id|nct_id|document_id|document_type|url|comment
2487189|NCT00460707|NKV109990|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491472|NCT00452686|108638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487190|NCT00460707|NKV109990|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487191|NCT00460707|NKV109990|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487192|NCT00460707|NKV109990|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487193|NCT00460707|NKV109990|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489316|NCT01112787|114571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491473|NCT00452686|108638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491474|NCT00452686|108638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491475|NCT00452686|108638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491476|NCT00452686|108638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491477|NCT00452686|108638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491478|NCT00452686|108638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491479|NCT00306982|106622|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491480|NCT00306982|106622|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491481|NCT00306982|106622|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491482|NCT00306982|106622|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491483|NCT00306982|106622|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491484|NCT00306982|106622|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489317|NCT01112787|114571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487194|NCT00460707|NKV109990|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487195|NCT00460707|NKV109990|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489318|NCT01112787|114571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489319|NCT01112787|114571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489320|NCT01112787|114571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487196|NCT00954512||CSR Synospsi Links|http://www.merck.com/clinical-trials/study.html?id=P04722&kw=P04722&tab=access|
2489321|NCT01112787|114571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489322|NCT01112787|114571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487197|NCT03347734||Clinical Study Report|https://en.wikipedia.org/wiki/Bates_method|
2487198|NCT06623838|HNYZ6|Study Protocol|https://doi.org/10.17605/OSF.IO/HNYZ6|
2491485|NCT01218126|113006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491486|NCT01218126|113006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491487|NCT01218126|113006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493605|NCT01313637|113361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493606|NCT01313637|113361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493607|NCT01313637|113361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489323|NCT04119180||Study Protocol|https://bmcoralhealth.biomedcentral.com/articles/10.1186/s12903-021-01594-0|
2489324|NCT01053988|112206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489325|NCT01053988|112206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493608|NCT01313637|113361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495753|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
2495754|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
2495755|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
2487199|NCT00984139|112682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489326|NCT01053988|112206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489327|NCT01053988|112206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489328|NCT01053988|112206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489329|NCT01053988|112206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489330|NCT01053988|112206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495756|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
2495757|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
2489331|NCT02371603|200229|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489332|NCT02371603|200229|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489333|NCT02371603|200229|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489334|NCT02371603|200229|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495758|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.
2495759|NCT01294709||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-014&kw=0974-014&tab=access|
2487200|NCT00984139|112682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487201|NCT00984139|112682|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487202|NCT00984139|112682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487203|NCT00984139|112682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489335|NCT02371603|200229|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489336|NCT02371603|200229|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489337|NCT01957202|200286|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489338|NCT01957202|200286|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489339|NCT01957202|200286|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489340|NCT01957202|200286|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489341|NCT01957202|200286|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495760|NCT00633217|111117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489342|NCT01957202|200286|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489343|NCT01957202|200286|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491488|NCT01218126|113006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491489|NCT01218126|113006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491490|NCT01218126|113006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491491|NCT01218126|113006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491492|NCT02254447|201713|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491493|NCT02254447|201713|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487204|NCT00984139|112682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495761|NCT00633217|111117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495762|NCT00633217|111117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489344|NCT06040853|doi: 10.1371|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28282425/|
2489345|NCT00240500|100448|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495763|NCT00633217|111117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495764|NCT00633217|111117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489346|NCT00240500|100448|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489347|NCT00240500|100448|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489348|NCT00240500|100448|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489349|NCT00240500|100448|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491494|NCT02254447|201713|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493609|NCT01313637|113361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493610|NCT01313637|113361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493611|NCT01313637|113361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493612|NCT00398645|FFA106783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495765|NCT00633217|111117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495766|NCT00633217|111117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493613|NCT00398645|FFA106783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493614|NCT00398645|FFA106783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495767|NCT00364273|B2F104300|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487205|NCT00984139|112682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487206|NCT05336292||Individual Participant Data Set|https://drive.google.com/drive/folders/1Z6K71rEcfJHXIzsurwREdgHRweFwgFW3|Data will be made available upon reasonable request
2489350|NCT01324362|SAM40065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489351|NCT01324362|SAM40065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491495|NCT02254447|201713|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491496|NCT02254447|201713|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491497|NCT02254447|201713|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491498|NCT02254447|201713|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491499|NCT06901193||Study Protocol|https://orapps.osu.edu/buck-irb/index/view/study/64513|
2491500|NCT01337674||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4618-010&kw=4618-010&tab=access|
2491501|NCT01477853||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431E-211&kw=0431E-211&tab=access|
2491502|NCT00453986|109067|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493615|NCT00398645|FFA106783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493616|NCT00398645|FFA106783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491503|NCT00453986|109067|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491504|NCT00453986|109067|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495768|NCT00364273|B2F104300|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491505|NCT00453986|109067|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493617|NCT00398645|FFA106783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493618|NCT00398645|FFA106783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489352|NCT01324362|SAM40065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491506|NCT00453986|109067|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493619|NCT01808482|116702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493620|NCT01808482|116702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493621|NCT01808482|116702|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493622|NCT01808482|116702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493623|NCT01808482|116702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493624|NCT01808482|116702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489353|NCT01324362|SAM40065|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491507|NCT00453986|109067|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491508|NCT00453986|109067|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491509|NCT04322123||Study Protocol|https://www.medrxiv.org/content/10.1101/2020.05.19.20106997v1|Preprint of the Protocol
2491510|NCT05435352||Study Protocol|https://www.pearbio.com/peartnbc|
2491511|NCT06599567|sample size|Individual Participant Data Set|https://bmjopen.bmj.com/content/10/11/e039976|reference article to see sample size with g power
2491512|NCT06599567|Nintendo Wii protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28330586/|
2491513|NCT06599567|Graded motor imagery protocol|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32003812/|
2491514|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."
2491515|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."
2491516|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."
2491517|NCT01506895|115403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491518|NCT01506895|115403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493625|NCT01808482|116702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493626|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
2493627|NCT05981599||Clinical Study Report|https://doi.org/10.1371/journal.pone.0281544|
2493628|NCT00451100||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493629|NCT01287065|114624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493630|NCT01287065|114624|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493631|NCT01287065|114624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491519|NCT01506895|115403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491520|NCT01506895|115403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491521|NCT01506895|115403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493632|NCT01287065|114624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493633|NCT01287065|114624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493634|NCT01287065|114624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493635|NCT01287065|114624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493636|NCT01323634|113109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491522|NCT01506895|115403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491523|NCT01506895|115403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493637|NCT01323634|113109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493638|NCT01323634|113109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489354|NCT01324362|SAM40065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489355|NCT01324362|SAM40065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491524|NCT00118716|SFA100314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491525|NCT00118716|SFA100314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491526|NCT00118716|SFA100314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491527|NCT00118716|SFA100314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491528|NCT00118716|SFA100314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491529|NCT00118716|SFA100314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491530|NCT01777321|116760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493639|NCT01323634|113109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493640|NCT01323634|113109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493641|NCT01323634|113109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493642|NCT01323634|113109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493643|NCT00753272|106372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493644|NCT00753272|106372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493645|NCT00753272|106372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495769|NCT00364273|B2F104300|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495770|NCT00364273|B2F104300|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495771|NCT00364273|B2F104300|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495772|NCT00364273|B2F104300|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495773|NCT00364273|B2F104300|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495774|NCT02677675||Study Protocol|http://www.nmrr.gov.my|
2495775|NCT00479739|SAM40056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487207|NCT00345878|105926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487208|NCT00345878|105926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487209|NCT00345878|105926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487210|NCT00345878|105926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487211|NCT00345878|105926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489356|NCT01324362|SAM40065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489357|NCT00274677|SCA100223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495776|NCT00479739|SAM40056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487212|NCT00345878|105926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487213|NCT00831545||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487214|NCT02262689|201402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487215|NCT02262689|201402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487216|NCT02262689|201402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487217|NCT02262689|201402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491531|NCT01777321|116760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487218|NCT02262689|201402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487219|NCT02262689|201402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487220|NCT02262689|201402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487221|NCT00197002|208109/220|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491532|NCT01777321|116760|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491533|NCT01777321|116760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493646|NCT00753272|106372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493647|NCT00753272|106372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493648|NCT00753272|106372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493649|NCT00753272|106372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493650|NCT01294683||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-118&kw=0524B-118&tab=access|
2493651|NCT01138007|113351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493652|NCT01138007|113351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493653|NCT01138007|113351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493654|NCT01138007|113351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493655|NCT01138007|113351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493656|NCT01128894|114179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493657|NCT01128894|114179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493658|NCT01128894|114179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493659|NCT01128894|114179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493660|NCT01128894|114179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495777|NCT00479739|SAM40056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495778|NCT00479739|SAM40056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495779|NCT00479739|SAM40056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495780|NCT00479739|SAM40056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495781|NCT00479739|SAM40056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495782|NCT01563029|106855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495783|NCT01563029|106855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495784|NCT01563029|106855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495785|NCT01563029|106855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495786|NCT01563029|106855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495787|NCT01563029|106855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495788|NCT01563029|106855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495789|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.
2495790|NCT00005274||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
2495791|NCT00005274||Study Forms|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
2487222|NCT00197002|208109/220|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487223|NCT00197002|208109/220|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487224|NCT00197002|208109/220|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487225|NCT00197002|208109/220|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495792|NCT00005274||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
2487226|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
2487227|NCT00514904|109495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487228|NCT00514904|109495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487229|NCT00514904|109495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487230|NCT00514904|109495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487231|NCT00514904|109495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487232|NCT00514904|109495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489358|NCT00274677|SCA100223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489359|NCT00274677|SCA100223|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489360|NCT00274677|SCA100223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489361|NCT00274677|SCA100223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489362|NCT00274677|SCA100223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489363|NCT00274677|SCA100223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489364|NCT00954993||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-029&kw=7009-029&tab=access|
2491534|NCT01777321|116760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491535|NCT01777321|116760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491536|NCT01777321|116760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495793|NCT00607906|AXO110461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487233|NCT00514904|109495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489365|NCT01870115||Publication|http://www.aging-us.com/article/101158|
2491537|NCT00508261|109835|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491538|NCT00508261|109835|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491539|NCT00508261|109835|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491540|NCT00508261|109835|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491541|NCT00508261|109835|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491542|NCT00508261|109835|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495794|NCT00607906|AXO110461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495795|NCT00607906|AXO110461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495796|NCT00607906|AXO110461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495797|NCT00607906|AXO110461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495798|NCT00607906|AXO110461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495799|NCT00607906|AXO110461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495800|NCT02691312||FDA 501(k)|https://www.accessdata.fda.gov/cdrh_docs/pdf10/K101935.pdf|
2495801|NCT05016765|2y7fs|Study Protocol|https://osf.io/2y7fs/|
2495802|NCT06565754||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563562/|
2495803|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"
2495804|NCT00981409|106206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491543|NCT00508261|109835|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487234|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.
2495805|NCT00981409|106206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495806|NCT00981409|106206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489366|NCT00398099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491544|NCT02614443|10.1186/s40814-016-0068-9|Study Protocol|https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-016-0068-9|
2491545|NCT00796250||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491546|NCT01376323|114728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491547|NCT01376323|114728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491548|NCT01376323|114728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491549|NCT01376323|114728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491550|NCT01376323|114728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491551|NCT01376323|114728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491552|NCT01376323|114728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491553|NCT01879423|115207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491554|NCT01879423|115207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495807|NCT04845451|Cluster Headaches-Neuroma|Clinical Study Report|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
2495808|NCT04845451|Cluster Headaches-Neuroma|Statistical Analysis Plan|https://curemymigraine.com/|Data access on-demand only by research clinician and participating individuals
2495809|NCT00627458|111344|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495810|NCT00627458|111344|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495811|NCT00627458|111344|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495812|NCT00627458|111344|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495813|NCT00627458|111344|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495814|NCT00627458|111344|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487235|NCT00005300||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/csscd/|
2487236|NCT00005300||Study Forms|http://biolincc.nhlbi.nih.gov/studies/csscd/|
2487237|NCT02920541||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2487238|NCT02920541||Study Protocol|https://clinicaltrials.servier.com/|
2489367|NCT07061483||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/JKAXZ|
2489368|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|
2491555|NCT01879423|115207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491556|NCT01879423|115207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491557|NCT01879423|115207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495815|NCT00627458|111344|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495816|NCT04355767||Individual Participant Data Set|https://biodatacatalyst.nhlbi.nih.gov/|
2495817|NCT01336608|113108|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495818|NCT01336608|113108|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495819|NCT01336608|113108|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495820|NCT01336608|113108|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495821|NCT01336608|113108|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495822|NCT01336608|113108|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495823|NCT01336608|113108|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487239|NCT02920541||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2489369|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.
2489370|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.
2489371|NCT06921174||Study Protocol|https://www.isemu.es|
2489372|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:"
2491558|NCT01879423|115207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491559|NCT01879423|115207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491560|NCT06579820||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|pubmed
2491561|NCT01678131||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-048&kw=7009-048&tab=access|
2491562|NCT07165366||Informed Consent Form|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EalUzspTf7VClbHYAyBlJg4BVp2wl1gK8uHn7MzUbZ4tbA?e=1vfYnE|
2491563|NCT07165366||Statistical Analysis Plan|https://indiana-my.sharepoint.com/:w:/g/personal/tmatis_iu_edu/EbDir0nT8JNAlpv4-vfnOxMBCBxsvrV2UjY2_ua4APTs2g?e=zJdPmF|
2491564|NCT03117725|31098|Study Protocol|https://ezdrug.mfds.go.kr|
2495824|NCT02524665|114553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491565|NCT04699955||Individual Participant Data Set|https://osf.io/akef9/|
2491566|NCT00361959|SCO40036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491567|NCT00361959|SCO40036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491568|NCT00361959|SCO40036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487240|NCT02920541||Informed Consent Form|https://clinicaltrials.servier.com/|
2487241|NCT02920541||study-level clinical trial data|https://clinicaltrials.servier.com/|
2487242|NCT02920541||Clinical Study Report|https://clinicaltrials.servier.com/|
2487243|NCT01639066|25800784|pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25800784|Publication for the primary study results
2487244|NCT00483704||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-031&kw=0974-031&tab=access|
2487245|NCT05546216||REFERENCE|https://doi.org/10.1016/j.ctcp.2019.101068|
2489373|NCT01196026|114451|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489374|NCT01196026|114451|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495825|NCT02524665|114553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495826|NCT02524665|114553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495827|NCT02524665|114553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495828|NCT02524665|114553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487246|NCT05546216||REFERENCE|http://dx.doi.org/10.1016/j.ijcard.2016.11.043|
2491569|NCT00361959|SCO40036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491570|NCT00361959|SCO40036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495829|NCT02524665|114553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495830|NCT00443131|107731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495831|NCT00443131|107731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495832|NCT00443131|107731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495833|NCT00443131|107731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487247|NCT05546216||REFERENCE|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540812/|
2487248|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30367542/|
2487249|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/18065335/|
2487250|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/35307131/|
2487251|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/17056770/|
2487252|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/27252099/|
2487253|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/33632127/|
2487254|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/26171374/|
2487255|NCT05546216||REFERENCE|https://pubmed.ncbi.nlm.nih.gov/29476940/|
2487256|NCT03273465||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
2487257|NCT01485445|115440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487258|NCT01485445|115440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495834|NCT00443131|107731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495835|NCT00443131|107731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495836|NCT00552617||CSr Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495837|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
2495838|NCT00549120|MAB104954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495839|NCT00549120|MAB104954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495840|NCT00549120|MAB104954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487259|NCT01485445|115440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495841|NCT00549120|MAB104954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495842|NCT00549120|MAB104954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495843|NCT00549120|MAB104954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487260|NCT01485445|115440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489375|NCT01196026|114451|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489376|NCT01196026|114451|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489377|NCT01196026|114451|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489378|NCT01196026|114451|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491454|NCT00428090|105640|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491455|NCT00428090|105640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495844|NCT00549120|MAB104954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495845|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.
2487261|NCT01485445|115440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487262|NCT01485445|115440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487263|NCT01485445|115440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487264|NCT02064465|200697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487265|NCT02064465|200697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487266|NCT02064465|200697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495846|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|
2487267|NCT02064465|200697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487268|NCT02064465|200697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487269|NCT02064465|200697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487270|NCT02064465|200697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487271|NCT00322361||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487272|NCT05442606||Full Paper|https://www.e-arm.org/journal/view.php?doi=10.5535/arm.23058|
2487273|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.
2487274|NCT00005159|NLMS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nlms/|Public-use IPD through BioLINCC. Registration is required for access.
2491571|NCT00361959|SCO40036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493661|NCT01128894|114179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493662|NCT01128894|114179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495847|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.
2495848|NCT01480271|114450|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495849|NCT01480271|114450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495850|NCT01480271|114450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493663|NCT04140383||Clinical Study Report|http://rdcu.be/bUabz|
2493664|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)
2493665|NCT03761511|NICOFA|Study Protocol|https://ukaachen.sharepoint.com/:b:/s/NICOFA/ESUAT8h1fTBHlTcsdu48LrQBbvvAABdsy81bvQ4Egq696g?e=8Xliis|
2493666|NCT03434782|60622416.1.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
2495851|NCT01480271|114450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495852|NCT01480271|114450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495853|NCT01480271|114450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495854|NCT01480271|114450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487275|NCT04928469||Statistical Analysis Plan|https://docs.google.com/document/d/11uN0slg6N6K_10vm4BuXVtB7_QcZOAf5M6P0I-okGkU/edit#|
2487276|NCT00282386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487277|NCT01009255|110651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487278|NCT01009255|110651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487279|NCT01009255|110651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487280|NCT01009255|110651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487281|NCT01009255|110651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487282|NCT01009255|110651|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487283|NCT01009255|110651|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491572|NCT00361959|SCO40036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491573|NCT06320626|37369395|Study Protocol|http://bmjopen.bmj.com/content/13/6/e072363.long|Published study protocol
2493667|NCT01323621|112352|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493668|NCT01323621|112352|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493669|NCT01323621|112352|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493670|NCT01323621|112352|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491574|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
2491575|NCT06453655||Study Protocol|https://doi.org/10.1097/MEG.0b013e328333fca6|
2491576|NCT03681574|study protocol|Study Protocol|https://www.justbeamit.com/k7ciq|study protocol
2493671|NCT01323621|112352|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487284|NCT01573767|106853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487285|NCT01573767|106853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491577|NCT03681574|data set|Individual Participant Data Set|https://www.justbeamit.com/nwxjr|individual participant data set
2493672|NCT01323621|112352|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487286|NCT01573767|106853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487287|NCT01573767|106853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487288|NCT01573767|106853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487289|NCT01573767|106853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487290|NCT01573767|106853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487291|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.\[http://dx.doi.org/10.1097/PRS.0000000000002852\] \[PMID: 28027253\]
2487292|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.
2487293|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.
2487294|NCT00005131||Study Forms|http://www2.cscc.unc.edu/aric/cohort-forms|
2487295|NCT00005131||Study Manuals|http://www2.cscc.unc.edu/aric/cohort-forms|
2487296|NCT05591924||C3RP Laboratory Website|https://c3rp.org/leligdowiczlab|
2487297|NCT03707366||Individual Participant Data Set|https://osf.io/673eu/|
2487298|NCT05416645|post LSG GERD|Study Protocol|http://www.mans.edu.eg/|Postlaparoscopic sleeve gastrectomy
2487299|NCT01440387|115418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487300|NCT01440387|115418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487301|NCT01440387|115418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487302|NCT01440387|115418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487303|NCT01440387|115418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487304|NCT01440387|115418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487305|NCT01920867||Clinical Study Report|http://mdstemcells.com/scots-ii/|http://mdstemcells.com/scots-ii/
2491578|NCT03681574|informed consent form|Informed Consent Form|https://www.justbeamit.com/n2c2d|consert form
2491579|NCT03681574|statistical plan|Statistical Analysis Plan|https://www.justbeamit.com/43kxq|statistical plan
2491580|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.
2491581|NCT07165613||thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp
2491582|NCT00441701||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04592&kw=7123-012&tab=access|
2491583|NCT03077464||preliminary results|http://hdl.handle.net/2097/19148|Rodicheva master's thesis document with preliminary analyses
2491584|NCT03408275||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data available to researchers on application through the website
2491585|NCT05525936|University of Sydney|Individual Participant Data Set|https://redcap.sydney.edu.au/|
2491586|NCT00652938|111507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491587|NCT00652938|111507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491588|NCT00652938|111507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491589|NCT00652938|111507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491590|NCT00652938|111507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491591|NCT00652938|111507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491592|NCT00652938|111507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491593|NCT00682643|FFR110537|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491594|NCT00682643|FFR110537|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491595|NCT00682643|FFR110537|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495855|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."
2495856|NCT00803673|110106|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495857|NCT00803673|110106|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495858|NCT00803673|110106|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495859|NCT00803673|110106|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495860|NCT00803673|110106|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487306|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
2487307|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
2487308|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
2495861|NCT00803673|110106|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495862|NCT00803673|110106|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495863|NCT04688814||Study Protocol|http://www.med.alexu.edu.eg|
2487309|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
2487310|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
2487311|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
2495864|NCT01440595||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-012&kw=5172-012&tab=access|
2495865|NCT01294605|263855/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495866|NCT01294605|263855/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495867|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
2495868|NCT01294605|263855/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495869|NCT01294605|263855/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487312|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
2487313|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
2487314|NCT00092339||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487315|NCT01362244|111782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487316|NCT01362244|111782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487317|NCT01362244|111782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487318|NCT01362244|111782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487319|NCT01362244|111782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487320|NCT01362244|111782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491596|NCT00682643|FFR110537|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491597|NCT00682643|FFR110537|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491598|NCT00682643|FFR110537|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487321|NCT01362244|111782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487322|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
2495870|NCT01294605|263855/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495871|NCT00975884|113630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495872|NCT00975884|113630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487323|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
2487324|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
2487325|NCT02839564||Study Protocol|http://gmail.com|Study data can be requested by mailing to mjmolegraaf@gmail.com
2487326|NCT04909372||Study Protocol|https://osf.io/du58k/|
2487327|NCT04909372||Statistical Analysis Plan|https://osf.io/du58k/|
2495873|NCT00975884|113630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495874|NCT00975884|113630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495875|NCT00975884|113630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495876|NCT00975884|113630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495877|NCT01077531|111601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495878|NCT01077531|111601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491456|NCT00428090|105640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491457|NCT00428090|105640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495879|NCT01077531|111601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495880|NCT01077531|111601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495881|NCT01077531|111601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495882|NCT01077531|111601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495883|NCT01077531|111601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495884|NCT00297206|HS210914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495885|NCT00297206|HS210914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495886|NCT00297206|HS210914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495887|NCT00297206|HS210914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495888|NCT00297206|HS210914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495889|NCT00297206|HS210914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495890|NCT00297206|HS210914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495891|NCT00386100|AVT105913|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495892|NCT00386100|AVT105913|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495893|NCT00386100|AVT105913|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495894|NCT00386100|AVT105913|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495895|NCT00386100|AVT105913|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495896|NCT00386100|AVT105913|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491599|NCT00682643|FFR110537|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491600|NCT01691521|115588|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491601|NCT01691521|115588|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491602|NCT01691521|115588|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491603|NCT01691521|115588|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493673|NCT01323621|112352|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495897|NCT00386100|AVT105913|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491604|NCT01691521|115588|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493674|NCT01177787||Individual Participant Data Set|http://dx.doi.org/10.4172/2165-7904.1000203|
2493675|NCT00402363|OM8 Afib|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495898|NCT03284073|NCT01844362|Study Protocol|http://clinicaltrials.gov|
2495899|NCT00370396|107046|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495900|NCT00370396|107046|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495901|NCT00370396|107046|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495902|NCT00370396|107046|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495903|NCT00370396|107046|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487328|NCT04909372||Individual Participant Data Set|https://osf.io/du58k/|
2487329|NCT00103922|CIL103657|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487330|NCT00103922|CIL103657|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489379|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
2487331|NCT00103922|CIL103657|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487332|NCT00103922|CIL103657|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487333|NCT00103922|CIL103657|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487334|NCT00103922|CIL103657|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487335|NCT02713438||Study Protocol|https://drive.google.com/file/d/1bosgzFmvKglMyMjhELiSg-fqzw1pn1nf/view?usp=sharing|The handbook with the protocol for experimenters (in English)
2489380|NCT00799903|100601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489381|NCT00799903|100601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489382|NCT00799903|100601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491605|NCT01691521|115588|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491606|NCT01691521|115588|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493676|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
2493677|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
2493678|NCT00402363|OM8 Afib|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493679|NCT00402363|OM8 Afib|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495904|NCT00370396|107046|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495905|NCT02647554||Study Protocol|http://pan.baidu.com/s/1eQJUJDK|
2487336|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
2487337|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
2489383|NCT00799903|100601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489384|NCT00799903|100601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489385|NCT00799903|100601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489386|NCT00799903|100601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489387|NCT00812773|112356|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489388|NCT00812773|112356|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491607|NCT02786264||Statistical Analysis Plan|https://docs.google.com/document/d/1SUzYG_9aKT5sSkPXEmhvRTqvhXRflQLBiXJe59inDh4/edit?usp=sharing|
2491608|NCT00116844|VLX103596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491609|NCT00116844|VLX103596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491610|NCT00116844|VLX103596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491611|NCT00116844|VLX103596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491612|NCT00116844|VLX103596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491613|NCT00116844|VLX103596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491614|NCT00116844|VLX103596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493680|NCT00402363|OM8 Afib|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493681|NCT00402363|OM8 Afib|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493682|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
2493683|NCT01372410|115321|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493684|NCT01372410|115321|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495906|NCT00140738|100633|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495907|NCT00140738|100633|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495908|NCT00140738|100633|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493685|NCT01372410|115321|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493686|NCT01372410|115321|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495909|NCT00140738|100633|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495910|NCT00140738|100633|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495911|NCT00140738|100633|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493687|NCT01372410|115321|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493688|NCT01372410|115321|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493689|NCT01372410|115321|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489389|NCT00812773|112356|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493690|NCT01313650|113373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493691|NCT01313650|113373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493692|NCT01313650|113373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493693|NCT01313650|113373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495912|NCT00550420|AVA102677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487338|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
2489390|NCT00812773|112356|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489391|NCT00812773|112356|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491615|NCT00327184|106388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491616|NCT00327184|106388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493694|NCT01313650|113373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493695|NCT01313650|113373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495913|NCT00550420|AVA102677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489392|NCT00812773|112356|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489393|NCT00812773|112356|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489394|NCT00892775|108760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489395|NCT00892775|108760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489396|NCT00892775|108760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489397|NCT00892775|108760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493696|NCT01313650|113373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493697|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
2493698|NCT00390910|107737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493699|NCT00390910|107737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493700|NCT00390910|107737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495914|NCT00550420|AVA102677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495915|NCT00550420|AVA102677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495916|NCT00550420|AVA102677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495917|NCT00550420|AVA102677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495918|NCT00550420|AVA102677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489398|NCT00892775|108760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493701|NCT00390910|107737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493702|NCT00390910|107737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493703|NCT00390910|107737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493704|NCT00390910|107737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493705|NCT05512637||Study Protocol|https://bmjopen.bmj.com/content/14/11/e084110|
2493706|NCT00530868||Clinical Study Report|https://doi.org/10.1186/s13058-020-01258-x|Bevacizumab and Letrozole
2493707|NCT03992469||Individual Participant Data Set|https://vivli.org/|
2493708|NCT05833087||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08079-9|
2493709|NCT05833087||Statistical Analysis Plan|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
2493710|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
2493711|NCT05833087||Analytic Code|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-025-09012-4|
2493712|NCT00992511|113809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487339|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
2487340|NCT00411073|SB 480848/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491617|NCT00327184|106388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493713|NCT00992511|113809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493714|NCT00992511|113809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489399|NCT00892775|108760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493715|NCT00992511|113809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493716|NCT00992511|113809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491458|NCT00428090|105640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491459|NCT00428090|105640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491460|NCT00428090|105640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491461|NCT06038760||Study Protocol|https://www.pearbio.com/pearglio|
2491462|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"
2491618|NCT00327184|106388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491619|NCT00327184|106388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491620|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.
2491621|NCT02948881|BON103593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493717|NCT00992511|113809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493718|NCT00992511|113809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495919|NCT01416376|115830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495920|NCT01416376|115830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495921|NCT01416376|115830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487341|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
2491463|NCT06182306||Study Protocol|https://www.pearbio.com/pearmet|Company website with background and information and links to protocol, etc.
2491464|NCT06264479||Study Protocol|https://www.pearbio.com/peartree2|
2491465|NCT02920697||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2491466|NCT02920697||Study Protocol|https://clinicaltrials.servier.com/|
2491467|NCT02920697||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2491468|NCT02920697||Informed Consent Form|https://clinicaltrials.servier.com/|
2491469|NCT02920697||study-level clinical trial data|https://clinicaltrials.servier.com/|
2493719|NCT01405937||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-044&kw=7009-044&tab=access|
2493720|NCT01545570|114403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495922|NCT01416376|115830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491470|NCT02920697||Clinical Study Report|https://clinicaltrials.servier.com/|
2491471|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"
2495923|NCT01416376|115830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495924|NCT01416376|115830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495925|NCT00969059|112967|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495926|NCT00969059|112967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495927|NCT00969059|112967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495928|NCT00969059|112967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495929|NCT00969059|112967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495930|NCT00969059|112967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495931|NCT00969059|112967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491622|NCT02948881|BON103593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493721|NCT01545570|114403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487342|NCT00411073|SB 480848/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487343|NCT00849134|111383|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495932|NCT00289731|100382|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495933|NCT00289731|100382|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495934|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.
2495935|NCT00289731|100382|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495936|NCT00289731|100382|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495937|NCT00289731|100382|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493722|NCT01545570|114403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495938|NCT02094937|201135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487344|NCT00849134|111383|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487345|NCT00849134|111383|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487346|NCT00849134|111383|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487347|NCT00849134|111383|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487348|NCT00849134|111383|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487349|NCT00849134|111383|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489400|NCT02744092|AFT-28|Study Protocol|https://www.allianceforclinicaltrialsinoncology.org/main/public/standard.xhtml?path=%2FPublic%2FAFT|Email the study team at CANVAS@AllianceFoundationTrials.org.
2489401|NCT05347836||Study Protocol|https://www.degruyter.com/document/doi/10.1515/jpem-2015-0340/html|
2489402|NCT02636205|25014045|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25014045|
2489403|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|
2489404|NCT00857857|110762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489405|NCT00857857|110762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489406|NCT00857857|110762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489407|NCT00857857|110762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489408|NCT00857857|110762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489409|NCT00857857|110762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489410|NCT00857857|110762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489411|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.
2493723|NCT01545570|114403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493724|NCT01545570|114403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493725|NCT01545570|114403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493726|NCT01545570|114403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493727|NCT01387230|115408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493728|NCT01387230|115408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493729|NCT01387230|115408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495939|NCT02094937|201135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495940|NCT02094937|201135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495941|NCT02094937|201135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495942|NCT02094937|201135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487350|NCT00568334|109705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487351|NCT00568334|109705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491623|NCT02948881|BON103593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491624|NCT02948881|BON103593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491625|NCT02948881|BON103593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491626|NCT02948881|BON103593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491627|NCT02948881|BON103593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495943|NCT00524576|108988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495944|NCT00524576|108988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495945|NCT00524576|108988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495946|NCT00524576|108988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495947|NCT00524576|108988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487352|NCT00568334|109705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487353|NCT00568334|109705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487354|NCT00568334|109705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487355|NCT00568334|109705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487356|NCT02983916||Clinical Study Report|https://doi.org/10.1038/s41395-018-0158-9|
2487357|NCT00359177|NKT102785|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487358|NCT00359177|NKT102785|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487359|NCT00359177|NKT102785|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487360|NCT00359177|NKT102785|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487361|NCT00359177|NKT102785|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487362|NCT00359177|NKT102785|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487363|NCT00359177|NKT102785|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489412|NCT00000526||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/cast/|
2489413|NCT00000526||Study Forms|http://biolincc.nhlbi.nih.gov/studies/cast/|
2489414|NCT00938184|112811|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489415|NCT00938184|112811|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491628|NCT04599738||Study Protocol|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
2491629|NCT04599738||Informed Consent Form|https://drive.google.com/drive/u/0/folders/1wsl_6XU0myZgcXtOjRaemk414v9qgDaz|
2491630|NCT01036022|111407|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487364|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.
2487365|NCT00000589||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/trap/|
2487366|NCT00000589||Study Forms|http://biolincc.nhlbi.nih.gov/studies/trap/|
2489416|NCT00938184|112811|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491631|NCT01036022|111407|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495948|NCT00879970|111960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495949|NCT00879970|111960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495950|NCT00879970|111960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495951|NCT00879970|111960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487367|NCT01636947||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-225&kw=0869-225&tab=access|
2487368|NCT03532815||Study Protocol|https://sites.google.com/view/lifestyle-intervention-/home|
2487369|NCT03449992||Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.5873190.v1|
2487370|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,
2487371|NCT00603382|FFA109687|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487372|NCT00603382|FFA109687|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487373|NCT00603382|FFA109687|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487374|NCT00603382|FFA109687|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487375|NCT00603382|FFA109687|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487376|NCT00603382|FFA109687|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487377|NCT00603382|FFA109687|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487378|NCT00482599||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487379|NCT01716520|116133|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487380|NCT01716520|116133|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487381|NCT01716520|116133|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487382|NCT01716520|116133|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487383|NCT01716520|116133|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489417|NCT00938184|112811|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491632|NCT01036022|111407|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491633|NCT01036022|111407|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491634|NCT01036022|111407|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491635|NCT01036022|111407|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491636|NCT01036022|111407|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491637|NCT04599686|NCT04599686|Study Protocol|http://clinicaltrials.gov/ct2/results?cond=&term=NCT04599686&cntry=&state=&city=&dist=|Please see the clinical trials NCT04599686
2491638|NCT00979602|113480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487384|NCT01716520|116133|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487385|NCT01716520|116133|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487386|NCT00530790|107846|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487387|NCT00530790|107846|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487388|NCT00530790|107846|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489418|NCT06122506||Statistical Analysis Plan|https://drive.google.com/file/d/16iZkdhVtT_pnExSoUhJV5iprYyA1JYhx/view?usp=sharing|
2489419|NCT06122506||Study Protocol|https://drive.google.com/file/d/1Z_nDas-Emj7x3OnbkcmRl3Pujy0tjlmM/view?usp=sharing|
2489420|NCT04205721||Individual Participant Data Set|http://dataverse.unc.edu/dataverse/cpc|Search for South Africa Impact Evaluation
2495952|NCT00879970|111960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489421|NCT03110471||Publications|http://orcid.org/0000-0002-5691-2987|Prof Sue Jordan- publication list
2487389|NCT00530790|107846|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487390|NCT00034944||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489422|NCT01358825|115375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489423|NCT01358825|115375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489424|NCT01358825|115375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489425|NCT01358825|115375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489426|NCT01358825|115375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489427|NCT01358825|115375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489428|NCT01358825|115375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489429|NCT00985673|113536|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489430|NCT00985673|113536|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489431|NCT00985673|113536|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489432|NCT00985673|113536|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489433|NCT00985673|113536|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489434|NCT00985673|113536|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489435|NCT00985673|113536|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489436|NCT00127023|104389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495953|NCT00879970|111960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495954|NCT00879970|111960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489437|NCT00127023|104389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489438|NCT00127023|104389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489439|NCT00127023|104389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489440|NCT00127023|104389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491639|NCT00979602|113480|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491640|NCT00979602|113480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495955|NCT02169583|201022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495956|NCT02169583|201022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495957|NCT02169583|201022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495958|NCT02169583|201022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495959|NCT02169583|201022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495960|NCT02169583|201022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487391|NCT01648192|116681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489441|NCT00127023|104389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489442|NCT00985465|113166|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489443|NCT00985465|113166|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489444|NCT00985465|113166|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491641|NCT00979602|113480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495961|NCT02169583|201022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495962|NCT03567330||Study Protocol|https://link-springer-com.udel.idm.oclc.org/article/10.1186/s12885-018-5052-8|
2495963|NCT04716673||Individual Participant Data Set|https://info.swissubase.ch|
2495964|NCT05709054||Clinical Study Report|https://doi.org/10.1016/j.ijosm.2018.07.006|
2495965|NCT01332513|114552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491642|NCT00979602|113480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491643|NCT00979602|113480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491644|NCT00979602|113480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491645|NCT00980005|112999|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491646|NCT00980005|112999|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491647|NCT00980005|112999|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491648|NCT00980005|112999|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491649|NCT00980005|112999|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491650|NCT00980005|112999|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491651|NCT00980005|112999|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491652|NCT00144872|LAM100118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491653|NCT00144872|LAM100118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491654|NCT00144872|LAM100118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491655|NCT00144872|LAM100118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491656|NCT00144872|LAM100118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491657|NCT00144872|LAM100118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491658|NCT00144872|LAM100118|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491659|NCT01812382|117151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491660|NCT01812382|117151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495966|NCT01332513|114552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491661|NCT01812382|117151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493730|NCT01387230|115408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487392|NCT01648192|116681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489445|NCT00985465|113166|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489446|NCT00985465|113166|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489447|NCT00985465|113166|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489448|NCT00985465|113166|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489449|NCT06342817||Study Protocol|https://drive.google.com/file/d/1YWyRsHac1y9eqsmQXVHCsmYArWwAdMoq/view?usp=sharing|
2489450|NCT06342817||Informed Consent Form|https://drive.google.com/file/d/1TfBgnmUMvF4tFJu-a1lGXlcawu0k5YeJ/view?usp=sharing|
2489451|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
2489452|NCT00481702||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493731|NCT01387230|115408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489453|NCT00992758|104512|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491662|NCT01812382|117151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493732|NCT01387230|115408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489454|NCT00992758|104512|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495967|NCT01332513|114552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493733|NCT01387230|115408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493734|NCT07060235|fascial tarining|statics|https://www.anatomytrains.com/fascialfitness/fascial_fitness1.pdf|fascia and mobile app
2493735|NCT00863109||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05278&kw=P05278&tab=access|
2493736|NCT04024644|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
2495968|NCT01332513|114552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487393|NCT01648192|116681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487394|NCT01648192|116681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487395|NCT01648192|116681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487396|NCT01648192|116681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487397|NCT01648192|116681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487398|NCT00329745|107070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487399|NCT00329745|107070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487400|NCT00329745|107070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487401|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.
2487402|NCT00329745|107070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487403|NCT00329745|107070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487404|NCT01119846|111598|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489455|NCT00992758|104512|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489456|NCT00992758|104512|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489457|NCT00992758|104512|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489458|NCT00992758|104512|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489459|NCT00992758|104512|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489460|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.
2495969|NCT01332513|114552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489461|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.
2489462|NCT06239740||Study Protocol|https://doi.org/10.5281/zenodo.10488186|
2489463|NCT00496015|107137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489464|NCT00496015|107137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489465|NCT00496015|107137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489466|NCT00496015|107137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493737|NCT04024644|10.1016/j.joms.2011.09.034|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
2493738|NCT00437671||FDA approved labeling information|http://www.talecris-pi.info/inserts/hypertet.pdf|
2493739|NCT01829360||Treatment & Testing Scripts|http://doi.org/10.23641/asha.9745181|See item S4 and S7.
2493740|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.
2495970|NCT01332513|114552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495971|NCT01332513|114552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493741|NCT04561804||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/MOH_2017-06-07_000470.aspx|Israel Ministry of Health registration number
2493742|NCT00067951|712753/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493743|NCT00067951|712753/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493744|NCT00067951|712753/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495972|NCT02496221|201834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495973|NCT02496221|201834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495974|NCT02496221|201834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495975|NCT02496221|201834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495976|NCT02496221|201834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495977|NCT02496221|201834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495978|NCT02496221|201834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495979|NCT01165242|114249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487405|NCT01119846|111598|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487406|NCT01119846|111598|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489467|NCT00496015|107137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489468|NCT00496015|107137|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493745|NCT00067951|712753/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495980|NCT01165242|114249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487407|NCT01119846|111598|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489469|NCT00496015|107137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489470|NCT01342913|113107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489471|NCT01342913|113107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489472|NCT01342913|113107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489473|NCT01342913|113107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489474|NCT01342913|113107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491663|NCT01812382|117151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491664|NCT01812382|117151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491665|NCT01812382|117151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489475|NCT01342913|113107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489476|NCT01342913|113107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491666|NCT01678820||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-266&kw=0431D-266&tab=access|
2491667|NCT02777996||Study Protocol|http://www.ispo.it|In Italian, available under request
2491668|NCT01590771||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-253&kw=0431-253&tab=access|
2493746|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
2495981|NCT01165242|114249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495982|NCT01165242|114249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495983|NCT01165242|114249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495984|NCT01165242|114249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487408|NCT01119846|111598|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495985|NCT00411697|106789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487409|NCT01119846|111598|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487410|NCT01119846|111598|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487411|NCT01370616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0826-061&kw=0826-061&tab=access|
2487412|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
2487413|NCT01088711||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-004&kw=3102-004&tab=access|
2487414|NCT03602833||Summary of Product Characteristics|https://www.medicines.org.uk/emc/product/8453|
2487415|NCT01039805|112571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487416|NCT01039805|112571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487417|NCT01039805|112571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487418|NCT01039805|112571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487419|NCT01039805|112571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487420|NCT01039805|112571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487421|NCT01039805|112571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487422|NCT03075332|plataforma brasil|Ethics committee project|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|all project
2487423|NCT02696174||Study Protocol|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Total protocol FILE named protocol.pdf
2487424|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
2489477|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).
2489478|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/).
2489479|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_prep/|Source code for preprocessing prostate MRI data archives.
2489480|NCT05489341||Analytic Code|https://github.com/DIAGNijmegen/picai_baseline|Source code for training baseline diagnostic AI models.
2489481|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.
2489482|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).
2489483|NCT00387881|TXA107563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489484|NCT00387881|TXA107563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491669|NCT00674635|104972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491670|NCT00674635|104972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495986|NCT00411697|106789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489485|NCT00387881|TXA107563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487425|NCT02696174||Questionnaires|https://www.flipdrive.com/site/login|Username: HMI Password: insurance All questionnaires (English) uploaded
2487426|NCT02785562||Study Protocol|http://www.g-f-p-c.org|The login can be obtained directly on gfpc site.
2487427|NCT05543031||Study Protocol|http://dc.etsu.edu/etd/772|
2487428|NCT05543031||Study Protocol|http://encompass.eku.edu/honors_theses|
2487429|NCT01148459|112745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489486|NCT00387881|TXA107563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491671|NCT00674635|104972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487430|NCT01148459|112745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487431|NCT01148459|112745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487432|NCT01148459|112745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495987|NCT00411697|106789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487433|NCT01148459|112745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487434|NCT01148459|112745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491672|NCT00674635|104972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491673|NCT00674635|104972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491674|NCT00674635|104972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491675|NCT00674635|104972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493747|NCT00067951|712753/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493748|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
2489487|NCT00387881|TXA107563|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489488|NCT00387881|TXA107563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489489|NCT00387881|TXA107563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489490|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/22original18.pdf|
2489491|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/23original19.pdf|
2489492|NCT01387217|114070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493749|NCT01153802|112773|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493750|NCT01153802|112773|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495988|NCT00411697|106789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495989|NCT00411697|106789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495990|NCT00411697|106789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489493|NCT01387217|114070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489494|NCT01387217|114070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489495|NCT01387217|114070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489496|NCT01387217|114070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489497|NCT01387217|114070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489498|NCT01387217|114070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489499|NCT00102765|SFA103153|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491676|NCT00082537||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495991|NCT06538168||Informed Consent Form|https://www.facebook.com/gghgmabadfsd/?paipv=0&eav=AfbwgEmoehvAkH8F8E-KZ9WClHEgcLyNQwBOij0PYLNHpvrJZ1KZbTJdZYuWB21J8rA&_rdr|
2495992|NCT01663714|104514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495993|NCT01663714|104514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491677|NCT00352898|105909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495994|NCT01663714|104514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495995|NCT01663714|104514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495996|NCT01663714|104514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495997|NCT01663714|104514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489500|NCT00102765|SFA103153|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489501|NCT00102765|SFA103153|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491678|NCT00352898|105909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487435|NCT01934127|115415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491679|NCT00352898|105909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487436|NCT01934127|115415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489502|NCT00102765|SFA103153|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489503|NCT00102765|SFA103153|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489504|NCT00102765|SFA103153|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489505|NCT00102765|SFA103153|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489506|NCT00539994|ALB110247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489507|NCT00539994|ALB110247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491680|NCT00352898|105909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493751|NCT01153802|112773|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487437|NCT01934127|115415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493752|NCT01153802|112773|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487438|NCT01934127|115415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487439|NCT01934127|115415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487440|NCT01934127|115415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487441|NCT00657657|110071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487442|NCT00657657|110071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487443|NCT00657657|110071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487444|NCT00657657|110071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487445|NCT00657657|110071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491681|NCT00352898|105909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491682|NCT00352898|105909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491683|NCT06925763||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/?term=nitroglycerin+in+bone+regeneration|
2493753|NCT01153802|112773|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493754|NCT01153802|112773|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493755|NCT01153802|112773|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493756|NCT01436071|115283|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493757|NCT01436071|115283|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493758|NCT01436071|115283|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493759|NCT01436071|115283|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487446|NCT00657657|110071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491684|NCT06900699|Not available at moment|papers|https://pubmed.ncbi.nlm.nih.gov/|Most of thé informations available at This site and Google Scholar
2491685|NCT02726776||Study Protocol|https://cloud.scientificnet.org/index.php/s/7vKbCJ1vs0UOYNN|Unfortunately available only in German
2493760|NCT01436071|115283|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493761|NCT01436071|115283|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493762|NCT01436071|115283|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493763|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.
2493764|NCT01013766|111823|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489508|NCT00539994|ALB110247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489509|NCT00539994|ALB110247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489510|NCT00539994|ALB110247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489511|NCT00539994|ALB110247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489512|NCT00539994|ALB110247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489513|NCT00550407|SCA104779|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489514|NCT00550407|SCA104779|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489515|NCT00550407|SCA104779|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489516|NCT00550407|SCA104779|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489517|NCT06938126|TE-KEB/22/2023|Individual Participant Data Set|https://tf.hu/en/|For more information please email to: petridis.leonidas@tf.hu
2491686|NCT02726776||Informed Consent Form|https://cloud.scientificnet.org/index.php/s/9RXyWhRxEgUgbTd|Unfortunately available only in German or Italian
2491687|NCT03047122|P110006|U.S. Food and Drug Administration. somo-v Automated Breast Ultrasound System|http://www.accessdata.fda.gov/cdrh_docs/pdf11/P110006b.pdf|
2491688|NCT01147692|108366|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491689|NCT01147692|108366|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491690|NCT01147692|108366|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491691|NCT01147692|108366|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491692|NCT01147692|108366|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491693|NCT01147692|108366|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491694|NCT01147692|108366|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491695|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.
2491696|NCT01235975|113807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491697|NCT01235975|113807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491698|NCT01235975|113807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491699|NCT01235975|113807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491700|NCT01235975|113807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491701|NCT01235975|113807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491702|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
2491703|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
2491704|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
2491705|NCT00344006|CDA 714703/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491706|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
2493765|NCT01013766|111823|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495998|NCT01663714|104514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495999|NCT01162590|113545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489518|NCT01928927||Grading table|https://rsc.tech-res.com/clinical-research-sites/safety-reporting/daids-grading-tables|
2491707|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
2491708|NCT00344006|CDA 714703/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489519|NCT03847766|31484523|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31484523/|Data can be accessed by request from the corresponding author
2489520|NCT00988884||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-005&kw=V503-005&tab=access|
2491709|NCT01190215|114452|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487447|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
2487448|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
2487449|NCT00693615|580299/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489521|NCT00960063||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05883&kw=P05883&tab=access|
2489522|NCT00689390||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05063&kw=P05063&tab=access|
2489523|NCT00605852|HH3110161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489524|NCT00605852|HH3110161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489525|NCT00605852|HH3110161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489526|NCT00605852|HH3110161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489527|NCT00605852|HH3110161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489528|NCT00605852|HH3110161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491710|NCT01190215|114452|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491711|NCT01190215|114452|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491712|NCT01190215|114452|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493766|NCT01013766|111823|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493767|NCT01013766|111823|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493768|NCT01013766|111823|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493769|NCT01013766|111823|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493770|NCT01013766|111823|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493771|NCT01667107||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5592-105&kw=5592-105&tab=access|
2493772|NCT04100629||Study Protocol|https://drive.google.com/open?id=1vNjwT5j9Y32e7vdayZAMBp-3PvJWCiSK|
2493773|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.
