|111596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054961|NCT00783549|111596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054962|NCT00783549|111596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054963|NCT00783549|111596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054964|NCT00783549|111596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054965|NCT00783549|111596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054966|NCT01962467|200284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054967|NCT01962467|200284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054968|NCT01962467|200284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054969|NCT01962467|200284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054970|NCT01962467|200284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054971|NCT01962467|200284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054972|NCT01962467|200284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054973|NCT01160224|114312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054974|NCT01160224|114312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054975|NCT01160224|114312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054976|NCT01160224|114312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054977|NCT01160224|114312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054978|NCT01160224|114312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054979|NCT01160224|114312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054980|NCT03582969||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
3054981|NCT01899768|117270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054982|NCT01899768|117270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054983|NCT01899768|117270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054984|NCT01899768|117270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054985|NCT01899768|117270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054986|NCT01899768|117270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054987|NCT01899768|117270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054988|NCT02968966||Synopsis|http://www.medizin.uni-tuebingen.de/kinder/de/abteilungen/cpcs/projekte/|
3054989|NCT00469040|B2C108784|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054990|NCT00469040|B2C108784|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054991|NCT00469040|B2C108784|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054992|NCT00469040|B2C108784|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054993|NCT00469040|B2C108784|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054994|NCT00469040|B2C108784|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054995|NCT00469040|B2C108784|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054996|NCT04704206|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
3057341|NCT00784550|111114|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057342|NCT00784550|111114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057343|NCT00784550|111114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057344|NCT00784550|111114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057345|NCT00784550|111114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057346|NCT00784550|111114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054997|NCT00964249|112017|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054998|NCT00964249|112017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3054999|NCT00964249|112017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055000|NCT00964249|112017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055001|NCT00964249|112017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055002|NCT00772889|111738|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055003|NCT00772889|111738|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055004|NCT00772889|111738|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055005|NCT00772889|111738|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055006|NCT00772889|111738|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055007|NCT00772889|111738|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055008|NCT00772889|111738|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055009|NCT00345956|105722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055010|NCT00345956|105722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055011|NCT00345956|105722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055012|NCT00345956|105722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055013|NCT00345956|105722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055014|NCT00345956|105722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055015|NCT00419237|FFA10013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055016|NCT00419237|FFA10013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055017|NCT00419237|FFA10013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055018|NCT00419237|FFA10013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055019|NCT00419237|FFA10013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055020|NCT00419237|FFA10013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055021|NCT00419237|FFA10013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055022|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.
3055023|NCT01808365|114991|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055024|NCT01808365|114991|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055025|NCT01808365|114991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055026|NCT01808365|114991|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055027|NCT01808365|114991|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055028|NCT01808365|114991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055029|NCT01808365|114991|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055030|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
3055031|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
3055032|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
3055033|NCT00748306|111834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055034|NCT00748306|111834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055035|NCT00748306|111834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055036|NCT00748306|111834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055037|NCT00748306|111834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055038|NCT00748306|111834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055039|NCT00748306|111834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055040|NCT01722903||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25807199|
3055041|NCT00732472|105211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055042|NCT00732472|105211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055043|NCT00732472|105211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055044|NCT00732472|105211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055045|NCT00732472|105211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055046|NCT00732472|105211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055047|NCT00732472|105211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055048|NCT05859906||Clinical Study Report|http://doi.org/10.1093/bjaceaccp/mkh037|
3055049|NCT01086449|113819|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055050|NCT01086449|113819|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055051|NCT01086449|113819|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055052|NCT01086449|113819|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055053|NCT01086449|113819|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055054|NCT01086449|113819|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055055|NCT01086449|113819|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055056|NCT00067444|29060/874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055057|NCT00067444|29060/874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055058|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
3055059|NCT00067444|29060/874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055060|NCT00067444|29060/874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055061|NCT00067444|29060/874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055062|NCT00034697||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
3055063|NCT02202161|201351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055064|NCT02202161|201351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055065|NCT02202161|201351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055066|NCT02202161|201351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055067|NCT02202161|201351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055068|NCT02202161|201351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055069|NCT02202161|201351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055070|NCT00518336|109616 (Y7)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055071|NCT00518336|109616 (Y7)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055072|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.
3055073|NCT00518336|109616 (Y7)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055074|NCT00518336|109616 (Y7)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055075|NCT00518336|109616 (Y7)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055076|NCT00686699||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04628&kw=P04628&tab=access|
3055077|NCT00290355|249553/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055078|NCT00290355|249553/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055079|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
3055080|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
3055081|NCT00290355|249553/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055082|NCT00290355|249553/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055083|NCT00290355|249553/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055084|NCT00829010|111634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055085|NCT00829010|111634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055086|NCT00829010|111634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055087|NCT00829010|111634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055088|NCT00829010|111634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055089|NCT00829010|111634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055090|NCT00829010|111634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055091|NCT02685839||Clinical Study Report|http://goo.gl/FilVtL|
3055092|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
3055093|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
3055094|NCT01021553|109059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055095|NCT01021553|109059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055096|NCT01021553|109059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055097|NCT01021553|109059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055098|NCT01021553|109059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055099|NCT01021553|109059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055100|NCT01021553|109059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055101|NCT05399836||Study Protocol|https://osf.io/hx75k/|Protocol on the Open Science Framework (OSF)
3055102|NCT05399836||Statistical Analysis Plan|https://osf.io/hx75k/|
3055103|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.