2487450|NCT00693615|580299/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489529|NCT00605852|HH3110161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489530|NCT01969708|PB2016-103333|Study Protocol|https://ntrl.ntis.gov/NTRL/|SCORE2 Protocol Version 3.0 (the Identifier for the appendices is PB2016-103334)
2491713|NCT01190215|114452|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491714|NCT01190215|114452|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491715|NCT03176446|1.941.369|Approval of the ethics committee|http://plataformabrasil.saude.gov.br|
2491716|NCT05051332|NCT03545269|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Efficacy and Safety of Treatment of Articular Cartilage Lesions With CartiLife®
2491717|NCT05051332|NCT03517046|Clinical Study Report|https://clinicaltrials.gov/|Study to Assess the Safety of Treatment of Articular Cartilage Lesions With CartiLife®
2491718|NCT01868035|393229/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491719|NCT01868035|393229/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491720|NCT01868035|393229/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491721|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
2491722|NCT01868035|393229/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493774|NCT02509104|201897|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489531|NCT00938158|108370|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489532|NCT00938158|108370|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489533|NCT00938158|108370|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489534|NCT00938158|108370|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489535|NCT00938158|108370|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489536|NCT00938158|108370|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491723|NCT01868035|393229/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487451|NCT00693615|580299/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487452|NCT00693615|580299/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489537|NCT00938158|108370|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489538|NCT01009060|113147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489539|NCT01009060|113147|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489540|NCT01009060|113147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489541|NCT01009060|113147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489542|NCT01009060|113147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489543|NCT01009060|113147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489544|NCT01009060|113147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489545|NCT06555185|10.17632/2cwcz2vx4v.1|Individual Participant Data Set|https://data.mendeley.com/datasets/2cwcz2vx4v/1|
2489546|NCT01527123|115959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489547|NCT01527123|115959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489548|NCT01527123|115959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489549|NCT01527123|115959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489550|NCT01527123|115959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489551|NCT01527123|115959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489552|NCT00382772|107876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489553|NCT00382772|107876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489554|NCT00382772|107876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489555|NCT00382772|107876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489556|NCT00382772|107876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489557|NCT00382772|107876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489558|NCT00405080|NKV105091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489559|NCT00405080|NKV105091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489560|NCT00405080|NKV105091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489561|NCT00405080|NKV105091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489562|NCT00405080|NKV105091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491724|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
2491725|NCT02378402|ClinicalTrials.gov/NCT02378402|Clinical Study Report|http://jcmr-online.biomedcentral.com/articles/10.1186/s12968-016-0228-3|
2491726|NCT00460148|ROP109087|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491727|NCT00460148|ROP109087|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496000|NCT01162590|113545|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496001|NCT01162590|113545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496002|NCT01162590|113545|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496003|NCT01162590|113545|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496004|NCT01162590|113545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496005|NCT00950833|112801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496006|NCT00950833|112801|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489563|NCT00405080|NKV105091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489564|NCT00506350|109817|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489565|NCT00506350|109817|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489566|NCT00506350|109817|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489567|NCT00506350|109817|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489568|NCT00506350|109817|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491728|NCT00460148|ROP109087|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491729|NCT00460148|ROP109087|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491730|NCT00460148|ROP109087|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491731|NCT00460148|ROP109087|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491732|NCT00460148|ROP109087|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491733|NCT00196989|ADG20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487453|NCT00693615|580299/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487454|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."
2487455|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.
2491734|NCT00196989|ADG20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491735|NCT00196989|ADG20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491736|NCT00196989|ADG20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491737|NCT00196989|ADG20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491738|NCT00196989|ADG20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491739|NCT00196989|ADG20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491740|NCT00197028|103967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491741|NCT00197028|103967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491742|NCT00197028|103967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491743|NCT00197028|103967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491744|NCT00197028|103967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491745|NCT00197028|103967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491746|NCT00044460|49653/326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491747|NCT00044460|49653/326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493775|NCT02509104|201897|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493776|NCT02509104|201897|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493777|NCT02509104|201897|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493778|NCT02509104|201897|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493779|NCT02509104|201897|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493780|NCT02509104|201897|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493781|NCT00378833||CSR synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493782|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
2493783|NCT00108914|FFR30008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493784|NCT00108914|FFR30008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493785|NCT00108914|FFR30008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493786|NCT00108914|FFR30008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493787|NCT00108914|FFR30008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493788|NCT00108914|FFR30008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493789|NCT00108914|FFR30008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493790|NCT01159912|112059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493791|NCT01159912|112059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493792|NCT01159912|112059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493793|NCT01159912|112059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493794|NCT01159912|112059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493795|NCT01159912|112059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493796|NCT01159912|112059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493797|NCT06725225||Individual Participant Data Set|https://vivli.org|
2493798|NCT01086410|106851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493799|NCT01086410|106851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493800|NCT01086410|106851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493801|NCT01086410|106851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493802|NCT01086410|106851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493803|NCT01086410|106851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496007|NCT00950833|112801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496008|NCT00950833|112801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496009|NCT00950833|112801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496010|NCT00950833|112801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496011|NCT00950833|112801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487456|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.
2493804|NCT01086410|106851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493805|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.
2493806|NCT01177384||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-130&kw=0431-130&tab=access|
2493807|NCT00279019|AC2103473|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493808|NCT00279019|AC2103473|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493809|NCT00279019|AC2103473|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493810|NCT00279019|AC2103473|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493811|NCT00279019|AC2103473|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493812|NCT00279019|AC2103473|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493813|NCT00279019|AC2103473|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493814|NCT00766090|112202|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493815|NCT00766090|112202|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493816|NCT00766090|112202|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493817|NCT00766090|112202|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493818|NCT00766090|112202|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493819|NCT00766090|112202|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493820|NCT00766090|112202|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495698|NCT00297063|AVD104742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495699|NCT00297063|AVD104742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495700|NCT00297063|AVD104742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495701|NCT00297063|AVD104742|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495702|NCT00297063|AVD104742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495703|NCT00109278||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495704|NCT03052374||Informed Consent Form|http://childstudies.ca/contact|
2495705|NCT03052374||Study Protocol|http://childstudies.ca/contact|
2495706|NCT03052374||Statistical Analysis Plan|http://childstudies.ca/contact|
2495707|NCT00538473|110223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495708|NCT00538473|110223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495709|NCT00538473|110223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495710|NCT00538473|110223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489569|NCT00506350|109817|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489570|NCT00506350|109817|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489571|NCT02481154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2489572|NCT02481154||Study Protocol|https://clinicaltrials.servier.com/|
2489573|NCT02481154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2489574|NCT02481154||Informed Consent Form|https://clinicaltrials.servier.com/|
2489575|NCT02481154||Clinical Study Report|https://clinicaltrials.servier.com/|
2489576|NCT02481154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2489577|NCT06357481|doi: 10.1111/iej.13304|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/32266988/|
2489578|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.
2489579|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
2489580|NCT02257398|115775|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489581|NCT02257398|115775|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489582|NCT02257398|115775|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489583|NCT02257398|115775|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493821|NCT02689531|VIV00008648|Individual Participant Data Set|https://doi.org/10.25934/PR00008648|
2493822|NCT00082524||CSRSynopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493823|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
2493824|NCT04160169|doi:10.15139/S3/XEXQXO|Individual Participant Data Set|https://dataverse.unc.edu/dataset.xhtml?persistentId=doi:10.15139/S3/XEXQXO|
2493825|NCT05689970|PubMed ID: 34763217|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/34763217/|
2496012|NCT00964223|114547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496013|NCT00964223|114547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496014|NCT00964223|114547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496015|NCT00964223|114547|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496016|NCT00964223|114547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496017|NCT00964223|114547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496018|NCT00964223|114547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496019|NCT00345683|105988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496020|NCT00345683|105988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496021|NCT00345683|105988|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496022|NCT00345683|105988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496023|NCT00345683|105988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496024|NCT00345683|105988|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496025|NCT00345683|105988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493826|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
2487457|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.
2487458|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.
2487459|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.
2487460|NCT05880095||Study Protocol|https://ensati.wixsite.com/ensati/qu%C3%A9-es-ensati|
2487461|NCT00481767|106069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487462|NCT00481767|106069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487463|NCT00481767|106069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491748|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
2491749|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
2491750|NCT00044460|49653/326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491751|NCT00044460|49653/326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491752|NCT00044460|49653/326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491753|NCT01607385|116511|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493827|NCT00139347|444563/024|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493828|NCT00139347|444563/024|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493829|NCT00139347|444563/024|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493830|NCT00139347|444563/024|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493831|NCT00139347|444563/024|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493832|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
2493833|NCT00370227|107706|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493834|NCT00370227|107706|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493835|NCT00370227|107706|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493836|NCT00370227|107706|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493837|NCT00370227|107706|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493838|NCT00370227|107706|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493839|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.
2493840|NCT00000551||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/act/|
2493841|NCT00000551||Study Forms|http://biolincc.nhlbi.nih.gov/studies/act/|
2493842|NCT00000551||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/act/|
2493843|NCT00674583|111414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493844|NCT00674583|111414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493845|NCT00674583|111414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493846|NCT00674583|111414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493847|NCT00674583|111414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493848|NCT00674583|111414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493849|NCT00674583|111414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493850|NCT00376584||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493851|NCT00330395||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493852|NCT03662165||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/UULS6T|
2493853|NCT00768326|2006-003739-57|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2006-003739-57/results|
2493854|NCT00861250||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25303369|First study article: http://www.ncbi.nlm.nih.gov/pubmed/23206270
2493855|NCT00282295|105753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493856|NCT00282295|105753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493857|NCT00282295|105753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487464|NCT00481767|106069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487465|NCT00481767|106069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487466|NCT00481767|106069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493858|NCT00282295|105753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493859|NCT00282295|105753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493860|NCT00282295|105753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493861|NCT00169455|103477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493862|NCT00169455|103477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493863|NCT00169455|103477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493864|NCT00169455|103477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493865|NCT00169455|103477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493866|NCT00169455|103477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493867|NCT00449670|109630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493868|NCT00449670|109630|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493869|NCT00449670|109630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493870|NCT00449670|109630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493871|NCT00449670|109630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493872|NCT00449670|109630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493873|NCT00449670|109630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493874|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.
2493875|NCT01086462|114041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493876|NCT01086462|114041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493877|NCT01086462|114041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493878|NCT01086462|114041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493879|NCT01086462|114041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493880|NCT01086462|114041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487467|NCT00481767|106069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487468|NCT01147718|111680|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493881|NCT01086462|114041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487469|NCT01147718|111680|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487470|NCT01147718|111680|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487471|NCT01147718|111680|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493882|NCT00714285|111295|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493883|NCT00714285|111295|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493884|NCT00714285|111295|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493885|NCT00714285|111295|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493886|NCT00714285|111295|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493887|NCT00714285|111295|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493888|NCT00714285|111295|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493889|NCT00309634|106750|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493890|NCT00309634|106750|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493891|NCT00309634|106750|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493892|NCT00309634|106750|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493893|NCT00309634|106750|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493894|NCT00309634|106750|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493895|NCT05820633||Study Protocol|https://www.sealedenvelope.com/simple-randomiser/v1/lists|
2493896|NCT07171515||Study Protocol|https://data.doi.or.kr/10.22694/CANCERDATA032018070101|1\. 1. Guidelines for the Pancreatic Cancer Registry, National Cancer Center Big Data
2493897|NCT07171515||Study Protocol|https://cancerportal.kr/ncc/clinicalLibraryInfo.do|2\. CONNECT Cancer Big Data Library: Pancreatic Cancer Section
2493898|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
2493899|NCT01717287||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-248&kw=0518-248&tab=access|
2493900|NCT00111800|100925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493901|NCT00111800|100925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493902|NCT00111800|100925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493903|NCT00111800|100925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493904|NCT00111800|100925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493905|NCT00111800|100925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493906|NCT00111800|100925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493907|NCT03686436||Study Protocol|https://www.clinicaltrials.gov|
2493908|NCT03715153||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2493909|NCT03715153||Study Protocol|https://clinicaltrials.servier.com/|
2493910|NCT03715153||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2493911|NCT03715153||Informed Consent Form|https://clinicaltrials.servier.com/|
2493912|NCT03715153||Clinical Study Report|https://clinicaltrials.servier.com/|
2493913|NCT03715153||study-level clinical trial data]|https://clinicaltrials.servier.com/|
2493914|NCT06089148|Cairo unversity|Study Protocol|https://medicine.cu.edu.eg/index.php/en/postgraduate/32-research/161-research-ethics-committee|upon requirement
2493915|NCT02699957|Data Collection Form|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|
2493916|NCT02699957|Data Dictionary|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|Element definitions and coding instructions.
2493917|NCT01147744|112186|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493918|NCT01147744|112186|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493919|NCT01147744|112186|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493920|NCT01147744|112186|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493921|NCT01147744|112186|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493922|NCT01147744|112186|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493923|NCT01147744|112186|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493924|NCT00346073|106316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493925|NCT00346073|106316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496026|NCT00606684|B2C111045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496027|NCT00606684|B2C111045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496028|NCT00606684|B2C111045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496029|NCT00606684|B2C111045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496030|NCT00606684|B2C111045|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496031|NCT00606684|B2C111045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496032|NCT00606684|B2C111045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496033|NCT03189797||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed|
2496034|NCT05163379||Study Protocol|https://khgmekodemedb.saglik.gov.tr/Eklenti/23273/0/fizik-tedavi-ve-rehabilitasyon-islemleri-degerlendirme-olcekleripdf.pdf|
2496035|NCT00229112||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487472|NCT01147718|111680|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487473|NCT01147718|111680|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487474|NCT01147718|111680|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487475|NCT00547248|109509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487476|NCT00547248|109509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487477|NCT00547248|109509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487478|NCT00547248|109509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487479|NCT00547248|109509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487480|NCT00547248|109509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487481|NCT00547248|109509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487482|NCT00435461|FFU109045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487483|NCT00435461|FFU109045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496036|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.
2496037|NCT00000531||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/avid/|
2496038|NCT00000531||Study Forms|http://biolincc.nhlbi.nih.gov/studies/avid/|
2496039|NCT00000531||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/avid/|
2496040|NCT02879747||Study Protocol|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
2496041|NCT02879747||Statistical Analysis Plan|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
2496042|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.
2496043|NCT00000606||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nett/|
2496044|NCT00000606||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nett/|
2496045|NCT00616928|110464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496046|NCT00616928|110464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496047|NCT00616928|110464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496048|NCT00616928|110464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496049|NCT00616928|110464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496050|NCT00616928|110464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496051|NCT00616928|110464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496052|NCT04517006||Individual Participant Data Set|https://osf.io/63yg9/|Not yet available, but will be posted once study is complete.
2496053|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.
2496054|NCT04517006||Informed Consent Form|https://osf.io/63yg9/|
2493926|NCT00346073|106316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493927|NCT00346073|106316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493928|NCT00346073|106316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493929|NCT00346073|106316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493930|NCT02938884||Study Protocol|https://oncore.umn.edu/login/|
2493931|NCT00290342|104871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493932|NCT00290342|104871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493933|NCT00290342|104871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493934|NCT00290342|104871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493935|NCT00290342|104871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493936|NCT00290342|104871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493937|NCT04630587||Study Protocol|http://www.oulu.fi/medicine/node/52771|
2493938|NCT05705609|Kim H, Kim S, Choe K, Kim JS|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/29579508/|web site is provided
2493939|NCT00316680|104489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487484|NCT00435461|FFU109045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487485|NCT00435461|FFU109045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487486|NCT00435461|FFU109045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487487|NCT00435461|FFU109045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487488|NCT03126253||Report of the survey along with sampling plan|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|
2487489|NCT02588664||Full Data Package|https://www.pcori.org/about-us/governance/policy-data-management-and-data-sharing|
2487490|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|
2487491|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.|
2487492|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.|
2487493|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|
2487494|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/15008827|
2487495|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|
2489584|NCT02257398|115775|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491754|NCT01607385|116511|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491755|NCT01607385|116511|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491756|NCT01607385|116511|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491757|NCT01607385|116511|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491758|NCT01607385|116511|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491759|NCT01607385|116511|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491760|NCT00318149|104886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491761|NCT00318149|104886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491762|NCT00318149|104886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491763|NCT00318149|104886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493940|NCT00316680|104489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489585|NCT02257398|115775|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491764|NCT00318149|104886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491765|NCT00318149|104886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491766|NCT00517309||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491767|NCT00240526|100450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491768|NCT00240526|100450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491769|NCT00240526|100450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491770|NCT00240526|100450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491771|NCT00240526|100450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491772|NCT00240526|100450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491773|NCT01751113|116572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491774|NCT01751113|116572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491775|NCT01751113|116572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491776|NCT01751113|116572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491777|NCT01751113|116572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491778|NCT00034645||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491779|NCT03877705|Pubmed|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/m/pubmed/30455769/?i=6&from=xylitol%20review|
2491780|NCT06233123||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/32021311/|
2491781|NCT01017120|114576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493941|NCT00316680|104489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493942|NCT00316680|104489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493943|NCT00316680|104489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493944|NCT00316680|104489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487496|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|
2487497|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|
2487498|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/20606205|
2487499|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22699609|
2487500|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|
2487501|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|
2487502|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|
2487503|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|
2489586|NCT02257398|115775|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489587|NCT02855476||Study Protocol|http://hdclarity.net/study-information/|
2489588|NCT02855476||Informed Consent Form|http://hdclarity.net/study-information/|Draft informed consent form, not yet approved by an Institutional Review Board for clinical use
2489589|NCT01673529|115246|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489590|NCT01673529|115246|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489591|NCT01673529|115246|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491782|NCT01017120|114576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491783|NCT01017120|114576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491784|NCT01017120|114576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493945|NCT00122681|580299/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493946|NCT00122681|580299/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493947|NCT00122681|580299/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493948|NCT00122681|580299/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493949|NCT00122681|580299/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493950|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
2489592|NCT01673529|115246|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489593|NCT01673529|115246|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489594|NCT01673529|115246|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489595|NCT01673529|115246|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493951|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
2493952|NCT01018628|114011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493953|NCT01018628|114011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493954|NCT01018628|114011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493955|NCT01018628|114011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493956|NCT01018628|114011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493957|NCT01018628|114011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489596|NCT00551317|LPL110077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489597|NCT00551317|LPL110077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489598|NCT00551317|LPL110077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489599|NCT00551317|LPL110077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489600|NCT00551317|LPL110077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489601|NCT00551317|LPL110077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489602|NCT00551317|LPL110077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489603|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)
2489604|NCT06644573|Virtual Consultation SOAP Note|Individual Participant Data Set|https://drive.google.com/file/d/1uAAbC0gRFOthwnUiWz3O2sDyLgkGkiKf/view?usp=sharing|Virtual Consultation SOAP Note
2493958|NCT01018628|114011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493959|NCT00315744|102318|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493960|NCT00315744|102318|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493961|NCT00315744|102318|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493962|NCT00315744|102318|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493963|NCT00315744|102318|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493964|NCT00315744|102318|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493965|NCT00695448|PIK111051|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493966|NCT00695448|PIK111051|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493967|NCT00695448|PIK111051|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493968|NCT00695448|PIK111051|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493969|NCT00695448|PIK111051|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493970|NCT00695448|PIK111051|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493971|NCT00695448|PIK111051|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493972|NCT02134483||Article|https://www.ncbi.nlm.nih.gov/pubmed/26375142|
2493973|NCT00996268|113412|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493974|NCT00996268|113412|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493975|NCT00996268|113412|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493976|NCT00996268|113412|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493977|NCT00996268|113412|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493978|NCT00996268|113412|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493979|NCT00996268|113412|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493980|NCT00980200|113310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493981|NCT00980200|113310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493982|NCT00980200|113310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493983|NCT00980200|113310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493984|NCT00980200|113310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493985|NCT00980200|113310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493986|NCT00980200|113310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493987|NCT02257372|201314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493988|NCT02257372|201314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493989|NCT02257372|201314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493990|NCT02257372|201314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493991|NCT02257372|201314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493992|NCT02257372|201314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493993|NCT02257372|201314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493994|NCT01669070|115441|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493995|NCT01669070|115441|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496055|NCT04517006||Analytic Code|https://osf.io/63yg9/|Will be posted after study is complete.
2489605|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
2489606|NCT06644573|PROSOMNIA Sleep Quiz|Individual Participant Data Set|https://drive.google.com/file/d/1XWzVYL0L2OR8FzFUGtd0vggjwBflBAFa/view?usp=sharing|PROSOMNIA Sleep Quiz
2491785|NCT01017120|114576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491786|NCT01017120|114576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489607|NCT06644573|Sleep Quiz Evaluation|Clinical Study Report|https://drive.google.com/file/d/1Hzw1OvpbAn44nCbvqbtPwC25clwCbclW/view?usp=sharing|PSHES Sleep Quiz Scoring System
2489608|NCT06644573|Mood/Emotion Quality Scale|Individual Participant Data Set|https://drive.google.com/file/d/1-UzkVbn7UG57aZMg9d1LRB9yoLkjUlWS/view?usp=sharing|Mood/Emotion Quality Scale
2489609|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
2489610|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
2489611|NCT00674817|MAB110123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489612|NCT00674817|MAB110123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489613|NCT00674817|MAB110123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489614|NCT00674817|MAB110123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489615|NCT00674817|MAB110123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489616|NCT00674817|MAB110123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489617|NCT00674817|MAB110123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489618|NCT03941470|IRB17200056|Study Protocol|http://Email:ethics_committee12@yahoo.com|
2489619|NCT06471972||Study Protocol|http://stepcare.org/biomarkers|Lab manuals and sample collection form
2491787|NCT01017120|114576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489620|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/18426039|
2489621|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/19952380|
2489622|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/20922783|
2489623|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/?term=In+vitro+effects+of+detergent+sclerosants+on+coagulation%2C+platelets+and+microparticles.|
2489624|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/21725957|
2489625|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/16226898|
2489626|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/11231246|
2489627|NCT06602661||Study Protocol|https://docs.google.com/document/d/1-NMx1lP-_x1KHA0t49yEG7tNsFgepmyWPkbdFfWMPMc/edit?usp=sharing|
2489628|NCT06602661||Informed Consent Form|https://drive.google.com/file/d/1rON8VADRvws1J_I_rmqAAy2sNgL0I9c5/view?usp=sharing|
2489629|NCT00269217||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489630|NCT00390143|108595 Mth18|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489631|NCT00390143|108595 Mth18|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489632|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
2489633|NCT00390143|108595 Mth18|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489634|NCT00390143|108595 Mth18|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489635|NCT00390143|108595 Mth18|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489636|NCT00360230|106367|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489637|NCT00360230|106367|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489638|NCT00360230|106367|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489639|NCT00360230|106367|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489640|NCT00360230|106367|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489641|NCT00360230|106367|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489642|NCT03435250||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2489643|NCT03435250||Study-level clinical trial data|https://clinicaltrials.servier.com/wp-content/uploads/AG270-C-001-anonymised-synopsis-2023.11.10.pdf|Results synopsis
2489644|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
2496056|NCT04413747|guest_1|Study Protocol|http://giardinostlucia.it|
2496057|NCT04413747|guest_2|Informed Consent Form|http://giardinostlucia.it|
2496058|NCT04413747|guest_3|Individual Participant Data Set|http://giardinostlucia.it|
2496059|NCT02224521|112071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496060|NCT02224521|112071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496061|NCT02224521|112071|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496062|NCT02224521|112071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496063|NCT02224521|112071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496064|NCT02224521|112071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496065|NCT02224521|112071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496066|NCT01001169|113847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496067|NCT01001169|113847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496068|NCT01001169|113847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496069|NCT01001169|113847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496070|NCT01001169|113847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496071|NCT01001169|113847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496072|NCT01001169|113847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496073|NCT00551564|DIX110434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496074|NCT00551564|DIX110434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496075|NCT00551564|DIX110434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496076|NCT00551564|DIX110434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496077|NCT00551564|DIX110434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496078|NCT00551564|DIX110434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496079|NCT00551564|DIX110434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496080|NCT00743067|MET111648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496081|NCT00743067|MET111648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496082|NCT00743067|MET111648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496083|NCT00743067|MET111648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496084|NCT00743067|MET111648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496085|NCT00743067|MET111648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496086|NCT00743067|MET111648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496087|NCT01000857|112812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496088|NCT01000857|112812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496089|NCT01000857|112812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496090|NCT01000857|112812|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496091|NCT03556917||Statistical Analysis Plan|http://www.unopar.com.br/|
2496092|NCT03974633||Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1dEjSUmhIkqAOvh30WaJ0svs6jrdEGDyU5FXHeBuTOF8/edit?usp=sharing|
2496093|NCT01928914|114582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496094|NCT01928914|114582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487504|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.|
2487505|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/9794114|
2487506|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|
2487507|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Zinc+as+a+potential+coadjuvant+in+therapy+for+type+2+diabetes.|
2487508|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|
2487509|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/25284151|
2487510|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/27915988|
2487511|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Insulino-mimetic+and+anti-diabetic+effects+of+zinc|
2487512|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/28615382|
2487513|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/12502486|
2487514|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22375253|
2487515|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|
2487516|NCT01400906|114748|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487517|NCT01400906|114748|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487518|NCT01400906|114748|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487519|NCT01400906|114748|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487520|NCT01400906|114748|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487521|NCT01400906|114748|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487522|NCT01400906|114748|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487523|NCT00610168|110806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487524|NCT00610168|110806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487525|NCT00610168|110806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487526|NCT00610168|110806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487527|NCT00610168|110806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487528|NCT00610168|110806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487529|NCT00610168|110806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487530|NCT03249168||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/26705527|
2487531|NCT00370591|SAM40104|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487532|NCT00370591|SAM40104|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487533|NCT00370591|SAM40104|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487534|NCT00370591|SAM40104|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487535|NCT00370591|SAM40104|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487536|NCT00370591|SAM40104|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487537|NCT00370591|SAM40104|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487538|NCT00370097|FAS106533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487539|NCT00370097|FAS106533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487540|NCT00370097|FAS106533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487541|NCT00370097|FAS106533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487542|NCT00370097|FAS106533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487543|NCT00370097|FAS106533|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487544|NCT00370097|FAS106533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493996|NCT01669070|115441|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493997|NCT01669070|115441|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493998|NCT01669070|115441|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493999|NCT01669070|115441|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494000|NCT01669070|115441|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494001|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.
2494002|NCT01225731||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05495&kw=P05495&tab=access|
2494003|NCT00490568|AVA102675|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489645|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. While politics intentionally create lengthy barriers in Federal grants funding, including impeding the opportunity to serve as a Medicaid and/or Medicare Provider, I understand the difference between politics and culture. Inclusion involves optional access to all healthcare services without financial assistance. As a licensed referral, ordering, and nonclinical prescribing Holistic Medicine provider only, cost-effective pastoral counseling serve its purpose.
2489646|NCT00951353|SDY951|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study identifier is SDY951.
2489647|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."
2489648|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.
2489649|NCT03038061||Informed Consent Form|http://ventilation.fbmi.cvut.cz/wp-content/uploads/2017/01/Informed-Consent-Form.pdf|Informed Consent
2489650|NCT01424384|105012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489651|NCT01424384|105012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489652|NCT01424384|105012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489653|NCT01424384|105012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489654|NCT01424384|105012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489655|NCT01424384|105012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489656|NCT01424384|105012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489657|NCT01353898||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1972-003&kw=1972-003&tab=access|
2489658|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,
2489659|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)
2489660|NCT00379964||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489661|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
2489662|NCT06591234||Study Protocol|https://www.ausl.bologna.it/|To send a request by mail
2494004|NCT00490568|AVA102675|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494005|NCT00490568|AVA102675|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494006|NCT00490568|AVA102675|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494007|NCT00490568|AVA102675|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494008|NCT00490568|AVA102675|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494009|NCT00490568|AVA102675|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494010|NCT00996944|113079|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494011|NCT00996944|113079|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489663|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|
2489664|NCT06999954||Informed Consent Form|https://www.sdsalliance.org/sds-gps|Available from the SDS-GPS program team at gps@sdsalliance.org
2489665|NCT06700473|10.1097/JNR.0000000000000129.|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/28277391/|https://pubmed.ncbi.nlm.nih.gov/28277391/
2489666|NCT06473740||Individual Participant Data Set|https://patientdatabase.ishemii.net/login|
2489667|NCT01054885|112207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489668|NCT01054885|112207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489669|NCT01054885|112207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489670|NCT01054885|112207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489671|NCT01054885|112207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489672|NCT01054885|112207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489673|NCT01054885|112207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491788|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
2489675|NCT01656408||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-002&kw=8150-002&tab=access|
2489676|NCT01929317|116991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489677|NCT01929317|116991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489678|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
2489679|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
2489680|NCT03173248||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2489681|NCT03173248||Study Protocol|https://clinicaltrials.servier.com/|
2489682|NCT03173248||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2489683|NCT03173248||Informed Consent Form|https://clinicaltrials.servier.com/|
2489684|NCT03173248||Clinical Study Report|https://clinicaltrials.servier.com/|
2489685|NCT03173248||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2489686|NCT06595771||Study Protocol|https://haydarpasanumuneah.saglik.gov.tr/|
2489687|NCT05350397|REFERENCE|REFERENCE|https://pubmed.ncbi.nlm.nih.gov/30982782/|
2489688|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_35_70_76_127.pdf|
2489689|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/30982782/|
2489690|NCT05350397|REFERENCE|REFERENCE|http://dergipark.org.tr/tr/pub/ikcusbfd/issue/60165/705219|
2489691|NCT05350397|REFERENCE|REFERENCE|http://www.journalagent.com/tkd/pdfs/TKDA_37_60_1_10.pdf|
2489692|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/18992625/|
2489693|NCT05350397|REFERENCE|REFERENCE|http://www.ncbi.nlm.nih.gov/books/NBK72567/|
2489694|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1016/j.ctcp.2021.101304|
2489695|NCT05350397|REFERENCE|REFERENCE|http://doi.org/10.1097/HNP.0000000000000384|
2489696|NCT05350397|REFERENCE|REFERENCE|http://pubmed.ncbi.nlm.nih.gov/23981400/|
2489697|NCT00090207||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489698|NCT06081816|10.4314/ahs.v19i1.55|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
2489699|NCT06081816|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
2489700|NCT03584789||Study Protocol|https://www.researchprotocols.org/2021/4/e24342|
2489701|NCT01128634|113950|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489702|NCT01128634|113950|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489703|NCT01128634|113950|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489704|NCT01128634|113950|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489705|NCT01128634|113950|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489706|NCT01128634|113950|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489707|NCT01128634|113950|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489708|NCT01357850|112670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489709|NCT01357850|112670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496095|NCT01928914|114582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496096|NCT01928914|114582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496097|NCT01928914|114582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496098|NCT01928914|114582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496099|NCT01928914|114582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496100|NCT02058628|200398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496101|NCT02058628|200398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496102|NCT02058628|200398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496103|NCT02058628|200398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496104|NCT02058628|200398|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496105|NCT02058628|200398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496106|NCT02058628|200398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496107|NCT01626820|116664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496108|NCT01626820|116664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496109|NCT01626820|116664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496110|NCT01626820|116664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496111|NCT01626820|116664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496112|NCT01626820|116664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496113|NCT01626820|116664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496114|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
2496115|NCT00425737|444563/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496116|NCT00425737|444563/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496117|NCT00425737|444563/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496118|NCT00425737|444563/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496119|NCT00425737|444563/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496120|NCT00376779|106786|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489710|NCT01357850|112670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489711|NCT01357850|112670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489712|NCT01357850|112670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489713|NCT01357850|112670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489714|NCT01357850|112670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489715|NCT01587924|116582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489716|NCT01587924|116582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489717|NCT01587924|116582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489718|NCT01587924|116582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489719|NCT01587924|116582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496121|NCT00376779|106786|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496122|NCT00376779|106786|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496123|NCT00376779|106786|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496124|NCT00376779|106786|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496125|NCT00376779|106786|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496126|NCT00035009||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2496127|NCT00946257|112438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496128|NCT00946257|112438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496129|NCT00946257|112438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496130|NCT00946257|112438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496131|NCT00946257|112438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496132|NCT00946257|112438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491789|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.
2491790|NCT00289770|100551 (EXT Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496133|NCT00946257|112438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491791|NCT00289770|100551 (EXT Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491792|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
2491793|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)
2491794|NCT00451217||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2496134|NCT00996671|113581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496135|NCT00996671|113581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496136|NCT00996671|113581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496137|NCT00996671|113581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496138|NCT00996671|113581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496139|NCT00996671|113581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496140|NCT00996671|113581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496141|NCT00274703|MEE103226|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496142|NCT00274703|MEE103226|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496143|NCT00274703|MEE103226|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496144|NCT00274703|MEE103226|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496145|NCT00274703|MEE103226|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496146|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/33036555/|
2496147|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/32247709/|
2496148|NCT05899790||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/34252034/|
2496149|NCT00684671|111572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496150|NCT00684671|111572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491795|NCT01929330|117342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496151|NCT00684671|111572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496152|NCT00684671|111572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496153|NCT00684671|111572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496154|NCT00684671|111572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491796|NCT01929330|117342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491797|NCT01929330|117342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491798|NCT01929330|117342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491799|NCT01929330|117342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491800|NCT01929330|117342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491801|NCT01929330|117342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491802|NCT00453479|AC2108378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491803|NCT00453479|AC2108378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491804|NCT00453479|AC2108378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491805|NCT00453479|AC2108378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491806|NCT00453479|AC2108378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491807|NCT00453479|AC2108378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491808|NCT00453479|AC2108378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491809|NCT00535743||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491810|NCT04020003|mengxinke|Individual Participant Data Set|http://www.chictr.org.cn|
2491811|NCT00224523|FFR104503|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491812|NCT00224523|FFR104503|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491813|NCT00224523|FFR104503|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491814|NCT00224523|FFR104503|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491815|NCT00224523|FFR104503|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491816|NCT00224523|FFR104503|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491817|NCT00224523|FFR104503|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491818|NCT01424436|113043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491819|NCT01424436|113043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491820|NCT01424436|113043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491821|NCT01424436|113043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491822|NCT01424436|113043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491823|NCT01424436|113043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491824|NCT01424436|113043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491825|NCT06480682|RED-D|Individual Participant Data Set|https://figshare.com/account/home|All anonymised data will be published on figshare
2491826|NCT06480682|RED-D|Study Protocol|https://figshare.com/account/home|Study protocol will be published on figshare
2491827|NCT01648179|116595|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491828|NCT01648179|116595|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491829|NCT01648179|116595|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491830|NCT01648179|116595|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491831|NCT01648179|116595|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491832|NCT01648179|116595|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491833|NCT01648179|116595|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491834|NCT00432679|AVD105248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491835|NCT00432679|AVD105248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491836|NCT00432679|AVD105248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491837|NCT00432679|AVD105248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491838|NCT00432679|AVD105248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491839|NCT00432679|AVD105248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491840|NCT00432679|AVD105248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491841|NCT00579982|LBI108884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487545|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.
2491842|NCT00579982|LBI108884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491843|NCT00579982|LBI108884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491844|NCT00579982|LBI108884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491845|NCT00579982|LBI108884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491846|NCT00579982|LBI108884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491847|NCT00579982|LBI108884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491848|NCT00092170||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491849|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
2491850|NCT00742885|111756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491851|NCT00742885|111756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491852|NCT00742885|111756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491853|NCT00742885|111756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491854|NCT00742885|111756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491855|NCT00742885|111756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491856|NCT00742885|111756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491857|NCT00317174|759346/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491858|NCT00317174|759346/002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491859|NCT00317174|759346/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491860|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
2491861|NCT00317174|759346/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491862|NCT00317174|759346/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491863|NCT01340911|115444|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491864|NCT01340911|115444|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487546|NCT01046331||Study Forms|http://biolincc.nhlbi.nih.gov/studies/h1n1/|
2487547|NCT01808261|104615|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491865|NCT01340911|115444|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491866|NCT01340911|115444|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491867|NCT01340911|115444|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491868|NCT01340911|115444|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491869|NCT00697554|208129/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487548|NCT01808261|104615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487549|NCT01808261|104615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487550|NCT01808261|104615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487551|NCT01808261|104615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487552|NCT01808261|104615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487553|NCT01808261|104615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487554|NCT00519467|714703/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487555|NCT00519467|714703/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487556|NCT00519467|714703/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487557|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
2487558|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
2487559|NCT00519467|714703/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487560|NCT00519467|714703/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487561|NCT01236040|114371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487562|NCT01236040|114371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487563|NCT01236040|114371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487564|NCT01236040|114371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487565|NCT01236040|114371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487566|NCT01236040|114371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487567|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.
2487568|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.
2487569|NCT00346749|ADC105931|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487570|NCT00346749|ADC105931|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487571|NCT00346749|ADC105931|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487572|NCT00346749|ADC105931|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487573|NCT00346749|ADC105931|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487574|NCT00346749|ADC105931|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487575|NCT00534638|106636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487576|NCT00534638|106636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487577|NCT00534638|106636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487578|NCT00534638|106636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487579|NCT00534638|106636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487580|NCT00534638|106636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487581|NCT00534638|106636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487582|NCT00107757|FFR100010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487583|NCT00107757|FFR100010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487584|NCT00107757|FFR100010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491870|NCT00697554|208129/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491871|NCT00697554|208129/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491872|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
2491873|NCT00697554|208129/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491874|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.
2491875|NCT00000556||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/affirm/|
2491876|NCT00000556||Study Forms|http://biolincc.nhlbi.nih.gov/studies/affirm/|
2491877|NCT00551213||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04721&kw=P04721&tab=access|
2491878|NCT00992160|111364|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491879|NCT00992160|111364|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491880|NCT00992160|111364|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491881|NCT00992160|111364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491882|NCT00992160|111364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491883|NCT00992160|111364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491884|NCT00992160|111364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491885|NCT00519636|FFU105927|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491886|NCT00519636|FFU105927|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491887|NCT00519636|FFU105927|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491888|NCT00519636|FFU105927|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491889|NCT00519636|FFU105927|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491890|NCT00519636|FFU105927|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491891|NCT00519636|FFU105927|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491892|NCT00605371|LEP111102|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491893|NCT00605371|LEP111102|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491894|NCT00605371|LEP111102|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491895|NCT00605371|LEP111102|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491896|NCT00605371|LEP111102|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491897|NCT00605371|LEP111102|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491898|NCT00605371|LEP111102|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491899|NCT00090272||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491900|NCT00933062|113140|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491901|NCT00933062|113140|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491902|NCT00933062|113140|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491903|NCT00933062|113140|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491904|NCT00933062|113140|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491905|NCT00933062|113140|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491906|NCT00933062|113140|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491907|NCT03904082||Clinical Study Report|http://doi.org/10.1016/j.jclinane.2018.06.033|
2491908|NCT01627340|115918|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487585|NCT00107757|FFR100010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487586|NCT00107757|FFR100010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487587|NCT00107757|FFR100010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487588|NCT00107757|FFR100010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487589|NCT00920959|SAS30021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487590|NCT00920959|SAS30021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487591|NCT00920959|SAS30021|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487592|NCT00920959|SAS30021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487593|NCT00920959|SAS30021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487594|NCT00920959|SAS30021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487595|NCT00920959|SAS30021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487596|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."
2487597|NCT00354965|AUG102821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487598|NCT00354965|AUG102821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487599|NCT00354965|AUG102821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487600|NCT00354965|AUG102821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487601|NCT00354965|AUG102821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487602|NCT00354965|AUG102821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489720|NCT01587924|116582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489721|NCT01587924|116582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489722|NCT02581410|201198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489723|NCT02581410|201198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489724|NCT02581410|201198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489725|NCT02581410|201198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489726|NCT02581410|201198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489727|NCT02581410|201198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489728|NCT02581410|201198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489729|NCT01416324|114985|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489730|NCT01416324|114985|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489731|NCT01416324|114985|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489732|NCT01416324|114985|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489733|NCT01416324|114985|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489734|NCT01416324|114985|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489735|NCT01416324|114985|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489736|NCT00345358|107058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487603|NCT00792909|111736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487604|NCT00792909|111736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487605|NCT00792909|111736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487606|NCT00792909|111736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487607|NCT00792909|111736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491909|NCT01627340|115918|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491910|NCT01627340|115918|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491911|NCT01627340|115918|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491912|NCT01627340|115918|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491913|NCT01627340|115918|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491914|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.
2491915|NCT04731714|mtbzf|Individual Participant Data Set|https://osf.io/mtbzf/|IPD, study protocol, SAP, and ICF will all be posted at this location.
2491916|NCT01577732|115389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491917|NCT01577732|115389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491918|NCT01577732|115389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491919|NCT01577732|115389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491920|NCT01577732|115389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491921|NCT01577732|115389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487608|NCT00792909|111736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487609|NCT03180203|Study Intensive Care|Study Protocol|https://www.catharinaziekenhuis.nl/contact.html|Contact can be made to request the study protocol (Dutch)
2487610|NCT00268983|393229/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487611|NCT00268983|393229/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487612|NCT00268983|393229/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487613|NCT00268983|393229/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487614|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
2487615|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
2487616|NCT00268983|393229/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487617|NCT01061541|208108/091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487618|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.
2487619|NCT01061541|208108/091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491922|NCT00410384|HGS1006-C1056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491923|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
2491924|NCT00410384|HGS1006-C1056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491925|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
2491926|NCT00410384|HGS1006-C1056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491927|NCT00410384|HGS1006-C1056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491928|NCT00410384|HGS1006-C1056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491929|NCT03205020||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25118503|
2491930|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.
2491931|NCT01125774||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-065&kw=0974-065&tab=access|
2491932|NCT00097370|100901|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491933|NCT00097370|100901|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494012|NCT00996944|113079|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494013|NCT00996944|113079|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494014|NCT04411355|10128359|National Thesis Center|https://tez.yok.gov.tr/UlusalTezMerkezi|thesis Number: 494582
2494015|NCT00034658||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494016|NCT00385255|106323|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494017|NCT00385255|106323|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494018|NCT00385255|106323|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494019|NCT00385255|106323|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494020|NCT00385255|106323|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494021|NCT00385255|106323|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494022|NCT00513409|110031|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494023|NCT00513409|110031|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494024|NCT00513409|110031|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494025|NCT00513409|110031|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494026|NCT00513409|110031|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494027|NCT00513409|110031|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494028|NCT00548496|CR9108914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494029|NCT00548496|CR9108914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494030|NCT00548496|CR9108914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494031|NCT00548496|CR9108914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494032|NCT00548496|CR9108914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494033|NCT00548496|CR9108914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494034|NCT00548496|CR9108914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494035|NCT03177772|dtp38|Study Protocol|https://osf.io/dtp38/|Open Science Framework. we are registered
2494036|NCT02467933|449|Study Protocol|https://www.socialscienceregistry.org/trials/729|Study protocol archived on American Economic Association Social Science Registry page.
2494037|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)"
2494038|NCT02692495|10.17632/8bk6h6bmkr.1|Individual Participant Data Set|https://data.mendeley.com/datasets/8bk6h6bmkr/1|
2494039|NCT02692495||Clinical Study Report|http://www.aurametrix.com/nct02692495|
2494040|NCT00092430||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494041|NCT00317109|104756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494042|NCT00317109|104756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494043|NCT00317109|104756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494044|NCT00317109|104756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494045|NCT00317109|104756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494046|NCT00317109|104756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494047|NCT00976066|111848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491934|NCT00097370|100901|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491935|NCT00097370|100901|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491936|NCT00097370|100901|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491937|NCT00097370|100901|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491938|NCT00097370|100901|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491939|NCT02985697|DEXProtocol|Study Protocol|https://drive.google.com/open?id=0BwBFaEmsvS0PYnlzVDUyMGREWFk|Protocol for the study; includes introduction, design, and references/citations.
2491940|NCT00920374|113018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491941|NCT00920374|113018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491942|NCT00920374|113018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491943|NCT00920374|113018|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491944|NCT00920374|113018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491945|NCT00920374|113018|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491946|NCT00920374|113018|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491947|NCT01161160|114495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491948|NCT01161160|114495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491949|NCT01161160|114495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491950|NCT01161160|114495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491951|NCT01161160|114495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491952|NCT01161160|114495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491953|NCT01161160|114495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491954|NCT04610203||Study Protocol|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2491955|NCT04610203||Informed Consent Form|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2491956|NCT04610203||Clinical Study Report|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2491957|NCT04610203||Individual Participant Data Set|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|
2491958|NCT04610203||Statistical Analysis Plan|http://drive.google.com/drive/folders/1H_y4bMle13r4wOG8YyapreznKUFG8cT_|Included in the Study Protocol and Clinical Study report
2491959|NCT01323660|114418|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491960|NCT01323660|114418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491961|NCT01323660|114418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491962|NCT01323660|114418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491963|NCT01323660|114418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491964|NCT01323660|114418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491965|NCT01323660|114418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491966|NCT01114620|114270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491967|NCT01114620|114270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491968|NCT01114620|114270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491969|NCT01114620|114270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491970|NCT01114620|114270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494048|NCT00976066|111848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494049|NCT00976066|111848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491971|NCT01114620|114270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491972|NCT01114620|114270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491973|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.
2491974|NCT06919211||Study Protocol|https://eyewiki.org/Retinal_Detachment|
2491975|NCT00578227|110886|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491976|NCT00578227|110886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491977|NCT00578227|110886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487620|NCT01061541|208108/091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491978|NCT00578227|110886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491979|NCT00578227|110886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491980|NCT00578227|110886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491981|NCT00578227|110886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491982|NCT03668067||Individual Participant Data Set|http://www.abcd-vision.org/references/2WIN%20Bus%20de-identified%209-6-18.pdf|Public de-identified ongoing
2491983|NCT00263679|100406/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491984|NCT00263679|100406/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491985|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
2491986|NCT00263679|100406/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491987|NCT00263679|100406/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491988|NCT00263679|100406/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491989|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
2491990|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
2491991|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
2491992|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
2491993|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
2491994|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
2491995|NCT00119743|347414/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491996|NCT00119743|347414/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491997|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
2491998|NCT00119743|347414/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491999|NCT00119743|347414/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492000|NCT00119743|347414/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492001|NCT01738867|116753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492002|NCT01738867|116753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492003|NCT01738867|116753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492004|NCT01738867|116753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492005|NCT01738867|116753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492006|NCT01738867|116753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494050|NCT00976066|111848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494051|NCT00976066|111848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494052|NCT00976066|111848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494053|NCT00976066|111848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494054|NCT01425203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08160&kw=P08160&tab=access|
2494055|NCT00382993|TRX106573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494056|NCT00382993|TRX106573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494057|NCT00382993|TRX106573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494058|NCT00382993|TRX106573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494059|NCT00382993|TRX106573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494060|NCT00382993|TRX106573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494061|NCT00382993|TRX106573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494062|NCT01857869|117014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494063|NCT01857869|117014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494064|NCT01857869|117014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494065|NCT01857869|117014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494066|NCT01857869|117014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494067|NCT01857869|117014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494068|NCT01857869|117014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494069|NCT02931058||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2366-9|
2494070|NCT02931058||Clinical Study Report|https://www.clinicalkey.com/#!/content/journal/1-s2.0-S1063458422007154|
2494071|NCT00731250|111611|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494072|NCT00731250|111611|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494073|NCT00731250|111611|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494074|NCT00731250|111611|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494075|NCT00731250|111611|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494076|NCT00731250|111611|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494077|NCT00731250|111611|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494078|NCT00790907|108888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494079|NCT00790907|108888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494080|NCT00790907|108888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494081|NCT00790907|108888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494082|NCT00790907|108888|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494083|NCT00790907|108888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494084|NCT00790907|108888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494085|NCT00092846||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494086|NCT02700490|10.17863/CAM.43399|Complete Data Set|https://doi.org/10.17863/CAM.43399|
2494087|NCT00835237|111413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494088|NCT00835237|111413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494089|NCT00835237|111413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487621|NCT01061541|208108/091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487622|NCT01061541|208108/091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487623|NCT01630135|116364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487624|NCT01630135|116364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487625|NCT01630135|116364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487626|NCT01630135|116364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487627|NCT00230243||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487628|NCT02689804||Publication|http://dx.doi.org/10.1016/j.contraception.2017.01.004|Results Reference: Yes
2487629|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.
2487630|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.
2487631|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
2487632|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
2487633|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.
2487634|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.
2487635|NCT02527629||Study results|https://pubmed.ncbi.nlm.nih.gov/32386409/|
2487636|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.
2487637|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
2487638|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
2487639|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
2487640|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
2487641|NCT00371735|CDA 714703/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487642|NCT00371735|CDA 714703/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487643|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
2487644|NCT00523913|AVD105720|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487645|NCT00523913|AVD105720|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487646|NCT00523913|AVD105720|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487647|NCT00523913|AVD105720|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487648|NCT00523913|AVD105720|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492007|NCT01738867|116753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492008|NCT01096056|114182|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492009|NCT01096056|114182|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492010|NCT01096056|114182|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492011|NCT01096056|114182|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492012|NCT01096056|114182|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492013|NCT01096056|114182|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492014|NCT01244984|113989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494090|NCT00835237|111413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494091|NCT00835237|111413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494092|NCT00835237|111413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494093|NCT00835237|111413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494094|NCT01110200|113874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489737|NCT00345358|107058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489738|NCT00345358|107058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489739|NCT00345358|107058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489740|NCT00345358|107058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489741|NCT00345358|107058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494095|NCT01110200|113874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494096|NCT01110200|113874|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494097|NCT01110200|113874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494098|NCT01110200|113874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494099|NCT01110200|113874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494100|NCT01110200|113874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494101|NCT04106648||Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/|
2494102|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
2494103|NCT00861744|111870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494104|NCT00861744|111870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494105|NCT00861744|111870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494106|NCT00861744|111870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494107|NCT00861744|111870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494108|NCT00861744|111870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494109|NCT00861744|111870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494110|NCT00452699|ADA109055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494111|NCT00452699|ADA109055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494112|NCT00452699|ADA109055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494113|NCT00452699|ADA109055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494114|NCT00452699|ADA109055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494115|NCT00452699|ADA109055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494116|NCT00452699|ADA109055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494117|NCT01014117|114009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494118|NCT01014117|114009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494119|NCT01014117|114009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489742|NCT02094924|200957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489743|NCT02094924|200957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489744|NCT02094924|200957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496155|NCT01209052|112483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496156|NCT01209052|112483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496157|NCT01209052|112483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496158|NCT01209052|112483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496159|NCT01209052|112483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496160|NCT01209052|112483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496161|NCT01209052|112483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496162|NCT04956666||Individual Participant Data Set|https://clinicaltrials.servier.com|
2496163|NCT04956666||Study Protocol|https://clinicaltrials.servier.com|
2496164|NCT04956666||Statistical Analysis Plan|https://clinicaltrials.servier.com|
2496165|NCT04956666||Informed Consent Form|https://clinicaltrials.servier.com|
2496166|NCT04956666||Clinical Study Report|https://clinicaltrials.servier.com|
2496167|NCT04956666||Study-level clinical trial data|https://clinicaltrials.servier.com|
2496168|NCT00317161|100480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496169|NCT00317161|100480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496170|NCT00317161|100480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496171|NCT00317161|100480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496172|NCT00317161|100480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496173|NCT00317161|100480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496174|NCT01047345||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-006&kw=V503-006&tab=access|
2496175|NCT01974895|200806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496176|NCT01974895|200806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496177|NCT01974895|200806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496178|NCT01974895|200806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496179|NCT01974895|200806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496180|NCT01974895|200806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496181|NCT01974895|200806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496182|NCT00197275|104733|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496183|NCT00197275|104733|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496184|NCT00197275|104733|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496185|NCT00197275|104733|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496186|NCT00197275|104733|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496187|NCT00197275|104733|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496188|NCT01691508|115575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496189|NCT01691508|115575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496190|NCT01691508|115575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496191|NCT01691508|115575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496192|NCT01691508|115575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496193|NCT01691508|115575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496194|NCT01691508|115575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496195|NCT00861809|111809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496196|NCT00861809|111809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489745|NCT02094924|200957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489746|NCT02094924|200957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489747|NCT02094924|200957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489748|NCT02094924|200957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489749|NCT00742261|MET111516|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489750|NCT00742261|MET111516|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489751|NCT00742261|MET111516|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489752|NCT00742261|MET111516|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489753|NCT00742261|MET111516|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489754|NCT00742261|MET111516|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489755|NCT00742261|MET111516|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496197|NCT00861809|111809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496198|NCT00861809|111809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489756|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.
2489757|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.
2489758|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.
2489759|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|
2489760|NCT05345652||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31571625/|
2489761|NCT00976560|113009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489762|NCT00976560|113009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489763|NCT00976560|113009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489764|NCT00976560|113009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489765|NCT00976560|113009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489766|NCT00976560|113009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489767|NCT00976560|113009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489768|NCT04591808||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2489769|NCT04591808||Study Protocol|https://clinicaltrials.servier.com/|
2489770|NCT04591808||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2489771|NCT04591808||Informed Consent Form|https://clinicaltrials.servier.com/|
2489772|NCT04591808||Clinical Study Report|https://clinicaltrials.servier.com/|
2489773|NCT04591808||[study-level clinical trial data]|https://clinicaltrials.servier.com/|
2489774|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.
2489775|NCT00760617|111737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489776|NCT00760617|111737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489777|NCT00760617|111737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489778|NCT00760617|111737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489779|NCT00760617|111737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489780|NCT00760617|111737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494120|NCT01014117|114009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494121|NCT01014117|114009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494122|NCT01014117|114009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494123|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
2494124|NCT02889458|BrCA.risk.001|Study Protocol|http://www.hkuctr.com/Study/Show/b122235f3995420a97d570a85d03b542|
2494125|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.
2494126|NCT00972673|112018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494127|NCT00972673|112018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494128|NCT00972673|112018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494129|NCT00972673|112018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494130|NCT01353742|114957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494131|NCT01353742|114957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494132|NCT01353742|114957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494133|NCT01353742|114957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494134|NCT01353742|114957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494135|NCT01353742|114957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494136|NCT01353742|114957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494137|NCT01627587|115893|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494138|NCT01627587|115893|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494139|NCT01627587|115893|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494140|NCT01627587|115893|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494141|NCT01627587|115893|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494142|NCT01627587|115893|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494143|NCT01627587|115893|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494144|NCT01209026|102936|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494145|NCT01209026|102936|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494146|NCT01209026|102936|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494147|NCT01209026|102936|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494148|NCT01209026|102936|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494149|NCT01209026|102936|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494150|NCT01209026|102936|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494151|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
2494152|NCT00368576|LPL107629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494153|NCT00368576|LPL107629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494154|NCT00368576|LPL107629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494155|NCT00368576|LPL107629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494156|NCT00368576|LPL107629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487649|NCT00523913|AVD105720|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487650|NCT00523913|AVD105720|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487651|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.
2487652|NCT00612820|IPR110723|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487653|NCT00612820|IPR110723|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487654|NCT00612820|IPR110723|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487655|NCT00612820|IPR110723|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487656|NCT00612820|IPR110723|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487657|NCT00612820|IPR110723|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487658|NCT00612820|IPR110723|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487659|NCT00731822|HZC111348|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487660|NCT00731822|HZC111348|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487661|NCT00731822|HZC111348|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487662|NCT00731822|HZC111348|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487663|NCT00731822|HZC111348|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487664|NCT00731822|HZC111348|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487665|NCT00731822|HZC111348|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487666|NCT00903201|110399|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487667|NCT00903201|110399|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487668|NCT00903201|110399|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487669|NCT00903201|110399|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487670|NCT00903201|110399|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487671|NCT00903201|110399|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487672|NCT00903201|110399|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487673|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.
2487674|NCT00933595||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
2487675|NCT00933595||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
2487676|NCT00933595||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
2487677|NCT00092196||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487678|NCT01545388||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-136&kw=0431A-136&tab=access|
2487679|NCT00358358|SCO104925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487680|NCT00358358|SCO104925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487681|NCT00358358|SCO104925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487682|NCT00358358|SCO104925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487683|NCT00358358|SCO104925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487684|NCT00358358|SCO104925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496199|NCT00861809|111809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487685|NCT00358358|SCO104925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487686|NCT01725685|116524|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489781|NCT00760617|111737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489782|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.
2489783|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
2489784|NCT06947681|Not available at moment|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|Most of the informations available at This site and Google Scholar
2489785|NCT00533676||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489786|NCT00555061|TOC106489|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489787|NCT00555061|TOC106489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489788|NCT00555061|TOC106489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489789|NCT00555061|TOC106489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489790|NCT00555061|TOC106489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489791|NCT00555061|TOC106489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489792|NCT00555061|TOC106489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489793|NCT01318980|114604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489794|NCT01318980|114604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489795|NCT01318980|114604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489796|NCT01318980|114604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489797|NCT01318980|114604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489798|NCT01318980|114604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489799|NCT01318980|114604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489800|NCT06940778|blenti|Study Protocol|https://hcor.com.br|blenti
2489801|NCT07156396|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
2489802|NCT01818011|116266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489803|NCT01818011|116266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489804|NCT01818011|116266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489805|NCT01818011|116266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489806|NCT01818011|116266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489807|NCT01818011|116266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489808|NCT01818011|116266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489809|NCT01485172|111662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489810|NCT01485172|111662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489811|NCT01485172|111662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489812|NCT01485172|111662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489813|NCT01485172|111662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489814|NCT01485172|111662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489815|NCT00329355|TRX105852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496200|NCT00861809|111809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489816|NCT00329355|TRX105852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489817|NCT00329355|TRX105852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494157|NCT00368576|LPL107629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494158|NCT00368576|LPL107629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494159|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."
2494160|NCT00505453|110502|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494161|NCT00505453|110502|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494162|NCT00505453|110502|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494163|NCT00505453|110502|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494164|NCT00505453|110502|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494165|NCT00505453|110502|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494166|NCT00505453|110502|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494167|NCT01017952|102970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494168|NCT01017952|102970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494169|NCT01017952|102970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494170|NCT01017952|102970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494171|NCT01017952|102970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494172|NCT01017952|102970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494173|NCT01017952|102970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494174|NCT01353703|111157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494175|NCT01353703|111157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494176|NCT01353703|111157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494177|NCT01353703|111157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494178|NCT01353703|111157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494179|NCT01353703|111157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494180|NCT00920660|113161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494181|NCT00920660|113161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494182|NCT00920660|113161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494183|NCT00920660|113161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494184|NCT00920660|113161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494185|NCT00920660|113161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494186|NCT00920660|113161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494187|NCT03276611||Statistical Analysis Plan|http://www.ncbi.nlm.nih.gov/|
2494188|NCT00808444|111654|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494189|NCT00808444|111654|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494190|NCT00808444|111654|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494191|NCT00808444|111654|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494192|NCT00808444|111654|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494193|NCT00808444|111654|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494194|NCT00808444|111654|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487687|NCT01725685|116524|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487688|NCT01725685|116524|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487689|NCT01725685|116524|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492015|NCT01244984|113989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487690|NCT01725685|116524|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487691|NCT01725685|116524|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487692|NCT01725685|116524|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487693|NCT01405560||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-045&kw=7009-045&tab=access|
2487694|NCT01702467|116698|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487695|NCT01702467|116698|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487696|NCT01702467|116698|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487697|NCT01702467|116698|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487698|NCT01702467|116698|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487699|NCT01702467|116698|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487700|NCT01702467|116698|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487701|NCT00427908|108658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487702|NCT00427908|108658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487703|NCT00427908|108658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487704|NCT00427908|108658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487705|NCT00427908|108658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487706|NCT00427908|108658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492016|NCT01244984|113989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492017|NCT01244984|113989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492018|NCT01244984|113989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492019|NCT01244984|113989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492020|NCT01244984|113989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492021|NCT01013974|113377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492022|NCT01013974|113377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487707|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
2487708|NCT04087239||Individual Participant Data Set|http://www.redcap.uzchs.ac.zw/redcap|Data being entered, now verification of enrolment case report forms
2487709|NCT00896064|112993|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492023|NCT01013974|113377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496201|NCT00861809|111809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487710|NCT00896064|112993|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487711|NCT00896064|112993|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487712|NCT00896064|112993|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487713|NCT00896064|112993|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487714|NCT01299558|102934|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492024|NCT01013974|113377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492025|NCT01013974|113377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492026|NCT01013974|113377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492027|NCT01013974|113377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492028|NCT06103422||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/26935213/|
2492029|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/26935213/|
2492030|NCT06103422||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/11078134/|
2492031|NCT00364442|SAS10019|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492032|NCT00364442|SAS10019|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492033|NCT00364442|SAS10019|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492034|NCT00364442|SAS10019|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492035|NCT00364442|SAS10019|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496202|NCT00442936||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-011&kw=0974-011&tab=access|
2496203|NCT00569062|PKI108574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496204|NCT00569062|PKI108574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496205|NCT00569062|PKI108574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496206|NCT00569062|PKI108574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496207|NCT00569062|PKI108574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496208|NCT00109109||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2496209|NCT00329602|ROR104836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496210|NCT00329602|ROR104836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496211|NCT00329602|ROR104836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496212|NCT00329602|ROR104836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496213|NCT00329602|ROR104836|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496214|NCT00329602|ROR104836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494195|NCT02480933|https://doi.org/10.3892/mco.20|Study Protocol|http://www.spandidos-publications.com/mco|feasibility of the protocol paper
2494196|NCT00814957|110269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494197|NCT00814957|110269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494198|NCT00814957|110269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494199|NCT00814957|110269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494200|NCT00814957|110269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494201|NCT00814957|110269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489818|NCT00329355|TRX105852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494202|NCT00814957|110269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494203|NCT01471665|115134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487166|NCT00325156|100917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494204|NCT01471665|115134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494205|NCT01471665|115134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489819|NCT00329355|TRX105852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494206|NCT01471665|115134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494207|NCT01471665|115134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494208|NCT01471665|115134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494209|NCT01471665|115134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489820|NCT00329355|TRX105852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489821|NCT00329355|TRX105852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489822|NCT01192191|114156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489823|NCT01192191|114156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489824|NCT01192191|114156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489825|NCT01192191|114156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489826|NCT01192191|114156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489827|NCT01192191|114156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489828|NCT01192191|114156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489829|NCT02914301|FWA00005945|Informed Consent Form|https://files.acrobat.com/a/preview/c262292c-6de1-4f73-bae3-689555b8c77f|
2489830|NCT02914301|Post-Partum Survey|Individual Participant Data Set|https://files.acrobat.com/a/preview/5ec925dd-52ad-4b07-b6fc-2084d2f751d5|
2489831|NCT02914301|Prenatal Participant Data -22|Individual Participant Data Set|https://files.acrobat.com/a/preview/984213bb-ccef-419b-8f56-87336004ec5a|
2489832|NCT01175083|114056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489833|NCT01175083|114056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489834|NCT01175083|114056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489835|NCT01175083|114056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489836|NCT01175083|114056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489837|NCT01175083|114056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489838|NCT01175083|114056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492036|NCT00364442|SAS10019|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492037|NCT00364442|SAS10019|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492038|NCT02808442||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2492039|NCT02808442||Study Protocol|https://clinicaltrials.servier.com/|
2492040|NCT02808442||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2492041|NCT02808442||Informed Consent Form|https://clinicaltrials.servier.com/|
2492042|NCT02808442||Clinical Study Report|https://clinicaltrials.servier.com/|
2487167|NCT00325156|100917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487168|NCT01446237|115576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487169|NCT01446237|115576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487170|NCT01446237|115576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487171|NCT01446237|115576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487172|NCT01446237|115576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487173|NCT01446237|115576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487174|NCT01446237|115576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487175|NCT05544773||Study Protocol|https://drive.google.com/file/d/1gKwThkhpbD7eQxFYL4CkTEhzWtcLS1jZ/view?usp=sharing|
2487176|NCT00742508|CRV110734|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487177|NCT00742508|CRV110734|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487178|NCT00742508|CRV110734|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487179|NCT00742508|CRV110734|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487180|NCT00742508|CRV110734|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487181|NCT00035295||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487182|NCT00381238|AVA104617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487183|NCT00381238|AVA104617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487184|NCT00381238|AVA104617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492043|NCT02808442||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2492044|NCT01078233||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-058&kw=0518-058&tab=access|
2492045|NCT04553302||Clinical Study Report|http://ard.bmj.com/content/79/Suppl_1/555.2|
2492046|NCT00502593|107066|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492047|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.
2492048|NCT00502593|107066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492049|NCT00502593|107066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492050|NCT00502593|107066|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492051|NCT00502593|107066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492052|NCT00502593|107066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492053|NCT00586339|107863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492054|NCT00586339|107863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492055|NCT00586339|107863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492056|NCT00586339|107863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492057|NCT00586339|107863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492058|NCT00586339|107863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492059|NCT00197236|208109/232|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492060|NCT00197236|208109/232|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492061|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
2492062|NCT00197236|208109/232|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492063|NCT00197236|208109/232|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492064|NCT00197236|208109/232|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492065|NCT00140673|444563/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492066|NCT00140673|444563/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492067|NCT00140673|444563/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492068|NCT00140673|444563/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492069|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
2492070|NCT00140673|444563/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492071|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
2492072|NCT01457560|217744/060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492073|NCT01457560|217744/060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492074|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
2492075|NCT01457560|217744/060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492076|NCT01457560|217744/060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492077|NCT04405713|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
2492078|NCT04401722|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|through elnakeebayman@yahoo.com
2492079|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.
2492080|NCT00004560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pad/|
2494210|NCT05506397||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/|
2492081|NCT00420316|109810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492082|NCT00420316|109810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492083|NCT00420316|109810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492084|NCT00420316|109810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492085|NCT00420316|109810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492086|NCT00420316|109810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492087|NCT00420316|109810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496215|NCT00329602|ROR104836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496216|NCT00436007|106369|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496217|NCT00436007|106369|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496218|NCT00436007|106369|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496219|NCT00436007|106369|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496220|NCT00436007|106369|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496221|NCT00436007|106369|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496222|NCT00404274|NKV105097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496223|NCT00404274|NKV105097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496224|NCT00404274|NKV105097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496225|NCT00404274|NKV105097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496226|NCT00404274|NKV105097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496227|NCT00404274|NKV105097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496228|NCT00404274|NKV105097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496229|NCT00394056|NKP106254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496230|NCT00394056|NKP106254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496231|NCT00394056|NKP106254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492088|NCT01196988|113275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492089|NCT01196988|113275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496232|NCT00394056|NKP106254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496233|NCT00394056|NKP106254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496234|NCT00394056|NKP106254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496235|NCT02746952||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2496236|NCT02746952||Study Protocol|https://clinicaltrials.servier.com/|
2496237|NCT02746952||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2496238|NCT02746952||Informed Consent Form|https://clinicaltrials.servier.com/|
2496239|NCT02746952||Clinical Study Report|https://clinicaltrials.servier.com/|
2496240|NCT02746952||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2496241|NCT04025034||Informed Consent Form|http://microsoftwindows.com|Navigator
2496242|NCT00269048|LPL104884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496243|NCT00269048|LPL104884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496244|NCT00269048|LPL104884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496245|NCT00269048|LPL104884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496246|NCT00269048|LPL104884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496247|NCT00269048|LPL104884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496248|NCT00269048|LPL104884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496249|NCT00622609|MAG103114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496250|NCT00622609|MAG103114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496251|NCT00622609|MAG103114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496252|NCT00622609|MAG103114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496253|NCT00622609|MAG103114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496254|NCT00622609|MAG103114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496255|NCT00950807|113073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496256|NCT00950807|113073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496257|NCT00950807|113073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496258|NCT00950807|113073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496259|NCT00950807|113073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496260|NCT00950807|113073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496261|NCT00950807|113073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496262|NCT02197468||Clinical Study Report|https://www.frontiersin.org/articles/10.3389/fped.2018.00347/full|Publication from this study
2496263|NCT00502775|FFU109047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496264|NCT00502775|FFU109047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496265|NCT00502775|FFU109047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496266|NCT00502775|FFU109047|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496267|NCT00502775|FFU109047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496268|NCT00502775|FFU109047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496269|NCT00502775|FFU109047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496270|NCT01385033||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3328-002&kw=3328-002&tab=access|
2496271|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.
2496272|NCT00000619||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/escape/|
2496273|NCT00000619||Study Forms|http://biolincc.nhlbi.nih.gov/studies/escape/|
2496274|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, \[osf.io/d5t4m/\].
2496275|NCT04437693||Clinical Study Report|https://www.worldometers.info/coronavirus/|https://www.worldometers.info/coronavirus/
2496276|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
2496277|NCT01019603|114565|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496278|NCT01019603|114565|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496279|NCT01019603|114565|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496280|NCT01019603|114565|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496281|NCT01019603|114565|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496282|NCT01019603|114565|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496283|NCT01019603|114565|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496284|NCT01866319||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3475-006&kw=3475-006&tab=access|
2496285|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."
2496286|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
2496287|NCT01030965|113589|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496288|NCT01030965|113589|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496289|NCT01030965|113589|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496290|NCT01030965|113589|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496291|NCT01030965|113589|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496292|NCT01030965|113589|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496293|NCT01030965|113589|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496294|NCT06000280|Repositorio|Informed Consent Form|http://repositorio.bc.ufg.br|Repositorio da Biblioteca Central da Universidade Federal de Goias
2496295|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.
2496296|NCT00000566||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pioped/|
2496297|NCT00000566||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pioped/|
2496298|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
2496299|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
2496300|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
2496301|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.
2496302|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
2496303|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
2496304|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"
2496305|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"
2496306|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.
2492090|NCT01196988|113275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492091|NCT01196988|113275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492092|NCT01196988|113275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492093|NCT01196988|113275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492094|NCT01196988|113275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492095|NCT00843193|106870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492096|NCT00843193|106870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492097|NCT00843193|106870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492098|NCT00843193|106870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492099|NCT00843193|106870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492100|NCT00843193|106870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487715|NCT01299558|102934|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496307|NCT01295372|2010-022181-28|EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2010-022181-28/result|
2496308|NCT03044171|57655916.3.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
2496309|NCT00993187||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-202&kw=NCT00993187&tab=access|
2496310|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.
2496311|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.
2496312|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).
2496313|NCT03167671|ISBN-10: 1886039224|Book|https://www.amazon.com/Prescription-Drug-Abuse-Epidemic-Understanding/dp/1886039224|
2496314|NCT07025395|28 May 2025|Study Protocol|https://youtu.be/ql8SD07abnI|Core Training Protocol by Ioannis Tsartsapakis Ph.D.
2496315|NCT00693966|580299/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496316|NCT00693966|580299/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496317|NCT00693966|580299/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496318|NCT00693966|580299/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496319|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
2496320|NCT00693966|580299/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496321|NCT01954264|200187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496322|NCT01954264|200187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496323|NCT01954264|200187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487716|NCT01299558|102934|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487717|NCT01299558|102934|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487718|NCT01299558|102934|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487719|NCT01299558|102934|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487720|NCT01299558|102934|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487721|NCT01573000|104515|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487722|NCT01573000|104515|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487723|NCT01573000|104515|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487724|NCT01573000|104515|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487725|NCT01573000|104515|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487726|NCT01573000|104515|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487727|NCT01573000|104515|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489846|NCT01449799|113423|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496324|NCT01954264|200187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496325|NCT01954264|200187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496326|NCT01954264|200187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496327|NCT00454909|109377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496328|NCT00454909|109377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496329|NCT00454909|109377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489847|NCT01449799|113423|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489848|NCT01449799|113423|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489849|NCT01449799|113423|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489850|NCT01449799|113423|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489851|NCT01449799|113423|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489852|NCT01449799|113423|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489853|NCT00389987||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489854|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."
2489855|NCT01049009|26285691|Publication|https://www.ncbi.nlm.nih.gov/pubmed/26285691|
2489856|NCT02758483|63683417.1.0000.5257|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
2489857|NCT01696604|116715|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489858|NCT01696604|116715|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489859|NCT01696604|116715|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489860|NCT01696604|116715|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489861|NCT01696604|116715|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489862|NCT01696604|116715|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489863|NCT01696604|116715|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489864|NCT01702493|117041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489865|NCT01702493|117041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489866|NCT01702493|117041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489867|NCT01702493|117041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489868|NCT01702493|117041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489869|NCT01702493|117041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489870|NCT01702493|117041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489871|NCT00435045|OM9L|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489872|NCT00435045|OM9L|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489873|NCT00435045|OM9L|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489874|NCT00435045|OM9L|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489875|NCT00435045|OM9L|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489876|NCT00435045|OM9L|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489877|NCT00435045|OM9L|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489878|NCT01015638|114546|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489879|NCT01015638|114546|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489880|NCT01015638|114546|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489881|NCT01015638|114546|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489882|NCT01015638|114546|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489883|NCT06757920|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2489884|NCT07144891||article|https://pmc.ncbi.nlm.nih.gov/articles/PMC7488296/|
2489885|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
2489886|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
2496330|NCT00454909|109377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496331|NCT00454909|109377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496332|NCT00454909|109377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496333|NCT00454909|109377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496334|NCT01376167|112582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496335|NCT01376167|112582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496336|NCT01376167|112582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496337|NCT01376167|112582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496338|NCT01376167|112582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496339|NCT01376167|112582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496340|NCT02578953|204646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496341|NCT02578953|204646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496342|NCT02578953|204646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2496343|NCT04752592||Study Protocol|https://www.seroselecttb.org/resources|
2496344|NCT00861705||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov|
2496345|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
2496346|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
2496347|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)
2496348|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)
2496349|NCT07199218||Informed Consent Form|https://osf.io/f69ds/files/osf|
2487728|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.
2487729|NCT00097006|REDS II-CORE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/core/|
2489887|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
2489888|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
2489889|NCT00265148|BRL-49653/461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489890|NCT00265148|BRL-49653/461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489891|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
2489892|NCT00776919|114677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489893|NCT00776919|114677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489894|NCT00776919|114677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489895|NCT00776919|114677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489896|NCT00776919|114677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489897|NCT00776919|114677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489898|NCT00776919|114677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489899|NCT07131241||Individual Participant Data Set|https://www.fjmu.edu.cn|For more information, please contact: dajunchai@126.com
2489900|NCT00470834|AVO108943|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492101|NCT00843193|106870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492102|NCT06615128||Study Protocol|https://doi.org/10.1371/journal.pone.0047748|
2492103|NCT00197015|208109/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492104|NCT00197015|208109/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492105|NCT00197015|208109/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492106|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
2492107|NCT00197015|208109/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492108|NCT00197015|208109/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492109|NCT00961142||Results|https://www.clinicaltrialsregister.eu/ctr-search/search?query=2007-006016-33|
2492110|NCT06706882||INFORMATION SHEET|https://drive.google.com/file/d/1Y90Fr8O30tFqNL_OjAjMfrayrK8-KKxt/view?usp=sharing|
2492111|NCT06706882|Informed Consent Form|Informed Consent Form|https://drive.google.com/file/d/1eQLHRV80sIPlZNoHR5HFS4uauF8RWoDI/view?usp=sharing|
2492112|NCT01651949||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-003&kw=V503-003&tab=access|
2492113|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
2492114|NCT00501020|49653/284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492115|NCT00501020|49653/284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492116|NCT00501020|49653/284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492117|NCT00501020|49653/284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492118|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
2492119|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
2492120|NCT00501020|49653/284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492121|NCT02281318|200862|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492122|NCT02281318|200862|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492123|NCT02281318|200862|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492124|NCT02281318|200862|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492125|NCT02281318|200862|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492126|NCT02281318|200862|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492127|NCT02281318|200862|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492128|NCT00937846|110771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492129|NCT00937846|110771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492130|NCT00937846|110771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492131|NCT00937846|110771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492132|NCT00937846|110771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492133|NCT00937846|110771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492134|NCT00937846|110771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492135|NCT01235949|112921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492136|NCT01235949|112921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492137|NCT01235949|112921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492138|NCT01235949|112921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494211|NCT00982904||Publication of results|http://www.dndi.org/wp-content/uploads/2009/06/ClinicalPK_Tarral_FexinidazoleHAT_2014.pdf|Publication of results
2487730|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.
2487731|NCT00097006|REDS II-LAPS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/laps/|
2487732|NCT00097006|REDS II-LAPS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/laps/|
2487733|NCT00097006|REDS II-LAPS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/laps/|
2487734|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.
2487735|NCT00097006|REDS II-MS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/redsms/|
2487736|NCT00097006|REDS II-MS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/redsms/|
2487737|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.
2487738|NCT00097006|REDS II-RISE|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rise/|
2487739|NCT00097006|REDS II-RISE|Study Forms|http://biolincc.nhlbi.nih.gov/studies/rise/|
2487740|NCT00097006|REDS II-RISE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/rise/|
2487741|NCT00969228|112269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487742|NCT00969228|112269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487743|NCT00969228|112269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487744|NCT00969228|112269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487745|NCT00969228|112269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487746|NCT00969228|112269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487747|NCT00969228|112269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487748|NCT01035749|113883|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487749|NCT01035749|113883|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487750|NCT01035749|113883|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487751|NCT01035749|113883|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487752|NCT01035749|113883|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487753|NCT01035749|113883|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489901|NCT00470834|AVO108943|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489902|NCT00470834|AVO108943|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489903|NCT00470834|AVO108943|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489904|NCT00470834|AVO108943|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489905|NCT00470834|AVO108943|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489906|NCT00470834|AVO108943|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489907|NCT06947330||Study Protocol|https://www.ilovepdf.com/download/6bhl069fp1wzcttl2h9kympvwcw0z348Az4p933p7tx6gm77hss9dbx3gbxjvm9ypjzwt97hdptj659jxht28ybgh1m4lyj34sth4k980tx1wzvm0A2pjghl7rs70r7pk67kblvbcfl9fn68lp5c06pjtdd07x9jqh7grqdl8b1kkp3b6271/88w|
2489908|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.
2489909|NCT07145281||Individual Participant Data Set|https://doi.org/10.17605/OSF.IO/TCRUW|
2489910|NCT00368199||Individual Participant Data Set|https://peerj.com/articles/2037/|
2489911|NCT01115322|114573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489912|NCT01115322|114573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489913|NCT01115322|114573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489914|NCT01115322|114573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489915|NCT01115322|114573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489916|NCT01115322|114573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494212|NCT00684515||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05005&kw=P05005&tab=access|
2494213|NCT00783393||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494214|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
2494215|NCT00137917|710158/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494216|NCT00137917|710158/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494217|NCT00137917|710158/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494218|NCT00137917|710158/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494219|NCT00132730||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-005&kw=0873-005&tab=access|
2487754|NCT00103454|FFR30002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487755|NCT00103454|FFR30002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487756|NCT00103454|FFR30002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487757|NCT00103454|FFR30002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487758|NCT00103454|FFR30002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487759|NCT00103454|FFR30002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487760|NCT00103454|FFR30002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487761|NCT03074695|Pro00079368|Informed Consent Form|https://eirb.mc.duke.edu/|
2487762|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.
2487763|NCT04801251|Sarah bakry|Study Protocol|https://www.outlook.com/aun.edu.eg|All data or information will be uploaded on the website
2487764|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
2487765|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.
2487766|NCT00887484|114544|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487767|NCT00887484|114544|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487768|NCT00887484|114544|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487769|NCT00887484|114544|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487770|NCT00887484|114544|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487771|NCT01204671|114269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487772|NCT01204671|114269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487773|NCT01204671|114269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487774|NCT01204671|114269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487775|NCT01204671|114269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487776|NCT01204671|114269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487777|NCT01204671|114269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487778|NCT01494636|115419|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487779|NCT01494636|115419|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487780|NCT01494636|115419|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487781|NCT01494636|115419|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487782|NCT01494636|115419|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487783|NCT01494636|115419|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487784|NCT01494636|115419|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487785|NCT00526474||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04737&kw=P04737&tab=access|
2487786|NCT00413023|NKF100096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487787|NCT00413023|NKF100096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487788|NCT00413023|NKF100096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487789|NCT00413023|NKF100096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494220|NCT01462266||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-260&kw=0431-260&tab=access|
2487790|NCT00413023|NKF100096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487791|NCT00413023|NKF100096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487792|NCT00413023|NKF100096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487793|NCT01218308|114541|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487794|NCT01218308|114541|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487795|NCT01218308|114541|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487796|NCT01218308|114541|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487797|NCT01218308|114541|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487798|NCT01218308|114541|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487799|NCT01218308|114541|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492139|NCT01235949|112921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492140|NCT01235949|112921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487800|NCT02944292||Study Protocol|https://drive.google.com/open?id=0B-XpW352z4ZJMFdseHNwTWI2clU|
2487801|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
2487802|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
2487803|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
2487804|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
2487805|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.
2487806|NCT00423046|108933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487807|NCT00423046|108933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487808|NCT00423046|108933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487809|NCT00423046|108933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487810|NCT00423046|108933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487811|NCT00423046|108933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487812|NCT00423046|108933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487813|NCT01704261||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-022&kw=3102-022&tab=access|
2487814|NCT01663389|112167|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487815|NCT01663389|112167|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487816|NCT01663389|112167|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487817|NCT01663389|112167|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487818|NCT01663389|112167|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487819|NCT01663389|112167|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487820|NCT01663389|112167|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487821|NCT00706563|111631|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487822|NCT00706563|111631|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487823|NCT00706563|111631|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487824|NCT00706563|111631|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487825|NCT00706563|111631|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492141|NCT02289560||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
2489917|NCT01115322|114573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489918|NCT03111186|HS-15-00706|Study Protocol|http://istar.usc.edu|
2489919|NCT03111186|HS-15-00706|Informed Consent Form|http://istar.usc.edu|
2489920|NCT00363545|107077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489921|NCT00363545|107077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489922|NCT00363545|107077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489923|NCT00363545|107077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489924|NCT00363545|107077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489925|NCT00363545|107077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489926|NCT03673397||Individual Participant Data Set|https://doi.org/10.7910/DVN/WASN36|
2489927|NCT01144299|114292|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489928|NCT01144299|114292|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489929|NCT01144299|114292|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489930|NCT01144299|114292|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489931|NCT01144299|114292|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489932|NCT01144299|114292|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489933|NCT01144299|114292|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489934|NCT01209104|113722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489935|NCT01209104|113722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489936|NCT01209104|113722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489937|NCT01209104|113722|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489938|NCT01209104|113722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489939|NCT01209104|113722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494221|NCT02000804|117326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494222|NCT02000804|117326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494223|NCT02000804|117326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494224|NCT02000804|117326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494225|NCT02000804|117326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494226|NCT02000804|117326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494227|NCT02000804|117326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494228|NCT01827631|116416|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494229|NCT01827631|116416|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494230|NCT01827631|116416|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494231|NCT01827631|116416|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494232|NCT01827631|116416|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494233|NCT01827631|116416|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494234|NCT01827631|116416|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494235|NCT02899858|140503|Study Protocol|https://www4.vanderbilt.edu/irb/|
2494236|NCT04106622||Pubmed|https://www.ncbi.nlm.nih.gov/pubmed/|
2494237|NCT03311048|Sistema Nacional de Informação|Informed Consent Form|http://portal2.saude.gov.br/sisnep/pesquisador|
2494238|NCT03194984|27045285|Metanalysis, systematic review|https://www.ncbi.nlm.nih.gov/pubmed/?term=27045285|
2494239|NCT03194984|21740236|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21740236|
2494240|NCT03194984|21488723|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21488723|
2494241|NCT03194984|27007348|Informed Consent Form|https://www.ncbi.nlm.nih.gov/pubmed/?term=27007348|
2494242|NCT00609596|ARI111402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494243|NCT00609596|ARI111402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494244|NCT00609596|ARI111402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494245|NCT00609596|ARI111402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494246|NCT00609596|ARI111402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494247|NCT00609596|ARI111402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494248|NCT00609596|ARI111402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494249|NCT01097629||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-029&kw=4305-029&tab=access|
2494250|NCT04719351||Individual Participant Data Set|https://osf.io/uz3b7/?view_only=ba37189d0b594529b159ba27564dfb81|
2494251|NCT01648231|116797|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494252|NCT01648231|116797|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494253|NCT01648231|116797|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494254|NCT01648231|116797|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494255|NCT01648231|116797|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494256|NCT01648231|116797|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494257|NCT01648231|116797|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494258|NCT00600171|B2C109575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494259|NCT00600171|B2C109575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494260|NCT00600171|B2C109575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494261|NCT00600171|B2C109575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492142|NCT00538213|110263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492143|NCT00538213|110263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492144|NCT00538213|110263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492145|NCT00538213|110263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492146|NCT00538213|110263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492147|NCT00538213|110263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492148|NCT00538213|110263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494262|NCT00600171|B2C109575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494263|NCT00600171|B2C109575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494264|NCT00600171|B2C109575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494265|NCT00849017|112756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494266|NCT00849017|112756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494267|NCT00849017|112756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494268|NCT00849017|112756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494269|NCT00849017|112756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494270|NCT00849017|112756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494271|NCT00849017|112756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494272|NCT00379951||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494273|NCT01879410|114951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494274|NCT01879410|114951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494275|NCT01879410|114951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494276|NCT01879410|114951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494277|NCT01879410|114951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492149|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.
2492150|NCT00241644|102248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492151|NCT00241644|102248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492152|NCT00241644|102248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492153|NCT00241644|102248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492154|NCT00241644|102248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492155|NCT00241644|102248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492156|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25939657|Report of vascular function testing
2492157|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/24548114|Report of platelet function and physiology
2494278|NCT01879410|114951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494279|NCT01879410|114951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494280|NCT04523532||Study Protocol|http://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s13148-017-0407-6|
2494281|NCT00976144|113208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494282|NCT00976144|113208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494283|NCT00976144|113208|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494284|NCT00976144|113208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494285|NCT00976144|113208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494286|NCT00976144|113208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494287|NCT00976144|113208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494288|NCT03289130||Individual Participant Data Set|https://pcap.bioinf.unc.edu/|
2494289|NCT02698098||Study Protocol|http://dx.doi.org/10.7910/DVN/RO34OK|
2494290|NCT02698098||Individual Participant Data Set|http://dx.doi.org/10.7910/DVN/RO34OK|
2494291|NCT02698098||Analytic Code|http://dx.doi.org/10.7910/DVN/RO34OK|
2494292|NCT00792298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-006&kw=4305-006&tab=access|
2494293|NCT01086436|113552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494294|NCT01086436|113552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494295|NCT01086436|113552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494296|NCT01086436|113552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494297|NCT01086436|113552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494298|NCT01086436|113552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492158|NCT00711126|B2C106180|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492159|NCT00711126|B2C106180|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492160|NCT00711126|B2C106180|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492161|NCT00711126|B2C106180|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492162|NCT00711126|B2C106180|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492163|NCT00711126|B2C106180|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492164|NCT00711126|B2C106180|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492165|NCT01406262|107085|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492166|NCT01406262|107085|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492167|NCT01406262|107085|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492168|NCT01406262|107085|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492169|NCT01406262|107085|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492170|NCT01406262|107085|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492171|NCT01406262|107085|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492172|NCT02918916||Tables. Training program, Phototherapy parameters, Time point of outcomes|https://pt.scribd.com/document/325401697/Documents-ClinicalTrials-ID-2015-25219-0|
2492173|NCT00972504|112864|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492174|NCT00972504|112864|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492175|NCT00972504|112864|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492176|NCT00972504|112864|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492177|NCT00972504|112864|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492178|NCT00972504|112864|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492179|NCT00972504|112864|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492180|NCT01123083|115494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492181|NCT01123083|115494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492182|NCT01123083|115494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492183|NCT01123083|115494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492184|NCT01123083|115494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492185|NCT01123083|115494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492186|NCT01123083|115494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492187|NCT01984086|200921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492188|NCT01984086|200921|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492189|NCT01984086|200921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492190|NCT01984086|200921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492191|NCT01984086|200921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492192|NCT01984086|200921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492193|NCT01984086|200921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492194|NCT01025843||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5478-001&kw=5478-001&tab=access|
2492195|NCT01648140|115879|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492196|NCT01648140|115879|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492197|NCT01648140|115879|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492198|NCT01648140|115879|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492199|NCT01648140|115879|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492200|NCT01648140|115879|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492201|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.
2492202|NCT00970307|112157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492203|NCT00970307|112157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492204|NCT00970307|112157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492205|NCT00970307|112157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492206|NCT00970307|112157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492207|NCT00970307|112157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492208|NCT00970307|112157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492209|NCT01370694||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=8808-001&kw=8808-001&tab=access|
2492210|NCT02683811||Study Protocol|http://www.diariodellasalute.it|Study protocol (Italian version) can be requested by contacting the project manager (lmarinaro@aslcn2.it)
2492211|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.
2492212|NCT05171218||Individual Participant Data Set|https://osf.io/efya2/|
2492213|NCT05171218||Study Protocol|https://doi.org/10.17605/OSF.IO/VHCA5|
2492214|NCT05171218||Statistical Analysis Plan|https://doi.org/10.17605/OSF.IO/VHCA5|
2492215|NCT05171218||Informed Consent Form|https://osf.io/efya2/|
2492216|NCT03912948||Web site for patient information on studies bases on patients data (RGPD)|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|
2492217|NCT06210334||Clinical Study Report|https://www.researchdata.org.cn/|
2492218|NCT00465816|109063|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492219|NCT00465816|109063|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492220|NCT00465816|109063|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492221|NCT00465816|109063|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492222|NCT00465816|109063|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492223|NCT00465816|109063|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492224|NCT00465816|109063|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492225|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.
2492226|NCT00723450|SCA102833|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492227|NCT00723450|SCA102833|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494299|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.
2492228|NCT00723450|SCA102833|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492229|NCT00723450|SCA102833|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492230|NCT00723450|SCA102833|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492231|NCT00723450|SCA102833|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492232|NCT00723450|SCA102833|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492233|NCT05888155|01095697530|Clinical Study Report|http://Shaimaa4796@gmail.com|
2492234|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.
2492235|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.
2492236|NCT00891176|112830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492237|NCT00891176|112830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492238|NCT00891176|112830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492239|NCT00891176|112830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492240|NCT00891176|112830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492241|NCT00891176|112830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492242|NCT00622830|LPL110736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492243|NCT00622830|LPL110736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492244|NCT00622830|LPL110736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492245|NCT00622830|LPL110736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492246|NCT00622830|LPL110736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492247|NCT00622830|LPL110736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492248|NCT00622830|LPL110736|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492249|NCT01930045||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-295&kw=0518-295&tab=access|
2492250|NCT01405924||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-030&kw=0517-030&tab=access|
2492251|NCT00880477|217744/069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492252|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
2492253|NCT00880477|217744/069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492254|NCT00880477|217744/069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492255|NCT00880477|217744/069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492256|NCT04893213||Study Protocol|https://osf.io/yku5q/|Protocol on the Open Science Framework (OSF)
2492257|NCT04893213||Statistical Analysis Plan|https://osf.io/yku5q/|
2492258|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.
2492259|NCT02744521|Study protocol|Study Protocol|https://sites.google.com/site/relevantdocuments2016|I shared this protocol on Google Plus.
2492260|NCT00202865||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492261|NCT01424397|111924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492262|NCT01424397|111924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492263|NCT01424397|111924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492264|NCT01424397|111924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492265|NCT01424397|111924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492266|NCT01424397|111924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492267|NCT01424397|111924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492268|NCT01831791|114264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492269|NCT01831791|114264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492270|NCT01831791|114264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492271|NCT01831791|114264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492272|NCT01831791|114264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492273|NCT01831791|114264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494300|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.
2494301|NCT01475734|108372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494302|NCT01475734|108372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485890|NCT02841488||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
2485891|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
2485892|NCT01536405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V221-027&kw=V221-027&tab=access|
2485893|NCT00624065|COR111096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485894|NCT00624065|COR111096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485895|NCT00624065|COR111096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485896|NCT00624065|COR111096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485897|NCT00624065|COR111096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485898|NCT00624065|COR111096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485899|NCT00624065|COR111096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485900|NCT01171963|113808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494303|NCT01475734|108372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494304|NCT01475734|108372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485901|NCT01171963|113808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485902|NCT01171963|113808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485903|NCT01171963|113808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485904|NCT01171963|113808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485905|NCT01171963|113808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485906|NCT01171963|113808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485907|NCT03306394||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2485908|NCT03306394||Study Protocol|https://clinicaltrials.servier.com/|
2485909|NCT03306394||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2485910|NCT03306394||Informed Consent Form|https://clinicaltrials.servier.com/|
2485911|NCT03306394||Clinical Study Report|https://clinicaltrials.servier.com/|
2485912|NCT03306394||study-level clinical trial data|https://clinicaltrials.servier.com/|
2485913|NCT00062790|ARI40014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485914|NCT00062790|ARI40014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485915|NCT00062790|ARI40014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485916|NCT00062790|ARI40014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485917|NCT00062790|ARI40014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485918|NCT00062790|ARI40014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485919|NCT00062790|ARI40014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485920|NCT03222765||Study Protocol|http://www.epredice.eu|Study Protocol Version 5.0
2485921|NCT00358449|MEE103219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485922|NCT00358449|MEE103219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485923|NCT00358449|MEE103219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485924|NCT00358449|MEE103219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489940|NCT01209104|113722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489941|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.
2489942|NCT00000590||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pactg/|
2489943|NCT00000590||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/pactg/|
2489944|NCT01451437||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=P07649&kw=P07649&tab=access|
2489945|NCT00535288||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06472&kw=P06472&tab=access|
2489946|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
2489947|NCT04727489||Study Protocol|http://www.inserm.fr|
2489948|NCT04727489||Informed Consent Form|http://www.inserm.fr|
2489949|NCT00794898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489950|NCT01128621|113132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489951|NCT01128621|113132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489952|NCT01128621|113132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489953|NCT01128621|113132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489954|NCT01128621|113132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487826|NCT00706563|111631|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487827|NCT00706563|111631|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487828|NCT00764790|111751|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487829|NCT00764790|111751|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487830|NCT00764790|111751|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487831|NCT00764790|111751|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487832|NCT00764790|111751|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487833|NCT00764790|111751|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487834|NCT00764790|111751|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487835|NCT00545025|110674|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487836|NCT00545025|110674|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487837|NCT00545025|110674|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487838|NCT00545025|110674|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487839|NCT00545025|110674|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489955|NCT01128621|113132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489956|NCT01128621|113132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489957|NCT01328444|114417|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489958|NCT01328444|114417|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489959|NCT01328444|114417|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489960|NCT01328444|114417|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489961|NCT01328444|114417|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489962|NCT01328444|114417|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487840|NCT00545025|110674|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487841|NCT01416571|112691|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487842|NCT01416571|112691|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487843|NCT01416571|112691|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487844|NCT01416571|112691|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487845|NCT01416571|112691|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487846|NCT01416571|112691|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487847|NCT00420745|106481|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487848|NCT00420745|106481|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487849|NCT00420745|106481|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487850|NCT00420745|106481|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487851|NCT00420745|106481|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487852|NCT00420745|106481|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487853|NCT00420745|106481|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487854|NCT01027845|112640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487855|NCT01027845|112640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487856|NCT01027845|112640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487857|NCT01027845|112640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487858|NCT01027845|112640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487859|NCT01027845|112640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487860|NCT06523712||Informed Consent Form|https://schoolsplus.pk/schools/sharif-education-complex/|
2487861|NCT06523712||Informed Consent Form|https://apseducation123.wixsite.com/website|
2487862|NCT06523712||Informed Consent Form|https://apsaskarixi.pk/|
2487863|NCT07155863||Study Protocol|https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-024-06091-6|
2487864|NCT00325169|104962|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487865|NCT00325169|104962|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487866|NCT00325169|104962|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487867|NCT00325169|104962|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487868|NCT00325169|104962|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487869|NCT00325169|104962|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487870|NCT00325169|104962|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487871|NCT00481663||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487872|NCT00687700|MAB110553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487873|NCT00687700|MAB110553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487874|NCT00687700|MAB110553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487875|NCT00687700|MAB110553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487876|NCT00687700|MAB110553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487877|NCT00687700|MAB110553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487878|NCT00687700|MAB110553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487879|NCT00478621|109836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489963|NCT01328444|114417|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492274|NCT01831791|114264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492275|NCT00478738|MAB104958|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492276|NCT00478738|MAB104958|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492277|NCT00478738|MAB104958|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492278|NCT00478738|MAB104958|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492279|NCT00478738|MAB104958|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492280|NCT00478738|MAB104958|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492281|NCT00478738|MAB104958|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492282|NCT00327665|106068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492283|NCT00327665|106068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492284|NCT00327665|106068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492285|NCT00327665|106068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492286|NCT00327665|106068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492287|NCT00327665|106068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492288|NCT00688519|114741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492289|NCT00688519|114741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492290|NCT00688519|114741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492291|NCT00688519|114741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492292|NCT00688519|114741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492293|NCT00688519|114741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492294|NCT00688519|114741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492295|NCT00687011||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492296|NCT06613204||data set|http://www.ohsu.edu/alzheimers-disease-research-center/data-resources|
2492297|NCT00126997|104020|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492298|NCT00126997|104020|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492299|NCT00126997|104020|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492300|NCT00126997|104020|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492301|NCT00126997|104020|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492302|NCT00126997|104020|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492303|NCT06972433||Study Protocol|http://www.scd.edu.pk|
2492304|NCT05782231|VIV0001019|Individual Participant Data Set|https://doi.org/10.25934/PR00010109|
2492305|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.