3055104|NCT04746027||Study Protocol|https://www.stmarys.ac.uk/staff-directory/jonathan-nixon|
3055105|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
3055106|NCT00329459|TRX105850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055107|NCT00329459|TRX105850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055108|NCT00329459|TRX105850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055109|NCT00329459|TRX105850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055110|NCT00329459|TRX105850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055111|NCT00329459|TRX105850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055112|NCT00329459|TRX105850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055113|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.
3055114|NCT00998985||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-004&kw=5172-004&tab=access|
3055115|NCT01619176|GSE59526|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/geo|
3055116|NCT05386641|18192154|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3055117|NCT05386641|25977305|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
3055118|NCT05386641|26079868|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3055119|NCT05386641|29332760|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3055120|NCT05386641|32031629|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3055121|NCT05386641|32767329|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3055122|NCT05386641||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
3055123|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)
3055124|NCT01371799|113746|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055125|NCT01371799|113746|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055126|NCT01371799|113746|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055127|NCT01371799|113746|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055128|NCT01371799|113746|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055129|NCT01371799|113746|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055130|NCT07100288||preprint|https://www.researchsquare.com/article/rs-283444/v1|
3055131|NCT01021293|112679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055132|NCT01021293|112679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055133|NCT01021293|112679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055134|NCT01021293|112679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055135|NCT01021293|112679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055136|NCT01021293|112679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055137|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.
3055138|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.
3055139|NCT01428479|115070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055140|NCT01428479|115070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055141|NCT01428479|115070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055142|NCT01428479|115070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055143|NCT01428479|115070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055144|NCT01428479|115070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055145|NCT05327309||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/22456397/|
3055146|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.
3055147|NCT02356770|PMID: 28107560|2. publicaton|https://www.ncbi.nlm.nih.gov/pubmed/28107560|2\. publication concerning the volumetric changes of the soft tissue
3055148|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.
3055149|NCT00005128||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrcps/|
3055150|NCT02896686||Study Protocol|https://cirurgiahj23.wordpress.com|
3055151|NCT00354991||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
3059555|NCT00532298|110620|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059556|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
3059557|NCT02964767||Epidemiological report|http://www.who.int|
3059558|NCT02964767||Clinical Study Report|http://www.Wiley.com|
3059559|NCT00954993||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-029&kw=7009-029&tab=access|
3059560|NCT01112787|114571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059561|NCT01112787|114571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059562|NCT01112787|114571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059563|NCT01112787|114571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059564|NCT01112787|114571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059565|NCT01112787|114571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059566|NCT01112787|114571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059567|NCT01853878|116389|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059568|NCT01853878|116389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059569|NCT01853878|116389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059570|NCT01853878|116389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059571|NCT01853878|116389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059572|NCT01853878|116389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059573|NCT01853878|116389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059574|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
3055152|NCT00750360|218352/054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055153|NCT00750360|218352/054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055154|NCT00750360|218352/054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055155|NCT00750360|218352/054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055156|NCT00750360|218352/054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055157|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
3055158|NCT00104299|SDY91|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY91|ImmPort study identifier is SDY91.
3055159|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.
3055160|NCT00104299|ITN021AI|Individual Participant Data Set|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
3055161|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.
3055162|NCT02671786||Pilot Study Research Paper|http://www.worldwidejournals.com/ijar/file.php?val=April_2015_1427896145__152.pdf|
3059575|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
3059576|NCT00500955|BRL-49653/137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3059577|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
3059578|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
3059579|NCT00500955|BRL-49653/137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055163|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
3055164|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
3055165|NCT00989664|104504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055166|NCT00989664|104504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055167|NCT00989664|104504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055168|NCT00989664|104504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055169|NCT00989664|104504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055170|NCT00989664|104504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055171|NCT00989664|104504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055172|NCT04340804||Study Protocol|https://osf.io/k369t/|
3055173|NCT04340804||Statistical Analysis Plan|https://osf.io/k369t/|
3055174|NCT04340804||Informed Consent Form|https://osf.io/k369t/|
3055175|NCT04340804||Individual Participant Data Set|https://osf.io/k369t/|When results will be published
3055176|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
3055177|NCT00381472|101468/169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055178|NCT00381472|101468/169|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055179|NCT00381472|101468/169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055180|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
3055181|NCT00381472|101468/169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055182|NCT00381472|101468/169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055183|NCT00115622|FFR30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055184|NCT00115622|FFR30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055185|NCT00115622|FFR30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055186|NCT00115622|FFR30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055187|NCT00115622|FFR30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055188|NCT00115622|FFR30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055189|NCT00115622|FFR30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055190|NCT04308668||Individual Participant Data Set|http://www.covidpep.umn.edu/data|
3055191|NCT02619942||Study Protocol|http://www.trialsjournal.com/content/17/1/582|
3055192|NCT01979250||Manuscript|http://www.ncbi.nlm.nih.gov/pubmed/27273977|To acces the results, please go to the above mentioned manuscript.
3055193|NCT02135848|114272|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055194|NCT02135848|114272|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055195|NCT02135848|114272|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055196|NCT02135848|114272|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055197|NCT02135848|114272|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055198|NCT02135848|114272|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055199|NCT02135848|114272|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055200|NCT01213849|102932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055201|NCT01213849|102932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055202|NCT01213849|102932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3055203|NCT01213849|102932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057393|NCT01899742|116960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057394|NCT01446237|115576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057395|NCT01446237|115576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057396|NCT01446237|115576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057397|NCT01446237|115576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057398|NCT01446237|115576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057399|NCT01446237|115576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057400|NCT01446237|115576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
3057401|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