2492306|NCT01607372|116392|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492307|NCT01607372|116392|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492308|NCT01607372|116392|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492309|NCT01607372|116392|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492310|NCT01607372|116392|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492311|NCT01607372|116392|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494305|NCT01475734|108372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494306|NCT01475734|108372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494307|NCT01475734|108372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494308|NCT05521737||Protocol reapproval report|https://drive.google.com/file/d/1P3sbgleW3murWJq_FIaerBlFU12aga9z/view?usp=sharing|
2494309|NCT04067518||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2494310|NCT04067518||Study Protocol|https://clinicaltrials.servier.com/|
2494311|NCT04067518||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2494312|NCT04067518||Informed Consent Form|https://clinicaltrials.servier.com/|
2494313|NCT04067518||Clinical Study Report|https://clinicaltrials.servier.com/|
2494314|NCT04067518||study-level clinical trial data|https://clinicaltrials.servier.com/|
2494315|NCT02706938|Clinical Trial Protocol|Study Protocol|https://drive.google.com/open?id=0B6Uam9x9PtiiV2xUcDBKU3RHYU0|
2494316|NCT01428466|114849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494317|NCT01428466|114849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494318|NCT01428466|114849|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494319|NCT01428466|114849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494320|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.
2494321|NCT00707798|111651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494322|NCT00707798|111651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489964|NCT01106092|113264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489965|NCT01106092|113264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489966|NCT01106092|113264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489967|NCT01106092|113264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489968|NCT01106092|113264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489969|NCT01106092|113264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489970|NCT01106092|113264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489971|NCT00376714|AC2105333|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489972|NCT00376714|AC2105333|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489973|NCT00376714|AC2105333|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489974|NCT00376714|AC2105333|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489975|NCT00376714|AC2105333|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489976|NCT00376714|AC2105333|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489977|NCT00376714|AC2105333|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489978|NCT04570059|Booklet of recommendation|intervention material|https://hal.archives-ouvertes.fr/|Booklet of recommendation provided to the intervention group (in French)
2489979|NCT00406562|107924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489980|NCT00406562|107924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489981|NCT00406562|107924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489982|NCT00406562|107924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489983|NCT00406562|107924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489984|NCT00406562|107924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489985|NCT00406562|107924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489986|NCT02184624|200301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489987|NCT02184624|200301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489988|NCT02184624|200301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489989|NCT02184624|200301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489990|NCT02184624|200301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489991|NCT02184624|200301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489992|NCT02184624|200301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489993|NCT00456807|109801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489994|NCT00456807|109801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489995|NCT00456807|109801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489996|NCT00456807|109801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489997|NCT00456807|109801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489998|NCT00456807|109801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489999|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)."
2490000|NCT00920803|113221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490001|NCT00920803|113221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490002|NCT00920803|113221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490003|NCT00920803|113221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490004|NCT00920803|113221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490005|NCT00920803|113221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490006|NCT00169442|104065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490007|NCT00169442|104065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490008|NCT00169442|104065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490009|NCT00169442|104065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490010|NCT00169442|104065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490011|NCT00169442|104065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490012|NCT00627575|LEP108937|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490013|NCT00627575|LEP108937|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490014|NCT00627575|LEP108937|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490015|NCT00627575|LEP108937|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490016|NCT00627575|LEP108937|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490017|NCT00627575|LEP108937|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490018|NCT00627575|LEP108937|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490019|NCT05053373||Individual Participant Data Set|http://www.medresman.org.cn/pub/en/proj/projectshow.aspx?proj=1282|
2490020|NCT02691585||Study Protocol|http://rguhs.ac.in/|
2490021|NCT02003274||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov|
2490022|NCT00067938|SCA40917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490023|NCT00067938|SCA40917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490024|NCT00067938|SCA40917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490025|NCT00067938|SCA40917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490026|NCT00067938|SCA40917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490027|NCT00067938|SCA40917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490028|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.
2490029|NCT00000485||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hdfp/|
2490030|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/34004390/|This article is from the National Library of Medicine.
2490031|NCT06078150||Systematic Review|https://pubmed.ncbi.nlm.nih.gov/32375184/|This article is from the National Library of Medicine.
2490032|NCT06078150||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/24905451/|This article is from the National Library of Medicine.
2490033|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.
2490034|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.
2490035|NCT06995794||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/|
2490036|NCT06995794||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
2490037|NCT00400478||Clinical Study Report|https://www.clinicaltrialsregister.eu/ctr-search/search;jsessionid=cJHnlkSBP30JjfQV2K-KXCK3mdjOE64o0FAsUcmzHmslzlaX5yhQ!675812678|
2490038|NCT01587898|116581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490039|NCT01587898|116581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490040|NCT01587898|116581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492312|NCT01607372|116392|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492313|NCT02916758||Individual Participant Data Set|http://grad.kean.edu/ot/faculty|Please contact cmulry@kean.edu to request the data set
2492314|NCT03343197||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2492315|NCT03343197||Study Protocol|https://clinicaltrials.servier.com/|
2492316|NCT03343197||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2492317|NCT03343197||Informed Consent Form|https://clinicaltrials.servier.com/|
2492318|NCT03343197||Clinical Study Report|https://clinicaltrials.servier.com/|
2492319|NCT03343197||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2492320|NCT00704184||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-007&kw=7009-007&tab=access|
2492321|NCT00123903|COR103560|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492322|NCT00123903|COR103560|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492323|NCT00123903|COR103560|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492324|NCT00123903|COR103560|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492325|NCT00123903|COR103560|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492326|NCT00123903|COR103560|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492327|NCT00123903|COR103560|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492328|NCT00529516|109821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492329|NCT00529516|109821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492330|NCT00529516|109821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492331|NCT00529516|109821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492332|NCT00529516|109821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492333|NCT00529516|109821|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492334|NCT00529516|109821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492335|NCT02439827||Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-015-2543-2|Study design paper
2492336|NCT02439827||Individual Participant Data Set|http://www.scielo.br/scielo.php?pid=S1980-00372016000200207&script=sci_arttext|Instrument validation study
2492337|NCT02439827||Individual Participant Data Set|http://journals.humankinetics.com/doi/abs/10.1123/jpah.2016-0113|Intervention results
2492338|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.
2492339|NCT06973135||Statistical Analysis Plan|https://dent.alexu.edu.eg/index.php/ar/|
2492340|NCT03997916||Individual Participant Data Set|http://redcap.uhhospitals.org/redcap|
2492341|NCT01780298||Individual Participant Data Set|https://doi.org/10.12688/f1000research.11698.2|
2492342|NCT01673555|116008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492343|NCT01673555|116008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492344|NCT01673555|116008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492345|NCT01673555|116008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492346|NCT01673555|116008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492347|NCT01673555|116008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492348|NCT01673555|116008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487880|NCT00478621|109836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492349|NCT00802464|112077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492350|NCT00802464|112077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492351|NCT00802464|112077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492352|NCT00802464|112077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492353|NCT00802464|112077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492354|NCT00802464|112077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492355|NCT00802464|112077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487881|NCT00478621|109836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492356|NCT01000597|113477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492357|NCT01000597|113477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492358|NCT01000597|113477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492359|NCT01000597|113477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492360|NCT01000597|113477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492361|NCT01000597|113477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492362|NCT01000597|113477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492363|NCT01808339|117156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492364|NCT01808339|117156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492365|NCT01808339|117156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492366|NCT01808339|117156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492367|NCT01808339|117156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492368|NCT01808339|117156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492369|NCT01808339|117156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492370|NCT04641741|FGBMEP202001|Study Protocol|https://www.idisantiago.es/|The study protocol was added to clinicaltrials.gov
2492371|NCT00314860|101468/204|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492372|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
2492373|NCT00314860|101468/204|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492374|NCT00314860|101468/204|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492375|NCT00314860|101468/204|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492376|NCT00314860|101468/204|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492377|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
2492378|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|
2492379|NCT05489250||Informed Consent Form|https://platon-network.de/contact|
2492380|NCT05489250||See Use & Access Regulation|https://platon-network.de/contact|
2492381|NCT06783530||Study Protocol|https://dentfac.mans.edu.eg|Faculty of Dentistry, Mansoura University - Ethical Committee Information.
2492382|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"
2492383|NCT00792636|110948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492384|NCT00792636|110948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492385|NCT00792636|110948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492386|NCT00792636|110948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487882|NCT00478621|109836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492387|NCT00792636|110948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492388|NCT00792636|110948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492389|NCT00792636|110948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492390|NCT03181711||Study Protocol|http://mah.se|can be requested by mail Karin.Ridell@mah.se
2492391|NCT07065084|dilek.cecen@cbu.edu.tr|Clinical Study Report|https://cdn.clinicaltrials.gov/large-docs/02/NCT04069702/ICF_000.pdf|
2492392|NCT04649008||Individual Participant Data Set|https://www.ieeg.org/|
2492393|NCT05909618||Nature Communications manuscript|https://www.nature.com/articles/s41467-021-22186-0|
2492394|NCT01017146|114575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492395|NCT01017146|114575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492396|NCT01017146|114575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487883|NCT00478621|109836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487884|NCT00478621|109836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487885|NCT01725672|116806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492397|NCT01017146|114575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492398|NCT01017146|114575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492399|NCT01017146|114575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492400|NCT01017146|114575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492401|NCT00976105|111849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492402|NCT00976105|111849|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492403|NCT00976105|111849|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492404|NCT00976105|111849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492405|NCT00976105|111849|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492406|NCT00976105|111849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492407|NCT07048717||General information about the study plus information about application for data|https://www.umu.se/en/research/groups/the-mauritius-study/|
2492408|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)
2492409|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)
2492410|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)
2492411|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
2492412|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
2492413|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
2492414|NCT05179200||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-024-08035-7|
2492415|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
2492416|NCT03172468||Informed Consent Form|https://box.medunigraz.at/s/QuTYym3xsqXybWI|
2492417|NCT03172468||Study Protocol|https://box.medunigraz.at/s/YbufqAn3DBI1f4Q|
2492418|NCT06447519||Study Protocol|https://ikee.lib.auth.gr|https://ikee.lib.auth.gr
2492419|NCT06791993||Individual Participant Data Set|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op|https://drive.google.com/drive/folders/1C-CfBwEXCHEXl86ePRO4o4opAShsa9Op
2492420|NCT00611559|110478|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492421|NCT00611559|110478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487886|NCT01725672|116806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492422|NCT00611559|110478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492423|NCT00611559|110478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492424|NCT00611559|110478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492425|NCT00611559|110478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492426|NCT00611559|110478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492427|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
2492428|NCT04119284||Informed Consent Form|http://irbnet.org|The Informed consent form can be obtained while the patient is seen for scoliosis at Nemours-AIDHC.
2492429|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
2492430|NCT03739450|602d|Individual Participant Data Set|https://www.tbindsc.org/StaticFiles/SOP/602d%20-%20External%20Use%20TBIMS%20National%20Database%20Notification.pdf|
2492431|NCT02073994||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2492432|NCT03423303||Statistical Analysis Plan|https://bmjopen.bmj.com/content/bmjopen/14/1/e075595.full.pdf|
2492433|NCT03111290||Summary Data Set|http://dx.doi.org/10.5281/zenodo.45811|Dataset supporting Alagapan et al. 2016 PLoS Biology
2492434|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
2492435|NCT06795880||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/33062451/|
2492436|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
2492437|NCT02240472||Study Protocol|http://senomac.se/Home/study%20protocol.html|Study protocol and patient information (English)
2492438|NCT06830330||ethics committee approval|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
2492439|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.
2492440|NCT05162755||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2492441|NCT05162755||Study Protocol|https://clinicaltrials.servier.com/|
2492442|NCT05162755||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2492443|NCT05162755||Informed Consent Form|https://clinicaltrials.servier.com/|
2492444|NCT05162755||Clinical Study Report|https://clinicaltrials.servier.com/|
2492445|NCT05162755||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2492446|NCT06188754||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/38762486/|
2492447|NCT06786429||Clinical Study Report|https://www.nust.ac.zw|
2494323|NCT00707798|111651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494324|NCT00707798|111651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494325|NCT00707798|111651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494326|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
2494327|NCT00348140|AVA102670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494328|NCT00348140|AVA102670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494329|NCT00348140|AVA102670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494330|NCT00348140|AVA102670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494331|NCT00348140|AVA102670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494332|NCT00348140|AVA102670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494333|NCT00348140|AVA102670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494334|NCT02069002||Study Protocol|http://bmjopen.bmj.com/content/6/6/e011003.full.pdf+html|
2494335|NCT00868790||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3577-009&kw=3577-009&tab=access|
2494336|NCT00358813|NKT102783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494337|NCT00358813|NKT102783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494338|NCT00358813|NKT102783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494339|NCT00358813|NKT102783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494340|NCT00358813|NKT102783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494341|NCT00358813|NKT102783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494342|NCT00358813|NKT102783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494343|NCT01495026|115708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494344|NCT01495026|115708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494345|NCT01495026|115708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494346|NCT01495026|115708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494347|NCT01495026|115708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494348|NCT01495026|115708|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492448|NCT06786429|tba|Clinical Study Report|https://www.nust.ac.zw|
2492449|NCT04522375||Study Protocol|http://clinicaltrials.gov|clinicaltrials.gov
2492450|NCT04522375||Statistical Analysis Plan|http://clinicaltrials.gov|clinicaltrials.gov
2492451|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.
2492452|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.
2492453|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.
2492454|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.
2492455|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.
2485925|NCT00358449|MEE103219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485926|NCT00358449|MEE103219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485927|NCT00358449|MEE103219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485928|NCT02605395|201528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485929|NCT02605395|201528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485930|NCT02605395|201528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485931|NCT02605395|201528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485932|NCT01171989|113978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485933|NCT01171989|113978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485934|NCT01171989|113978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485935|NCT01171989|113978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485936|NCT01171989|113978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485937|NCT01171989|113978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485938|NCT01171989|113978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487887|NCT01725672|116806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487888|NCT01725672|116806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487889|NCT01725672|116806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487890|NCT01725672|116806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487891|NCT01725672|116806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487892|NCT04434508|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
2487893|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
2487894|NCT00849056|112755|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492456|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.
2492457|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.
2492458|NCT05459688||Trial Results Summary|https://www.trialsummaries.com/Study/StudyDetails?id=25790&tenant=MT_MED_9011|Trial Results Summary
2492459|NCT02132936||Clinical Study Report|https://www.leopharmatrials.com/en|Clinical Trials at LEO Pharma
2492460|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
2492461|NCT03060421||Study Protocol|http://www.parkerinst.dk|
2492462|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
2492463|NCT07063940||Study Protocol|http://www.birmingham.ac.uk/ExaLT|
2485939|NCT01472341||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-113&kw=0000-113&tab=access|
2487895|NCT00849056|112755|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487896|NCT00849056|112755|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487897|NCT00849056|112755|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487898|NCT00849056|112755|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487899|NCT00849056|112755|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487900|NCT00849056|112755|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487901|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
2492464|NCT07063940||Informed Consent Form|http://www.birmingham.ac.uk/ExaLT|
2492465|NCT06272903|MBRU IRB-2023-228|Study Protocol|http://www.mbru.ac.ae|
2492466|NCT04979351||Review|https://dergipark.org.tr/tr/download/article-file/117117|
2487902|NCT00453687|AC2108380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487903|NCT00453687|AC2108380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487904|NCT00453687|AC2108380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487905|NCT00453687|AC2108380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487906|NCT00453687|AC2108380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487907|NCT00453687|AC2108380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487908|NCT00453687|AC2108380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487909|NCT00544271|263855/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487910|NCT00544271|263855/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487911|NCT00544271|263855/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487912|NCT00544271|263855/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487913|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
2487914|NCT00544271|263855/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487915|NCT00355641|101468/206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487916|NCT00355641|101468/206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487917|NCT00355641|101468/206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487918|NCT00355641|101468/206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487919|NCT00355641|101468/206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487920|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
2487921|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
2487922|NCT00126945|104702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487923|NCT00126945|104702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487924|NCT00126945|104702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487925|NCT00126945|104702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487926|NCT00126945|104702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487927|NCT00126945|104702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487928|NCT00034632||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2487929|NCT00321763|107192|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487930|NCT00321763|107192|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487931|NCT00321763|107192|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487932|NCT00321763|107192|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487933|NCT00321763|107192|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487934|NCT00113165|LAM100034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487935|NCT00113165|LAM100034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487936|NCT00113165|LAM100034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487937|NCT00113165|LAM100034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492467|NCT04979351||Clinical Study Report|https://dergipark.org.tr/tr/download/article-file/29524|
2492468|NCT06852430|042025201171|Study Protocol|https://docs.google.com/document/d/18-WWwL8l_EB2nHv4wr1-Q1cslJ1VUYUf/edit?usp=drivesdk&ouid=111849282554145262325&rtpof=true&sd=true|
2492469|NCT02733159||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/PePS2/index.aspx|
2490041|NCT01587898|116581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490042|NCT01587898|116581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490043|NCT01587898|116581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490044|NCT01587898|116581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490045|NCT02045953|201092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490046|NCT02045953|201092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490047|NCT02045953|201092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490048|NCT02045953|201092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490049|NCT02045953|201092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490050|NCT02045953|201092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490051|NCT02045953|201092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490052|NCT02700087|Consent form cycle 3|Informed Consent Form|https://eprotocol.stanford.edu/irb/ControlServlet?updateFlag=Y|
2490053|NCT03009370||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26806685|
2490054|NCT00400608|SAS105519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490055|NCT00400608|SAS105519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490056|NCT00400608|SAS105519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490057|NCT00400608|SAS105519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490058|NCT00400608|SAS105519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490059|NCT00400608|SAS105519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490060|NCT00400608|SAS105519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490061|NCT00197158|104387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490062|NCT00197158|104387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490063|NCT00197158|104387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490064|NCT00197158|104387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490065|NCT00197158|104387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490066|NCT00197158|104387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485940|NCT00379600|ARA102198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490067|NCT05386628|26079868|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2490068|NCT05386628|16225693|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2490069|NCT05386628|12924842|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2490070|NCT05386628|31864435|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2490071|NCT05386628|22018755|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2490072|NCT05386628|18192154|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2492470|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
2492471|NCT04817761||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2492472|NCT04817761||Study Protocol|https://clinicaltrials.servier.com/|
2492473|NCT04817761||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2492474|NCT04817761||Informed Consent Form|https://clinicaltrials.servier.com/|
2492475|NCT04817761||Clinical Study Report|https://clinicaltrials.servier.com/|
2492476|NCT04817761||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2492477|NCT06821919|2022-09-22_012059|Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
2492478|NCT06836102|drmostafanasr1988@gmail.com|Study Protocol|https://doi.org/10.1016/j.hermed.2021.100468|
2492479|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"
2492480|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"
2492481|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"
2492482|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"
2492483|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"
2492484|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"
2492485|NCT01385189||Clinical Study Report|http://smhs.gwu.edu/mitm-crg/clinical-trials|
2492486|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)
2492487|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).
2492488|NCT06814223||Study Protocol|https://my.health.gov.il/CliniTrials/Pages/Home.aspx|
2492489|NCT06817746||Study Protocol|https://www.fsm.unipi.it|
2492490|NCT06805448|2024-516715-25-00|Study Protocol|https://euclinicaltrials.eu/|
2492491|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
2492492|NCT06824558|Fear of Childbirth Scale|Individual Participant Data Set|https://gcris.pau.edu.tr/bitstream/11499/6124/1/7ba3f584-23f9-4af0-9a4a-56f72570f94d.pdf|
2492493|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"
2492494|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
2492495|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.
2492496|NCT06824922|Protocolo_ECA_piloto|Study Protocol|https://drive.google.com/file/d/1PhNe1G9PVs2FkOmKeyXazMLW3l-sxRR7/view?usp=sharing|
2492497|NCT06863207||Individual Participant Data Set|https://vivli.org/|
2492498|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
2492499|NCT06997874|COMBAT trial|Study Protocol|https://nictu.hscni.net/service/combat/|
2492500|NCT02415933||Study Protocol|https://knowledge.uchicago.edu/handle/11417/69|
2492501|NCT06883916|Ethics Committee Approval|Informed Consent Form|https://tip.cu.edu.tr/storage/Mevzuat/Kurullar%20Y%C3%B6nergesi.pdf|
2492502|NCT04098276|10.1186/s12889-021-11930-2|Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-021-11930-2|
2492503|NCT06886594||Study Protocol|https://bap.ksu.edu.tr/|
2492504|NCT06744946|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2492505|NCT06692621|Yöktez|Individual Participant Data Set|https://tez.yok.gov.tr/UlusalTezMerkezi/tezlerim.jsp?sira=0|You can reach us at harunzengin71@gmail.com
2492506|NCT06739343||Study Protocol|https://www.ecwaeyehospitalkano.com/|
2492507|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
2492508|NCT06881381||Study Protocol|https://docs.google.com/document/d/19ZwAv6y0UUaSa_Hjb3jlzuhMfTro0Y6p/edit?usp=drive_link&ouid=101334879348395838064&rtpof=true&sd=true|STUDY PROTOKOL DIAGRAM
2494349|NCT01495026|115708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490073|NCT05386628|25977305|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2487938|NCT00113165|LAM100034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487939|NCT00113165|LAM100034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487940|NCT00113165|LAM100034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487941|NCT00090103|ARI40005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487942|NCT00090103|ARI40005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487943|NCT00090103|ARI40005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487944|NCT00090103|ARI40005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487945|NCT00090103|ARI40005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487946|NCT00090103|ARI40005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487947|NCT00090103|ARI40005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487948|NCT00358488|B2E106359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487949|NCT00358488|B2E106359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487950|NCT00358488|B2E106359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487951|NCT00358488|B2E106359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487952|NCT00358488|B2E106359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487953|NCT00358488|B2E106359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487954|NCT00358488|B2E106359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487955|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."
2487956|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.
2487957|NCT06108921||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
2487958|NCT06956586|Research|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37330438/|"There is no additional information."
2487959|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.
2487960|NCT00689741|580299/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487961|NCT00689741|580299/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487962|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
2487963|NCT00689741|580299/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487964|NCT00689741|580299/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487965|NCT00689741|580299/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487966|NCT01134042|106829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487967|NCT01134042|106829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487968|NCT01134042|106829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487969|NCT01134042|106829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487970|NCT01134042|106829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487971|NCT01134042|106829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487972|NCT01134042|106829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487973|NCT01192178|113872|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487974|NCT01192178|113872|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487975|NCT01192178|113872|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487976|NCT01192178|113872|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487977|NCT01192178|113872|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487978|NCT01192178|113872|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487979|NCT01192178|113872|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487980|NCT03641729||Study Protocol|http://aline.priori.fioritto@gmail.com|More information contact the principal investigator
2487981|NCT02035540||Study results|http://pubmed.ncbi.nlm.nih.gov/30879050/|
2487982|NCT04744181||Individual Participant Data Set|https://redcap-irccs.policlinicogemelli.it/|
2487983|NCT01431976|115377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487984|NCT01431976|115377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490074|NCT05386628|20068255|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2490075|NCT05905003||Individual Participant Data Set|https://nda.nih.gov/ampscz/|
2490076|NCT03016676||Study Protocol|http://www.ijpbs.net/abstract.php?article=5240|
2490077|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"
2490078|NCT00541463||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490079|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."
2490080|NCT02848443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490081|NCT02848443||Study Protocol|https://clinicaltrials.servier.com/|
2490082|NCT02848443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490083|NCT02848443||Informed Consent Form|https://clinicaltrials.servier.com/|
2490084|NCT02848443||Clinical Study Report|https://clinicaltrials.servier.com/|
2490085|NCT02848443||study-level clinical trial data|https://clinicaltrials.servier.com/|
2490086|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.
2490087|NCT00005132||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nghs/|
2490088|NCT00005132||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nghs/|
2490089|NCT02393586||Link to Pubmed (Final publication)|https://www.ncbi.nlm.nih.gov/pubmed/28333342|
2490090|NCT01067443||Study Protocol|http://journals.plos.org/plosntds/article/file?type=supplementary&id=info:doi/10.1371/journal.pntd.0004880.s002|Final Study Protocol
2490091|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
2490092|NCT03121027||Individual Participant Data Set|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|Detail about sampling and BDHS 2011 report
2490093|NCT00371007||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490094|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.
2487985|NCT01431976|115377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487986|NCT01431976|115377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490095|NCT01155479||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05664&kw=P05664&tab=access|
2490096|NCT00955383|112359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490097|NCT00955383|112359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490098|NCT00955383|112359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490099|NCT00955383|112359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490100|NCT00955383|112359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490101|NCT00955383|112359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490102|NCT00955383|112359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490103|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 \[there-on other citations are referenced 1 citation later\]
2490104|NCT01277042|114590|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490105|NCT01277042|114590|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490106|NCT01277042|114590|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490107|NCT01277042|114590|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485941|NCT00379600|ARA102198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485942|NCT00379600|ARA102198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485943|NCT00379600|ARA102198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485944|NCT00379600|ARA102198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485945|NCT00379600|ARA102198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485946|NCT00379600|ARA102198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485947|NCT03579303|123|Individual Participant Data Set|http://bethesda.org?data-id=123|De-identified data for primary and secondary outcome measures
2485948|NCT04391933|CPR|Informed Consent Form|https://komite.regionsyddanmark.dk/wm258128|
2485949|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
2485950|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
2485951|NCT01421277||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-076&kw=0974-076&tab=access|
2485952|NCT01639092|25596179|Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25596179|Publication for the primary study results
2485953|NCT01037114|112266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485954|NCT01037114|112266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485955|NCT01037114|112266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485956|NCT01037114|112266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485957|NCT01037114|112266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485958|NCT01037114|112266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485959|NCT01037114|112266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485960|NCT00609674|FFU111439|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485961|NCT00609674|FFU111439|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485962|NCT00609674|FFU111439|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485963|NCT00609674|FFU111439|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485964|NCT00609674|FFU111439|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485965|NCT00609674|FFU111439|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485966|NCT00609674|FFU111439|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485967|NCT02197481|PMID:25925431|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25925431|
2485968|NCT01899755|116987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485969|NCT01899755|116987|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485970|NCT01899755|116987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485971|NCT01899755|116987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485972|NCT01899755|116987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485973|NCT01899755|116987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485974|NCT01899755|116987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485975|NCT00385320|444563/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485976|NCT00385320|444563/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485977|NCT00385320|444563/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485978|NCT00385320|444563/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492509|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.
2492510|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.
2492511|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
2492512|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.
2492513|NCT06762756||Analytic Code|https://osf.io/v5deq/?view_only=d5dd1f5903a0480d94402c7c6528c6a4|Scripts are available on Open Science Framework
2492514|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
2492515|NCT07038772|EAT-40|Study Protocol|https://www.eat-26.com/|
2492516|NCT03869892||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2492517|NCT03869892||Study Protocol|https://clinicaltrials.servier.com/|
2492518|NCT03869892||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2492519|NCT03869892||Informed Consent Form|https://clinicaltrials.servier.com/|
2492520|NCT03869892||Clinical Study Report|https://clinicaltrials.servier.com/|
2492521|NCT03869892||study-level clinical trial data|https://clinicaltrials.servier.com/|
2492522|NCT05018143|GUID|Individual Participant Data Set|https://nda.nih.gov/|
2492523|NCT06764238|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
2492524|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.
2492525|NCT06828367|not necessary|Study Protocol|https://docs.google.com/document/d/1hvjyp_RfCDDpHWkrTv_s7qhztM4Pqw9T/edit|is a public document
2492526|NCT06776536||institutional review board|https://camsakurasehir.saglik.gov.tr/|
2492527|NCT06744270|Inonu University Clinical Rese|Clinical Study Report|https://www.inonu.edu.tr/klinik.etik|https://www.inonu.edu.tr/klinik.etik
2492528|NCT06762743||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|registered clinical trial about Brivaracetam oral solution on Chinese website
2492529|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.
2492530|NCT00979121||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/sails/|
2492531|NCT00979121||Study Forms|http://biolincc.nhlbi.nih.gov/studies/sails/|
2492532|NCT06667661||NIH Reporter Information|https://reporter.nih.gov/search/w2y2LWuI50aTEgDfuqR7lg/project-details/11017278|Final Data set will be deposited into NICHD DASH database.
2492533|NCT06861205||Study Protocol|https://doi.org/10.3389/fnut.2024.1438740|
2492534|NCT01128595|113126|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492535|NCT01128595|113126|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492536|NCT01128595|113126|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492537|NCT01128595|113126|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492538|NCT01128595|113126|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492539|NCT01128595|113126|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492540|NCT01128595|113126|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492541|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.
2492542|NCT00309166|580299/011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492543|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
2492544|NCT00309166|580299/011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494350|NCT06896929|permethrin|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/21860157/|Comparison of permethrin and ivermectin in scabies was done
2494351|NCT00312013|FRX106365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494352|NCT00312013|FRX106365|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494353|NCT00312013|FRX106365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494354|NCT00312013|FRX106365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494355|NCT00312013|FRX106365|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494356|NCT00312013|FRX106365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494357|NCT00312013|FRX106365|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494358|NCT00537719|GLP107030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494359|NCT00537719|GLP107030|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494360|NCT00537719|GLP107030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494361|NCT00537719|GLP107030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494362|NCT00537719|GLP107030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494363|NCT00537719|GLP107030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494364|NCT00537719|GLP107030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494365|NCT01154101|114296|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494366|NCT01154101|114296|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494367|NCT01154101|114296|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494368|NCT01154101|114296|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494369|NCT01154101|114296|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494370|NCT01154101|114296|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494371|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
2495711|NCT00538473|110223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495712|NCT00538473|110223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495713|NCT02437175||Methodology paper|https://www.dovepress.com/articles.php?article_id=25534|
2495714|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/106014|
2495715|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/143046|
2495716|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889771|
2495717|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889781|
2495718|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889773|
2495719|NCT00539006|FFU105924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495720|NCT00539006|FFU105924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495721|NCT00539006|FFU105924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495722|NCT00539006|FFU105924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495723|NCT00539006|FFU105924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495724|NCT00539006|FFU105924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495725|NCT00539006|FFU105924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495726|NCT01153685|110628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495727|NCT01153685|110628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495728|NCT01153685|110628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490108|NCT01277042|114590|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490109|NCT01277042|114590|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490110|NCT00042029||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490111|NCT04488107|ICH topic S9|ICH topic S9 - nonclinical evaluation for anticancer pharmaceuticals. 2009|https://database.ich.org/sites/default/files/S9_Guideline.pdf|
2490112|NCT04488107|IBRANCE® (palbociclib) capsule|label for IBRANCE® (palbociclib) capsules|https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/207103s000lbl.pdf|
2490113|NCT04488107|IBRANCE® (palbociclib) tablets|label for IBRANCE® (palbociclib) tablets,|https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf|
2490114|NCT04488107|KISQALI® (ribociclib) tablets|Label for KISQALI® (ribociclib) tablets|https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209092s005lbl.pdf|
2490115|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|
2490116|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|
2490117|NCT01286831|106181|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490118|NCT01286831|106181|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490119|NCT01286831|106181|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490120|NCT01286831|106181|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490121|NCT01286831|106181|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490122|NCT01286831|106181|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490123|NCT01286831|106181|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490124|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
2490125|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
2490126|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
2490127|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
2490128|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
2490129|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
2490130|NCT04335422||Device website|https://www.hocoma.com/solutions/armeo-spring/|
2490131|NCT04335422||references|https://www.ncbi.nlm.nih.gov/pubmed/28540536|
2490132|NCT00688207|AVA109941|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490133|NCT00688207|AVA109941|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490134|NCT00688207|AVA109941|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492545|NCT00309166|580299/011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492546|NCT00309166|580299/011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492547|NCT00309166|580299/011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492548|NCT06753526|ahmed-mahmoud@sohag.med.edu.eg|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/9008325/|
2492549|NCT06662136||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2492550|NCT06750744|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2492551|NCT06950970|tetinstitute.rn@gmail.com|Informed Consent Form|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
2492552|NCT06950970|tetinstitute.rn@gmail.com|Statistical Analysis Plan|https://tionemoorg.wordpress.com/wp-admin/site-editor.php?canvas=edit&p=/|
2492553|NCT00756067|111652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492554|NCT00756067|111652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492555|NCT00756067|111652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492556|NCT00756067|111652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492557|NCT00756067|111652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492558|NCT05201599|zxt4|Study Protocol|https://pan.baidu.com/s/1PNKfPWrpeJtodX1RwH8k-w|
2490135|NCT00688207|AVA109941|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490136|NCT00688207|AVA109941|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490137|NCT00688207|AVA109941|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490138|NCT00688207|AVA109941|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490139|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
2490140|NCT01266941|111789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490141|NCT01266941|111789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490142|NCT01266941|111789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490143|NCT01266941|111789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490144|NCT01266941|111789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490145|NCT01266941|111789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490146|NCT01266941|111789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490147|NCT05749770||Individual Participant Data Set|https://zenodo.org/records/5913009|
2490148|NCT02777736||Study Protocol|http://www.lymphoma.cz/docs/studies/dlbcl/CLSG-CNS-01_en.pdf|
2490149|NCT05648071|[ PMID ]31560378|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31560378/|
2490150|NCT05648071|PMID:30285222|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30285222/|
2490151|NCT05648071|PMID:31378236|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31378236/|
2490152|NCT05648071|PMID:32997907|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32997907/|
2490153|NCT05648071|PMID:30955977|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30955977/|
2490154|NCT05648071|PMID:31402780|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/31402780/|
2490155|NCT05648071|PMID:32781263|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/32781263/|
2490156|NCT05648071|PMID: 34358724|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34358724/|
2490157|NCT05648071|PMID: 29229461|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29229461/|
2490158|NCT05648071|PMID: 30119083|Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/30119083/|
2490159|NCT01323946|109825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490160|NCT01323946|109825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490161|NCT01323946|109825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490162|NCT01323946|109825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490163|NCT01323946|109825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490164|NCT01323946|109825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490165|NCT01323946|109825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490166|NCT02826850||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
2490167|NCT02826850||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
2490168|NCT00510874|110028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490169|NCT00510874|110028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490170|NCT00510874|110028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490171|NCT00510874|110028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494372|NCT00818259||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=0869-134&kw=0869-134&tab=access|
2494373|NCT00996840|111592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494374|NCT00996840|111592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494375|NCT00996840|111592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494376|NCT00996840|111592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494377|NCT00996840|111592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487987|NCT01431976|115377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487988|NCT01405859||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983677/|Final Study Results, Published in Tremor and Other Hyperkinetic Disorders
2487989|NCT01014091|113810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487990|NCT01014091|113810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487991|NCT01014091|113810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487992|NCT01014091|113810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487993|NCT01014091|113810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487994|NCT01014091|113810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487995|NCT01014091|113810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487996|NCT05704309|DPPOS|Individual Participant Data Set|https://repository.niddk.nih.gov/studies/dppos/|
2487997|NCT05704309||Individual Participant Data Set|https://naccdata.org/requesting-data/data-request-process|will be available in 2025
2487998|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.
2487999|NCT00385840|108708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488000|NCT00385840|108708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488001|NCT00385840|108708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488002|NCT00385840|108708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488003|NCT00385840|108708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488004|NCT00385840|108708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488005|NCT01706328|116974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488006|NCT01706328|116974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488007|NCT01706328|116974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488008|NCT01706328|116974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488009|NCT01706328|116974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488010|NCT01706328|116974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488011|NCT01706328|116974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488012|NCT07130370|fabatool@numl.edu.pk|Informed Consent Form|https://pakjmcr.com/index.php/1/article/view/67|It is not applicable at this time.
2488013|NCT07011264||Study Protocol|https://reporter.nih.gov/search/xHobiVLiPU68u-6wSogmsA/project-details/11052906|
2488014|NCT00765076|112147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488015|NCT00765076|112147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488016|NCT00765076|112147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492559|NCT01702376|113789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488017|NCT00765076|112147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488018|NCT00765076|112147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488019|NCT00765076|112147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488020|NCT06855810|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
2488021|NCT06882057|CCCG-ALL|Individual Participant Data Set|http://cccg.nipher.com/cccg/|CCCG-ALL-2025 DATASET
2488022|NCT07080528||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2024-515545-41-00|
2488023|NCT07121348|END-7-25-3400|Study Protocol|http://www.tanta.edu.eg|
2490172|NCT00510874|110028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485979|NCT00385320|444563/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485980|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
2485981|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
2485982|NCT00268203|BEX104545|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485983|NCT00268203|BEX104545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485984|NCT00268203|BEX104545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485985|NCT00268203|BEX104545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485986|NCT01039961|113022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485987|NCT01039961|113022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485988|NCT01039961|113022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485989|NCT01039961|113022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485990|NCT01039961|113022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485991|NCT01039961|113022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485992|NCT01039961|113022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485993|NCT01929863|200185|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485994|NCT01929863|200185|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485995|NCT01929863|200185|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485996|NCT01929863|200185|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485997|NCT01929863|200185|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485998|NCT01929863|200185|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2485999|NCT01929863|200185|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486000|NCT01494532|111569|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486001|NCT01494532|111569|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486002|NCT01494532|111569|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486003|NCT01494532|111569|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486004|NCT01494532|111569|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486005|NCT01494532|111569|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486006|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.
2486007|NCT00005292||Study Forms|https://biolincc.nhlbi.nih.gov/studies/aadr/Forms/|
2486008|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|
2486009|NCT02045849|117349|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486010|NCT02045849|117349|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486011|NCT02045849|117349|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486012|NCT02045849|117349|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486013|NCT02045849|117349|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486014|NCT02045849|117349|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486015|NCT02045849|117349|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488024|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.
2488025|NCT05104346|COVID and acute appendicitis|Study Protocol|http://www.mans.edu.eg/|
2488026|NCT00536835|PLK107427|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488027|NCT00536835|PLK107427|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488028|NCT00536835|PLK107427|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488029|NCT00536835|PLK107427|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488030|NCT00536835|PLK107427|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488031|NCT00536835|PLK107427|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488032|NCT00536835|PLK107427|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492560|NCT01702376|113789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492561|NCT01702376|113789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492562|NCT01702376|113789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492563|NCT01702376|113789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492564|NCT01702376|113789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492565|NCT01702376|113789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492566|NCT06952582|doi.org/10.17605/OSF.IO/SE8M7|Individual Participant Data Set|https://osf.io/puxgw/|
2492567|NCT00449774|LBI108617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492568|NCT00449774|LBI108617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492569|NCT00449774|LBI108617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492570|NCT00449774|LBI108617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492571|NCT00449774|LBI108617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492572|NCT00449774|LBI108617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492573|NCT00449774|LBI108617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492574|NCT00857766|112355|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492575|NCT00857766|112355|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492576|NCT00857766|112355|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492577|NCT00857766|112355|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492578|NCT00857766|112355|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492579|NCT00857766|112355|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492580|NCT00857766|112355|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492581|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"
2492582|NCT00985088|113440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492583|NCT00985088|113440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492584|NCT00985088|113440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492585|NCT00985088|113440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492586|NCT00985088|113440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492587|NCT00985088|113440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486016|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/31353554/|
2486017|NCT07067515||PMC article.|https://pubmed.ncbi.nlm.nih.gov/30734608/|
2486018|NCT07067515||Free PMC article.|https://pubmed.ncbi.nlm.nih.gov/35508275/|
2486019|NCT01818024|116343|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486020|NCT01818024|116343|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486021|NCT01818024|116343|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486022|NCT01818024|116343|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486023|NCT01818024|116343|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486024|NCT01818024|116343|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486025|NCT01818024|116343|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486026|NCT03192163||Survey|http://j.mp/2qdz7P2|This is the RedCap survey that subjects will take.
2486027|NCT01934205|116666|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486028|NCT01934205|116666|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486029|NCT01934205|116666|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486030|NCT01934205|116666|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486031|NCT01934205|116666|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486032|NCT01934205|116666|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488033|NCT01371682|112771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488034|NCT01371682|112771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488035|NCT01371682|112771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488036|NCT01371682|112771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488037|NCT01371682|112771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488038|NCT01371682|112771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488039|NCT01371682|112771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488040|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
2488041|NCT00386698|104887|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488042|NCT00386698|104887|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488043|NCT00386698|104887|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488044|NCT00386698|104887|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488045|NCT00386698|104887|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488046|NCT00386698|104887|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488047|NCT01899703|117213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488048|NCT01899703|117213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488049|NCT01899703|117213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488050|NCT01899703|117213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488051|NCT01899703|117213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488052|NCT01899703|117213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486033|NCT01934205|116666|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486034|NCT00196963|103532|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486035|NCT00196963|103532|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492588|NCT00985088|113440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492589|NCT01119651|114574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492590|NCT01119651|114574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492591|NCT01119651|114574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492592|NCT01119651|114574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492593|NCT01119651|114574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492594|NCT01119651|114574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492595|NCT01119651|114574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492596|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
2492597|NCT01332552|115040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492598|NCT01332552|115040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492599|NCT01332552|115040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492600|NCT01332552|115040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492601|NCT01332552|115040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492602|NCT01332552|115040|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492603|NCT01332552|115040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492604|NCT03019835||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/7880668|
2492605|NCT01491815||Study Protocol|http://www.biomedcentral.com/search?query=glinatsi&searchType=publisherSearch|Publication of the protocol. Glinatsi et al. Trials (2017) 18:161
2492606|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|
2492607|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|
2492608|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.
2492609|NCT01827839|116796|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492610|NCT01827839|116796|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492611|NCT01827839|116796|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492612|NCT01827839|116796|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492613|NCT01827839|116796|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492614|NCT01827839|116796|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492615|NCT01827839|116796|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492616|NCT04091347|37478967|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37478967/|
2492617|NCT04091347|38094930|Outcomes Manuscript|https://pubmed.ncbi.nlm.nih.gov/38094930/|
2492618|NCT01074242||CSR Synopsis|http://www.merck.com/clinical-trials/search.html?kw=V260-037|
2492619|NCT01957163|200109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492620|NCT01957163|200109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492621|NCT01957163|200109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492622|NCT01957163|200109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492623|NCT01957163|200109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492624|NCT01957163|200109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492625|NCT01957163|200109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492626|NCT00614614|110870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492627|NCT00614614|110870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492628|NCT00614614|110870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492629|NCT00614614|110870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490173|NCT00510874|110028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490174|NCT00510874|110028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490175|NCT03272230||Study Protocol|https://data.mendeley.com/datasets/mv8hndcd95/2|The ECOCAPTURE ethograms: apathy ethogram and disinhibition ethogram
2490176|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
2490177|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
2490178|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
2490179|NCT01036061|108414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490180|NCT01036061|108414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490181|NCT01036061|108414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490182|NCT01036061|108414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490183|NCT01036061|108414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490184|NCT01036061|108414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488053|NCT01899703|117213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488054|NCT01610388|113376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488055|NCT01610388|113376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488056|NCT01610388|113376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488057|NCT01610388|113376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488058|NCT01610388|113376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488059|NCT01610388|113376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488060|NCT01610388|113376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488061|NCT01248975|114387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488062|NCT01248975|114387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486036|NCT00196963|103532|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486037|NCT00196963|103532|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486038|NCT00196963|103532|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486039|NCT00429481|444563/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490185|NCT06933992||Study Protocol|http://www.chinadrugtrials.org.cn/clinicaltrials.searchlistdetail.dhtml|
2494378|NCT00996840|111592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494379|NCT00996840|111592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494380|NCT01164878||Individual Participant Data Set|https://dfzljdn9uc3pi.cloudfront.net/2016/2483/1/SPSS_repa_et_al.sav|SPSS Data Set for Analysis
2494381|NCT03322358||Individual Participant Data Set|https://www.sleepdata.org/datasets/urbanpoor|
2494382|NCT00684177|TOC110977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494383|NCT00684177|TOC110977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494384|NCT00684177|TOC110977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494385|NCT00684177|TOC110977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494386|NCT00684177|TOC110977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494387|NCT00684177|TOC110977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494388|NCT00684177|TOC110977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494389|NCT03094247||Individual Participant Data Set|https://openscholarship.wustl.edu/data/101/|
2494390|NCT00291343|105239 (mth24-30)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494391|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
2494392|NCT00291343|105239 (mth24-30)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494393|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
2494394|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.
2494395|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
2494396|NCT06935851||Study Protocol|https://osf.io|signing a data agreement
2494397|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.
2494398|NCT02184637|200951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494399|NCT02184637|200951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494400|NCT02184637|200951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494401|NCT02184637|200951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494402|NCT02184637|200951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494403|NCT02184637|200951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494404|NCT02184637|200951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494405|NCT00463437|109507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494406|NCT00463437|109507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494407|NCT00463437|109507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494408|NCT00463437|109507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494409|NCT00463437|109507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494410|NCT00463437|109507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494411|NCT00463437|109507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494412|NCT02740309|Sala Institute|Sala Institute for Child & Family Centered Care|http://nyulangone.org/locations/hassenfeld-childrens-hospital/sala-institute-for-child-family-centered-care|
2494413|NCT03184948||Statistical Analysis Plan|http://ketkisheth.weebly.com/|
2494414|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.
2494415|NCT01583036|116216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494416|NCT01583036|116216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488063|NCT01248975|114387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492630|NCT00614614|110870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492631|NCT00614614|110870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492632|NCT00614614|110870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492633|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
2488064|NCT01248975|114387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488065|NCT01248975|114387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488066|NCT01248975|114387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492634|NCT01767688||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-031&kw=3102-031&tab=access|
2492635|NCT02224469|k9f10|Individual Participant Data Set|http://datadryad.org/resource/doi:10.5061/dryad.k9f10|
2492636|NCT00273052|COR103561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488067|NCT01248975|114387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492637|NCT00273052|COR103561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488068|NCT02836769||Study Protocol|http://www.implementationscience.com/content/10/1/6|Publication of the initial project protocol
2492638|NCT00273052|COR103561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492639|NCT00273052|COR103561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492640|NCT00273052|COR103561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492641|NCT00273052|COR103561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492642|NCT00273052|COR103561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492643|NCT00489554|109661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492644|NCT00489554|109661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492645|NCT00489554|109661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492646|NCT00489554|109661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492647|NCT00489554|109661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492648|NCT00489554|109661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492649|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.
2492650|NCT00907933|111610|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492651|NCT00907933|111610|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492652|NCT00907933|111610|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492653|NCT00907933|111610|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492654|NCT00907933|111610|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492655|NCT00907933|111610|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492656|NCT00907933|111610|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488069|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
2488070|NCT01996995||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/s13063-015-0622-4|
2488071|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.
2488072|NCT00005123||Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/hhp/|
2488073|NCT04976725||Statistical Analysis Plan|https://doi.org/10.1016/J.JCM.2019.12.001|
2488074|NCT01059851||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-023&kw=4305-023&tab=access|
2488075|NCT01039675|113120|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488076|NCT01039675|113120|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488077|NCT01039675|113120|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490186|NCT01039974|112648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490187|NCT01039974|112648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490188|NCT01039974|112648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490189|NCT01039974|112648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490190|NCT01039974|112648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490191|NCT01039974|112648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490192|NCT01039974|112648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490193|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.
2490194|NCT00887406|104865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490195|NCT00887406|104865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490196|NCT00887406|104865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490197|NCT00887406|104865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490198|NCT00887406|104865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490199|NCT00887406|104865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490200|NCT05377203|PMID: 37276913|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/37276913|
2490201|NCT00679055||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0736-006&kw=0736-006&tab=access|
2490202|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.
2490203|NCT00290277|104951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490204|NCT00290277|104951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490205|NCT00290277|104951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490206|NCT00290277|104951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490207|NCT00290277|104951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494417|NCT01583036|116216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488078|NCT01039675|113120|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490208|NCT00290277|104951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490209|NCT00290277|104951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490210|NCT03075046||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
2490211|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)."
2490212|NCT00135564|711202/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490213|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
2490214|NCT00135564|711202/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490215|NCT00135564|711202/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490216|NCT00135564|711202/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490217|NCT00135564|711202/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490218|NCT06934850||Clinical Study Report|https://etik.inonu.edu.tr/panel/index|
2490219|NCT06935032||Statistical Analysis Plan|http://academic.oup.com/ejo/article-abstract/31/2/174/468205|
2490220|NCT00334607|107531|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490221|NCT00334607|107531|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490222|NCT00334607|107531|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490223|NCT00334607|107531|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486040|NCT00429481|444563/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486041|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
2486042|NCT00429481|444563/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486043|NCT00429481|444563/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486044|NCT00429481|444563/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486045|NCT05866263||Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/23405164/|
2486046|NCT05866263||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/23405164/|
2486047|NCT00294047|104820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486048|NCT00294047|104820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486049|NCT00294047|104820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486050|NCT00294047|104820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486051|NCT00294047|104820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486052|NCT00294047|104820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486053|NCT01717950||Clinical Study Report|https://smhs.gwu.edu/mitm-crg/|
2486054|NCT00197249|270362/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486055|NCT00197249|270362/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486056|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
2486057|NCT00197249|270362/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486058|NCT00197249|270362/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486059|NCT07138755||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/39489090/|
2486060|NCT05341453||Study Protocol|https://www.chmirakl.cz/aktuality/study-protokol|
2486061|NCT05341453||Statistical Analysis Plan|https://www.chmirakl.cz/aktuality/statistical-analysis-plan|
2486062|NCT05341453||Informed Consent Form|https://www.chmirakl.cz/aktuality/type-informed-consent-form|
2486063|NCT00985751|113171|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490224|NCT00334607|107531|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490225|NCT00334607|107531|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490226|NCT00289718|100556 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494418|NCT01583036|116216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494419|NCT01583036|116216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494420|NCT01583036|116216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490227|NCT00289718|100556 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490228|NCT00289718|100556 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490229|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.
2490230|NCT00289718|100556 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490231|NCT01453725||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07642&kw=8259-006&tab=access|
2490232|NCT00543543||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-001&kw=V503-001&tab=access|
2490233|NCT00699764|208141/017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490234|NCT00699764|208141/017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490235|NCT00699764|208141/017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490236|NCT00699764|208141/017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490237|NCT00699764|208141/017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490238|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
2490239|NCT00857883|111314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490240|NCT00857883|111314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490241|NCT00857883|111314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490242|NCT00857883|111314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490243|NCT00857883|111314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490244|NCT00857883|111314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490245|NCT00857883|111314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490246|NCT00118690|SFA100316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490247|NCT00118690|SFA100316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490248|NCT00118690|SFA100316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490249|NCT00118690|SFA100316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490250|NCT00118690|SFA100316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490251|NCT00397215|108251|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490252|NCT00397215|108251|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494421|NCT01583036|116216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494422|NCT01471327|115705|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494423|NCT01471327|115705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494424|NCT01471327|115705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494425|NCT01471327|115705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494426|NCT01471327|115705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494427|NCT01471327|115705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494428|NCT01471327|115705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494429|NCT00473694||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494430|NCT00942162|111476|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494431|NCT00942162|111476|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494432|NCT00942162|111476|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494433|NCT00942162|111476|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494434|NCT00942162|111476|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494435|NCT00942162|111476|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494436|NCT00942162|111476|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494437|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.
2494438|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.
2494439|NCT00499707|712753/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494440|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
2494441|NCT00499707|712753/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494442|NCT00499707|712753/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494443|NCT00499707|712753/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494444|NCT00499707|712753/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494445|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
2494446|NCT07030387||Study Protocol|https://www.precis-2.org/Help/Documentation/Help|
2494447|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.
2494448|NCT01772134|116135|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494449|NCT01772134|116135|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494450|NCT01772134|116135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494451|NCT01772134|116135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494452|NCT01772134|116135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494453|NCT01772134|116135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494454|NCT01772134|116135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494455|NCT00920543|SAM40086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494456|NCT00920543|SAM40086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494457|NCT00920543|SAM40086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494458|NCT00920543|SAM40086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494459|NCT00920543|SAM40086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494460|NCT00920543|SAM40086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494461|NCT00920543|SAM40086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494462|NCT00410371|LBI108614|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494463|NCT00410371|LBI108614|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494464|NCT00410371|LBI108614|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494465|NCT00410371|LBI108614|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488079|NCT01039675|113120|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488080|NCT01039675|113120|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488081|NCT01039675|113120|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488082|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.
2488083|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.
2488084|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
2488085|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
2488086|NCT00134719|102370 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488087|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.
2488088|NCT00134719|102370 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488089|NCT00127010|103388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488090|NCT00127010|103388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488091|NCT00127010|103388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488092|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.
2488093|NCT00127010|103388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488094|NCT00127010|103388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488095|NCT00985790|113237|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488096|NCT00985790|113237|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488097|NCT00985790|113237|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488098|NCT00985790|113237|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488099|NCT00985790|113237|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488100|NCT00985790|113237|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488101|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.
2488102|NCT00335075||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488103|NCT01245933||general information|http://www.asconet.net|
2488104|NCT00729001|444563/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488105|NCT00729001|444563/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492657|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
2492658|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32532623/|Study scientific background
2492659|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.
2492660|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32727835/|Study scientific background.
2492661|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/32769063/|Study scientific background.
2492662|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/25636714/|Study scientific background.
2492663|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/24444048/|Alemtuzumab medication
2492664|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/27766281/|Alemtuzumab medication
2492665|NCT05075499|PMID|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/31898276/|Alemtuzumab medication
2492666|NCT05075499|PMID|Study Protocol|http://products.sanofi.us/aubagio/aubagio.html|Aubagio (teriflunomide) \[prescribing information\]. Cambridge (MA): Genzyme Corporation; September 2012.
2492667|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/31898276/|Aubagio (teriflunomide) medication
2492668|NCT05075499|PMID|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/29275977/|Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria.
2492669|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.
2492670|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.
2492671|NCT01772199|116477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492672|NCT01772199|116477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492673|NCT01772199|116477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492674|NCT01772199|116477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492675|NCT01772199|116477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488106|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
2488107|NCT00729001|444563/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488108|NCT00729001|444563/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492676|NCT01772199|116477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488109|NCT00729001|444563/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488110|NCT00496327||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488111|NCT04967703||Full Paper|http://www.europeanreview.org/article/32287|
2488112|NCT03496675||Individual Participant Data Set|https://osf.io/tpdhu/|
2488113|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.
2488114|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
2488115|NCT00676052|AC2110664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488116|NCT00676052|AC2110664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488117|NCT00676052|AC2110664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488118|NCT00676052|AC2110664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488119|NCT00676052|AC2110664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488120|NCT00676052|AC2110664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488121|NCT00676052|AC2110664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488122|NCT07055932||Study Protocol|https://theses.gla.ac.uk/1017/|
2488123|NCT00976391|108486|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492677|NCT01772199|116477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492678|NCT00910962|111810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492679|NCT00910962|111810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492680|NCT00910962|111810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486064|NCT00985751|113171|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486065|NCT00985751|113171|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486066|NCT00985751|113171|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486067|NCT00985751|113171|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486068|NCT04748991||Product monograph - Vernakalant|https://pdf.hres.ca/dpd_pm/00038441.PDF|
2486069|NCT04748991||Product monograph - Amiodarone|https://pdf.hres.ca/dpd_pm/00035425.PDF|
2486070|NCT00363077|107975|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486071|NCT00363077|107975|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486072|NCT00363077|107975|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494466|NCT00410371|LBI108614|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494467|NCT00410371|LBI108614|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494468|NCT00410371|LBI108614|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494469|NCT00693706|110127|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494470|NCT00693706|110127|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490253|NCT00397215|108251|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490254|NCT00397215|108251|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490255|NCT00397215|108251|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490256|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.
2490257|NCT01926015||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-060&kw=V260-060&tab=access|
2490258|NCT00851344|110163|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490259|NCT00851344|110163|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490260|NCT00851344|110163|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490261|NCT00851344|110163|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490262|NCT00851344|110163|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494471|NCT00693706|110127|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490263|NCT00851344|110163|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490264|NCT00851344|110163|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490265|NCT00318058|104540|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490266|NCT00318058|104540|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490267|NCT00318058|104540|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490268|NCT00318058|104540|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490269|NCT00318058|104540|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490270|NCT00318058|104540|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490271|NCT06652529||Study Protocol|https://www.aromics.es/en/|
2490272|NCT02714907||Study Protocol|http://cortrium.com|In Danish language
2490273|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
2490274|NCT00094172|ITN020AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN020AI
2490275|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.
2490276|NCT00968890|113525|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490277|NCT00968890|113525|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490278|NCT00968890|113525|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490279|NCT00968890|113525|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494472|NCT00693706|110127|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494473|NCT00693706|110127|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494474|NCT00693706|110127|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494475|NCT00693706|110127|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494476|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.
2494477|NCT06961422|0009-0009-61|Individual Participant Data Set|https://orcid.org/0009-0009-6142-6201|
2494478|NCT04457921|Mary Colleen Simonelli|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/30102886/|web site is provided
2494479|NCT04160403||Study Protocol|https://www.ncbi.nlm.nih.gov/|
2494480|NCT05446675|EC/EH/220608-SK|Individual Participant Data Set|https://ehs-hernia-registry.com|
2494481|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
2494482|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
2494483|NCT04406038|ID|Individual Participant Data Set|http://github.com/eusporg/spb_covid_study20|Please consult with the README.md for the repository.
2494484|NCT00971321|113462|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494485|NCT00971321|113462|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494486|NCT00971321|113462|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494487|NCT00971321|113462|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494488|NCT00971321|113462|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494489|NCT00971321|113462|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494490|NCT00971321|113462|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494491|NCT01857895|200016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494492|NCT01857895|200016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494493|NCT01857895|200016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494494|NCT01857895|200016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488124|NCT00976391|108486|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492681|NCT00910962|111810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492682|NCT00910962|111810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492683|NCT00910962|111810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492684|NCT00910962|111810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492685|NCT01316913|113374|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492686|NCT01316913|113374|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492687|NCT01316913|113374|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492688|NCT01316913|113374|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492689|NCT01316913|113374|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492690|NCT01316913|113374|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492691|NCT01316913|113374|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492692|NCT00718120|110584|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492693|NCT00718120|110584|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492694|NCT00718120|110584|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492695|NCT00718120|110584|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492696|NCT00718120|110584|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492697|NCT00718120|110584|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492698|NCT00718120|110584|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492699|NCT07044193||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521375-31-00|
2492700|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
2488125|NCT00976391|108486|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492701|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"
2492702|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
2492703|NCT00035048||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492704|NCT07013123|2025-521258-41-00|Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en|avalable after authorization of competent authorities
2492705|NCT02236611|201315|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492706|NCT02236611|201315|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492707|NCT02236611|201315|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492708|NCT02236611|201315|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492709|NCT02236611|201315|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492710|NCT02236611|201315|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492711|NCT02236611|201315|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492712|NCT03928665||DDLS - reference|https://www.sign.ac.uk/assets/sign144_disc_chart_colour.pdf|
2492713|NCT00470483|TMT106386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492714|NCT00470483|TMT106386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492715|NCT00470483|TMT106386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492716|NCT00470483|TMT106386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486073|NCT00363077|107975|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486074|NCT00363077|107975|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486075|NCT03045458||Clinical Study Report|http://mc.manuscriptcentral.com/jperio|
2486076|NCT00533507|109861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486077|NCT00533507|109861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486078|NCT00533507|109861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486079|NCT00533507|109861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486080|NCT00533507|109861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486081|NCT00533507|109861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486082|NCT00533507|109861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486083|NCT01989884||Clinical Study Report|https://doi.org/10.1007/s11060-019-03116-z|
2486084|NCT05895435||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/12841881/|
2486085|NCT00279045|49653/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486086|NCT00279045|49653/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486087|NCT00279045|49653/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486088|NCT00279045|49653/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486089|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
2486090|NCT00279045|49653/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486091|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
2492717|NCT00470483|TMT106386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486092|NCT00139815|103420|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486093|NCT00139815|103420|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486094|NCT00139815|103420|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486095|NCT00139815|103420|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486096|NCT00139815|103420|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486097|NCT00139815|103420|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486098|NCT00139815|103420|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486099|NCT00268216|SCO30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486100|NCT00268216|SCO30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486101|NCT00268216|SCO30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486102|NCT00268216|SCO30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486103|NCT00268216|SCO30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486104|NCT00268216|SCO30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486105|NCT00268216|SCO30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492718|NCT00470483|TMT106386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494495|NCT01857895|200016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494496|NCT01857895|200016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487185|NCT00381238|AVA104617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494497|NCT01857895|200016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494498|NCT05957562|orcid.org/0000-0003-0558-6402|Study Protocol|http://orcid.org/0000-0003-0558-6402|
2490280|NCT00968890|113525|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490281|NCT00968890|113525|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490282|NCT00968890|113525|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494499|NCT00814710|111188|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494500|NCT00814710|111188|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494501|NCT00814710|111188|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494502|NCT00814710|111188|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494503|NCT00814710|111188|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494504|NCT00814710|111188|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494505|NCT00814710|111188|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494506|NCT01362322|114778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494507|NCT01362322|114778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494508|NCT01362322|114778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494509|NCT01362322|114778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494510|NCT01362322|114778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494511|NCT01362322|114778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488126|NCT00976391|108486|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494512|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.
2494513|NCT01009463|102871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494514|NCT01009463|102871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494515|NCT01009463|102871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494516|NCT01009463|102871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494517|NCT01009463|102871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492719|NCT00972686|112826|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492720|NCT00972686|112826|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492721|NCT00972686|112826|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492722|NCT00972686|112826|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486106|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)"
2486107|NCT05583097||Study Protocol|https://www.gu.se/forskning/tyreoideacancer|
2486108|NCT00452348|ADA109057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486109|NCT00452348|ADA109057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486110|NCT00452348|ADA109057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486111|NCT00452348|ADA109057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486112|NCT00452348|ADA109057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486113|NCT00452348|ADA109057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486114|NCT00452348|ADA109057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486115|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"
2486116|NCT03221972||Study Protocol|http://www.chinanutri.cn/gzrw_132/zgjmyyyjkzkjcxm/201412/t20141229_108493.html|
2486117|NCT06793592||More information on IPD sharing|https://osf.io/preprints/osf/6pwxe|
2486118|NCT00307541|105554|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486119|NCT00307541|105554|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486120|NCT00307541|105554|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486121|NCT00307541|105554|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486122|NCT00307541|105554|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486123|NCT00307541|105554|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486124|NCT01573819|115719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486125|NCT01573819|115719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486126|NCT01573819|115719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486127|NCT01573819|115719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486128|NCT01573819|115719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486129|NCT01573819|115719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486130|NCT01573819|115719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486131|NCT01119625|113266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486132|NCT01119625|113266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492723|NCT00972686|112826|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492724|NCT00972686|112826|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492725|NCT00972686|112826|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492726|NCT00929526|112949|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486133|NCT01119625|113266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486134|NCT01119625|113266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492727|NCT00929526|112949|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490283|NCT01254032|114169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490284|NCT01254032|114169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490285|NCT01254032|114169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490286|NCT01254032|114169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490287|NCT01254032|114169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490288|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
2490289|NCT01622231|116365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490290|NCT01622231|116365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490291|NCT01622231|116365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490292|NCT01622231|116365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490293|NCT01254071|114694|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490294|NCT01254071|114694|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490295|NCT01254071|114694|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490296|NCT01254071|114694|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490297|NCT01254071|114694|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490298|NCT01254071|114694|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490299|NCT01254071|114694|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490300|NCT01893203|25109244|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/|
2490301|NCT00347360|CFD105453|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490302|NCT00347360|CFD105453|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490303|NCT00347360|CFD105453|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490304|NCT00347360|CFD105453|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490305|NCT00347360|CFD105453|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490306|NCT00347360|CFD105453|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490307|NCT00347360|CFD105453|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490308|NCT00354536|GLP106073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490309|NCT00354536|GLP106073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486135|NCT01119625|113266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486136|NCT01119625|113266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486137|NCT01119625|113266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486138|NCT00333450|106623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486139|NCT00333450|106623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486140|NCT00333450|106623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486141|NCT00333450|106623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486142|NCT00333450|106623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486143|NCT00333450|106623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486144|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
2486145|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.
2486146|NCT00633022|PM1111138|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486147|NCT00633022|PM1111138|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486148|NCT00633022|PM1111138|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486149|NCT00633022|PM1111138|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486150|NCT00633022|PM1111138|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486151|NCT00633022|PM1111138|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486152|NCT00633022|PM1111138|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486153|NCT03211039|37114|Individual Participant Data Set|http://view.ncbi.nlm.nih.gov/dbgap-controlled|
2492728|NCT00929526|112949|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492729|NCT00929526|112949|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492730|NCT00929526|112949|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492731|NCT00929526|112949|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492732|NCT06699511||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/34847915/|
2492733|NCT04205669||Individual Participant Data Set|https://www.kaggle.com/julianmatthewman/grattigratta-data|
2492734|NCT06477549|Protocol version 1.0|Study Protocol|https://cloud.mail.ru/public/wQ1q/8amGwZdMb|Study protocol signed
2492735|NCT01381445|113435|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492736|NCT01381445|113435|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492737|NCT01381445|113435|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492738|NCT01381445|113435|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492739|NCT01381445|113435|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492740|NCT01381445|113435|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492741|NCT01381445|113435|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492742|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.
2492743|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.
2492744|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.
2494518|NCT01009463|102871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486154|NCT03211039|37114|Summary level phenotype data|http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs002094.v1.p1|
2494519|NCT01009463|102871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494520|NCT01516450|116119|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494521|NCT01516450|116119|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490310|NCT00354536|GLP106073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490311|NCT00354536|GLP106073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490312|NCT00354536|GLP106073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490313|NCT00354536|GLP106073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490314|NCT00354536|GLP106073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490315|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.
2490316|NCT00000488||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|
2490317|NCT06462885||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
2490318|NCT01148472|2004-005069-39|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2004-005069-39/results|
2490319|NCT00289783|103813|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490320|NCT00289783|103813|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490321|NCT00289783|103813|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490322|NCT00289783|103813|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487186|NCT00381238|AVA104617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490323|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.
2490324|NCT01323959|113060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490325|NCT01323959|113060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492745|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.
2492746|NCT04338568||Clinical Study Report|https://www.castoredc.com/|
2492747|NCT01602900|116038|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492748|NCT01602900|116038|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492749|NCT01602900|116038|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492750|NCT01602900|116038|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492751|NCT01602900|116038|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492752|NCT01602900|116038|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492753|NCT01602900|116038|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492754|NCT00103857||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492755|NCT05400525||Study Protocol|https://discoverthesecretofgoodhealth.weebly.com|
2492756|NCT04526171||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/Q3P4WX|
2492757|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.
2492758|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
2492759|NCT02795052||Clinical Study Report|http://mdstemcells.com/nest/|http://mdstemcells.com/nest/
2492760|NCT01072149|110946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492761|NCT01072149|110946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492762|NCT01072149|110946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492763|NCT01072149|110946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492764|NCT01072149|110946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492765|NCT01072149|110946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492766|NCT01072149|110946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492767|NCT04419571|285260|Individual Participant Data Set|https://www.myresearchproject.org.uk/|Data collection template available on IRAS (Integrated Research Application System) registration
2492768|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
2492769|NCT04419571|285260|Study Protocol|https://www.myresearchproject.org.uk/|Protocol available on IRAS (Integrated Research Application System) registration
2492770|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.
2492771|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.
2492772|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
2492773|NCT00632736|101468/248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492774|NCT00632736|101468/248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492775|NCT00632736|101468/248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492776|NCT00632736|101468/248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492777|NCT00632736|101468/248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492778|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
2492779|NCT00866619|110021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488127|NCT00976391|108486|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488128|NCT00976391|108486|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494522|NCT01516450|116119|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488129|NCT00976391|108486|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494523|NCT01516450|116119|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494524|NCT01516450|116119|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494525|NCT01516450|116119|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494526|NCT01516450|116119|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494527|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.
2494528|NCT00474253||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494529|NCT04752787||Study Protocol|http://files.eric.ed.gov/fulltext/EJ1086361.pdf|
2494530|NCT04752787||Study Protocol|https://mhealth.jmir.org/2018/4/e109/|
2494531|NCT00440128|NKV100781|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494532|NCT00440128|NKV100781|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494533|NCT00440128|NKV100781|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494534|NCT00440128|NKV100781|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494535|NCT00440128|NKV100781|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494536|NCT00440128|NKV100781|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494537|NCT00440128|NKV100781|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494538|NCT00984659|112989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494539|NCT00984659|112989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494540|NCT00984659|112989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488130|NCT00120848|580299/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488131|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
2488132|NCT00120848|580299/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488133|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
2488134|NCT00120848|580299/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488135|NCT00120848|580299/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488136|NCT00120848|580299/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488137|NCT05872945||Individual Participant Data Set|https://github.com/dradolfomunoz/PF12RED|
2488138|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.
2488139|NCT00000544||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dash/|
2488140|NCT00000544||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/dash/|
2488141|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"
2488142|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."
2490326|NCT01323959|113060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494541|NCT00984659|112989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494542|NCT00984659|112989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494543|NCT00984659|112989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492780|NCT00866619|110021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492781|NCT00866619|110021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492782|NCT00866619|110021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494544|NCT00984659|112989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494545|NCT03407391||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data is available for use by researchers on application through the website
2494546|NCT01972425||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1442-x|
2494547|NCT00196937|103514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494548|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.
2494549|NCT00196937|103514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494550|NCT00196937|103514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494551|NCT00196937|103514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494552|NCT00196937|103514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494553|NCT00196937|103514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494554|NCT04936672||Study Protocol|https://doi.org/10.1249/MSS.0b013e318213fefb|The protocol setting and data collection process is based on this reference
2494555|NCT03136705|STU00089165|Study Protocol|https://irb.northwestern.edu/contact|
2494556|NCT03136705|STU00089165|Informed Consent Form|https://irb.northwestern.edu/contact|
2494557|NCT00126451||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492783|NCT00866619|110021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492784|NCT00866619|110021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492785|NCT00424476|HGS1006-C1057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492786|NCT00424476|HGS1006-C1057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492787|NCT00424476|HGS1006-C1057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492788|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
2492789|NCT00424476|HGS1006-C1057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492790|NCT00424476|HGS1006-C1057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492791|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
2492792|NCT00197262|FFR104861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492793|NCT00197262|FFR104861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492794|NCT00197262|FFR104861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492795|NCT00197262|FFR104861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492796|NCT00197262|FFR104861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492797|NCT00197262|FFR104861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492798|NCT00197262|FFR104861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492799|NCT04883541||PhD thesis|http://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
2492800|NCT00879827|217744/049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492801|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
2492802|NCT00879827|217744/049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492803|NCT00879827|217744/049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492804|NCT00879827|217744/049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492805|NCT00787371||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492806|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.
2492807|NCT00000492||Study Forms|http://biolincc.nhlbi.nih.gov/studies/bhat/|
2492808|NCT02384122|27619827|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27619827|
2492809|NCT06700161|Study Protocol|Study Protocol|https://tipfakultesi.ksu.edu.tr/Default.aspx?SId=24451|
2492810|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
2492811|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
2492812|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
2492813|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
2492814|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
2492815|NCT05214248||Study Protocol|https://doi.org/10.1016/S0377-1237(10)80131-5|Article Title: Meconium Aspiration Syndrome: An Insight
2492816|NCT03884478||Study Protocol|https://www.researchprotocols.org/2021/4/e24647|available open access at URL provided
2492817|NCT03151694||Peer-Reviewed Article|http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12646/full|
2494558|NCT05700344||Summary of Product Characteristics|https://www.ema.europa.eu/en/documents/product-information/bavencio-epar-product-information_en.pdf|Summary of Product Characteristics
2494559|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
2494560|NCT01367743||Statistical Analysis Plan|http://cic-p-nancy.fr/wp-content/uploads/2019/01/revUS_SAP_OPTIMA_CC_KD_NG.pdf|
2494561|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.
2494562|NCT00945750||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0208-144&kw=0208-144&tab=access|
2494563|NCT01101568|113506|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494564|NCT01101568|113506|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494565|NCT01101568|113506|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494566|NCT01101568|113506|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494567|NCT01101568|113506|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494568|NCT01101568|113506|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494569|NCT01101568|113506|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494570|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
2494571|NCT06344520||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/22607780/|Dysfunctional movement patterns are directly related to the mechanism of injury
2494572|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
2494573|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.
2494574|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
2494575|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
2494576|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
2494577|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
2494578|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
2494579|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
2494580|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.
2495729|NCT01153685|110628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495730|NCT01153685|110628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495731|NCT01153685|110628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495732|NCT00903409|111818|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495733|NCT00903409|111818|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495734|NCT00903409|111818|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495735|NCT00903409|111818|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495736|NCT00903409|111818|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495737|NCT00903409|111818|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488143|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"
2488144|NCT01894360|117100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488145|NCT01894360|117100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488146|NCT01894360|117100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488147|NCT01894360|117100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488148|NCT01894360|117100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488149|NCT01894360|117100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488150|NCT01894360|117100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488151|NCT01691482|114956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488152|NCT01691482|114956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488153|NCT01691482|114956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488154|NCT01691482|114956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488155|NCT01691482|114956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488156|NCT01691482|114956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488157|NCT01691482|114956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488158|NCT00132912||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488159|NCT00705965||treatment manual and supplemental content|http://links.lww.com/PSYMED/A275|
2488160|NCT03142451||Study Protocol|http://foamix.co.il/|
2488161|NCT01370642||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-043&kw=7009-043&tab=access|
2492818|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529982|
2486155|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|
2492819|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529983|
2492820|NCT02907489||Study Protocol|https://www.scribd.com/document/328018560/Protocol-Omaia-Repaired-Autosaved|
2492821|NCT02404012||Website|https://ngletsum.wixsite.com/nito|
2492822|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.
2492823|NCT00092378||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492824|NCT00227422|102394|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495738|NCT00381667|B2C104604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495739|NCT00381667|B2C104604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488162|NCT00871000|111815|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495740|NCT00381667|B2C104604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486156|NCT02416180|201909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486157|NCT02416180|201909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486158|NCT02416180|201909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486159|NCT02416180|201909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486160|NCT02416180|201909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486161|NCT02416180|201909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486162|NCT00346892|444563/014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486163|NCT00346892|444563/014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486164|NCT00346892|444563/014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486165|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
2486166|NCT00346892|444563/014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486167|NCT00346892|444563/014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486168|NCT00296530|ADA103578|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486169|NCT00296530|ADA103578|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495741|NCT00381667|B2C104604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495742|NCT00381667|B2C104604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495743|NCT00381667|B2C104604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495744|NCT00381667|B2C104604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495745|NCT03196960||Scoring Sheet|https://docs.google.com/document/d/1pqYbMe4S-W-vgYRHzd1d4Is7s6ZbMt_MGDlWtndRRdM/edit?usp=sharing|Mobilization Quantification Score
2495746|NCT03011385||Study Protocol|https://drive.google.com/file/d/1xGrVkCeXwUZbih7NuOujjlNJcWvQ4j6H/view?usp=sharing|The file includes the protocol for data collection and intervention sessions
2495747|NCT02446496|201529|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495748|NCT02446496|201529|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495749|NCT02446496|201529|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495750|NCT02446496|201529|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495751|NCT02446496|201529|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495752|NCT02446496|201529|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488163|NCT00871000|111815|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488164|NCT00871000|111815|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494581|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
2494582|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
2494583|NCT02124798|200339|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494584|NCT02124798|200339|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494585|NCT02124798|200339|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488165|NCT00871000|111815|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488166|NCT00871000|111815|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488167|NCT00871000|111815|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488168|NCT00871000|111815|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488169|NCT01379937|115115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488170|NCT01379937|115115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488171|NCT01379937|115115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488172|NCT01379937|115115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488173|NCT01379937|115115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488174|NCT01379937|115115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494586|NCT02124798|200339|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494587|NCT02124798|200339|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494588|NCT02124798|200339|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494589|NCT02124798|200339|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494590|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.
2488175|NCT03755154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2488176|NCT03755154||Study Protocol|https://clinicaltrials.servier.com/|
2488177|NCT03755154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2488178|NCT03755154||Informed Consent Form|https://clinicaltrials.servier.com/|
2488179|NCT03755154||Clinical Study Report|https://clinicaltrials.servier.com/|
2494591|NCT00000530||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rts/|
2494592|NCT00000530||Study Forms|http://biolincc.nhlbi.nih.gov/studies/rts/|
2494593|NCT00866294|112810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494594|NCT00866294|112810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488180|NCT03755154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2488181|NCT01313676|113782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488182|NCT01313676|113782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488183|NCT01313676|113782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488184|NCT01313676|113782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494595|NCT00866294|112810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494596|NCT00866294|112810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494597|NCT00866294|112810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494598|NCT04552236||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/|
2494599|NCT01097616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-028&kw=4305-028&tab=access|
2494600|NCT00404768||Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494601|NCT00404768||Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494602|NCT00404768||Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494603|NCT00404768||Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494604|NCT00404768||Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494605|NCT00404768||Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494606|NCT00404768||Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494607|NCT03246035|CODIM-MBM-17-052|Study Protocol|http://www.ladydavis.ca/en/jonathanafilalo|Pilot study protocol
2494608|NCT03246035|CODIM-MBM-17-052|Informed Consent Form|http://www.ladydavis.ca/en/jonathanafilalo|Patient consent Caregiver consent French and English available
2494609|NCT01614769||CSR Snyposis Link|http://www.merck.com/clinical-trials/study.html?id=0000-253&kw=0000-253&tab=access|
2494610|NCT02345161|116853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494611|NCT02345161|116853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494612|NCT02345161|116853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494613|NCT02345161|116853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494614|NCT02345161|116853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494615|NCT02345161|116853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494616|NCT02345161|116853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494617|NCT00875784|103629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494618|NCT00875784|103629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494619|NCT00875784|103629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494620|NCT00875784|103629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494621|NCT00875784|103629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494622|NCT00875784|103629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494623|NCT00875784|103629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494624|NCT01147731|111681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488185|NCT01313676|113782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488186|NCT01313676|113782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494625|NCT01147731|111681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494626|NCT01147731|111681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494627|NCT01147731|111681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492825|NCT00227422|102394|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492826|NCT00227422|102394|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494628|NCT01147731|111681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494629|NCT01147731|111681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494630|NCT01147731|111681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494631|NCT01299597|109652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494632|NCT01299597|109652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494633|NCT01299597|109652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494634|NCT01299597|109652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494635|NCT01299597|109652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494636|NCT01299597|109652|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494637|NCT01299597|109652|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494638|NCT03102775||final report (Norwegian)|https://skriftserien.hioa.no/index.php/skriftserien/article/view/649|
2494639|NCT00828867|111341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494640|NCT00828867|111341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494641|NCT00828867|111341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494642|NCT00828867|111341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494643|NCT00828867|111341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494644|NCT00828867|111341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494645|NCT00828867|111341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494646|NCT01165203|112673|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494647|NCT01165203|112673|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494648|NCT01165203|112673|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494649|NCT01165203|112673|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494650|NCT01165203|112673|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494651|NCT01165203|112673|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494652|NCT01165203|112673|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494653|NCT06011005|MBRU IRB-2022-174|Study Protocol|http://www.mbru.ac.ae|
2494654|NCT01254604||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=2452-002&kw=2452-002&tab=access|
2494655|NCT01702363|115361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494656|NCT01702363|115361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494657|NCT01702363|115361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494658|NCT01702363|115361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486170|NCT00296530|ADA103578|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486171|NCT00296530|ADA103578|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486172|NCT00296530|ADA103578|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486173|NCT00296530|ADA103578|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486174|NCT00296530|ADA103578|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486175|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.
2486176|NCT00000516||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/solvd/|
2486177|NCT00000516||Study Forms|http://biolincc.nhlbi.nih.gov/studies/solvd/|
2486178|NCT00000516||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/solvd/|
2486179|NCT01706263|114551|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486180|NCT01706263|114551|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486181|NCT01706263|114551|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486182|NCT01706263|114551|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486183|NCT01706263|114551|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486184|NCT01706263|114551|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486185|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
2492827|NCT00227422|102394|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492828|NCT00227422|102394|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492829|NCT00227422|102394|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492830|NCT04503434||Informed Consent Form|https://enquesta.clinic.cat/index.php/admin/survey/sa/view/surveyid/818692|
2492831|NCT00475436|AC4106889|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492832|NCT00475436|AC4106889|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492833|NCT00475436|AC4106889|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492834|NCT00475436|AC4106889|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492835|NCT00475436|AC4106889|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492836|NCT00475436|AC4106889|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492837|NCT00475436|AC4106889|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492838|NCT00733577|111829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492839|NCT00733577|111829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492840|NCT00733577|111829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492841|NCT00733577|111829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492842|NCT00733577|111829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492843|NCT00733577|111829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492844|NCT00733577|111829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492845|NCT00733551|MOT109681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494659|NCT01702363|115361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494660|NCT01702363|115361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494661|NCT01702363|115361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494662|NCT03731416||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27283920|
2488187|NCT01313676|113782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488188|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.
2492846|NCT00733551|MOT109681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492847|NCT00733551|MOT109681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492848|NCT00733551|MOT109681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492849|NCT00733551|MOT109681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492850|NCT00733551|MOT109681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492851|NCT00352963|217744/097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492852|NCT00352963|217744/097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492853|NCT00352963|217744/097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492854|NCT00352963|217744/097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492855|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
2492856|NCT00352963|217744/097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492857|NCT06200480|NorHead|Study Protocol|https://www.ntnu.no/norhead/om|English Study protocol available by request to the Norwegian Centre of Headache Research (NorHead)
2492858|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)
2492859|NCT00603278|FFA109685|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492860|NCT00603278|FFA109685|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492861|NCT00603278|FFA109685|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492862|NCT00603278|FFA109685|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492863|NCT00603278|FFA109685|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492864|NCT00603278|FFA109685|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492865|NCT00603278|FFA109685|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492866|NCT00092365||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492867|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
2492868|NCT00938041|393229/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492869|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
2492870|NCT00938041|393229/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492871|NCT00938041|393229/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492872|NCT00938041|393229/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492873|NCT00938041|393229/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492874|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
2492875|NCT02033668|116891|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486186|NCT00363857|101468/249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486187|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
2486188|NCT00363857|101468/249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486189|NCT00363857|101468/249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486190|NCT00363857|101468/249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492876|NCT02033668|116891|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492877|NCT02033668|116891|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492878|NCT02033668|116891|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486191|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
2488189|NCT00000603||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coblt/|
2488190|NCT00000603||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coblt/|
2488191|NCT00000603||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coblt/|
2488192|NCT00202852||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488193|NCT02233088|PMC6589338|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/30234352|A manuscript summarizing the development of the intervention.
2488194|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.
2488195|NCT01934231|117150|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488196|NCT01934231|117150|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488197|NCT01934231|117150|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488198|NCT01934231|117150|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488199|NCT01934231|117150|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488200|NCT01934231|117150|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488201|NCT01934231|117150|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488202|NCT01362530||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-208&kw=0869-208&tab=access|
2488203|NCT04292496||Study Protocol|https://doi.org/10.1007/s00464-023-10025-w|
2488204|NCT01101555|113299|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492879|NCT02033668|116891|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492880|NCT02033668|116891|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492881|NCT02033668|116891|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492882|NCT00356564|106744|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492883|NCT00356564|106744|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486192|NCT00363857|101468/249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486193|NCT01873339|115678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486194|NCT01873339|115678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486195|NCT01873339|115678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486196|NCT01873339|115678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486197|NCT01873339|115678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486198|NCT01873339|115678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488205|NCT01101555|113299|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488206|NCT01101555|113299|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488207|NCT01101555|113299|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488208|NCT01101555|113299|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488209|NCT01101555|113299|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488210|NCT01101555|113299|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488211|NCT01316900|113360|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488212|NCT01316900|113360|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488213|NCT01316900|113360|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488214|NCT01316900|113360|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488215|NCT01316900|113360|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488216|NCT01316900|113360|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488217|NCT01316900|113360|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488218|NCT02100644|200776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488219|NCT02100644|200776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488220|NCT02100644|200776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488221|NCT02100644|200776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488222|NCT02100644|200776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488223|NCT00289900||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-024&kw=0524B-024&tab=access|
2488224|NCT02842671||Study Protocol|http://irb.psu.edu|
2488225|NCT02842671||Informed Consent Form|http://irb.psu.edu|for participants
2488226|NCT02842671||Accommodation Survey|http://irb.psu.edu|
2488227|NCT02842671||Patient Satisfaction Survey|http://irb.psu.edu|
2488228|NCT02842671||Medical Student Survey|http://irb.psu.edu|
2488229|NCT02842671||Summary Explanation of Research|http://irb.psu.edu|for medical students
2488230|NCT05600517|10.1016/j.ebiom.2017.11.019|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832611/|
2488231|NCT00970710||Study Protocol|http://bmcpediatr.biomedcentral.com/articles/10.1186/1471-2431-12-93|
2488232|NCT00970710||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=mustila+taina+vacopp|
2488233|NCT01703221||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-020&kw=3102-020&tab=access|
2488234|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
2488235|NCT00078195|CASALE ITN019AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
2488236|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
2488237|NCT00552279|109179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488238|NCT00552279|109179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488239|NCT00552279|109179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488240|NCT00552279|109179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488241|NCT00552279|109179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488242|NCT00552279|109179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488243|NCT00552279|109179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488244|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."
2488245|NCT02477046||Statistical Analysis Plan|https://idmod.sharepoint.com/projects/_layouts/15/guestaccess.aspx?guestaccesstoken=3%2bxJO%2bcBwXx6PfMuzCQmu8ESB0X7mhLPtowTTLaYTmY%3d&docid=02ab39752ccb14c10bdfd61c0a731e6ff&rev=1|
2488246|NCT00480025|109493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488247|NCT00480025|109493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488248|NCT00480025|109493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488249|NCT00480025|109493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494663|NCT00933335|393229/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488250|NCT00480025|109493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494664|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
2492884|NCT00356564|106744|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494665|NCT00933335|393229/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494666|NCT00933335|393229/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494667|NCT00933335|393229/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494668|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
2494669|NCT00933335|393229/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494670|NCT01323673|115054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494671|NCT01323673|115054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494672|NCT01323673|115054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494673|NCT01323673|115054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492885|NCT00356564|106744|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492886|NCT00356564|106744|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492887|NCT00356564|106744|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492888|NCT01031186|113324|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492889|NCT01031186|113324|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492890|NCT01031186|113324|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492891|NCT01031186|113324|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492892|NCT01031186|113324|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486199|NCT01873339|115678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486200|NCT00224484|208141/040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486201|NCT00224484|208141/040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486202|NCT00224484|208141/040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486203|NCT00224484|208141/040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486204|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
2486205|NCT00224484|208141/040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488251|NCT00480025|109493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488252|NCT00480025|109493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488253|NCT06694064||Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/36464977/|
2488254|NCT00434811|SDY1178|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study ID is SDY1178.
2488255|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.
2488256|NCT03495635|osf.io/8ukfv|Individual Participant Data Set|https://osf.io/|
2488257|NCT00979407|113535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488258|NCT00979407|113535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488259|NCT00979407|113535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488260|NCT00979407|113535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488261|NCT00979407|113535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488262|NCT00979407|113535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488263|NCT01266980|113970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488264|NCT01266980|113970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488265|NCT01266980|113970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488266|NCT01266980|113970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488267|NCT01266980|113970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488268|NCT01266980|113970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488269|NCT01266980|113970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488270|NCT02592655||Primary Outcome Ultrasound Images|https://doi.org/10.5281/zenodo.236263|NCT02592655 Primary Outcome Tourniquet Study
2492893|NCT01031186|113324|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492894|NCT01031186|113324|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492895|NCT02214017|doi: 10.1177/1357633X15608984|publication|https://www.ncbi.nlm.nih.gov/pubmed/26468213|
2492896|NCT00434577|108494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492897|NCT00434577|108494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492898|NCT00434577|108494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492899|NCT00434577|108494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492900|NCT00434577|108494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492901|NCT00434577|108494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492902|NCT00434577|108494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488271|NCT02592655||Individual Participant Data Set|https://doi.org/10.5281/zenodo.237773|NCT02592655 Individual level data set
2488272|NCT02592655||Informed Consent Form|https://doi.org/10.5281/zenodo.245150|Informed consent form containing description of study and procedures.
2488273|NCT02074839||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2488274|NCT02074839||Study Protocol|https://clinicaltrials.servier.com/|
2488275|NCT02074839||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2488276|NCT02074839||Informed Consent Form|https://clinicaltrials.servier.com/|
2488277|NCT02074839||Clinical Study Report|https://clinicaltrials.servier.com/|
2488278|NCT02074839||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2488279|NCT00911157|111436|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488280|NCT00911157|111436|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488281|NCT00911157|111436|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488282|NCT00298155||Paper with attached protocol and outcomes|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887479/|
2488283|NCT02988076|CNSR012 Protocol|Study Protocol|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of the protocol
2488284|NCT02988076|CNSR012 ICD|Informed Consent Form|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of ICD
2488285|NCT06791044||Study Protocol|https://eka-hosp.gr/|
2488286|NCT00459550|106006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488287|NCT00459550|106006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486206|NCT01098539|114130|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486207|NCT01098539|114130|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486208|NCT01098539|114130|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486209|NCT01098539|114130|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486210|NCT01098539|114130|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486211|NCT01098539|114130|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486212|NCT01098539|114130|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486213|NCT00396630|106260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486214|NCT00396630|106260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486215|NCT00396630|106260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486216|NCT00396630|106260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486217|NCT00396630|106260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490327|NCT01323959|113060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490328|NCT01323959|113060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490329|NCT01323959|113060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494674|NCT01323673|115054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494675|NCT01323673|115054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494676|NCT01323673|115054|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494677|NCT00169494|580299/012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494678|NCT00169494|580299/012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494679|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
2494680|NCT00169494|580299/012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494681|NCT00169494|580299/012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494682|NCT00169494|580299/012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494683|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.
2494684|NCT06253286||Study Protocol|https://drive.google.com/file/d/1edivKccFOAyt3_A6aNnNROe7JQnRmp4C/view?usp=sharing|
2494685|NCT06253286||Informed Consent Form|https://drive.google.com/file/d/1gA2nThyz6di3bSZKJQ7aQ_Usy1_wpOrR/view?usp=sharing|
2494686|NCT06527274||Study Protocol|https://nagano.umontreal.ca/login|Protocol and other documentation available upon request to the principal investigator email
2494687|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.
2494688|NCT00000567||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/hifi/|
2494689|NCT00000567||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hifi/|
2494690|NCT00000567||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hifi/|
2494691|NCT00726323|MET111644|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494692|NCT00726323|MET111644|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494693|NCT00726323|MET111644|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494694|NCT00726323|MET111644|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494695|NCT00726323|MET111644|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494696|NCT00726323|MET111644|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494697|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.
2494698|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
2494699|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
2494700|NCT01640990|115387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494701|NCT01640990|115387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494702|NCT01640990|115387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494703|NCT01640990|115387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494704|NCT01640990|115387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494705|NCT01640990|115387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494706|NCT01640990|115387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494707|NCT00139334|103992|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494708|NCT00139334|103992|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494709|NCT00139334|103992|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494710|NCT00139334|103992|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492903|NCT01697592||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=3102-015&kw=3102-015&tab=access|
2492904|NCT03037814|26161601|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/26161601|
2492905|NCT03037814|19953810|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/19953810|
2492906|NCT03037814|12542617|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/12542617|
2492907|NCT01772147|116136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492908|NCT01772147|116136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492909|NCT01772147|116136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492910|NCT01772147|116136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492911|NCT01772147|116136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492912|NCT01772147|116136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492913|NCT01772147|116136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486218|NCT00396630|106260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486219|NCT00396630|106260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486220|NCT00139932||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2486221|NCT02724826||Clinical Study Report|http://resolver.ebscohost.com/openurl?sid=Entrez%3aPubMed&id=pmid%3a18090079&site=ftf-live|
2486222|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.
2486223|NCT00000555||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/wave/|
2486224|NCT00000555||Study Forms|http://biolincc.nhlbi.nih.gov/studies/wave/|
2486225|NCT00000555||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/wave/|
2486226|NCT00108082|COR100216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486227|NCT00108082|COR100216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486228|NCT00108082|COR100216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486229|NCT00108082|COR100216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486230|NCT00108082|COR100216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486231|NCT00108082|COR100216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486232|NCT00108082|COR100216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486233|NCT00743860|LPL112498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486234|NCT00743860|LPL112498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486235|NCT00743860|LPL112498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486236|NCT00743860|LPL112498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486237|NCT00743860|LPL112498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486238|NCT00743860|LPL112498|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486239|NCT00743860|LPL112498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486240|NCT04056663|CONNECARE|Framework|http://www.connecare.eu|The ambition of the CONNECARE consortium is to co-design, develop, deploy, and evaluate a novel smart, adaptive integrated care system for chronic care management
2486241|NCT00476307|110221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486242|NCT00476307|110221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486243|NCT00476307|110221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486244|NCT00476307|110221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486245|NCT00476307|110221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486246|NCT00476307|110221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486247|NCT00476307|110221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486248|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.
2486249|NCT00725764|MET111646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486250|NCT00725764|MET111646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486251|NCT00725764|MET111646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486252|NCT00725764|MET111646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486253|NCT00725764|MET111646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486254|NCT00725764|MET111646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486255|NCT00725764|MET111646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486256|NCT00489099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488288|NCT00459550|106006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494711|NCT00139334|103992|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488289|NCT00459550|106006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494712|NCT00139334|103992|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488290|NCT00459550|106006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488291|NCT00459550|106006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494713|NCT00441441|SFA106484|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494714|NCT00441441|SFA106484|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494715|NCT00441441|SFA106484|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494716|NCT00441441|SFA106484|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494717|NCT00441441|SFA106484|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488292|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.
2488293|NCT00332566|106602|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488294|NCT00332566|106602|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488295|NCT00332566|106602|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488296|NCT00332566|106602|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488297|NCT00332566|106602|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488298|NCT00332566|106602|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488299|NCT01916226|200165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488300|NCT01916226|200165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488301|NCT01916226|200165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488302|NCT01916226|200165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488303|NCT01916226|200165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488304|NCT01916226|200165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488305|NCT01916226|200165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490330|NCT00043901|LAM40097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490331|NCT00043901|LAM40097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490332|NCT00043901|LAM40097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490333|NCT00043901|LAM40097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490334|NCT00043901|LAM40097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490335|NCT00043901|LAM40097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490336|NCT00043901|LAM40097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490337|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.
2490338|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.
2494718|NCT00441441|SFA106484|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494719|NCT00441441|SFA106484|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494720|NCT03167580||Study Protocol|https://sites.google.com/view/relaxtrial/study-details-and-documents/protocol|
2486257|NCT06899438||Clinical Study Report|https://tez.yok.gov.tr/UlusalTezMerkezi/tezDetay.jsp?id=ojJkM_gxQRaH4Sn9fMdQWw&no=8WIZbpBlZOGWvkUUwksxFg|
2486258|NCT00197080|101468/205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486259|NCT00197080|101468/205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486260|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
2486261|NCT00197080|101468/205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486262|NCT00197080|101468/205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486263|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
2486264|NCT00197080|101468/205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486265|NCT01077505|107032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486266|NCT01077505|107032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486267|NCT01077505|107032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486268|NCT01077505|107032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486269|NCT01077505|107032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486270|NCT01077505|107032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486271|NCT01077505|107032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486272|NCT01956487|116371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488306|NCT04164186|NSCLC Radiomics Interobserver|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics-Interobserver1|
2488307|NCT04164186|NSCLC Radiomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics|
2488308|NCT04164186|NSCLC Radiogenomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC+Radiogenomics|
2488309|NCT01817777|116086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488310|NCT01817777|116086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488311|NCT01817777|116086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488312|NCT01817777|116086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488313|NCT01817777|116086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488337|NCT02743221||Clinical Study Report|https://clinicaltrials.servier.com/|
2488338|NCT02743221||study-level clinical trial data|https://clinicaltrials.servier.com/|
2488339|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.
2488340|NCT01706315|116778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488341|NCT01706315|116778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488342|NCT01706315|116778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488343|NCT01706315|116778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488344|NCT01706315|116778|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488345|NCT01706315|116778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488346|NCT01706315|116778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488347|NCT06250257||Individual Participant Data Set|https://kf.kobotoolbox.org/#/forms/aSWyWhEb2TmCqshx54qTW7|
2488348|NCT01353729|114346|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488349|NCT01353729|114346|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488350|NCT01353729|114346|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488351|NCT01353729|114346|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492914|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
2492915|NCT00684203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04772&kw=P04772&tab=access|
2492916|NCT00522678|HZA102928|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492917|NCT00522678|HZA102928|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492918|NCT00522678|HZA102928|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492919|NCT00522678|HZA102928|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492920|NCT00522678|HZA102928|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492921|NCT00522678|HZA102928|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492922|NCT00522678|HZA102928|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488314|NCT01817777|116086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488315|NCT01817777|116086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488316|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
2488317|NCT03044899||Study Protocol|http://www.asos.org.za/|ASOS Protocol version 1.0
2488318|NCT00140920||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488319|NCT00680914|110808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488320|NCT00680914|110808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488321|NCT00680914|110808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488322|NCT00680914|110808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488323|NCT00680914|110808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488324|NCT00680914|110808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488325|NCT00680914|110808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488326|NCT00492544|110168|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488327|NCT00492544|110168|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488328|NCT00492544|110168|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488329|NCT00492544|110168|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488330|NCT00492544|110168|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488331|NCT00492544|110168|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488332|NCT00492544|110168|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488333|NCT02743221||Individual Participant Data Set|http://clinicaltrials.servier.com/|
2488334|NCT02743221||Study Protocol|https://clinicaltrials.servier.com/|
2488335|NCT02743221||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2488336|NCT02743221||Informed Consent Form|https://clinicaltrials.servier.com/|
2492923|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.
2492924|NCT00197119|100566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492925|NCT00197119|100566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492926|NCT00197119|100566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492927|NCT00197119|100566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492928|NCT00197119|100566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492929|NCT00383903|444563/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492930|NCT00383903|444563/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486273|NCT01956487|116371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486274|NCT01956487|116371|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486275|NCT01956487|116371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486276|NCT01956487|116371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486277|NCT01956487|116371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486278|NCT01956487|116371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486279|NCT01039454|109710|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488352|NCT01353729|114346|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488353|NCT01353729|114346|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488354|NCT01353729|114346|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488355|NCT04831229|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
2488356|NCT01051661|114000|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488357|NCT01051661|114000|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488358|NCT01051661|114000|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488359|NCT01051661|114000|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488360|NCT01051661|114000|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488361|NCT01051661|114000|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488362|NCT00323622|104297|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488363|NCT00323622|104297|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488364|NCT00323622|104297|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488365|NCT00323622|104297|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488366|NCT00323622|104297|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488367|NCT00323622|104297|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488368|NCT00157872||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488369|NCT00086515||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488370|NCT00005479||NCBI website|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724776/|
2488371|NCT00734032|LPL110118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488372|NCT00734032|LPL110118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488373|NCT00734032|LPL110118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488374|NCT00734032|LPL110118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488375|NCT00734032|LPL110118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488376|NCT00734032|LPL110118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488377|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.
2488378|NCT00005121|FHS-Cohort|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
2488379|NCT00005121|FHS-Cohort|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
2488380|NCT00005121|FHS-Cohort|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
2488381|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.
2488382|NCT00005121|FHS-OS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
2488383|NCT00005121|FHS-OS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
2488384|NCT00005121|FHS-OS|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
2488385|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.
2486280|NCT01039454|109710|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486281|NCT01039454|109710|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486282|NCT01039454|109710|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486283|NCT01039454|109710|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486284|NCT01039454|109710|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486285|NCT00129116|792014/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486286|NCT00129116|792014/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486287|NCT00129116|792014/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486288|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
2486289|NCT00129116|792014/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486290|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
2486291|NCT00749411|DB1111581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486292|NCT00749411|DB1111581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486293|NCT00749411|DB1111581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486294|NCT00749411|DB1111581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486295|NCT00749411|DB1111581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486296|NCT00749411|DB1111581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486297|NCT00749411|DB1111581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486298|NCT04828434||International Cognitive Stimulation Therapy Centre Website|http://www.ucl.ac.uk/international-cognitive-stimulation-therapy|
2486299|NCT00109486|FFR101747|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486300|NCT00109486|FFR101747|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486301|NCT00109486|FFR101747|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486302|NCT00109486|FFR101747|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486303|NCT00109486|FFR101747|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486304|NCT00109486|FFR101747|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486305|NCT00109486|FFR101747|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486306|NCT00480324|107625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486307|NCT00480324|107625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486308|NCT00480324|107625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486309|NCT00480324|107625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486310|NCT00480324|107625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486311|NCT00480324|107625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486312|NCT00480324|107625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486313|NCT02940678|10.6084/m9.figshare.4042572.v1|Study Protocol|https://dx.doi.org/10.6084/m9.figshare.4042572.v1|
2486314|NCT00792623|208133/178|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486315|NCT00792623|208133/178|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488386|NCT00005121|FHS-Gen III|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/gen3/|
2488387|NCT00005121|FHS-Gen III|Study Forms|http://biolincc.nhlbi.nih.gov/studies/gen3/|
2488388|NCT00005121|FHS-Gen III|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/gen3/|
2488389|NCT06835959|Informed consent form|Informed Consent Form|https://drive.google.com/file/d/1q09u34SVFOO2TXC7vXuDAE0MAjJfgVyA/view?usp=drive_link|
2494721|NCT00861484|111155|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494722|NCT00861484|111155|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494723|NCT00861484|111155|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494724|NCT00861484|111155|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494725|NCT00861484|111155|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494726|NCT00861484|111155|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494727|NCT00861484|111155|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494728|NCT01425190||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07614&kw=P07614&tab=access|
2494729|NCT01245426|114749|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494730|NCT01245426|114749|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494731|NCT01245426|114749|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494732|NCT01245426|114749|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494733|NCT01245426|114749|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494734|NCT01245426|114749|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494735|NCT01245426|114749|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494736|NCT00606697|NKI110334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494737|NCT00606697|NKI110334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494738|NCT00606697|NKI110334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494739|NCT00606697|NKI110334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486316|NCT00792623|208133/178|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486317|NCT00792623|208133/178|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486318|NCT00792623|208133/178|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486319|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
2486320|NCT01797926|116799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486321|NCT01797926|116799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486322|NCT01797926|116799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486323|NCT01797926|116799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486324|NCT01797926|116799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486325|NCT01797926|116799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486326|NCT01797926|116799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486327|NCT06290219||Study Protocol|https://www.vghtc.gov.tw/|Study Data/Document can be requested from the PI.
2486328|NCT02369120||Study Protocol|http://www.biomedcentral.com/1472-6947/15/97|
2494740|NCT00606697|NKI110334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494741|NCT00606697|NKI110334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486329|NCT01043926||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-017&kw=4305-017&tab=access|
2486330|NCT00240617|TRX103635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486331|NCT00240617|TRX103635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486332|NCT00240617|TRX103635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486333|NCT00240617|TRX103635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486334|NCT00240617|TRX103635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486335|NCT00240617|TRX103635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486336|NCT00240617|TRX103635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486337|NCT00964106|112684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486338|NCT00964106|112684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486339|NCT00964106|112684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486340|NCT00964106|112684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486341|NCT00964106|112684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486342|NCT00964106|112684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486343|NCT00964106|112684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486344|NCT02682147|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
2486345|NCT00784134|Data repository-VISTA|Data repository-VISTA|http://vista.gla.ac.uk|when available
2486346|NCT00784134||Study Protocol|http://vista.gla.ac.uk|when available
2486347|NCT00784134||Statistical Analysis Plan|http://vista.gla.ac.uk|when available
2486348|NCT01466322|114919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486349|NCT01466322|114919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486350|NCT01466322|114919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488390|NCT01999530||Publication|https://www.ncbi.nlm.nih.gov/pubmed/28233334|
2488391|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
2488392|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
2488393|NCT02989857||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2488394|NCT02989857||Study Protocol|https://clinicaltrials.servier.com/|
2488395|NCT02989857||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2488396|NCT02989857||Informed Consent Form|https://clinicaltrials.servier.com/|
2488397|NCT02989857||Clinical Study Report|https://clinicaltrials.servier.com/|
2488398|NCT02989857||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2488399|NCT01702298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-312&kw=0431D-312&tab=access|
2488400|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
2488401|NCT00140686|102247/036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488402|NCT00140686|102247/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488403|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
2488404|NCT00140686|102247/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488405|NCT00140686|102247/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488406|NCT00140686|102247/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492931|NCT00383903|444563/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486351|NCT01466322|114919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486352|NCT01466322|114919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486353|NCT01466322|114919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486354|NCT01466322|114919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486355|NCT02502734|107112|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488407|NCT00317122|759346/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488408|NCT00317122|759346/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488409|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
2486356|NCT02502734|107112|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486357|NCT02502734|107112|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486358|NCT02502734|107112|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492932|NCT00383903|444563/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492933|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
2492934|NCT00383903|444563/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492935|NCT02991781|neurofeedback-auth|Individual Participant Data Set|http://ckan.smokefreebrain.eu/|
2492936|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."
2492937|NCT04018547||Individual Participant Data Set|http://www.oxitone.com|De-identified data for primary and secondary outcome measures
2492938|NCT03116672|UABC|Clinical Study Report|http://www.uabc.mx|Clinical trial that evaluate drug and placebo
2492939|NCT03116672|protocol guide|Individual Participant Data Set|http://www.uabc.mx|Clinical Guide
2492940|NCT03013725||Study Protocol|http://husk.b.uib.no/prototest/|Protocol
2492941|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.
2492942|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.
2486359|NCT02502734|107112|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486360|NCT02502734|107112|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492943|NCT00005278|REDS-HTLV|Study Forms|http://biolincc.nhlbi.nih.gov/studies/reds/|
2492944|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.
2492945|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
2492946|NCT00118703|FFR30007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492947|NCT00118703|FFR30007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492948|NCT00118703|FFR30007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492949|NCT00118703|FFR30007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492950|NCT00118703|FFR30007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492951|NCT00118703|FFR30007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492952|NCT00118703|FFR30007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492953|NCT06244693|aparral|Individual Participant Data Set|http://www.redcap.med.uchile.cl|Data registry online system provided by sponsor
2492954|NCT00064428|103413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492955|NCT00064428|103413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492956|NCT00064428|103413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492957|NCT00064428|103413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492958|NCT00064428|103413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492959|NCT00064428|103413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492960|NCT00064428|103413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492961|NCT00591409||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2492962|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.
2494742|NCT00606697|NKI110334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492963|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.
2492964|NCT00038961|103414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492965|NCT00038961|103414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492966|NCT00038961|103414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492967|NCT00038961|103414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492968|NCT00038961|103414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492969|NCT00038961|103414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492970|NCT00721812|111406|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492971|NCT00721812|111406|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492972|NCT00721812|111406|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492973|NCT00721812|111406|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492974|NCT00721812|111406|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492975|NCT00721812|111406|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492976|NCT00721812|111406|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492977|NCT00372255|106252|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492978|NCT00372255|106252|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492979|NCT00372255|106252|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488410|NCT00317122|759346/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492980|NCT00372255|106252|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492981|NCT00372255|106252|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492982|NCT00372255|106252|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492983|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.
2492984|NCT00005541||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/heirs/|
2492985|NCT00005541||Study Forms|http://biolincc.nhlbi.nih.gov/studies/heirs/|
2492986|NCT00005541||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/heirs/|
2492987|NCT01274559||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0524A-133&kw=0524A-133&tab=access|
2492988|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 \[CIP\_PhD Rampidis Georgios\_1.1\]"
2492989|NCT04882748||Individual Participant Data Set|https://www.frontiersin.org/articles/10.3389/fnbot.2021.715632/full#supplementary-material|
2492990|NCT02348372|115385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492991|NCT02348372|115385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492992|NCT02348372|115385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492993|NCT02348372|115385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492994|NCT02348372|115385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492995|NCT02348372|115385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492996|NCT02348372|115385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492997|NCT01138098|113954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492998|NCT01138098|113954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2492999|NCT01138098|113954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486361|NCT02502734|107112|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486362|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
2486363|NCT01577693|115148|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486364|NCT01577693|115148|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486365|NCT01577693|115148|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486366|NCT01577693|115148|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486367|NCT01577693|115148|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486368|NCT01577693|115148|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486369|NCT01577693|115148|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486370|NCT02662231||Study Protocol|http://globalsurg.org/globalsurg-2-protocol/|GlobalSurg-II Study Protocol: available in multiple languages
2486371|NCT01294566|114422|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486372|NCT01294566|114422|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486373|NCT01294566|114422|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486374|NCT01294566|114422|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486375|NCT01294566|114422|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486376|NCT01294566|114422|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486377|NCT01294566|114422|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486378|NCT05917691||Individual Participant Data Set|https://www.facs.org/quality-programs/data-and-registries/acs-nsqip/participant-use-data-file/|
2486379|NCT01267006|114922|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486380|NCT01267006|114922|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486381|NCT01267006|114922|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486382|NCT01267006|114922|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486383|NCT01267006|114922|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486384|NCT01267006|114922|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486385|NCT01267006|114922|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486386|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
2486387|NCT00333723|49653/143|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486388|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
2486389|NCT00333723|49653/143|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486390|NCT00333723|49653/143|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486391|NCT00333723|49653/143|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486392|NCT00333723|49653/143|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486393|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
2486394|NCT00296491|ADA103575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486395|NCT00296491|ADA103575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486396|NCT00296491|ADA103575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486397|NCT00296491|ADA103575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486398|NCT00296491|ADA103575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493000|NCT01138098|113954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493001|NCT01138098|113954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486399|NCT00296491|ADA103575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486400|NCT00296491|ADA103575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486401|NCT01849016|Version 7.0 - 5/31/2016|Statistical Analysis Plan|http://www2.hematologie-amc.nl/nac_studie|
2486402|NCT00289757|100576 (Y11)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493002|NCT01138098|113954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493003|NCT00144846|SB030002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493004|NCT00144846|SB030002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493005|NCT00144846|SB030002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493006|NCT00144846|SB030002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493007|NCT00144846|SB030002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493008|NCT00144846|SB030002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493009|NCT00144846|SB030002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493010|NCT05907317||Study Protocol|https://www.rigshospitalet.dk/english/departments/juliane-marie-centre/department-of-neonatology/research/safeboosc-iiiv/Pages/protocol.aspx|
2493011|NCT00719043|110624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493012|NCT00719043|110624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486403|NCT00289757|100576 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486404|NCT00289757|100576 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486405|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
2486406|NCT00289757|100576 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486407|NCT00289757|100576 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486408|NCT00048204|NKD20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486409|NCT00048204|NKD20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486410|NCT00048204|NKD20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486411|NCT00048204|NKD20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486412|NCT00048204|NKD20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486413|NCT00048204|NKD20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486414|NCT00048204|NKD20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486415|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
2486416|NCT03182582||Study Protocol|https://eprotocol.stanford.edu/|
2486417|NCT00158756|104021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486418|NCT00158756|104021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486419|NCT00158756|104021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486420|NCT00158756|104021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486421|NCT00158756|104021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493013|NCT00719043|110624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493014|NCT00719043|110624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486422|NCT00158756|104021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486423|NCT02119286|200110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486424|NCT02119286|200110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486425|NCT02119286|200110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486426|NCT02119286|200110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486427|NCT02119286|200110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486428|NCT02119286|200110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486429|NCT02119286|200110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486430|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"
2486431|NCT02006537|117023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486432|NCT02006537|117023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486433|NCT02006537|117023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486434|NCT02006537|117023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486435|NCT02006537|117023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486436|NCT02006537|117023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486437|NCT02006537|117023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486438|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|
2486439|NCT00144911|SCO40043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486440|NCT00144911|SCO40043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486441|NCT00144911|SCO40043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486442|NCT00144911|SCO40043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486443|NCT00144911|SCO40043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486444|NCT00144911|SCO40043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486445|NCT00144911|SCO40043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486446|NCT00306943|104745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486447|NCT00306943|104745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486448|NCT00306943|104745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486449|NCT00306943|104745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486450|NCT00306943|104745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486451|NCT00316147|104005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486452|NCT00316147|104005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486453|NCT00316147|104005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486454|NCT00316147|104005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486455|NCT00316147|104005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486456|NCT00316147|104005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490339|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.
2486457|NCT00929331|110586|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486458|NCT00929331|110586|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486459|NCT00929331|110586|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486460|NCT00929331|110586|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486461|NCT00929331|110586|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486462|NCT00929331|110586|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486463|NCT00929331|110586|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486464|NCT03324321||Funder|http://dunhillmedical.org.uk/|Dunhill RTF Grant (RTF97/0117)
2486465|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.
2486466|NCT03762486||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/citmatch|
2486467|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.
2486468|NCT00000476||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dig/|
2486469|NCT00000476||Study Forms|http://biolincc.nhlbi.nih.gov/studies/dig/|
2486470|NCT00069836|712753/009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486471|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
2486472|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
2486473|NCT00069836|712753/009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486474|NCT00069836|712753/009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486475|NCT00069836|712753/009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486476|NCT00069836|712753/009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486477|NCT01195792|111850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486478|NCT01195792|111850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486479|NCT01195792|111850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486480|NCT01195792|111850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486481|NCT01195792|111850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486482|NCT01195792|111850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486483|NCT01195792|111850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486484|NCT00197288|104437|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486485|NCT00197288|104437|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486486|NCT00197288|104437|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486487|NCT00197288|104437|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486488|NCT00197288|104437|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486489|NCT00197288|104437|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486490|NCT00197288|104437|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486491|NCT00811356|111319|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486492|NCT00811356|111319|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486493|NCT00811356|111319|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486494|NCT00811356|111319|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486495|NCT00811356|111319|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494743|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.
2494744|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
2494745|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Forms|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
2494746|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.
2494747|NCT00000579|ARDSNet-LASRS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
2494748|NCT00000579|ARDSNet-LASRS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
2494749|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.
2494750|NCT00000579|ARDSNet-ALVEOLI|Study Forms|http://biolincc.nhlbi.nih.gov/studies/alveoli/|
2494751|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.
2494752|NCT00000579|ARDSNet-FACTT|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/factt/|
2494753|NCT00000579|ARDSNet-FACTT|Study Forms|http://biolincc.nhlbi.nih.gov/studies/factt/|
2494754|NCT01842620|117219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494755|NCT01842620|117219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494756|NCT01842620|117219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494757|NCT01842620|117219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494758|NCT01842620|117219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494759|NCT01842620|117219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494760|NCT01842620|117219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494761|NCT00048594||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494762|NCT00256867|AVS101946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494763|NCT00256867|AVS101946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494764|NCT00256867|AVS101946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494765|NCT00256867|AVS101946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494766|NCT00256867|AVS101946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494767|NCT00256867|AVS101946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494768|NCT00256867|AVS101946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494769|NCT01258530|115096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494770|NCT01258530|115096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494771|NCT01258530|115096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494772|NCT01258530|115096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494773|NCT01258530|115096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486496|NCT00811356|111319|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486497|NCT00811356|111319|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486498|NCT00307034|105539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486499|NCT00307034|105539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486500|NCT00307034|105539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486501|NCT00307034|105539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486502|NCT00307034|105539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486503|NCT00307034|105539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486504|NCT03274882||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2494774|NCT01258530|115096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494775|NCT01258530|115096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494776|NCT06459622||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/29337030/|
2486505|NCT03274882||Study Protocol|https://clinicaltrials.servier.com/|
2486506|NCT03274882||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2486507|NCT03274882||Informed Consent Form|https://clinicaltrials.servier.com/|
2486508|NCT03274882||Clinical Study Report|https://clinicaltrials.servier.com/|
2486509|NCT03274882||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2486510|NCT00541970|110659|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486511|NCT00541970|110659|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486512|NCT00541970|110659|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486513|NCT00541970|110659|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486514|NCT00541970|110659|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486515|NCT00541970|110659|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486516|NCT00541970|110659|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486517|NCT00273039|NKF100110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486518|NCT00273039|NKF100110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486519|NCT00273039|NKF100110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486520|NCT00273039|NKF100110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486521|NCT00273039|NKF100110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486522|NCT00273039|NKF100110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486523|NCT00273039|NKF100110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486524|NCT00169481|103488|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486525|NCT00169481|103488|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486526|NCT00169481|103488|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486527|NCT00169481|103488|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486528|NCT00169481|103488|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486529|NCT01874067|35110|Clinical Study Report|http://usir.salford.ac.uk/35110/|Conference Abstract: Hammond, A, Prior, Y, Jones, V, Dooley, M, Hough, Y and Jacklin, A 2015, 'A pre-post test pilot trial of compression gloves in early inflammatory and rheumatoid arthritis' , Rheumatology, 54 (S1) , i111-112
2486530|NCT00763438|2007-002160-10|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-002160-10/results|
2486531|NCT04838522||Breast Milk At the Dawn of New Discoveries|https://betterbeginnings.org/what-we-do/research/breast-milk/|
2486532|NCT01335997||CSR Synsopsi Link|http://www.merck.com/clinical-trials/study.html?id=0524B-143&kw=0524B-143&tab=access|
2486533|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.
2486534|NCT00548171|110804|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486535|NCT00548171|110804|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486536|NCT00548171|110804|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486537|NCT00548171|110804|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486538|NCT00548171|110804|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486539|NCT00548171|110804|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486540|NCT00548171|110804|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486541|NCT00117325|FFR30006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486542|NCT00117325|FFR30006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486543|NCT00117325|FFR30006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486544|NCT00117325|FFR30006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486545|NCT00117325|FFR30006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490340|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.
2493015|NCT00719043|110624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493016|NCT00719043|110624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493017|NCT04498988||Official study group website|https://tu-dresden.de/bereichsuebergreifendes/sfb940/|
2493018|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).
2493019|NCT01316887|113359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493020|NCT01316887|113359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493021|NCT01316887|113359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493022|NCT01316887|113359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493023|NCT01316887|113359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493024|NCT01316887|113359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493025|NCT01316887|113359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493026|NCT01006616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05575&kw=7123-019&tab=access|
2493027|NCT00197223|104438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486546|NCT00117325|FFR30006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486547|NCT00117325|FFR30006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486548|NCT02664935||Trial Website|https://www.birmingham.ac.uk/research/crctu/trials/lung-matrix/index.aspx|
2486549|NCT00871741|111761|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486550|NCT00871741|111761|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486551|NCT00871741|111761|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486552|NCT00871741|111761|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486553|NCT00871741|111761|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486554|NCT00871741|111761|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486555|NCT00871741|111761|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486556|NCT01711463|115199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486557|NCT01711463|115199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486558|NCT01711463|115199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486559|NCT01711463|115199|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486560|NCT01711463|115199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486561|NCT01711463|115199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486562|NCT01711463|115199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486563|NCT00678886|115495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490341|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.
2490342|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
2490343|NCT01471678|115707|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493028|NCT00197223|104438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486564|NCT00678886|115495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486565|NCT00678886|115495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486566|NCT00678886|115495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486567|NCT00678886|115495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486568|NCT00678886|115495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486569|NCT00678886|115495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486570|NCT00196924|580299/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486571|NCT00196924|580299/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486572|NCT00196924|580299/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486573|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.
2486574|NCT00196924|580299/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486575|NCT00196924|580299/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486576|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
2486577|NCT00883909|103094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486578|NCT00883909|103094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486579|NCT00883909|103094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486580|NCT00883909|103094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486581|NCT00883909|103094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486582|NCT00883909|103094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486583|NCT00883909|103094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486584|NCT02904824||Clinical Study Report|http://www.dynasolutions.com|CRO data base
2486585|NCT00224471|208141/042|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486586|NCT00224471|208141/042|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486587|NCT00224471|208141/042|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486588|NCT00224471|208141/042|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486589|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
2486590|NCT00224471|208141/042|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486591|NCT06989255|doi: 10.5281/zenodo.11371924|Study Protocol|https://zenodo.org/records/11371924|Study protocol including ICF
2486592|NCT06982014|lecturer|Individual Participant Data Set|https://kocaelisaglik.edu.tr/|
2486593|NCT00426361|108464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486594|NCT00426361|108464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486595|NCT00426361|108464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486596|NCT00426361|108464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486597|NCT00426361|108464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486598|NCT00426361|108464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486599|NCT00426361|108464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486600|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
2486601|NCT01590797||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-254&kw=0431-254&tab=access|
2486602|NCT02105974|200820|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490344|NCT01471678|115707|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490345|NCT01471678|115707|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490346|NCT01471678|115707|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486603|NCT02105974|200820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486604|NCT02105974|200820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486605|NCT02105974|200820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486606|NCT02105974|200820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486607|NCT02105974|200820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486608|NCT02105974|200820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486609|NCT04815889||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/35704376/|
2486610|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.
2486611|NCT00609180||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/omega/|
2486612|NCT00609180||Study Forms|http://biolincc.nhlbi.nih.gov/studies/omega/|
2486613|NCT01371812|114660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486614|NCT01371812|114660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490347|NCT01471678|115707|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490348|NCT01471678|115707|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490349|NCT01471678|115707|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490350|NCT00758836||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-046&kw=0974-046&tab=access|
2490351|NCT00109122||CSR Synopsiis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490352|NCT00963937|111035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490353|NCT00963937|111035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493029|NCT00197223|104438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493030|NCT00197223|104438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493031|NCT00197223|104438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493032|NCT00197223|104438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493033|NCT00197223|104438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493034|NCT04629443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2493035|NCT04629443||Study Protocol|https://clinicaltrials.servier.com/|
2493036|NCT04629443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2494777|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
2486615|NCT01371812|114660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486616|NCT01371812|114660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486617|NCT01371812|114660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486618|NCT01371812|114660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486619|NCT01371812|114660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486620|NCT00474266|109670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490354|NCT00963937|111035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490355|NCT00963937|111035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493037|NCT04629443||Informed Consent Form|https://clinicaltrials.servier.com/|
2493038|NCT04629443||Clinical Study Report|https://clinicaltrials.servier.com/|
2493039|NCT04629443||study-level clinical trial data|https://clinicaltrials.servier.com/|
2486621|NCT00474266|109670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486622|NCT00474266|109670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486623|NCT00474266|109670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486624|NCT00474266|109670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486625|NCT00474266|109670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486626|NCT00474266|109670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486627|NCT02152605|201211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493040|NCT01086384|106837|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493041|NCT01086384|106837|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493042|NCT01086384|106837|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486628|NCT02152605|201211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486629|NCT02152605|201211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486630|NCT02152605|201211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486631|NCT02152605|201211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486632|NCT02152605|201211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486633|NCT02152605|201211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486634|NCT02000765|115774|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486635|NCT02000765|115774|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486636|NCT02000765|115774|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486637|NCT02000765|115774|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486638|NCT02000765|115774|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486639|NCT02000765|115774|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486640|NCT02000765|115774|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486641|NCT00385008|TRX105848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486642|NCT00385008|TRX105848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486643|NCT00385008|TRX105848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486644|NCT00385008|TRX105848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486645|NCT00385008|TRX105848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486646|NCT00385008|TRX105848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486647|NCT00385008|TRX105848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486648|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
2486649|NCT00258700|103974 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486650|NCT00258700|103974 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493043|NCT01086384|106837|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486651|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
2486652|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
2493044|NCT01086384|106837|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493045|NCT01086384|106837|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486653|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
2487187|NCT00381238|AVA104617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487188|NCT00381238|AVA104617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488411|NCT00317122|759346/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488412|NCT00317122|759346/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488413|NCT02738463||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/pubmed|
2488414|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).
2488415|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
2488416|NCT07004348|PROM link|Statistical Analysis Plan|https://livenorthumbriaac-my.sharepoint.com/:w:/g/personal/frank_lai_northumbria_ac_uk/EbKJJ3cbnk5Ikr-NpppTxHoBmGuJLYpePT6qQ1ZnXA4P-w?e=ZZuX7U|
2488417|NCT07003204|msabry776@yahoo.com|Clinical Study Report|https://pmc.ncbi.nlm.nih.gov/articles/PMC8075197/|very good
2488418|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.
2488419|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.
2488420|NCT07150442||Study Protocol|https://bit.ly/45NuVGB|https://bit.ly/45NuVGB
2488421|NCT07161297||Study Protocol|https://www.humanitas-research.com/|Requests should be submitted to: ibd@humanitas.it Subject: REMI-IBD
2488422|NCT01128569|113090|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488423|NCT01128569|113090|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488424|NCT01128569|113090|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488425|NCT01128569|113090|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488426|NCT01128569|113090|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488427|NCT01128569|113090|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488428|NCT01128569|113090|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488429|NCT01495013|115317|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488430|NCT01495013|115317|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488431|NCT01495013|115317|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488432|NCT01495013|115317|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488433|NCT01495013|115317|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488434|NCT01495013|115317|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488435|NCT00445094||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488436|NCT01110057|113049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488437|NCT01110057|113049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488438|NCT01110057|113049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488439|NCT01110057|113049|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488440|NCT01110057|113049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488441|NCT01110057|113049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488442|NCT01110057|113049|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488443|NCT03150264||Study Protocol|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161575/|
2493046|NCT01086384|106837|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493047|NCT00823836|106066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493048|NCT00823836|106066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493049|NCT00823836|106066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493050|NCT00823836|106066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493051|NCT00823836|106066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493052|NCT01192776||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25536254|
2493053|NCT06254755||Individual Participant Data Set|http://competetrials@gmail.com|
2493054|NCT02075619|200561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493055|NCT02075619|200561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493056|NCT02075619|200561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493057|NCT02075619|200561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493058|NCT02075619|200561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493059|NCT02075619|200561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493060|NCT02075619|200561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493061|NCT01777334|117115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486654|NCT02549027||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-003&kw=1064-003&tab=access|
2486655|NCT01160003|113209|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486656|NCT01160003|113209|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486657|NCT01160003|113209|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486658|NCT01160003|113209|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486659|NCT01160003|113209|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486660|NCT01160003|113209|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486661|NCT01160003|113209|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486662|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.
2486663|NCT00000620||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/accord|
2486664|NCT00000620||Study Forms|http://biolincc.nhlbi.nih.gov/studies/accord|
2486665|NCT00000620||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/accord|
2486666|NCT00979641||Clinical Study Report|http://www.anticancerresearch.com|
2486667|NCT00315731|393229/027|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486668|NCT00315731|393229/027|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486669|NCT00315731|393229/027|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486670|NCT00315731|393229/027|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486671|NCT00315731|393229/027|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493062|NCT01777334|117115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486672|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
2486673|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
2486674|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"
2486675|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
2486676|NCT01887171|10.15825/1995-1191-2015-3-24|Clinical Study Report|http://journal.transpl.ru/vtio/article/view/561/488|
2486677|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|
2486678|NCT00366366|217744/075|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486679|NCT00366366|217744/075|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486680|NCT00366366|217744/075|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486681|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
2486682|NCT00366366|217744/075|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486683|NCT00366366|217744/075|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486684|NCT00323050|102547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486685|NCT00323050|102547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486686|NCT00323050|102547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486687|NCT00323050|102547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486688|NCT00323050|102547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486689|NCT00323050|102547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486690|NCT02257385|116961|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486691|NCT02257385|116961|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486692|NCT02257385|116961|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486693|NCT02257385|116961|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486694|NCT02257385|116961|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486695|NCT02257385|116961|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486696|NCT02257385|116961|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486697|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.
2494778|NCT00444509|HZA108799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486698|NCT00000474||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/paths/|
2486699|NCT00000474||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/paths/|
2486700|NCT00086593|101464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486701|NCT00086593|101464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486702|NCT00086593|101464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486703|NCT00086593|101464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486704|NCT00086593|101464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486705|NCT00086593|101464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486706|NCT01499446|FFA20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486707|NCT01499446|FFA20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486708|NCT01499446|FFA20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486709|NCT01499446|FFA20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486710|NCT01499446|FFA20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486711|NCT01499446|FFA20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486712|NCT01499446|FFA20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486713|NCT01890863|200260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486714|NCT01890863|200260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486715|NCT01890863|200260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486716|NCT01890863|200260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486717|NCT01890863|200260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486718|NCT01890863|200260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486719|NCT01890863|200260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486720|NCT02006602|201011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486721|NCT02006602|201011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486722|NCT02006602|201011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486723|NCT02006602|201011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486724|NCT02006602|201011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486725|NCT02006602|201011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486726|NCT02006602|201011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486727|NCT05088135||Clinical Study Report|https://doi.org/10.3389/fphys.2023.1215757|
2486728|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.
2486729|NCT00000591||Study Forms|http://biolincc.nhlbi.nih.gov/studies/tcd/|
2486730|NCT02872376||Study Protocol|https://sites.google.com/site/ridartstudy/|
2486731|NCT02872376||Informed Consent Form|https://sites.google.com/site/ridartstudy/|
2486732|NCT01295320|114825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486733|NCT01295320|114825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486734|NCT01295320|114825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486735|NCT01295320|114825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486736|NCT01295320|114825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486737|NCT01295320|114825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486738|NCT01295320|114825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486739|NCT00306995|102499|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486740|NCT00306995|102499|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486741|NCT00306995|102499|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486742|NCT00306995|102499|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486743|NCT00306995|102499|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486744|NCT00533312||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2486745|NCT00463697|B2C106996|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486746|NCT00463697|B2C106996|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486747|NCT00463697|B2C106996|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486748|NCT00463697|B2C106996|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486749|NCT00463697|B2C106996|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486750|NCT00463697|B2C106996|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486751|NCT00463697|B2C106996|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486752|NCT00307021|105874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486753|NCT00307021|105874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494779|NCT00444509|HZA108799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494780|NCT00444509|HZA108799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493063|NCT01777334|117115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486754|NCT00307021|105874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486755|NCT00307021|105874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486756|NCT00307021|105874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486757|NCT00307021|105874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486758|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.
2486759|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
2486760|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
2486761|NCT01332292|102942|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493064|NCT01777334|117115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493065|NCT01777334|117115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493066|NCT01777334|117115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488444|NCT00373542|RRL103660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488445|NCT00373542|RRL103660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488446|NCT00373542|RRL103660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493067|NCT01777334|117115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493068|NCT01841697||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-026&kw=3102-026&tab=access|
2488447|NCT00373542|RRL103660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488448|NCT00373542|RRL103660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488449|NCT00373542|RRL103660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488450|NCT00373542|RRL103660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488451|NCT06379828||Study Protocol|https://newborn-health-standards.org/about/project-overview/|
2488452|NCT00325143|217744/100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488453|NCT00325143|217744/100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488454|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
2488455|NCT00325143|217744/100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488456|NCT00325143|217744/100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488457|NCT00325143|217744/100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488458|NCT01073293||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-007&kw=V503-007&tab=access|
2488459|NCT01436110|115285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488460|NCT01436110|115285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493069|NCT01691547|116415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493070|NCT01691547|116415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488461|NCT01436110|115285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488462|NCT01436110|115285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488463|NCT01436110|115285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488464|NCT01436110|115285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488465|NCT01436110|115285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488466|NCT01978145|115646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488467|NCT01978145|115646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488468|NCT01978145|115646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488469|NCT01978145|115646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488470|NCT01978145|115646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488471|NCT01978145|115646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488472|NCT01978145|115646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488473|NCT00335881|106745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488474|NCT00335881|106745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488475|NCT00335881|106745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488476|NCT00335881|106745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488477|NCT00335881|106745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488478|NCT00335881|106745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486762|NCT01332292|102942|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486763|NCT01332292|102942|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486764|NCT01332292|102942|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486765|NCT01332292|102942|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486766|NCT01332292|102942|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486767|NCT01332292|102942|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493071|NCT01691547|116415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493072|NCT01691547|116415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493073|NCT01691547|116415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486768|NCT00562848|MOT107043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486769|NCT00562848|MOT107043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486770|NCT00562848|MOT107043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486771|NCT00562848|MOT107043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486772|NCT00562848|MOT107043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486773|NCT00562848|MOT107043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486774|NCT00562848|MOT107043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486775|NCT01198769|114351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486776|NCT01198769|114351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486777|NCT01198769|114351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486778|NCT01198769|114351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486779|NCT01198769|114351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486780|NCT01198769|114351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486781|NCT01198769|114351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486782|NCT00511823|NKV110483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486783|NCT00511823|NKV110483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486784|NCT00511823|NKV110483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486785|NCT00511823|NKV110483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486786|NCT00511823|NKV110483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493074|NCT01691547|116415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486787|NCT00511823|NKV110483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486788|NCT00511823|NKV110483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486789|NCT05063708||Analytic Code|http://zenodo.org|
2486790|NCT05063708||Statistical Analysis Plan|http://zenodo.org|
2486791|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.
2486792|NCT07192640||Study Protocol|https://doi.org/10.1590/acb370702|https://doi.org/10.1590/acb370702
2486793|NCT07192172|No. 1611-124-811|Study Protocol|http://cris.snuh.org|http://cris.snuh.org
2486794|NCT03718832|doi:10.7910/DVN/LZUTU0|Individual Participant Data Set|https://doi.org/10.7910/DVN/LZUTU0|
2486795|NCT03718832|doi:10.7910/DVN/LZUTU0|Analytic Code|https://doi.org/10.7910/DVN/LZUTU0|
2486796|NCT03173209|Calm Moments Cards program|intervention materials|http://www.everymomentcounts.org|Calm Moments Cards program
2486797|NCT00695305|LP2105521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486798|NCT00695305|LP2105521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486799|NCT00695305|LP2105521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486800|NCT00695305|LP2105521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486801|NCT00695305|LP2105521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486802|NCT00695305|LP2105521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486803|NCT00695305|LP2105521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486804|NCT00696423|111535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486805|NCT00696423|111535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486806|NCT00696423|111535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486807|NCT00696423|111535|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486808|NCT00696423|111535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486809|NCT00696423|111535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488479|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"
2488480|NCT06187857||Study Protocol|https://osf.io/cavkf/?view_only=cc219af15f614756b43742875b6b0b39|
2488481|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.
2488482|NCT00652743|111443|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488483|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.
2488484|NCT00652743|111443|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488485|NCT00652743|111443|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488486|NCT00652743|111443|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488487|NCT00652743|111443|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488488|NCT00730756|FFR111158|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488489|NCT00730756|FFR111158|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488490|NCT00730756|FFR111158|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488491|NCT00730756|FFR111158|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488492|NCT00730756|FFR111158|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488493|NCT00730756|FFR111158|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488494|NCT00730756|FFR111158|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488495|NCT03750019|10.5255/UKDA-SN-853370|Individual Participant Data Set|http://dx.doi.org/10.5255/UKDA-SN-853370|
2488496|NCT03750019|10.17605/OSF.IO/WYCKJ|Study Protocol|https://doi.org/10.17605/OSF.IO/WYCKJ|
2488497|NCT05173376||Study Protocol|https://osf.io/scjn6/|Protocol on the Open Science Framework (OSF)
2488498|NCT05173376||Statistical Analysis Plan|https://osf.io/scjn6/|
2488499|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.
2488500|NCT01030822|112909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488501|NCT01030822|112909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488502|NCT01030822|112909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488503|NCT01030822|112909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493075|NCT01691547|116415|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493076|NCT03034850||Study Protocol|https://drive.google.com/open?id=0B0qo2hDQpXhncWZFZkNfZXhZMjVuUGcxc0IzZll5TEtjaXdn|
2493077|NCT03034850|eudract/B-nr B37120154199|Advice Ethical Committee|https://drive.google.com/open?id=0B0qo2hDQpXhnU3AzRHY0d1NtVmlsSmx1cFhKOGtKLTVscno0|
2493078|NCT01648153|116378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493079|NCT01648153|116378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493080|NCT01648153|116378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493081|NCT01648153|116378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493082|NCT01648153|116378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493083|NCT01648153|116378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493084|NCT01648153|116378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493085|NCT01015677||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6913-004&kw=6913-004&tab=access|
2493086|NCT05394090||Individual Participant Data Set|http://www.pum.edu.pl|
2493087|NCT00749359|PCR111656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493088|NCT00749359|PCR111656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493089|NCT00749359|PCR111656|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493090|NCT00749359|PCR111656|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493091|NCT00749359|PCR111656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493092|NCT00749359|PCR111656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493093|NCT00749359|PCR111656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493094|NCT00157898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493095|NCT02446613|204509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493096|NCT02446613|204509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493097|NCT02446613|204509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493098|NCT02446613|204509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493099|NCT02446613|204509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493100|NCT02446613|204509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493101|NCT02446613|204509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493102|NCT01407276||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-009&kw=3102-009&tab=access|
2493103|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFNnVaQWlTakh5dEU|
2493104|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFazRhT1hZVm41RzA|05.01.2017 updated because of an amendment of ethnic proposal.
2493105|NCT02242643|201234|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493106|NCT02242643|201234|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493107|NCT02242643|201234|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493108|NCT02242643|201234|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493109|NCT02242643|201234|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493110|NCT02242643|201234|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493111|NCT02242643|201234|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493112|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.
2493113|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
2493114|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
2486810|NCT00696423|111535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486811|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.
2486812|NCT01557504||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-296&kw=0431A-296&tab=access|
2486813|NCT00810667|2008-001441-26|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-001441-26/results|
2486814|NCT00811967||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2486815|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.
2486816|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.
2486817|NCT03411161||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2486818|NCT03411161||Study Protocol|https://clinicaltrials.servier.com/|
2486819|NCT03411161||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2486820|NCT03411161||Informed Consent Form|https://clinicaltrials.servier.com/|
2486821|NCT03411161||Clinical Study Report|https://clinicaltrials.servier.com/|
2486822|NCT03411161||study-level clinical trial data|https://clinicaltrials.servier.com/|
2486823|NCT07097649||Clinical Study Report|https://pubmed.ncbi.nlm.nih.gov/33946001/|
2494781|NCT00444509|HZA108799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486824|NCT01847404|116480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486825|NCT01847404|116480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486826|NCT01847404|116480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486827|NCT01847404|116480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486828|NCT01847404|116480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486829|NCT01847404|116480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486830|NCT03494712||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2486831|NCT03494712||Study Protocol|https://clinicaltrials.servier.com/|
2486832|NCT03494712||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2486833|NCT03494712||Informed Consent Form|https://clinicaltrials.servier.com/|
2486834|NCT03494712||Clinical Study Report|https://clinicaltrials.servier.com/|
2486835|NCT03494712||study-level clinical trial data|https://clinicaltrials.servier.com/|
2486836|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
2486837|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
2486838|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
2486839|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
2486840|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
2486841|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
2486842|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
2494782|NCT00444509|HZA108799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486843|NCT06676878||Study Protocol|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
2486844|NCT06676878||Informed Consent Form|https://drive.google.com/file/d/1pTBiedgvBfyXRoGyx3W1kF5B8aNcpFML/view?usp=sharing|
2486845|NCT06881329|GSE290201|Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE290201|Gene Expression Omnibus repository
2486846|NCT01551771|115802|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486847|NCT01551771|115802|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486848|NCT01551771|115802|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486849|NCT01551771|115802|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486850|NCT01551771|115802|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486851|NCT01551771|115802|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486852|NCT01551771|115802|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486853|NCT01254643||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-008&kw=V503-008&tab=access|
2486854|NCT01110018|112008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486855|NCT01110018|112008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486856|NCT01110018|112008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486857|NCT01110018|112008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486858|NCT01110018|112008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486859|NCT01110018|112008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486860|NCT01110018|112008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486861|NCT02836002||Individual Participant Data Set|https://datadryad.org//resource/doi:10.5061/dryad.60h41|
2486862|NCT00661557|107408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494783|NCT00444509|HZA108799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494784|NCT00444509|HZA108799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494785|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
2494786|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
2486863|NCT00661557|107408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486864|NCT00661557|107408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486865|NCT00661557|107408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486866|NCT00661557|107408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486867|NCT00661557|107408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486868|NCT00661557|107408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486869|NCT06968286||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/39758269/|
2486870|NCT07089667||Study Protocol|https://drive.google.com/drive/folders/1QpzE6ACGieVNCGQ1nsLJHxUWtB-fUfLV?usp=sharing|
2486871|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
2486872|NCT01563042|114594|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486873|NCT01563042|114594|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486874|NCT01563042|114594|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486875|NCT01563042|114594|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486876|NCT01563042|114594|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486877|NCT01563042|114594|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486878|NCT01563042|114594|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486879|NCT00838903|112753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486880|NCT00838903|112753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486881|NCT00838903|112753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486882|NCT00838903|112753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488504|NCT01030822|112909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486883|NCT00838903|112753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486884|NCT00838903|112753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486885|NCT00838903|112753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486886|NCT00779935||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2486887|NCT00422604|AC2106956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486888|NCT00422604|AC2106956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486889|NCT00422604|AC2106956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486890|NCT00422604|AC2106956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486891|NCT00422604|AC2106956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486892|NCT00422604|AC2106956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486893|NCT00422604|AC2106956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486894|NCT00197171|100386 (EXT Y5)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486895|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
2486896|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.
2486897|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
2486898|NCT00197171|100386 (EXT Y5)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486899|NCT07111143||Health-Damaging Climate Events Highlight the Need for Interdisciplinary, Engaged Research|https://pubmed.ncbi.nlm.nih.gov/38371354/|
2486900|NCT06941233||Study Protocol|https://hjpwd.ahs.uic.edu|study protocol may be accessed by contacting the research team
2486901|NCT00226499|100388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486902|NCT00226499|100388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486903|NCT00226499|100388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486904|NCT00226499|100388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486905|NCT00226499|100388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486906|NCT00226499|100388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486907|NCT00485732|107291|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486908|NCT00485732|107291|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486909|NCT00485732|107291|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486910|NCT00485732|107291|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486911|NCT00485732|107291|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486912|NCT00485732|107291|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486913|NCT00485732|107291|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486914|NCT01894386|200587|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486915|NCT01894386|200587|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486916|NCT01894386|200587|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486917|NCT01894386|200587|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486918|NCT01894386|200587|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486919|NCT01894386|200587|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486920|NCT01894386|200587|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486921|NCT04616612||Clinical Study Report|https://www.usrds.org/annual-data-report/current-adr/|United States Renal Data System. USRDS annual data report: Epidemiology of kidney disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD. 2017.
2486922|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.
2486923|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.
2486924|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.
2486925|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.
2486926|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.
2486927|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.
2486928|NCT07111780|example study protokol|Study Protocol|https://www.nature.com/articles/s41598-024-79811-3|
2486929|NCT00471081|109375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486930|NCT00471081|109375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486931|NCT00471081|109375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486932|NCT00471081|109375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486933|NCT00471081|109375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486934|NCT00471081|109375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486935|NCT00471081|109375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486936|NCT01822639|116798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486937|NCT01822639|116798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486938|NCT01822639|116798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486939|NCT01822639|116798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486940|NCT01822639|116798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486941|NCT01822639|116798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486942|NCT01822639|116798|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486943|NCT04579848||Study Protocol|https://drive.google.com/file/d/1AKuis2zJlqhUqY4OEPyVhQPpIiuPnnhr/view?usp=sharing|
2486944|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1mB2pEgRmuMhaVM_eNnnyXdqsyev4wev5/view?usp=sharing|
2486945|NCT04579848||Informed Consent Form|https://drive.google.com/file/d/1oE_9J-5uwLpboVWEsUJL6tHn4st1ea9r/view?usp=sharing|
2486946|NCT00005235||NCBI website|http://www.ncbi.nlm.nih.gov/pubmed/8353919|
2486947|NCT06456775||Individual Participant Data Set|https://bit.ly/49RBPuQ|
2486948|NCT00133848|TOC103469|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486949|NCT00133848|TOC103469|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486950|NCT00133848|TOC103469|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486951|NCT00133848|TOC103469|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486952|NCT00133848|TOC103469|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486953|NCT00133848|TOC103469|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486954|NCT00133848|TOC103469|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486955|NCT07152041|CAMS-Ph+B-ALL|Individual Participant Data Set|https://login.imedidata.com|CAMS-Ph+ALL-2025 DATASET
2486956|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.
2486957|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
2486958|NCT01262872|114174|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486959|NCT01262872|114174|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486960|NCT01262872|114174|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486961|NCT01262872|114174|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493115|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
2493116|NCT00379769|BRL-049653/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493117|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
2493118|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
2493119|NCT00379769|BRL-049653/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493120|NCT00516139|LEP105972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486962|NCT01262872|114174|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486963|NCT01262872|114174|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486964|NCT00920439|112683|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486965|NCT00920439|112683|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486966|NCT00920439|112683|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486967|NCT00920439|112683|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486968|NCT00920439|112683|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486969|NCT00920439|112683|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493121|NCT00516139|LEP105972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486970|NCT02637206|200920|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486971|NCT02637206|200920|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486972|NCT02637206|200920|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486973|NCT02637206|200920|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486974|NCT02637206|200920|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486975|NCT02637206|200920|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486976|NCT02637206|200920|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486977|NCT06575504||Study Protocol|https://guides.lib.umich.edu/datamanagement/clinicaltrials|
2486978|NCT00996125|112022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486979|NCT00996125|112022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486980|NCT00996125|112022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486981|NCT00996125|112022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486982|NCT00996125|112022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486983|NCT00996125|112022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486984|NCT02006589|200956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486985|NCT02006589|200956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486986|NCT02006589|200956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486987|NCT02006589|200956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486988|NCT02006589|200956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486989|NCT02006589|200956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493122|NCT00516139|LEP105972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493123|NCT00516139|LEP105972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493124|NCT00516139|LEP105972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486990|NCT02006589|200956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486991|NCT01777282|116170|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486992|NCT01777282|116170|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486993|NCT01777282|116170|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486994|NCT01777282|116170|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486995|NCT01777282|116170|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486996|NCT01777282|116170|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486997|NCT00812981|111954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486998|NCT00812981|111954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2486999|NCT00812981|111954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487000|NCT00812981|111954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487001|NCT00812981|111954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487002|NCT00812981|111954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487003|NCT00812981|111954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487004|NCT01863667||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3102-027&kw=3102-027&tab=access|
2487005|NCT01154114|480848/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487006|NCT01154114|480848/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487007|NCT01154114|480848/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487008|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
2487009|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
2487010|NCT01154114|480848/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487011|NCT01154114|480848/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487012|NCT04132323||Study Protocol|https://www.venousregistry.org/index.php?f=1&id=97|
2487013|NCT00617890||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04720&kw=P04720&tab=access|
2487014|NCT00566020|SCA106052|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487015|NCT00566020|SCA106052|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487016|NCT00566020|SCA106052|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487017|NCT00566020|SCA106052|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487018|NCT02476578||Study Protocol|https://goo.gl/B6j1oF|LIMIT HEBREW PROTOCOL Version 3 (Final)
2487019|NCT05664360||Individual Participant Data Set|https://www.doi.org/10.17605/OSF.IO/TRU4N|
2487020|NCT06575127||Informed Consent Form|https://drive.google.com/file/d/1_CG_0wzCH_ZUxWXsfARsyWlcx37fOcRq/view?usp=drive_link|
2487021|NCT05497518||Study Protocol|https://tuftsmedicalcenter.box.com/s/bplcm9clgjsnnq23zcwwwuze6up368q4|
2487022|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
2487023|NCT00291876|100571 (M138)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487024|NCT00291876|100571 (M138)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487025|NCT00291876|100571 (M138)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487026|NCT00291876|100571 (M138)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487027|NCT00291876|100571 (M138)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487028|NCT00116818|FFR20002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493125|NCT00516139|LEP105972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493126|NCT00516139|LEP105972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488505|NCT01030822|112909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488506|NCT01030822|112909|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488507|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.
2488508|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.
2488509|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.
2488510|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.
2488511|NCT00688467||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05363&kw=P05363&tab=access|
2488512|NCT00538057|HZA105871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488513|NCT00538057|HZA105871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488514|NCT00538057|HZA105871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488515|NCT00538057|HZA105871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488516|NCT00538057|HZA105871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488517|NCT00538057|HZA105871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488518|NCT00538057|HZA105871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493127|NCT00092183||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493128|NCT01245140|117221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493129|NCT01245140|117221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488519|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
2488520|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
2488521|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
2488522|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
2488523|NCT00421148||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493130|NCT01245140|117221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493131|NCT01245140|117221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488524|NCT00363311|AVO105948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488525|NCT00363311|AVO105948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488526|NCT00363311|AVO105948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488527|NCT00363311|AVO105948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488528|NCT00363311|AVO105948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488529|NCT00363311|AVO105948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488530|NCT00363311|AVO105948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488531|NCT03910075||Study Protocol|http://www.nihstrokenet.org/i-acquire/resources|
2488532|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
2494787|NCT00380211|IDB-200-001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494788|NCT00380211|IDB-200-001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487029|NCT00116818|FFR20002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487030|NCT00116818|FFR20002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487031|NCT00116818|FFR20002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487032|NCT00116818|FFR20002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487033|NCT00116818|FFR20002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487034|NCT00116818|FFR20002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487035|NCT00839527|112757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487036|NCT00839527|112757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487037|NCT00839527|112757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487038|NCT00839527|112757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487039|NCT00839527|112757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487040|NCT00839527|112757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487041|NCT00839527|112757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487042|NCT04068129||Individual Participant Data Set|http://www.abcd-vision.org/references/index.html|
2487043|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
2487044|NCT00115492|SCO100250|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487045|NCT00115492|SCO100250|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487046|NCT00115492|SCO100250|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487047|NCT00115492|SCO100250|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487048|NCT00115492|SCO100250|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487049|NCT00115492|SCO100250|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487050|NCT00115492|SCO100250|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487051|NCT06968169||Study Protocol|https://doi.org/10.17605/OSF.IO/AJDZS|
2487052|NCT00347139|B2C106093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487053|NCT00347139|B2C106093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487054|NCT00347139|B2C106093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487055|NCT00347139|B2C106093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487056|NCT00347139|B2C106093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487057|NCT00347139|B2C106093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487058|NCT00347139|B2C106093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487059|NCT01521390|115487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487060|NCT01521390|115487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487061|NCT01521390|115487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487062|NCT01521390|115487|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494789|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
2494790|NCT01000727|480848/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487063|NCT01521390|115487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487064|NCT01521390|115487|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487065|NCT01521390|115487|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487066|NCT02064504|201010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487067|NCT02064504|201010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487068|NCT02064504|201010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487069|NCT02064504|201010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487070|NCT02064504|201010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487071|NCT02064504|201010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487072|NCT02064504|201010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487073|NCT00268177|SCO30005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487074|NCT00268177|SCO30005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487075|NCT00268177|SCO30005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487076|NCT00268177|SCO30005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487077|NCT00268177|SCO30005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487078|NCT00268177|SCO30005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487079|NCT00268177|SCO30005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487080|NCT01014988|113678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487081|NCT01014988|113678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487082|NCT01014988|113678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487083|NCT01014988|113678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487084|NCT01014988|113678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487085|NCT01014988|113678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487086|NCT01014988|113678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487087|NCT00256854|ROX104805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487088|NCT00256854|ROX104805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487089|NCT00256854|ROX104805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487090|NCT00256854|ROX104805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487091|NCT00256854|ROX104805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487092|NCT00256854|ROX104805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487093|NCT00256854|ROX104805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487094|NCT02004886||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0893-005&kw=0893-005&tab=access|
2487095|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
2487096|NCT00370318|107017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487097|NCT00370318|107017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487098|NCT00370318|107017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487099|NCT00370318|107017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487100|NCT00370318|107017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488533|NCT05223673||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2488534|NCT05223673||Study Protocol|https://clinicaltrials.servier.com/|
2488535|NCT05223673||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2488536|NCT05223673||Informed Consent Form|https://clinicaltrials.servier.com/|
2488537|NCT05223673||Clinical Study Report|https://clinicaltrials.servier.com/|
2488538|NCT05223673||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2488539|NCT00488514|TXA107977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488540|NCT00488514|TXA107977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488541|NCT00488514|TXA107977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488542|NCT00488514|TXA107977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488543|NCT00488514|TXA107977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488544|NCT00488514|TXA107977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488545|NCT00488514|TXA107977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488546|NCT01475721|115359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488547|NCT01475721|115359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488548|NCT01475721|115359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488549|NCT01475721|115359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488550|NCT01475721|115359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488551|NCT01475721|115359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488552|NCT01475721|115359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488553|NCT00225862|100310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488554|NCT00225862|100310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488555|NCT00225862|100310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488556|NCT00225862|100310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488557|NCT00225862|100310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488558|NCT00225862|100310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488559|NCT00225862|100310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488560|NCT00127855|792014/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488561|NCT00127855|792014/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488562|NCT00127855|792014/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488563|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
2488564|NCT00127855|792014/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488565|NCT02771405||Informed Consent Form|http://www.megafileupload.com/f3sT/Attachments_201656.zip|
2488566|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.
2488567|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.
2488568|NCT00400855|SIG103337|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488569|NCT00400855|SIG103337|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488570|NCT00400855|SIG103337|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488571|NCT00400855|SIG103337|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488572|NCT00400855|SIG103337|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488573|NCT00400855|SIG103337|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488574|NCT00400855|SIG103337|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488575|NCT01000506|112997|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488576|NCT01000506|112997|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493132|NCT01245140|117221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493133|NCT01245140|117221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493134|NCT01245140|117221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493135|NCT00443209||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-012&kw=0974-012&tab=access|
2493136|NCT01431950|114496|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493137|NCT01431950|114496|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493138|NCT01431950|114496|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488577|NCT01000506|112997|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488578|NCT01000506|112997|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488579|NCT01000506|112997|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488580|NCT01000506|112997|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488581|NCT01000506|112997|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488582|NCT01874548||Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1002/jmri.25386/abstract;jsessionid=86852D9FCBC14AF375566F8E7E214CB0.f01t04|
2488583|NCT00920556|113222|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488584|NCT00920556|113222|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488585|NCT00920556|113222|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488586|NCT00920556|113222|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488587|NCT00920556|113222|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488588|NCT00920556|113222|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488589|NCT01366573|115256|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488590|NCT01366573|115256|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488591|NCT01366573|115256|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488592|NCT01366573|115256|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488593|NCT01366573|115256|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488594|NCT01366573|115256|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488595|NCT01366573|115256|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488596|NCT00943761||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-028&kw=7009-028&tab=access|
2488597|NCT00292071||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488598|NCT03202433|ISSN 0124-8146|Study Protocol|http://scielo.org.co/scielo.php?script=sci_arttext&pid=S0124-81462013000200010|
2488599|NCT03202433||Clinical Practice Guide|http://www.criscancer.org|
2488600|NCT00412191|LAM105379|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488601|NCT00412191|LAM105379|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487101|NCT00370318|107017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487102|NCT01424514|114974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488602|NCT00412191|LAM105379|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488603|NCT00412191|LAM105379|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488604|NCT00412191|LAM105379|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488605|NCT00412191|LAM105379|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488606|NCT00412191|LAM105379|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488607|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.
2488608|NCT01453491|115951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493139|NCT01431950|114496|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493140|NCT01431950|114496|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493141|NCT01431950|114496|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493142|NCT01431950|114496|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493143|NCT01453023|112777|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493144|NCT01453023|112777|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493145|NCT01453023|112777|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493146|NCT01453023|112777|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493147|NCT01453023|112777|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493148|NCT01453023|112777|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493149|NCT01453023|112777|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493150|NCT00546078|109628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493151|NCT00546078|109628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493152|NCT00546078|109628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493153|NCT00546078|109628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493154|NCT00546078|109628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493155|NCT00546078|109628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493156|NCT00546078|109628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487103|NCT01424514|114974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487104|NCT01424514|114974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487105|NCT01424514|114974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487106|NCT01424514|114974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487107|NCT01424514|114974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487108|NCT01424514|114974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487109|NCT00784550|111114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487110|NCT00784550|111114|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487111|NCT00784550|111114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487112|NCT00784550|111114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487113|NCT00784550|111114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488609|NCT01453491|115951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488610|NCT01453491|115951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488611|NCT01453491|115951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488612|NCT01453491|115951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488613|NCT01453491|115951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488614|NCT01453491|115951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488615|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
2488616|NCT00289172|103792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488617|NCT00289172|103792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488618|NCT00289172|103792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488619|NCT00289172|103792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488620|NCT00289172|103792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488621|NCT00289172|103792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488622|NCT05711875|Sridhar A, Shiliang Z, Woodson|Informed Consent Form|https://pubmed.ncbi.nlm.nih.gov/33140989/|web site is provided
2488623|NCT01999842|201072|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488624|NCT01999842|201072|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488625|NCT01999842|201072|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488626|NCT01999842|201072|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488627|NCT01999842|201072|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488628|NCT01999842|201072|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488629|NCT01999842|201072|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488630|NCT00540592|110847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488631|NCT00540592|110847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488632|NCT00540592|110847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488633|NCT00540592|110847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488634|NCT00540592|110847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488635|NCT00540592|110847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488636|NCT00540592|110847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488637|NCT00906178||Intervention website|http://www.cybersenga.com|
2488638|NCT02833129||Study Protocol|http://arxiv.org/abs/1607.01756|
2488639|NCT00742131|MET111647|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488640|NCT00742131|MET111647|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488641|NCT00742131|MET111647|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488642|NCT00742131|MET111647|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488643|NCT00742131|MET111647|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488644|NCT00742131|MET111647|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488645|NCT00742131|MET111647|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488646|NCT00097929||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488647|NCT02052661|106793|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488648|NCT02052661|106793|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488649|NCT02052661|106793|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488650|NCT02052661|106793|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488651|NCT02052661|106793|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488652|NCT02052661|106793|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488653|NCT02052661|106793|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488654|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
2488655|NCT02726464||Patient Brochure|http://www.lightintegra.com/prism-study|
2488656|NCT01484496|112341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488657|NCT01484496|112341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488658|NCT01484496|112341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488659|NCT01484496|112341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488660|NCT01484496|112341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488661|NCT01484496|112341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488662|NCT01484496|112341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488663|NCT03160456|IPG598|"NICE guidance Hypoglossal Nerve Stimulation"|https://www.nice.org.uk/guidance/ipg598|National Institute for Health and Care Excellence
2488664|NCT06085235||Individual Participant Data Set|https://osf.io/y8e2r/|
2488665|NCT01018017|114010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488666|NCT01018017|114010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488667|NCT01018017|114010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488668|NCT01018017|114010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488669|NCT01018017|114010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488670|NCT01018017|114010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488671|NCT01018017|114010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488672|NCT01165125|105548|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488673|NCT01165125|105548|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488674|NCT01165125|105548|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488675|NCT01165125|105548|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488676|NCT01165125|105548|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488677|NCT01165125|105548|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488678|NCT01165125|105548|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488679|NCT00329576|106640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488680|NCT00329576|106640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488681|NCT00329576|106640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488682|NCT00329576|106640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488683|NCT00329576|106640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488684|NCT02947802||Study Instrument (Online Survey)|https://hbs.qualtrics.com/SE/?SID=SV_1LdkKR5P4DyCevH|This is the online survey participants will complete.
2488685|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.
2488686|NCT00883948||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/eden/|
2488687|NCT00883948||Study Forms|http://biolincc.nhlbi.nih.gov/studies/eden/|
2488688|NCT01899638|115380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488689|NCT01899638|115380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488690|NCT01899638|115380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488691|NCT01899638|115380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488692|NCT01899638|115380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488693|NCT01899638|115380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488694|NCT01899638|115380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493157|NCT00725712|MET111643|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493158|NCT00725712|MET111643|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488695|NCT01277705|711866/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488696|NCT01277705|711866/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488697|NCT01277705|711866/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488698|NCT01277705|711866/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488699|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
2488700|NCT01277705|711866/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488701|NCT02397915|201474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488702|NCT02397915|201474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488703|NCT02397915|201474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488704|NCT02397915|201474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488705|NCT02397915|201474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488706|NCT02397915|201474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488707|NCT02397915|201474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488708|NCT00456625|108984|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488709|NCT00456625|108984|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488710|NCT00456625|108984|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488711|NCT00456625|108984|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488712|NCT00456625|108984|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488713|NCT00456625|108984|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488714|NCT00456625|108984|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488715|NCT02993627|18039384|Clinical Study Report|http://lipidworld.biomedcentral.com/articles/10.1186/1476-511X-6-33/|
2488717|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.
2488718|NCT00434993||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/alta/|
2488719|NCT00434993||Study Forms|http://biolincc.nhlbi.nih.gov/studies/alta/|
2488720|NCT02218697|117276|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488721|NCT02218697|117276|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488722|NCT02218697|117276|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488723|NCT02218697|117276|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488724|NCT02218697|117276|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488725|NCT02218697|117276|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488726|NCT02218697|117276|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488727|NCT00466947|109563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488728|NCT00466947|109563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488729|NCT00466947|109563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488730|NCT00466947|109563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488731|NCT00466947|109563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488732|NCT00466947|109563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488733|NCT01534351||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0906A-149&kw=0906A-149&tab=access|
2488734|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
2488735|NCT00140712|101468/253|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488736|NCT00140712|101468/253|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488737|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
2488738|NCT00140712|101468/253|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488739|NCT00140712|101468/253|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488740|NCT00140712|101468/253|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488741|NCT00972517|113638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488742|NCT00972517|113638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488743|NCT00972517|113638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488744|NCT00972517|113638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488745|NCT00972517|113638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488746|NCT00972517|113638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488747|NCT00972517|113638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488748|NCT00104416|LAM100036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488749|NCT00104416|LAM100036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488750|NCT00104416|LAM100036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488751|NCT00104416|LAM100036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488752|NCT00104416|LAM100036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488753|NCT00104416|LAM100036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488754|NCT00104416|LAM100036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488755|NCT01536561|104728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488756|NCT01536561|104728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488757|NCT01536561|104728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488758|NCT01536561|104728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488759|NCT01536561|104728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488760|NCT01536561|104728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488761|NCT01536561|104728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488762|NCT00500461|AC2106213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488763|NCT00500461|AC2106213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488764|NCT00500461|AC2106213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488765|NCT00500461|AC2106213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488766|NCT00500461|AC2106213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488767|NCT00500461|AC2106213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488768|NCT00500461|AC2106213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488769|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.
2488770|NCT01762774|114068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488771|NCT01762774|114068|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488772|NCT01762774|114068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488773|NCT01762774|114068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488774|NCT01762774|114068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488775|NCT01762774|114068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488776|NCT01762774|114068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488777|NCT00404378|NKV105093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488778|NCT00404378|NKV105093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488779|NCT00404378|NKV105093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488780|NCT00404378|NKV105093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488781|NCT00404378|NKV105093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488782|NCT00404378|NKV105093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488783|NCT00404378|NKV105093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488784|NCT00758069||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488785|NCT00703846|114568|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488786|NCT00703846|114568|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488787|NCT00703846|114568|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488788|NCT00703846|114568|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488789|NCT00703846|114568|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488790|NCT00703846|114568|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490356|NCT00508365|CFD109701|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490357|NCT00508365|CFD109701|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490358|NCT00508365|CFD109701|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490359|NCT00508365|CFD109701|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487114|NCT00784550|111114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487115|NCT00784550|111114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487116|NCT00976820|113482|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487117|NCT00976820|113482|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487118|NCT00976820|113482|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487119|NCT00976820|113482|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487120|NCT00976820|113482|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487121|NCT00976820|113482|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487122|NCT01571999|114636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487123|NCT01571999|114636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487124|NCT01571999|114636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487125|NCT01571999|114636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487126|NCT01571999|114636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487127|NCT01571999|114636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487128|NCT01571999|114636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487129|NCT02184585|117057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487130|NCT02184585|117057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487131|NCT02184585|117057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487132|NCT02184585|117057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487133|NCT02184585|117057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487134|NCT02184585|117057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487135|NCT02184585|117057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487136|NCT01899742|116960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487137|NCT01899742|116960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487138|NCT01899742|116960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487139|NCT01899742|116960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487140|NCT01899742|116960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487141|NCT01899742|116960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487142|NCT01899742|116960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487143|NCT01154088|114248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487144|NCT01154088|114248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487145|NCT01154088|114248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487146|NCT01154088|114248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487147|NCT01154088|114248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487148|NCT01154088|114248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487149|NCT03228316||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/27208713|
2487150|NCT01453478|115550|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487151|NCT01453478|115550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494791|NCT01000727|480848/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494792|NCT01000727|480848/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494793|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
2494794|NCT01000727|480848/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488791|NCT00703846|114568|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488792|NCT01822899|116134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488793|NCT01822899|116134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488794|NCT01822899|116134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488795|NCT01822899|116134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488796|NCT01822899|116134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488797|NCT01822899|116134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488798|NCT01822899|116134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488799|NCT00875485|110699|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488800|NCT00875485|110699|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488801|NCT00875485|110699|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488802|NCT00875485|110699|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488803|NCT00875485|110699|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488804|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.
2488805|NCT02060344||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
2488806|NCT02060344||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
2488807|NCT03030352||Pilot Study of the How-to trial|http://link.springer.com/article/10.1007/s10826-013-9751-0|
2488808|NCT00473668|104977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488809|NCT00473668|104977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494795|NCT01000727|480848/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488810|NCT00473668|104977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488811|NCT00473668|104977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488812|NCT00473668|104977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488813|NCT00473668|104977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488814|NCT05896098||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/14616599/|
2488815|NCT00697866|208129/037|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488816|NCT00697866|208129/037|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488817|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
2488818|NCT00697866|208129/037|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488819|NCT00697866|208129/037|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488820|NCT00697866|208129/037|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488821|NCT03257202|HS-17-00319|Study Protocol|http://istar.usc.edu|
2494796|NCT00377611|107564|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494797|NCT00377611|107564|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494798|NCT00377611|107564|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494799|NCT00377611|107564|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488822|NCT03257202|HS-17-00319|Informed Consent Form|http://istar.usc.edu|
2488823|NCT00625196|HZA102940|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488824|NCT00625196|HZA102940|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488825|NCT00625196|HZA102940|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488826|NCT00625196|HZA102940|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488827|NCT00625196|HZA102940|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488828|NCT00625196|HZA102940|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488829|NCT00625196|HZA102940|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488830|NCT00758264|111393|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488831|NCT00758264|111393|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488832|NCT00758264|111393|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490360|NCT00508365|CFD109701|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488833|NCT00758264|111393|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488834|NCT00758264|111393|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488835|NCT00758264|111393|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488836|NCT00758264|111393|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488837|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.
2488838|NCT00000593||Study Forms|http://biolincc.nhlbi.nih.gov/studies/vats/|
2488839|NCT00344318|107007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488840|NCT00344318|107007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488841|NCT00344318|107007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488842|NCT00344318|107007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488843|NCT00344318|107007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488844|NCT00344318|107007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488845|NCT00500058|ILI105618|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488846|NCT00500058|ILI105618|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488847|NCT00500058|ILI105618|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488848|NCT00500058|ILI105618|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488849|NCT00500058|ILI105618|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488850|NCT00500058|ILI105618|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488851|NCT00500058|ILI105618|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490361|NCT00508365|CFD109701|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490362|NCT00508365|CFD109701|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490363|NCT01262911|115083|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490364|NCT01262911|115083|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490365|NCT01262911|115083|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490366|NCT01262911|115083|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490367|NCT01262911|115083|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488852|NCT03511508||Study Protocol|http://doi.org/10.1186/s13063-019-3405-5|Study Protocol
2488853|NCT00633074|111454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488854|NCT00633074|111454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488855|NCT00633074|111454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488856|NCT00633074|111454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488857|NCT00633074|111454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488858|NCT00633074|111454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488859|NCT00633074|111454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488860|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
2488861|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
2488862|NCT01431937|114347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488863|NCT01431937|114347|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488864|NCT01431937|114347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488865|NCT01431937|114347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488866|NCT01431937|114347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488867|NCT01431937|114347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488868|NCT01431937|114347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488869|NCT00519376|B2C110165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488870|NCT00519376|B2C110165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488871|NCT00519376|B2C110165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490368|NCT01262911|115083|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488872|NCT00519376|B2C110165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488873|NCT00519376|B2C110165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488874|NCT00519376|B2C110165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488875|NCT00519376|B2C110165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488876|NCT00306293|VLX105832|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488877|NCT00306293|VLX105832|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488878|NCT00306293|VLX105832|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488879|NCT00306293|VLX105832|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488880|NCT00306293|VLX105832|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488881|NCT00306293|VLX105832|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488882|NCT00306293|VLX105832|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488883|NCT04569136|DOI：10.6315/2009.37(4)06|Clinical Study Report|http://www.airitilibrary.com/Publication/alDetailedMesh?DocID=10253009-200912-201002050027-201002050027-261-268|
2488884|NCT03192020||Study Protocol|http://bmjopen.bmj.com/content/8/3/e019054|Protocol in BMJ Open access
2488885|NCT02998203||Manuscript and supplementary files|https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0219420|
2488886|NCT00964340|113312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488887|NCT00964340|113312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488888|NCT00964340|113312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488889|NCT00964340|113312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488890|NCT00964340|113312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488891|NCT00964340|113312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488892|NCT01165320||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0991-074&kw=0991-074&tab=access|
2493159|NCT00725712|MET111643|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488893|NCT05446792||Approval of the Ethics Committee for Research with Human Beings in Brazil|https://plataformabrasil.saude.gov.br/login.jsf|
2488894|NCT00908115|208355/128|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488895|NCT00908115|208355/128|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488896|NCT00908115|208355/128|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488897|NCT00908115|208355/128|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488898|NCT00908115|208355/128|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488899|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
2488900|NCT01155466||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04938&kw=P04938&tab=access|
2488901|NCT06896500|Ethics Committee Application|Clinical Study Report|https://drive.google.com/file/d/19dj7wMiq4mPOobklxuHQObULyObAOvgc/view?usp=sharing|
2488902|NCT06896500|informed consent form|Informed Consent Form|https://docs.google.com/document/d/1PuTtTRr_LxSuZvbzWyvw3EQZYQ0VyA7b/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
2488903|NCT06896500|Vaginal flatus status form|Forms|https://docs.google.com/document/d/1kFejPnvwa_N52yM8A2UKoAgZ3s1uPYuw/edit?usp=sharing&ouid=111712425749983896080&rtpof=true&sd=true|
2488904|NCT06896500|study main data|Study Protocol|https://drive.google.com/file/d/1yPsrrEh2E2eVLPD-_QtWy8F0rgT0dM9g/view?usp=sharing|
2488905|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.
2488906|NCT00316693|104798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488907|NCT00316693|104798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488908|NCT00316693|104798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488909|NCT00316693|104798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488910|NCT00316693|104798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488911|NCT00316693|104798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488912|NCT01245738||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-204&kw=0000-204&tab=access|
2488913|NCT06891469|https://doi.org/10.6084/m9.fig|Individual Participant Data Set|https://figshare.com|figshare
2488914|NCT00896363|109035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488915|NCT00896363|109035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488916|NCT00896363|109035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488917|NCT00896363|109035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488918|NCT00896363|109035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488919|NCT00896363|109035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488920|NCT00896363|109035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488921|NCT01691885|116601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488922|NCT01691885|116601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488923|NCT01691885|116601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493160|NCT00725712|MET111643|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493161|NCT00725712|MET111643|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493162|NCT00725712|MET111643|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488924|NCT01691885|116601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488925|NCT01691885|116601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488926|NCT01691885|116601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488927|NCT01691885|116601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488928|NCT03207321||Individual Participant Data Set|http://apcaps.lshtm.ac.uk/|
2488929|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27179664|
2488930|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27629371|
2488931|NCT06660953||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/37971133/|
2488932|NCT00937404|112581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488933|NCT00937404|112581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488934|NCT00937404|112581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488935|NCT00937404|112581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488936|NCT00937404|112581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488937|NCT00937404|112581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488938|NCT00559468||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2488939|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
2488940|NCT00871117|111852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488941|NCT00871117|111852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488942|NCT00871117|111852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488943|NCT00871117|111852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488944|NCT00871117|111852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488945|NCT00871117|111852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488946|NCT00871117|111852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488947|NCT00355342|SCO40041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488948|NCT00355342|SCO40041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488949|NCT00355342|SCO40041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488950|NCT00355342|SCO40041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488951|NCT00355342|SCO40041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488952|NCT00355342|SCO40041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488953|NCT00355342|SCO40041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488954|NCT01360398|114378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488955|NCT01360398|114378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488956|NCT01360398|114378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488957|NCT01360398|114378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488958|NCT01360398|114378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488959|NCT01360398|114378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488960|NCT01360398|114378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488961|NCT00549900|107336|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488962|NCT00549900|107336|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488963|NCT00549900|107336|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488964|NCT00549900|107336|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488965|NCT00549900|107336|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488966|NCT00549900|107336|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488967|NCT00624819|111345 (Mth 12)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488968|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
2488969|NCT00624819|111345 (Mth 12)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488970|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
2488971|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
2488972|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
2488973|NCT02014480|116132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488974|NCT02014480|116132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488975|NCT02014480|116132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488976|NCT02014480|116132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488977|NCT02014480|116132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488978|NCT02014480|116132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488979|NCT02014480|116132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488980|NCT01357135||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-201&kw=0431-201&tab=access|
2488981|NCT03630744||web page|http://fluidday.com|
2488982|NCT01224821|104731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488983|NCT01224821|104731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488984|NCT01224821|104731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488985|NCT01224821|104731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488986|NCT01224821|104731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488987|NCT01224821|104731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488988|NCT01224821|104731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488989|NCT06357091||results can be obtained from principal investigator|https://www.kh-schwaz.at/|results can be obtained from the principle investigator
2488990|NCT05455008||Individual Participant Data Set|https://iro.uiowa.edu/esploro/outputs/dataset/9984236057502771|
2488991|NCT01480609|115214|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488992|NCT01480609|115214|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488993|NCT01480609|115214|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488994|NCT01480609|115214|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488995|NCT01480609|115214|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488996|NCT01480609|115214|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488997|NCT01480609|115214|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2488998|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.
2488999|NCT03029078||Study Protocol|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003048-11/FR|
2489000|NCT00134732|103478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494800|NCT00377611|107564|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489001|NCT00134732|103478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489002|NCT00134732|103478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489003|NCT00134732|103478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489004|NCT00134732|103478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489005|NCT00134732|103478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489006|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
2489007|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
2489008|NCT00363727|101468/228|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489009|NCT00363727|101468/228|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489010|NCT00363727|101468/228|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489011|NCT00363727|101468/228|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490369|NCT01262911|115083|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490370|NCT03733470|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
2490371|NCT00169546|SAM40100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490372|NCT00169546|SAM40100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490373|NCT00169546|SAM40100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490374|NCT00169546|SAM40100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490375|NCT00169546|SAM40100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490376|NCT00169546|SAM40100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490377|NCT00169546|SAM40100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490378|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/auad/issue/60075/826745|
2490379|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/411491|
2490380|NCT06253572||Review|http://journalofomepturkey.org/index.php/eccd/article/view/78|
2490381|NCT06253572||Individual Participant Data Set|http://www.jstor.org/stable/1558435?casa_token=iq_3GDKvzp0AAAAA%3AirJftQ9Ewi5gyg9Tny2095o0KVV-33gvurOfsXyr0MiVZqrAHUcja3OeKJ8Cv6euyzIzkZ19Uz5FKxx7fYz7rZNS3v9_TUDfctQQuHRaeiFE2ki9_A|
2490382|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.
2490383|NCT06253572||Review|http://dergipark.org.tr/en/download/article-file/199140|
2490384|NCT06253572||Individual Participant Data Set|http://dergipark.org.tr/en/pub/rep/issue/63330/827844|
2490385|NCT02809612||Study Protocol|http://www.kbh.uu.se|
2490386|NCT05695209|VIV00009027|Individual Participant Data Set|https://vivli.org|https://doi.org/10.25934/PR00009027
2490387|NCT00043914|LAM40013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490388|NCT00043914|LAM40013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490389|NCT00043914|LAM40013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490390|NCT00043914|LAM40013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490391|NCT00043914|LAM40013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490392|NCT00043914|LAM40013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490393|NCT00043914|LAM40013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489012|NCT00363727|101468/228|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489013|NCT03745183||Study Protocol|https://drive.google.com/open?id=1ial1puH4ar075LyGcoWIrU1AXclt3FO-|
2489014|NCT03745183||Tables 1-5|https://drive.google.com/open?id=1pmZyUhTfoOPWRDJgEFjMsa_K9bvQ_Lon|
2489015|NCT03745183||Figure 1. Flow chart of the study procedure|https://drive.google.com/open?id=1MpUGMeNkzeOlThYZ_Zur4xTgt5cOvQNN|
2489016|NCT03745183||Informed Consent Form|https://drive.google.com/open?id=1kV91jvmtUDi_BA2paf-iszXb7bCnKHZO|
2489017|NCT03745183||Individual Participant Data Set|https://drive.google.com/open?id=1n3y-FDFc63KGyGfbkNBlpLJ-6HE9BBUZ|
2489018|NCT03745183||Appendix E. Illustrated checklist for the T'boli|https://drive.google.com/open?id=1t2b-wyQsJaTEy6qqJCiL4Opg-Hdvdxzj|
2490394|NCT01606800||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8908B-059&kw=8908B-059&tab=access|
2490395|NCT00684593||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04481&kw=7123-009&tab=access|
2490396|NCT05930912||Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
2489019|NCT03745183||Appendix F. Illustrated instruction on Senna alata decoction preparation|https://drive.google.com/open?id=17hMRr2-GhROnq7Gdw0Skd1KFApCpCgzy|
2489020|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
2489021|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
2489022|NCT00343915|101695 Ext. Mth30|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489023|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
2489024|NCT00343915|101695 Ext. Mth30|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489025|NCT00642148|MKI102428|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489026|NCT00642148|MKI102428|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489027|NCT00642148|MKI102428|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489028|NCT00642148|MKI102428|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489029|NCT00642148|MKI102428|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489030|NCT00642148|MKI102428|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490397|NCT05930912|zenodo.7382529|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7382529|
2490398|NCT05930912|zenodo.6942208|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6942208|
2490399|NCT05930912|zenodo.7188211|Social Circumstances and Events|http://doi.org/10.5281/zenodo.7188211|
2490400|NCT05930912|zenodo.6941906|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6941906|
2490401|NCT05930912|zenodo.6952516|Cyber-Social Circumstances and Events|http://doi.org/10.5281/zenodo.6952516|
2490402|NCT05930912|zenodo.7022873|Analytic Code|http://doi.org/10.5281/zenodo.7022873|The technological-psychoanalytic mass psychological observation and analysis schemes.
2490403|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
2490404|NCT00369824|107682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490405|NCT00369824|107682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490406|NCT00369824|107682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490407|NCT00369824|107682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490408|NCT00369824|107682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490409|NCT00369824|107682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490410|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.
2490411|NCT00000557||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
2490412|NCT00000557||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
2490413|NCT01762878|116617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490414|NCT01762878|116617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490415|NCT01762878|116617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490416|NCT01762878|116617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490417|NCT01762878|116617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490418|NCT01762878|116617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490419|NCT01762878|116617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490420|NCT01577680|114637|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490421|NCT01577680|114637|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490422|NCT01577680|114637|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490423|NCT01577680|114637|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494801|NCT00377611|107564|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494802|NCT01098461|110932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489031|NCT00642148|MKI102428|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489032|NCT00035360||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489033|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.
2489034|NCT00000558||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/peace/|
2489035|NCT00000558||Study Forms|http://biolincc.nhlbi.nih.gov/studies/peace/|
2489036|NCT00289198|FFR106080|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489037|NCT00289198|FFR106080|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494803|NCT01098461|110932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494804|NCT01098461|110932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489038|NCT00289198|FFR106080|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489039|NCT00289198|FFR106080|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489040|NCT00289198|FFR106080|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489041|NCT00289198|FFR106080|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489042|NCT00289198|FFR106080|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489043|NCT00307567|105555|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489044|NCT00307567|105555|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489045|NCT00307567|105555|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489046|NCT00307567|105555|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489047|NCT00307567|105555|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489048|NCT00307567|105555|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489049|NCT06367907|SM 68/6-1|Study Protocol|https://gepris.dfg.de/gepris/projekt/424869737|
2489050|NCT02011490||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-105&kw=8616-105&tab=access|
2489051|NCT04786418||Study Protocol|http://www.directclinicaltrial.org.uk|
2489052|NCT00379977|106345|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489053|NCT00379977|106345|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489054|NCT00379977|106345|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489055|NCT00379977|106345|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489056|NCT00379977|106345|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489057|NCT00379977|106345|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489058|NCT07041424||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28955539/|
2489059|NCT00969436|109995|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494805|NCT01098461|110932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494806|NCT01098461|110932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489060|NCT00969436|109995|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489061|NCT00969436|109995|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489062|NCT00969436|109995|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489063|NCT00969436|109995|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489064|NCT00969436|109995|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489065|NCT00969436|109995|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490424|NCT01577680|114637|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490425|NCT01577680|114637|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490426|NCT01577680|114637|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490427|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
2490428|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
2490429|NCT01648101|114855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490430|NCT01648101|114855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490431|NCT01648101|114855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490432|NCT01648101|114855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490433|NCT01648101|114855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490434|NCT01648101|114855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493163|NCT00725712|MET111643|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493164|NCT06509360||Individual Participant Data Set|https://www.castoredc.com/|Individual participant data is collected anonymously in Castor EDC.
2493165|NCT04240249||Individual Participant Data Set|https://github.com/hmep/r2fu/|
2493166|NCT04240249||Analytic Code|https://github.com/hmep/r2fu/|
2493167|NCT00383123|104858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493168|NCT00383123|104858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493169|NCT00383123|104858|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493170|NCT00383123|104858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493171|NCT00383123|104858|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493172|NCT00383123|104858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493173|NCT00383123|104858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490435|NCT01648101|114855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490436|NCT01168167|01168167|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT01168167|
2490437|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.
2490438|NCT02446483|201527|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490439|NCT02446483|201527|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490440|NCT02446483|201527|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490441|NCT02446483|201527|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490442|NCT02446483|201527|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490443|NCT04329871||Individual Participant Data Set|http://Metabolic-institute.com|
2490444|NCT04213079||Study Protocol|http://mdds.nyc/|
2493174|NCT00344032|104479|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493175|NCT00344032|104479|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493176|NCT00344032|104479|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489066|NCT00306644|49653/334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489067|NCT00306644|49653/334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489068|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
2489069|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
2489070|NCT00306644|49653/334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489071|NCT00306644|49653/334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489072|NCT00306644|49653/334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489073|NCT00353873|SAM104926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489074|NCT00353873|SAM104926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489075|NCT00353873|SAM104926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489076|NCT00353873|SAM104926|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489077|NCT00353873|SAM104926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489078|NCT00353873|SAM104926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489079|NCT00353873|SAM104926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489080|NCT01636713|114634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489081|NCT01636713|114634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489082|NCT01636713|114634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489083|NCT01636713|114634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489084|NCT01636713|114634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489085|NCT01636713|114634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489086|NCT01636713|114634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489087|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
2489088|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
2489089|NCT00126984|104703 (Primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489090|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
2489091|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.
2489092|NCT00126984|104703 (Primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489093|NCT00354666|B2E101312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489094|NCT00354666|B2E101312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489095|NCT00354666|B2E101312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489096|NCT00354666|B2E101312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489097|NCT00354666|B2E101312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489098|NCT00474617||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489099|NCT01762813||Study Protocol|http://translational-medicine.biomedcentral.com/articles/10.1186/s12967-016-0951-4|
2489100|NCT06979739||Informed Consent Form|https://www.hku.edu.tr/iletisim/|
2489101|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/0310250742582348|
2489102|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/1823080587913061|
2489103|NCT00307554|105553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489104|NCT00307554|105553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489105|NCT00307554|105553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489106|NCT00307554|105553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489107|NCT00307554|105553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489108|NCT00307554|105553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489109|NCT00422994|RRL103628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489110|NCT00422994|RRL103628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489111|NCT00422994|RRL103628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489112|NCT00422994|RRL103628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489113|NCT00422994|RRL103628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489114|NCT00422994|RRL103628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489115|NCT00422994|RRL103628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489116|NCT00320463|105910|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489117|NCT00320463|105910|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489118|NCT00320463|105910|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489119|NCT00320463|105910|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489120|NCT00320463|105910|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489121|NCT00320463|105910|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489122|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
2489123|NCT00475215||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2489124|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
2489125|NCT06103929||Individual Participant Data Set|https://le.ac.uk/people/sam-tromans|
2489126|NCT06103929||Study Protocol|https://le.ac.uk/people/sam-tromans|
2489127|NCT06103929||Statistical Analysis Plan|https://le.ac.uk/people/sam-tromans|
2489128|NCT06103929||Informed Consent Form|https://le.ac.uk/people/sam-tromans|
2489129|NCT01147900|113055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489130|NCT01147900|113055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489131|NCT01147900|113055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489132|NCT01147900|113055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489133|NCT01147900|113055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489134|NCT01147900|113055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489135|NCT00945932|112851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489136|NCT00945932|112851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489137|NCT00945932|112851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489138|NCT00945932|112851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489139|NCT00945932|112851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489140|NCT00945932|112851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489141|NCT00945932|112851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489142|NCT01381536|114243|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489143|NCT01381536|114243|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489144|NCT01381536|114243|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489145|NCT01381536|114243|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489146|NCT01381536|114243|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489147|NCT01381536|114243|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493177|NCT00344032|104479|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493178|NCT00344032|104479|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493179|NCT00344032|104479|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493180|NCT05688618||Study Protocol|https://drive.google.com/drive/u/0/folders/1JG22lkEchQULxW79ktlsVcM5uGNB4iVh|
2493181|NCT00263653|103954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493182|NCT00263653|103954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489148|NCT05936528||Individual Participant Data Set|https://drive.google.com/drive/folders/1CBAPVtAVYsi2x1iLQdWl48b9OowGSxw9|
2489149|NCT03696901|Xydalba|Study Protocol|https://awbdb.bfarm.de/ords/f?p=101:STARTSEITE::::::|BfArM AWB Datenbank
2489150|NCT01300455||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-036&kw=4305-036&tab=access|
2489151|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
2489152|NCT01521377|114635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489153|NCT01521377|114635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489154|NCT01521377|114635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489155|NCT01521377|114635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489156|NCT01521377|114635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489157|NCT01521377|114635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489158|NCT01521377|114635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489159|NCT00771615|111729|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489160|NCT00771615|111729|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489161|NCT00771615|111729|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489162|NCT00771615|111729|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489163|NCT00771615|111729|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489164|NCT00771615|111729|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489165|NCT00771615|111729|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489166|NCT04303299|Thai government data|Data references|https://ddc.moph.go.th|
2489167|NCT04303299||News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
2489168|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)
2489169|NCT04303299||Reference News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
2489170|NCT04892108||Study Protocol|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
2489171|NCT04892108||Statistical Analysis Plan|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
2489172|NCT04892108||Informed Consent Form|https://drive.google.com/drive/folders/10w8pl8TztkdTzafLc-M4wRyrHNZI1G-r?usp=sharing|
2489173|NCT01600092||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-035&kw=V260-035&tab=access|
2489174|NCT01669083|116741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489175|NCT01669083|116741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489176|NCT01669083|116741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489177|NCT01669083|116741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490445|NCT00617123||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05183&kw=P05183&tab=access|
2494807|NCT01098461|110932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494808|NCT01098461|110932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494809|NCT04987853|BR10965164|Study Protocol|https://is.ncste.kz/login|
2494810|NCT04987853|BR10965164|Informed Consent Form|https://is.ncste.kz/login|
2494811|NCT04987853|BR10965164|Clinical Study Report|https://is.ncste.kz/login|
2494812|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.
2494813|NCT01954251|117036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494814|NCT01954251|117036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494815|NCT01954251|117036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494816|NCT01954251|117036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494817|NCT01954251|117036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494818|NCT01954251|117036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494819|NCT01954251|117036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494820|NCT00718666|112021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494821|NCT00718666|112021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489178|NCT01669083|116741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489179|NCT01669083|116741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489180|NCT01669083|116741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489181|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
2489182|NCT00652951|110142|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489183|NCT00652951|110142|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489184|NCT00652951|110142|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489185|NCT00652951|110142|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489186|NCT00652951|110142|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489187|NCT00652951|110142|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489188|NCT01209078|113414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489189|NCT01209078|113414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489190|NCT01209078|113414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489191|NCT01209078|113414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489192|NCT01209078|113414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489193|NCT01209078|113414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489194|NCT01209078|113414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489195|NCT01462617|115117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489196|NCT01462617|115117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489197|NCT01462617|115117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494822|NCT00718666|112021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494823|NCT00718666|112021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494824|NCT00718666|112021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494825|NCT00718666|112021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494826|NCT01062074||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-059&kw=V501-059&tab=access|
2494827|NCT00043875|LAM20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494828|NCT00043875|LAM20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494829|NCT00043875|LAM20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494830|NCT00043875|LAM20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494831|NCT00043875|LAM20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494832|NCT00043875|LAM20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494833|NCT00043875|LAM20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494834|NCT00430521|107495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494835|NCT00430521|107495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494836|NCT00430521|107495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494837|NCT00430521|107495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494838|NCT00430521|107495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494839|NCT00430521|107495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494840|NCT00430521|107495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494841|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
2494842|NCT00757770|444563/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494843|NCT00757770|444563/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494844|NCT00757770|444563/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494845|NCT00757770|444563/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494846|NCT00757770|444563/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494847|NCT00992784|113094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489198|NCT01462617|115117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489199|NCT01462617|115117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489200|NCT01462617|115117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489201|NCT01462617|115117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489202|NCT00231413|102115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489203|NCT00231413|102115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489204|NCT00231413|102115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489205|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.
2489206|NCT00231413|102115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489207|NCT00231413|102115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489208|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.
2489209|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
2489210|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.
2489211|NCT01147848|113091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490446|NCT00783003|112146|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490447|NCT00783003|112146|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490448|NCT00783003|112146|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490449|NCT00783003|112146|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490450|NCT00783003|112146|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490451|NCT00783003|112146|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490452|NCT00783003|112146|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490453|NCT01916720|480848/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490454|NCT01916720|480848/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490455|NCT01916720|480848/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490456|NCT01916720|480848/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490457|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
2490458|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
2490459|NCT01916720|480848/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490460|NCT05792709||Study Protocol|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788277/|
2490461|NCT00907777|112807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490462|NCT00907777|112807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490463|NCT00907777|112807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493183|NCT00263653|103954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493184|NCT00263653|103954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493185|NCT00263653|103954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493186|NCT00263653|103954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493187|NCT04954326||Individual Participant Data Set|https://clinicaltrials.servier.com|
2493188|NCT04954326||Study Protocol|https://clinicaltrials.servier.com|
2493189|NCT04954326||Statistical Analysis Plan|https://clinicaltrials.servier.com|
2493190|NCT04954326||Informed Consent Form|https://clinicaltrials.servier.com|
2493191|NCT04954326||Clinical Study Report|https://clinicaltrials.servier.com|
2493192|NCT04954326||Study-level clinical trial data|https://clinicaltrials.servier.com|
2494848|NCT00992784|113094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494849|NCT00992784|113094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494850|NCT00992784|113094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494851|NCT00992784|113094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494852|NCT00992784|113094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494853|NCT00992784|113094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494854|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.
2494855|NCT00120289|AIM-HIGH|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
2494856|NCT00120289|AIM-HIGH|Study forms|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
2494857|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
2494858|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
2490464|NCT00907777|112807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493193|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
2494859|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
2494860|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
2494861|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
2494862|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
2494863|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
2494864|NCT00289185|104298|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494865|NCT00289185|104298|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494866|NCT00289185|104298|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494867|NCT00289185|104298|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494868|NCT00289185|104298|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494869|NCT00289185|104298|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494870|NCT00135486|711202/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494871|NCT00135486|711202/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494872|NCT00135486|711202/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489212|NCT01147848|113091|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489213|NCT01147848|113091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489214|NCT01147848|113091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489215|NCT01147848|113091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489216|NCT01147848|113091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489217|NCT01147848|113091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489218|NCT02747017||Study Protocol|http://insight.ccbr.umn.edu/official_documents/CDIFF/protocol_documents/I7-Protocol.pdf|
2489219|NCT06583694||Clinical Study Report|https://www.bangkoknoimodel.com/stat.|
2489220|NCT00343707|NKP102280|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489221|NCT00343707|NKP102280|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489222|NCT00343707|NKP102280|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489223|NCT00343707|NKP102280|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489224|NCT00343707|NKP102280|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489225|NCT00343707|NKP102280|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489226|NCT00778895|111635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489227|NCT00778895|111635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489228|NCT00778895|111635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489229|NCT00778895|111635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489230|NCT00778895|111635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489231|NCT00778895|111635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489232|NCT04904848||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/25437107/|
2489233|NCT05502510||Analytic Code|https://osf.io/bty8n/?view_only=f8bb6e5a7698443494d4c3788a45cc0f|The analytic code will be uploaded to OSF upon publishing the manuscript.
2489234|NCT01431963|115376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494873|NCT00135486|711202/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494874|NCT00135486|711202/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490465|NCT00907777|112807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490466|NCT00907777|112807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490467|NCT01802931|117016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490468|NCT01802931|117016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490469|NCT01802931|117016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490470|NCT01802931|117016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490471|NCT01802931|117016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490472|NCT01802931|117016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490473|NCT01802931|117016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490474|NCT00843024|107979|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490475|NCT00843024|107979|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490476|NCT00843024|107979|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490477|NCT00843024|107979|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490478|NCT00843024|107979|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490479|NCT00843024|107979|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490480|NCT00843024|107979|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490481|NCT00318630|104385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490482|NCT00318630|104385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490483|NCT00318630|104385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490484|NCT00318630|104385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490485|NCT00318630|104385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490486|NCT00318630|104385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490487|NCT00318630|104385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490488|NCT00694993|HHI110157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490489|NCT00694993|HHI110157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490490|NCT00694993|HHI110157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490491|NCT00694993|HHI110157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490492|NCT00694993|HHI110157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490493|NCT00694993|HHI110157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490494|NCT00694993|HHI110157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490495|NCT00811798|111712|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490496|NCT00811798|111712|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490497|NCT00811798|111712|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490498|NCT00811798|111712|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490499|NCT00811798|111712|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490500|NCT00811798|111712|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490501|NCT00811798|111712|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490502|NCT00530309|GLP107865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489235|NCT01431963|115376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489236|NCT01431963|115376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489237|NCT01431963|115376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489238|NCT01431963|115376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489239|NCT00383162|TRX106571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489240|NCT00383162|TRX106571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489241|NCT00383162|TRX106571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489242|NCT00383162|TRX106571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489243|NCT00383162|TRX106571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489244|NCT00383162|TRX106571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489245|NCT00383162|TRX106571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489246|NCT00148941|213503/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489247|NCT00148941|213503/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489248|NCT00148941|213503/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489249|NCT00148941|213503/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489250|NCT00148941|213503/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489251|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
2489252|NCT04657783||Study Protocol|https://drive.google.com/drive/my-drive|
2489253|NCT02964767||Epidemiological report|http://www.who.int|
2489254|NCT02964767||Clinical Study Report|http://www.Wiley.com|
2489255|NCT01853878|116389|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489256|NCT01853878|116389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489257|NCT01853878|116389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489258|NCT01853878|116389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489259|NCT01853878|116389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489260|NCT01853878|116389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489261|NCT01853878|116389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489262|NCT00348309|AVA102672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489263|NCT00348309|AVA102672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489264|NCT00348309|AVA102672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489265|NCT00348309|AVA102672|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489266|NCT00348309|AVA102672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489267|NCT00348309|AVA102672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489268|NCT00348309|AVA102672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489269|NCT02891382||Individual Participant Data Set|https://figshare.com/articles/REDEEM_Study_Feasibility_pilot_study/7180802|
2489270|NCT01000324|112267|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489271|NCT01000324|112267|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489272|NCT01000324|112267|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490503|NCT00530309|GLP107865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490504|NCT00530309|GLP107865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490505|NCT00530309|GLP107865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490506|NCT00530309|GLP107865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490507|NCT00530309|GLP107865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490508|NCT00530309|GLP107865|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490509|NCT07001969||Individual Participant Data Set|https://t.me/drmassoud77/24301|Book of author about technique
2493194|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.
2493195|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.
2493196|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.
2493197|NCT00390260||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493198|NCT02718261|NCT02467621|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT02467621?term=SUP-ICU&rank=1|SUP-ICU Website
2493199|NCT00632502||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05365&kw=7123-017&tab=access|
2493200|NCT01381575|114700|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493201|NCT01381575|114700|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493202|NCT01381575|114700|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493203|NCT01381575|114700|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493204|NCT01381575|114700|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493205|NCT01381575|114700|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493206|NCT00968526|113459|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493207|NCT00968526|113459|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493208|NCT00968526|113459|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493209|NCT00968526|113459|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493210|NCT00968526|113459|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493211|NCT00968526|113459|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493212|NCT00968526|113459|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493213|NCT00479882||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-063&kw=0524B-063&tab=access|
2493214|NCT01160237|114454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493215|NCT01160237|114454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493216|NCT01160237|114454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493217|NCT01160237|114454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493218|NCT01160237|114454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493219|NCT01160237|114454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493220|NCT01160237|114454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493221|NCT00334334|107005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493222|NCT00334334|107005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490510|NCT02877615||Study Protocol|https://clinicaltrials.servier.com/|
2490511|NCT02877615||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490512|NCT02877615||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490513|NCT02877615||Informed Consent Form|https://clinicaltrials.servier.com/|
2490514|NCT02877615||Clinical Study Report|https://clinicaltrials.servier.com/|
2490515|NCT02877615||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2490516|NCT00197132|49653/375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490517|NCT00197132|49653/375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490518|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
2490519|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
2490520|NCT00197132|49653/375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490521|NCT00197132|49653/375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490522|NCT00197132|49653/375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490523|NCT01366521|114092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490524|NCT01366521|114092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490525|NCT01366521|114092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490526|NCT01366521|114092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494875|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
2494876|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."
2490527|NCT01366521|114092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490528|NCT01366521|114092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490529|NCT01366521|114092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490530|NCT00356369|107386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490531|NCT00356369|107386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490532|NCT00356369|107386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490533|NCT00356369|107386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490534|NCT00356369|107386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490535|NCT00356369|107386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490536|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)."
2490537|NCT01366560|114639|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490538|NCT01366560|114639|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490539|NCT01366560|114639|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490540|NCT01366560|114639|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490541|NCT01366560|114639|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490542|NCT01366560|114639|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490543|NCT01366560|114639|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490544|NCT00044278|LAM20007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490545|NCT00044278|LAM20007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494877|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."
2489273|NCT01000324|112267|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489274|NCT01000324|112267|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489275|NCT01000324|112267|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489276|NCT01000324|112267|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489277|NCT00871338|111709|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489278|NCT00871338|111709|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489279|NCT00871338|111709|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489280|NCT00871338|111709|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489281|NCT00871338|111709|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489282|NCT00871338|111709|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489283|NCT00871338|111709|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489284|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
2489285|NCT00326248|NKT102553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489286|NCT00326248|NKT102553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489287|NCT00326248|NKT102553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489288|NCT00326248|NKT102553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489289|NCT00326248|NKT102553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489290|NCT00326248|NKT102553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489291|NCT00326248|NKT102553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489292|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
2489293|NCT03191227||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22984148|Cohort profile
2489294|NCT01140061||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-020&kw=0873-020&tab=access|
2489295|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
2489296|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
2489297|NCT00500955|BRL-49653/137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489298|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
2489299|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
2489300|NCT00500955|BRL-49653/137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489301|NCT00250276|104772|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489302|NCT00250276|104772|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489303|NCT00250276|104772|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489304|NCT00250276|104772|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489305|NCT00250276|104772|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489306|NCT00250276|104772|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489307|NCT00250276|104772|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489308|NCT00532298|110620|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493223|NCT00334334|107005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493224|NCT00334334|107005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493225|NCT00334334|107005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493226|NCT00334334|107005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489309|NCT00532298|110620|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489310|NCT00532298|110620|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489311|NCT00532298|110620|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489312|NCT00532298|110620|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489313|NCT00532298|110620|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489314|NCT00532298|110620|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2489315|NCT03214068||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282811/|
2490546|NCT00044278|LAM20007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490547|NCT00044278|LAM20007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493227|NCT00090155||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493228|NCT01939353||Poster Abstracts|https://apsard.org/wp-content/uploads/2016/11/Poster-Abstracts-Compiled1.pdf|Poster number 25
2493229|NCT00770744|2008-000479-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-000479-11/results|
2493230|NCT00388440|209762/147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494878|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."
2490548|NCT00044278|LAM20007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490549|NCT00044278|LAM20007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490550|NCT00044278|LAM20007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490551|NCT00609492|109621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490552|NCT00609492|109621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490553|NCT00609492|109621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490554|NCT00609492|109621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490555|NCT00609492|109621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490556|NCT00609492|109621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490557|NCT00609492|109621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490558|NCT01702454|116023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490559|NCT01702454|116023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490560|NCT01702454|116023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490561|NCT01702454|116023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490562|NCT01702454|116023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490563|NCT01702454|116023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490564|NCT01702454|116023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490565|NCT01077856||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-033&kw=V501-033&tab=access|
2490566|NCT01124422|113877|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493231|NCT00388440|209762/147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493232|NCT00388440|209762/147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490567|NCT01124422|113877|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490568|NCT01124422|113877|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490569|NCT01124422|113877|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490570|NCT01124422|113877|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490571|NCT01124422|113877|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490572|NCT01124422|113877|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490573|NCT03012802||Study Protocol|http://www.grupogerm.es/power|
2490574|NCT03012802||Statistical Analysis Plan|http://www.grupogerm.es/power|
2490575|NCT03012802||Clinical Study Report|http://www.grupogerm.es/power|
2490576|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.
2490577|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.
2490578|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.
2490579|NCT00372112|B2C108562|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490580|NCT00372112|B2C108562|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490581|NCT00372112|B2C108562|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493233|NCT00388440|209762/147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493234|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
2493235|NCT03567629||Individual Participant Data Set|https://en.wikipedia.org/wiki/United_States_National_Library_of_Medicine|
2493236|NCT03260478||Study Protocol|https://bmjopen.bmj.com/content/12/10/e067117.info|
2493237|NCT00678301|110521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493238|NCT00678301|110521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493239|NCT00678301|110521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493240|NCT00678301|110521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493241|NCT00678301|110521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493242|NCT00678301|110521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493243|NCT00678301|110521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493244|NCT01725126|116623|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493245|NCT01725126|116623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493246|NCT01725126|116623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493247|NCT01725126|116623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493248|NCT01725126|116623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493249|NCT01725126|116623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493250|NCT01725126|116623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493251|NCT07124052|SleeperOne2025|Informed Consent Form|https://clinicaltrials.gov/study-protocol-pending|Study protocol will be uploaded and publicly accessible upon final approval.
2493252|NCT01734239||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V110-018&kw=V110-018&tab=access|
2493253|NCT00972322||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8245-012&kw=8245-012&tab=access|
2493254|NCT03266926||Study Protocol|https://www.scribd.com/document/344597619/Study-Protocol|
2493255|NCT03266926||Informed Consent Form|https://www.scribd.com/document/344597523/Consent-Form|
2493256|NCT03266926||Individual Participant Data Set|https://www.scribd.com/document/344597573/Data-Collection-Spreadsheet|
2493257|NCT03266926||Participant Documents|https://www.scribd.com/document/344597424/Participant-Documents|
2493258|NCT04728139||Study Protocol|http://rehamhany809@gmail.com|
2490582|NCT00372112|B2C108562|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490583|NCT00372112|B2C108562|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490584|NCT00372112|B2C108562|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490585|NCT00372112|B2C108562|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490586|NCT01018186|106839|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490587|NCT01018186|106839|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490588|NCT01018186|106839|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490589|NCT01018186|106839|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490590|NCT01018186|106839|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490591|NCT01018186|106839|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490592|NCT01018186|106839|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490593|NCT01411111|112362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490594|NCT01411111|112362|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490595|NCT01411111|112362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490596|NCT01411111|112362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490597|NCT01411111|112362|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490598|NCT01411111|112362|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490599|NCT01411111|112362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490600|NCT04221009||Informed Consent Form|https://arc.research.usf.edu/Prod/sd/Doc/0/DDRU7K2KMHLK9ECT12FPTMA60B/3S78A88933BKN7869JO1NSMT62.pdf|
2490601|NCT04221009||Study Protocol|https://arc.research.usf.edu/Prod/sd/Doc/0/06USV5NTK2VKJ06CUK3TQJR578/Protocol%20v01%202019-10-24.docx|
2490602|NCT01428453|114458|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490603|NCT01428453|114458|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490604|NCT01428453|114458|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490605|NCT01428453|114458|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490606|NCT01428453|114458|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490607|NCT01428453|114458|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490608|NCT01428453|114458|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490609|NCT01030939|112861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490610|NCT01030939|112861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490611|NCT01030939|112861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490612|NCT01030939|112861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490613|NCT01030939|112861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490614|NCT01030939|112861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490615|NCT01030939|112861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493259|NCT01132443|115902|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493260|NCT01132443|115902|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493261|NCT01132443|115902|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493262|NCT01132443|115902|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494879|NCT05532995||Informed Consent Form|https://drive.google.com/file/d/1qiU0UgEzvPBntfA0lLWFe_AzOGngacl9/view?usp=sharing|
2490616|NCT00369993|SAS104449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490617|NCT00369993|SAS104449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490618|NCT00369993|SAS104449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490619|NCT00369993|SAS104449|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490620|NCT00369993|SAS104449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490621|NCT00369993|SAS104449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490622|NCT00369993|SAS104449|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490623|NCT04631081||Individual Participant Data Set|https://www.project-redcap.org/|
2490624|NCT00256893|ROF102100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490625|NCT00256893|ROF102100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490626|NCT00256893|ROF102100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490627|NCT00256893|ROF102100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490628|NCT00256893|ROF102100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490629|NCT00256893|ROF102100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490630|NCT00256893|ROF102100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490631|NCT01607086|111649|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490632|NCT01607086|111649|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490633|NCT01607086|111649|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490634|NCT01607086|111649|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490635|NCT01607086|111649|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490636|NCT01607086|111649|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490637|NCT01607086|111649|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490638|NCT00877877|111375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490639|NCT00877877|111375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490640|NCT00877877|111375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490641|NCT00877877|111375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490642|NCT00877877|111375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490643|NCT00877877|111375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490644|NCT00877877|111375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490645|NCT00102882|SFA100062|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490646|NCT00102882|SFA100062|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490647|NCT00102882|SFA100062|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490648|NCT00102882|SFA100062|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490649|NCT00102882|SFA100062|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494880|NCT00838916|112754|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490650|NCT00102882|SFA100062|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490651|NCT00102882|SFA100062|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490652|NCT04464369|LPDSItopride study|Study Protocol|http://www.targid.eu|
2494881|NCT00838916|112754|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490653|NCT01949051|200285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490654|NCT01949051|200285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490655|NCT01949051|200285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490656|NCT01949051|200285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490657|NCT01949051|200285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490658|NCT01949051|200285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490659|NCT01949051|200285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490660|NCT02028065||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-101&kw=8616-101&tab=access|
2490661|NCT02626520||Study Protocol|https://docs.google.com/viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxyZWFsd29ybGRvbmNvbG9neXxneDo2OGI0ZDgxMzdkZDIxYWJh|
2490662|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)
2490663|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf|CDC/NHSN Surveillance Definitions for Specific Types of Infections
2490664|NCT00503009|HZA109895|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490665|NCT00503009|HZA109895|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490666|NCT00503009|HZA109895|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490667|NCT00503009|HZA109895|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490668|NCT00503009|HZA109895|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490669|NCT00503009|HZA109895|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490670|NCT00496093||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490671|NCT00412854|104567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490672|NCT00412854|104567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490673|NCT00412854|104567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490674|NCT00412854|104567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490675|NCT00412854|104567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490676|NCT00412854|104567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490677|NCT00412854|104567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490678|NCT00268996|SB-480848/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490679|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
2490680|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
2490681|NCT00268996|SB-480848/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490682|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
2490683|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
2490684|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
2490685|NCT01847417|116498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490686|NCT01847417|116498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494882|NCT00838916|112754|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490687|NCT01847417|116498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490688|NCT01847417|116498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490689|NCT01847417|116498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490690|NCT01847417|116498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490691|NCT01777256|115919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490692|NCT01777256|115919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490693|NCT01777256|115919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490694|NCT01777256|115919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490695|NCT01777256|115919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490696|NCT01777256|115919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490697|NCT01777256|115919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490698|NCT03715166||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490699|NCT03715166||Study Protocol|https://clinicaltrials.servier.com/|
2490700|NCT03715166||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490701|NCT03715166||Informed Consent Form|https://clinicaltrials.servier.com/|
2490702|NCT03715166||Clinical Study Report|https://clinicaltrials.servier.com/|
2490703|NCT03715166||study-level clinical trial data|https://clinicaltrials.servier.com/|
2490704|NCT05069454||Study Protocol|http://www.isim.az|
2490705|NCT03019133|201609843|Informed Consent Form|http://hawkirb.research.uiowa.edu|
2490706|NCT02982967||Individual Participant Data Set|https://figshare.com/s/8f238bd02ca631cfe5fd|
2490707|NCT02369341|201959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490708|NCT02369341|201959|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490709|NCT02369341|201959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490710|NCT02369341|201959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490711|NCT02369341|201959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490712|NCT02369341|201959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490713|NCT02369341|201959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490714|NCT00451321|115493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490715|NCT00451321|115493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490716|NCT00451321|115493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490717|NCT00451321|115493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490718|NCT00451321|115493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490719|NCT00451321|115493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490720|NCT00451321|115493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490721|NCT01686633|116863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490722|NCT01686633|116863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490723|NCT01686633|116863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490724|NCT01686633|116863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490725|NCT01686633|116863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490726|NCT01686633|116863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490727|NCT01686633|116863|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490728|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
2490729|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
2490730|NCT02045797|116704|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490731|NCT02045797|116704|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490732|NCT02045797|116704|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490733|NCT02045797|116704|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490734|NCT02045797|116704|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490735|NCT02045797|116704|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490736|NCT02045797|116704|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490737|NCT03578081||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|
2490738|NCT04742101||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490739|NCT04742101||Study Protocol|https://clinicaltrials.servier.com/|
2490740|NCT04742101||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490741|NCT04742101||Informed Consent Form|https://clinicaltrials.servier.com/|
2490742|NCT04742101||Clinical Study Report|https://clinicaltrials.servier.com/|
2490743|NCT04742101||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2490744|NCT03577743|BMTN|Study Protocol|http://clinicaltrials.gov/NCT03577743|Phase 2 study to evaluate the effect of bevacizumab in metastatic triple negative breast cancer patients
2490745|NCT04999150|B0710118|Study Protocol|https://irbrcm.rcm.upr.edu/|
2490746|NCT00527943||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04736&kw=P04736&tab=access|
2490747|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
2490748|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
2490749|NCT00197041|257049/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490750|NCT00197041|257049/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490751|NCT00197041|257049/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490752|NCT00197041|257049/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490753|NCT00197041|257049/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490754|NCT00056407|ARI40006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490755|NCT00056407|ARI40006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490756|NCT00056407|ARI40006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490757|NCT00056407|ARI40006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490758|NCT00056407|ARI40006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490759|NCT00056407|ARI40006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490760|NCT00056407|ARI40006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490761|NCT01641692|116402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490762|NCT01641692|116402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490763|NCT01641692|116402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490764|NCT01641692|116402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490765|NCT01641692|116402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490766|NCT01641692|116402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490767|NCT01641692|116402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490768|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.
2490769|NCT00060476||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490770|NCT00873509||Individual Participant Data Set|https://ndar.nih.gov|
2493263|NCT01132443|115902|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490771|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.
2490772|NCT04644614||Study Protocol|https://doi.org/10.1016/j.urols.2015.06.286|
2490773|NCT03141281|https://osf.io/dp8n5/|Statistical Analysis Plan|https://osf.io/kq8yz/register/565fb3678c5e4a66b5582f67|Open Science Foundation registration of Data Analysis Plan
2490774|NCT06906133||Information site for participants (in Icelandic)|https://www.unak.is/is/rannsoknir/rannsoknir-vid-ha/svefn|
2490775|NCT04608500||Study Protocol|http://foamix.co.il/|
2490776|NCT01010906||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-005&kw=7009-005&tab=access|
2490777|NCT01107587|113518|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490778|NCT01107587|113518|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490779|NCT01107587|113518|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490780|NCT01107587|113518|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490781|NCT01107587|113518|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493264|NCT01132443|115902|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493265|NCT01132443|115902|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494883|NCT00838916|112754|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494884|NCT00838916|112754|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494885|NCT00838916|112754|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494886|NCT00838916|112754|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494887|NCT01842607|115661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494888|NCT01842607|115661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494889|NCT01842607|115661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494890|NCT01842607|115661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494891|NCT01842607|115661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494892|NCT01842607|115661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490782|NCT01107587|113518|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490783|NCT01756495|116628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490784|NCT01756495|116628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490785|NCT01756495|116628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490786|NCT01756495|116628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490787|NCT01756495|116628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490788|NCT01756495|116628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490789|NCT01756495|116628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490790|NCT01782664|116679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490791|NCT01782664|116679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490792|NCT01782664|116679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490793|NCT01782664|116679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490794|NCT01782664|116679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494893|NCT01842607|115661|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494894|NCT01245764||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-046&kw=V501-046&tab=access|
2494895|NCT00731393|100351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494896|NCT00731393|100351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494897|NCT00731393|100351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494898|NCT00731393|100351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494899|NCT00731393|100351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494900|NCT00731393|100351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494901|NCT00731393|100351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494902|NCT01551758|115151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490795|NCT01782664|116679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490796|NCT01782664|116679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490797|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.
2490798|NCT00000586||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/MSH/|
2490799|NCT00000586||Study Forms|http://biolincc.nhlbi.nih.gov/studies/MSH/|
2490800|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.
2490801|NCT00451386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490802|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.
2490803|NCT00000560||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/best/|
2490804|NCT00000560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/best/|
2490805|NCT01948739||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25570900|
2490806|NCT00048607||CSR Synospis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490807|NCT00751348|110876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490808|NCT00751348|110876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490809|NCT00751348|110876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490810|NCT00751348|110876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490811|NCT00751348|110876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490812|NCT00751348|110876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490813|NCT04187560||Clinical Study Report|http://lbpharma.us/wp-content/uploads/2020/12/lb-102-001-clinical-study-report-final.pdf|
2490814|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.
2490815|NCT07171762||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/18166260/|
2490816|NCT07180485|t780927t@yahoo.com.tw|Study Protocol|https://orcid.org/0000-0002-8823-6901|t780927t@yahoo.com.tw
2490817|NCT00454987|109664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490818|NCT00454987|109664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494903|NCT01551758|115151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494904|NCT01551758|115151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494905|NCT01551758|115151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494906|NCT01551758|115151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494907|NCT01551758|115151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494908|NCT01551758|115151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490819|NCT00454987|109664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490820|NCT00454987|109664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490821|NCT00454987|109664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490822|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
2490823|NCT01330485||Individual Participant Data Set|https://osf.io/426pd|
2490824|NCT01330485||All study files|https://osf.io/uhwnb|
2490825|NCT02319031|PMID: 26822022|Primary Publication|http://www.ncbi.nlm.nih.gov/pubmed/26822022|
2490826|NCT01075698||Study Protocol|https://prsinfo.clinicaltrials.gov/definitions.html|
2490827|NCT00129129|101858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490828|NCT00129129|101858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490829|NCT00129129|101858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490830|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.
2490831|NCT00129129|101858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490832|NCT01462669|115860|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490833|NCT01462669|115860|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490834|NCT01462669|115860|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490835|NCT01462669|115860|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490836|NCT01462669|115860|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490837|NCT01462669|115860|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490838|NCT01462669|115860|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490839|NCT01147861|114187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490840|NCT01147861|114187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490841|NCT01147861|114187|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490842|NCT01147861|114187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490843|NCT01147861|114187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490844|NCT01147861|114187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490845|NCT01147861|114187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490846|NCT00322335|106672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490847|NCT00322335|106672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490848|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.
2490849|NCT00322335|106672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490850|NCT00322335|106672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490851|NCT00322335|106672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490852|NCT01984775|117191|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490853|NCT01984775|117191|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490854|NCT01984775|117191|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490855|NCT01984775|117191|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493266|NCT00091559||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493267|NCT02145468|116197|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490856|NCT01984775|117191|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490857|NCT01984775|117191|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490858|NCT00907985|112676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490859|NCT00907985|112676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490860|NCT00907985|112676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490861|NCT00907985|112676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490862|NCT00907985|112676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490863|NCT00907985|112676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490864|NCT00907985|112676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490865|NCT02735083||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490866|NCT02735083||Study Protocol|https://clinicaltrials.servier.com/|
2490867|NCT02735083||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490868|NCT02735083||Informed Consent Form|https://clinicaltrials.servier.com/|
2490869|NCT02735083||Clinical Study Report|https://clinicaltrials.servier.com/|
2490870|NCT02735083||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2490871|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
2490872|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
2490873|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
2490874|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.
2490875|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.
2493268|NCT02145468|116197|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493269|NCT02145468|116197|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493270|NCT02145468|116197|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493271|NCT02145468|116197|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493272|NCT02145468|116197|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490876|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.
2490877|NCT00116831|AVD100521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490878|NCT00116831|AVD100521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490879|NCT00116831|AVD100521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490880|NCT00116831|AVD100521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490881|NCT00116831|AVD100521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490882|NCT00116831|AVD100521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490883|NCT00116831|AVD100521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490884|NCT00380393|106464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490885|NCT00380393|106464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490886|NCT00380393|106464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490887|NCT00380393|106464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490888|NCT00380393|106464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490889|NCT00380393|106464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490890|NCT00779012||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2490891|NCT01391065||Published article|https://doi.org/10.1016/j.ijrobp.2019.10.037|
2490892|NCT04164901||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490893|NCT00228917|103812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490894|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.
2490895|NCT00228917|103812|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490896|NCT00228917|103812|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490897|NCT00228917|103812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490898|NCT00228917|103812|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490899|NCT01165138|106827|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490900|NCT01165138|106827|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490901|NCT01165138|106827|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490902|NCT01165138|106827|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490903|NCT01165138|106827|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490904|NCT01165138|106827|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490905|NCT01165138|106827|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490906|NCT00896558|112668|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490907|NCT00896558|112668|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490908|NCT00896558|112668|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490909|NCT00896558|112668|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494909|NCT01021852||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6096-011&kw=6096-011&tab=access|
2490910|NCT00896558|112668|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490911|NCT00896558|112668|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490912|NCT00896558|112668|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490913|NCT07110077|vanesssatob@gmail.com|Study Protocol|https://drive.google.com/drive/folders/1oaz8ewLKW--cX5Nm7Y0I_j0jPhJzwzVS?usp=sharing|
2490914|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.
2490915|NCT00000514||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/shep/|
2490916|NCT00000514||Study Forms|http://biolincc.nhlbi.nih.gov/studies/shep/|
2490917|NCT00000514||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/shep/|
2490918|NCT00603746|FFA109684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490919|NCT00603746|FFA109684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490920|NCT00603746|FFA109684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490921|NCT00603746|FFA109684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490922|NCT00603746|FFA109684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490923|NCT00603746|FFA109684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490924|NCT00603746|FFA109684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490925|NCT00133874|TOC100224|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490926|NCT00133874|TOC100224|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490927|NCT00133874|TOC100224|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490928|NCT00133874|TOC100224|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490929|NCT00133874|TOC100224|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490930|NCT00133874|TOC100224|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490931|NCT00133874|TOC100224|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490932|NCT07044180||Study Protocol|https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en&EUCT=2025-521373-13-00|
2490933|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.
2490934|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.
2490935|NCT03672695||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490936|NCT03672695||Study Protocol|https://clinicaltrials.servier.com/|
2490937|NCT03672695||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490938|NCT03672695||Informed Consent Form|https://clinicaltrials.servier.com/|
2490939|NCT03672695||Clinical Study Report|https://clinicaltrials.servier.com/|
2490940|NCT03672435||Individual Participant Data Set|http://www.abcd-vision.org/OCR/OCR%20proparacaine%20de-identified.pdf|deidentified OCR topical anesthetic recovery outcomes
2490941|NCT00578175|110058|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490942|NCT00578175|110058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490943|NCT00578175|110058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490944|NCT00578175|110058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490945|NCT00578175|110058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490946|NCT00578175|110058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490947|NCT00578175|110058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490948|NCT03900299||Study Protocol|http://www.med.alexu.edu.eg/ethics-committee/|
2490949|NCT00924911|112034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490950|NCT00924911|112034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490951|NCT00924911|112034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490952|NCT00924911|112034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490953|NCT00924911|112034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490954|NCT00924911|112034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490955|NCT00924911|112034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490956|NCT00945503|109731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490957|NCT00945503|109731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490958|NCT00945503|109731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494910|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.
2490959|NCT00945503|109731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490960|NCT00945503|109731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490961|NCT00945503|109731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490962|NCT00945503|109731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490963|NCT00196950|134612/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490964|NCT00196950|134612/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490965|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.
2490966|NCT00196950|134612/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490967|NCT00196950|134612/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490968|NCT00196950|134612/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490969|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.
2490970|NCT04126785|CAAE 96882818.3.0000.5398|Brazil Research Ethics Committees|http://plataformabrasil.saude.gov.br/|
2490971|NCT02632708||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2490972|NCT02632708||Study Protocol|https://clinicaltrials.servier.com/|
2490973|NCT02632708||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2490974|NCT02632708||Informed Consent Form|https://clinicaltrials.servier.com/|
2490975|NCT02632708||Clinical Study Report|https://clinicaltrials.servier.com/|
2490976|NCT02632708||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2490977|NCT02016963|HGS1021-C1069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490978|NCT02016963|HGS1021-C1069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490979|NCT02016963|HGS1021-C1069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490980|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
2490981|NCT02016963|HGS1021-C1069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490982|NCT02016963|HGS1021-C1069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490983|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
2490984|NCT01494610|114334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490985|NCT01494610|114334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490986|NCT01494610|114334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490987|NCT01494610|114334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490988|NCT01494610|114334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490989|NCT01494610|114334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490990|NCT01494610|114334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494911|NCT00377585|104888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494912|NCT00377585|104888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494913|NCT00377585|104888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494914|NCT00377585|104888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494915|NCT00377585|104888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494916|NCT00989404|113625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494917|NCT00989404|113625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494918|NCT00989404|113625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494919|NCT00989404|113625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494920|NCT00989404|113625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494921|NCT00989404|113625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494922|NCT00989404|113625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494923|NCT01153893|113199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494924|NCT01153893|113199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494925|NCT01153893|113199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494926|NCT01153893|113199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494927|NCT01153893|113199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490991|NCT06876779||Study Protocol|https://www.ugc.edu.hk/eng/rgc/funding_opport/fds/funded%20research/fds2425.html|
2490992|NCT00394030|GLP107724|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490993|NCT00394030|GLP107724|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490994|NCT00394030|GLP107724|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490995|NCT00394030|GLP107724|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490996|NCT00394030|GLP107724|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490997|NCT00394030|GLP107724|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490998|NCT00394030|GLP107724|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2490999|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|
2491000|NCT01573624|115938|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494928|NCT01153893|113199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491001|NCT01573624|115938|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491002|NCT01573624|115938|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491003|NCT01573624|115938|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491004|NCT01573624|115938|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491005|NCT01573624|115938|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491006|NCT01573624|115938|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491007|NCT00689481|114742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491008|NCT00689481|114742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491009|NCT00689481|114742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491010|NCT00689481|114742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491011|NCT00689481|114742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491012|NCT00689481|114742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491013|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).
2491014|NCT00637195|111567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491015|NCT00637195|111567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491016|NCT00637195|111567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491017|NCT00637195|111567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491018|NCT00637195|111567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491019|NCT00637195|111567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491020|NCT00637195|111567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491021|NCT06919185|2025-01028-01|Study Protocol|https://slmf.se/forskning/lungmedicinsk-forskning/sparc/|
2491022|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).
2491023|NCT01934153|117157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491024|NCT01934153|117157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491025|NCT01934153|117157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491026|NCT01934153|117157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491027|NCT01934153|117157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491028|NCT01934153|117157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491029|NCT01934153|117157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491030|NCT00586469|111258|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491031|NCT00586469|111258|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491032|NCT00586469|111258|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491033|NCT00586469|111258|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491034|NCT00586469|111258|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491035|NCT00586469|111258|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491036|NCT00586469|111258|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491037|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.
2491038|NCT01114841|114572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491039|NCT01114841|114572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491040|NCT01114841|114572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491041|NCT01114841|114572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491042|NCT01114841|114572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491043|NCT01114841|114572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491044|NCT01114841|114572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491045|NCT01462357|115411|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491046|NCT01462357|115411|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491047|NCT01462357|115411|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491048|NCT01462357|115411|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491049|NCT01462357|115411|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491050|NCT01462357|115411|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491051|NCT07086287|rhBNP|Study Protocol|https://www.chictr.org.cn/|China Clinical Trial Registration Center
2491052|NCT00519649|110474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491053|NCT00519649|110474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491054|NCT00519649|110474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491055|NCT00519649|110474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491056|NCT00519649|110474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491057|NCT00519649|110474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491058|NCT00519649|110474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491059|NCT01930058||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8876-003&kw=8876-003|
2491060|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)
2491061|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.
2493273|NCT02145468|116197|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493274|NCT00635128|110947|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493275|NCT00635128|110947|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493276|NCT00635128|110947|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493277|NCT00635128|110947|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493278|NCT00635128|110947|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493279|NCT00635128|110947|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493280|NCT00635128|110947|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493281|NCT01333813|112688|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493282|NCT01333813|112688|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493283|NCT01333813|112688|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493284|NCT01333813|112688|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493285|NCT01333813|112688|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493286|NCT01333813|112688|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493287|NCT01376232|113634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493288|NCT01376232|113634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493289|NCT01376232|113634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493290|NCT01376232|113634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493291|NCT01376232|113634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491062|NCT01837316|116592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491063|NCT01837316|116592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491064|NCT01837316|116592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491065|NCT01837316|116592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491066|NCT01837316|116592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491067|NCT01837316|116592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491068|NCT01837316|116592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491069|NCT03125265||Study Protocol|http://bmjopen.bmj.com/content/5/3/e006897.long|
2491070|NCT05007457|Benedetta Isani|Study Protocol|http://aosp.bo.it|
2491071|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.
2491072|NCT00779766|107638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491073|NCT00779766|107638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491074|NCT00779766|107638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491075|NCT00779766|107638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491076|NCT00779766|107638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491077|NCT00779766|107638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491078|NCT00779766|107638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491079|NCT01706250|114550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491080|NCT01706250|114550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491081|NCT01706250|114550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491082|NCT01706250|114550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491083|NCT01706250|114550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491084|NCT00812929|112025|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491085|NCT00812929|112025|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491086|NCT00812929|112025|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491087|NCT00812929|112025|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491088|NCT00812929|112025|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491089|NCT00812929|112025|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491090|NCT00812929|112025|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491091|NCT05776030||Statistical Analysis Plan|https://osf.io/87wfq/files/osfstorage|
2491092|NCT00263692|213503/047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491093|NCT00263692|213503/047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491094|NCT00263692|213503/047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491095|NCT00263692|213503/047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491096|NCT00263692|213503/047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491097|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
2491098|NCT00812812|112487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491099|NCT00812812|112487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491100|NCT00812812|112487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491101|NCT00812812|112487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491102|NCT05262205||Study Protocol|http://irb.mans.edu.eg|
2491103|NCT01310413|114464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491104|NCT01310413|114464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491105|NCT01310413|114464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491106|NCT01310413|114464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491107|NCT01310413|114464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491108|NCT01310413|114464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491109|NCT00482079||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491110|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.
2491111|NCT00075829|BMT CTN-0102|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
2491112|NCT00075829|BMT CTN-0102|Study Forms|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
2491113|NCT00774995|110073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491114|NCT00774995|110073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491115|NCT00774995|110073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491116|NCT00774995|110073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491117|NCT00774995|110073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491118|NCT00774995|110073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491119|NCT02143518||Clinical Study Report|https://gwvru.smhs.gwu.edu/clinical|
2491120|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.
2491121|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.
2491122|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.
2491123|NCT01957189|200254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491124|NCT01957189|200254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491125|NCT01957189|200254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491126|NCT01957189|200254|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491127|NCT01957189|200254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491128|NCT01957189|200254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491129|NCT01957189|200254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491130|NCT04891679|PATIENT INFORMATION SHEET|Informed Consent Form|https://figshare.com/s/a6c10a2a4be65f30144b|
2491131|NCT04891679|STUDY PROTOCOL|Study Protocol|https://figshare.com/s/3f978a10eee4e90173bb|
2491132|NCT00298831||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491133|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.
2491134|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.
2491135|NCT00338351|106208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491136|NCT00338351|106208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493292|NCT01376232|113634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493293|NCT01376232|113634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493294|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.
2493295|NCT00586612|110215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493296|NCT00586612|110215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493297|NCT00586612|110215|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493298|NCT00586612|110215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493299|NCT00586612|110215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493300|NCT00586612|110215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493301|NCT00109330|776423/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493302|NCT00109330|776423/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493303|NCT00109330|776423/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493304|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
2493305|NCT00109330|776423/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493306|NCT00109330|776423/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493307|NCT00056277|SCA30924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493308|NCT00056277|SCA30924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493309|NCT00056277|SCA30924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493310|NCT00056277|SCA30924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493311|NCT00056277|SCA30924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493312|NCT00056277|SCA30924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493313|NCT00056277|SCA30924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493314|NCT04110704|IRAS 261294|Study Protocol|http://preview-kcl.cloud.contensis.com/Preview/1/research/project?id=478a6e61-4446-4a12-945e-c41a3879371d|
2493315|NCT00359983|107824|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493316|NCT00359983|107824|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493317|NCT00359983|107824|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493318|NCT00359983|107824|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493319|NCT00359983|107824|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493320|NCT00359983|107824|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493321|NCT04445727|vitamin c|Clinical Study Report|http://www.bonusan.es/vademecum/vitamina_c1000_complejo_de_ascorbatos.html|
2493322|NCT01353768|115008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493323|NCT01353768|115008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493324|NCT01353768|115008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493325|NCT01353768|115008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494929|NCT01299610|113434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494930|NCT01299610|113434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494931|NCT01299610|113434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493326|NCT01353768|115008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493327|NCT01353768|115008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493328|NCT01353768|115008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493329|NCT03091231|mpUS2016|Study Protocol|http://www.martini-klinik.de|to request an electronic copy send an email to a.renter@uke.de
2493330|NCT04340791||Study Protocol|https://osf.io/kq9c8/|
2493331|NCT04340791||Statistical Analysis Plan|https://osf.io/kq9c8/|
2493332|NCT04340791||Informed Consent Form|https://osf.io/kq9c8/|
2493333|NCT04340791||Individual Participant Data Set|https://osf.io/kq9c8/|When results will be published
2493334|NCT00989625|108504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493335|NCT00989625|108504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493336|NCT00989625|108504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493337|NCT00989625|108504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493338|NCT00989625|108504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493339|NCT00989625|108504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493340|NCT00989625|108504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493341|NCT02963025||Study Protocol|http://prothor.info|
2493342|NCT05931913||Individual Participant Data Set|https://nda.nih.gov/|
2493343|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
2493344|NCT00225823|FFR103184|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494932|NCT01299610|113434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493345|NCT00225823|FFR103184|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493346|NCT00225823|FFR103184|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493347|NCT00225823|FFR103184|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493348|NCT00225823|FFR103184|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493349|NCT00225823|FFR103184|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493350|NCT00225823|FFR103184|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493351|NCT02615002||Study website|http://www.recognitionstudy.com|
2493352|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/22118062/|
2493353|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/20673234/|
2493354|NCT00095420||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076578/|
2493355|NCT00095420||Clinical Study Report|http://pubmed.ncbi.nlm.nih.gov/27620949/|
2493356|NCT00537654|ARI109882|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493357|NCT00537654|ARI109882|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493358|NCT00537654|ARI109882|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493359|NCT00537654|ARI109882|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493360|NCT00537654|ARI109882|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493361|NCT00537654|ARI109882|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493362|NCT00537654|ARI109882|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493363|NCT00552929||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493364|NCT06906354|msabry776@yahoo.com|Study Protocol|https://pubmed.ncbi.nlm.nih.gov/17482984/|very good
2493365|NCT01198756|113314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493366|NCT01198756|113314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493367|NCT01198756|113314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493368|NCT01198756|113314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493369|NCT01198756|113314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493370|NCT01198756|113314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493371|NCT01198756|113314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493372|NCT00599911|2007-001071-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001071-11/results|
2493373|NCT01978327|200592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493374|NCT01978327|200592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493375|NCT01978327|200592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493376|NCT01978327|200592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493377|NCT01978327|200592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493378|NCT01978327|200592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493379|NCT01978327|200592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493380|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
2493381|NCT01498679|113719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493382|NCT01498679|113719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493383|NCT01498679|113719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493384|NCT01498679|113719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493385|NCT01498679|113719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493386|NCT01498679|113719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493387|NCT01498679|113719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493388|NCT01035645|110040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493389|NCT01035645|110040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493390|NCT01035645|110040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493391|NCT01035645|110040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493392|NCT01035645|110040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493393|NCT01035645|110040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493394|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
2493395|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
2493396|NCT02688218|STUDY00015452|Study Protocol|http://eirb.ohsu.edu|Institutionally reviewed and accepted protocol for this study.
2493397|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.
2493398|NCT03789448||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2128-8|
2493399|NCT00092352||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2493400|NCT00116883|FFR100012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493401|NCT00116883|FFR100012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493402|NCT00116883|FFR100012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493403|NCT00116883|FFR100012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493404|NCT00116883|FFR100012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493405|NCT00116883|FFR100012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493406|NCT00116883|FFR100012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493407|NCT02960750|4382156|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382156/?report=classic|
2493408|NCT02960750|4323230|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323230/?report=classic|
2493409|NCT02960750|4266209|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266209/|
2493410|NCT01139580|114743|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493411|NCT01139580|114743|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493412|NCT01139580|114743|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493413|NCT01139580|114743|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493414|NCT01139580|114743|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493415|NCT01139580|114743|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493416|NCT01139580|114743|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493417|NCT00662818||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-034&kw=0974-034&tab=access|
2493418|NCT00659178|ILI108621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493419|NCT00659178|ILI108621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493420|NCT00659178|ILI108621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493421|NCT00659178|ILI108621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493422|NCT00659178|ILI108621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493423|NCT00659178|ILI108621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493424|NCT00659178|ILI108621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493425|NCT00353288|105908|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493426|NCT00353288|105908|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493427|NCT00353288|105908|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493428|NCT00353288|105908|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493429|NCT00353288|105908|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493430|NCT00353288|105908|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493431|NCT02437253||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=28119823|
2493432|NCT06729515||Individual Participant Data Set|https://figshare.com/s/46ea85c406ec97afc17a|
2493433|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.
2493434|NCT00005130||Study Protocol|http://www.cardia.dopm.uab.edu/exam-materials2/protocols|
2493435|NCT00005130||Informed Consent Form|http://www.cardia.dopm.uab.edu/exam-materials2/consent-forms|
2493436|NCT00005130||Data Collection Forms|http://www.cardia.dopm.uab.edu/exam-materials2/data-collection-forms|
2493437|NCT00005130||Study Manuals|http://www.cardia.dopm.uab.edu/exam-materials2/manual-of-operations|
2493438|NCT00852540|110978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493439|NCT00852540|110978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493440|NCT00852540|110978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493441|NCT00852540|110978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493442|NCT00852540|110978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491137|NCT00338351|106208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491138|NCT00338351|106208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491139|NCT00338351|106208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491140|NCT00338351|106208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491141|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
2491142|NCT01978119|115645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491143|NCT01978119|115645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491144|NCT01978119|115645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491145|NCT01978119|115645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491146|NCT01978119|115645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491147|NCT01978119|115645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491148|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.
2491149|NCT01814722||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-266&kw=0518-266&tab=access|
2491150|NCT00420680||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491151|NCT01181895|112060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491152|NCT01181895|112060|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491153|NCT01181895|112060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491154|NCT01181895|112060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491155|NCT01181895|112060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491156|NCT01181895|112060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491157|NCT01181895|112060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491158|NCT00560833||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06459&kw=P06459&tab=access|
2491159|NCT01003418|113629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491160|NCT01003418|113629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491161|NCT01003418|113629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491162|NCT01003418|113629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491163|NCT01003418|113629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491164|NCT01003418|113629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491165|NCT02696850|CGI scale|Questionnaire|https://www.psywellness.com.sg/docs/CGI.pdf|
2493443|NCT00852540|110978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493444|NCT00852540|110978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493445|NCT01156792|114255|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493446|NCT01156792|114255|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493447|NCT01156792|114255|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493448|NCT01156792|114255|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493449|NCT01156792|114255|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493450|NCT01156792|114255|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493451|NCT01156792|114255|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493452|NCT00158860|HS2100275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491166|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.
2491167|NCT00345579|105987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491168|NCT00345579|105987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491169|NCT00345579|105987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491170|NCT00345579|105987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491171|NCT00345579|105987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491172|NCT00345579|105987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491173|NCT01827904||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
2491174|NCT00432380|109216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491175|NCT00432380|109216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491176|NCT00432380|109216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491177|NCT00432380|109216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491178|NCT00432380|109216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491179|NCT00432380|109216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491180|NCT00432380|109216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491181|NCT00264615|LEP103944|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491182|NCT00264615|LEP103944|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491183|NCT00264615|LEP103944|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493453|NCT00158860|HS2100275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493454|NCT00158860|HS2100275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493455|NCT00158860|HS2100275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493456|NCT00158860|HS2100275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493457|NCT00158860|HS2100275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493458|NCT00158860|HS2100275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493459|NCT01476098|114693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493460|NCT01476098|114693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493461|NCT01476098|114693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494933|NCT01299610|113434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494934|NCT01299610|113434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494935|NCT01299610|113434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494936|NCT00671216|DB1111509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494937|NCT00671216|DB1111509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491184|NCT00264615|LEP103944|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493462|NCT01476098|114693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493463|NCT01476098|114693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493464|NCT01476098|114693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493465|NCT01476098|114693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493466|NCT00950586|110792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493467|NCT00950586|110792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493468|NCT00950586|110792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493469|NCT00950586|110792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493470|NCT00950586|110792|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493471|NCT00950586|110792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493472|NCT00950586|110792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493473|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
2493474|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
2493475|NCT00603252|111149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493476|NCT00603252|111149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493477|NCT00603252|111149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493478|NCT00603252|111149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493479|NCT00603252|111149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493480|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.
2493481|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.
2493482|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.
2493483|NCT01711723|115676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493484|NCT01711723|115676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493485|NCT01711723|115676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493486|NCT01711723|115676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493487|NCT01711723|115676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493488|NCT01711723|115676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493489|NCT01711723|115676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493490|NCT01323972|113398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493491|NCT01323972|113398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493492|NCT01323972|113398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493493|NCT01323972|113398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493494|NCT01323972|113398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493495|NCT01323972|113398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493496|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/.
2493497|NCT00363870|108134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493498|NCT00363870|108134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491185|NCT00264615|LEP103944|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491186|NCT00264615|LEP103944|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491187|NCT00264615|LEP103944|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491188|NCT00701389||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-026&kw=0974-026&tab=access|
2491189|NCT01267071|114136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491190|NCT01267071|114136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491191|NCT01267071|114136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491192|NCT01267071|114136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491193|NCT01267071|114136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491194|NCT01267071|114136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491195|NCT01267071|114136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491196|NCT01319006|114703|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491197|NCT01319006|114703|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491198|NCT01319006|114703|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491199|NCT01319006|114703|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491200|NCT01319006|114703|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491201|NCT01319006|114703|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491202|NCT01319006|114703|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491203|NCT00996996|104517|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491204|NCT00996996|104517|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491205|NCT00996996|104517|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491206|NCT00996996|104517|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491207|NCT00996996|104517|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491208|NCT00996996|104517|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491209|NCT00996996|104517|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491210|NCT00289796|210602-002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491211|NCT00289796|210602-002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491212|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
2491213|NCT00289796|210602-002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491214|NCT00289796|210602-002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491215|NCT00289796|210602-002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491216|NCT02207829|201316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491217|NCT02207829|201316|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491218|NCT02207829|201316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491219|NCT02207829|201316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491220|NCT02207829|201316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491221|NCT02207829|201316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491222|NCT02207829|201316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491223|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.
2491224|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
2491225|NCT02019719|116099|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491226|NCT02019719|116099|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491227|NCT02019719|116099|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491228|NCT02019719|116099|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491229|NCT02019719|116099|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491230|NCT02019719|116099|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491231|NCT02019719|116099|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491232|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
2491233|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
2491234|NCT01059617|113483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491235|NCT01059617|113483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491236|NCT01059617|113483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491237|NCT01059617|113483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491238|NCT01059617|113483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491239|NCT01059617|113483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491240|NCT00605241|DAN106593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491241|NCT00605241|DAN106593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491242|NCT00605241|DAN106593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491243|NCT00605241|DAN106593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491244|NCT00605241|DAN106593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491245|NCT00605241|DAN106593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491246|NCT00605241|DAN106593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491247|NCT01476046|110951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491248|NCT01476046|110951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491249|NCT01476046|110951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491250|NCT01476046|110951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491251|NCT01476046|110951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491252|NCT01476046|110951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491253|NCT01476046|110951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491254|NCT00941603||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05675&kw=P05675&tab=access|
2491255|NCT06635343||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28990891|
2491256|NCT00797667||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-049&kw=0974-049&tab=access|
2491257|NCT05166018|SUMO|Individual Participant Data Set|https://sumo.doc.cortexxmi.com/|
2491258|NCT06633263||Study Protocol|https://osf.io/dhmj8/|
2491259|NCT06633263||Individual Participant Data Set|https://osf.io/dhmj8/|
2491260|NCT03793101||Clinical Study Report|http://eyemed.pl|
2491261|NCT00920192|111645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491262|NCT00920192|111645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491263|NCT00920192|111645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491264|NCT00920192|111645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491265|NCT00920192|111645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491266|NCT00920192|111645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491267|NCT06333444||Informed Consent Form|https://docs.google.com/forms/d/e/1FAIpQLScX9N2R8xP62390ly7vV8Ixyy_yfQsUUmUG3QCm_M-ZriXAnA/viewform|
2491268|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."
2493499|NCT00363870|108134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493500|NCT00363870|108134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493501|NCT00363870|108134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493502|NCT00363870|108134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493503|NCT00363870|108134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493504|NCT00196976|103533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493505|NCT00196976|103533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493506|NCT00196976|103533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491269|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. \[Epub ahead of print\]"
2491270|NCT02679690||Informed Consent Form|http://www.osiris.pitt.edu|
2491271|NCT02701218|ENT-2558-03601|Study Protocol|http://ros.med.cmu.ac.th/Security/SignIn.aspx|Research administration section website
2491272|NCT00833989|111539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491273|NCT00833989|111539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491274|NCT00833989|111539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491275|NCT00833989|111539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491276|NCT00833989|111539|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491277|NCT00833989|111539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491278|NCT00833989|111539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491279|NCT01462344|115358|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491280|NCT01462344|115358|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491281|NCT01462344|115358|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491282|NCT01462344|115358|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491283|NCT01462344|115358|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491284|NCT01462344|115358|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491285|NCT01462344|115358|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491286|NCT00263666|444563/022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491287|NCT00263666|444563/022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491288|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
2491289|NCT00263666|444563/022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493507|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.
2493508|NCT00196976|103533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493509|NCT00196976|103533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493510|NCT00321373|107022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493511|NCT00321373|107022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493512|NCT00321373|107022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493513|NCT00321373|107022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493514|NCT00321373|107022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493515|NCT01323647|114306|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493516|NCT01323647|114306|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493517|NCT01323647|114306|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493518|NCT01323647|114306|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493519|NCT01323647|114306|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493520|NCT01323647|114306|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493521|NCT00071747|SCA30926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493522|NCT00071747|SCA30926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493523|NCT00071747|SCA30926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493524|NCT00071747|SCA30926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493525|NCT00071747|SCA30926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493526|NCT00071747|SCA30926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493527|NCT00306696|49653/342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493528|NCT00306696|49653/342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493529|NCT00306696|49653/342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493530|NCT00306696|49653/342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493531|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
2494938|NCT00671216|DB1111509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494939|NCT00671216|DB1111509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494940|NCT00671216|DB1111509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494941|NCT00671216|DB1111509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494942|NCT00671216|DB1111509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494943|NCT01615796|115198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494944|NCT01615796|115198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494945|NCT01615796|115198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494946|NCT01615796|115198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494947|NCT01615796|115198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494948|NCT01615796|115198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494949|NCT01615796|115198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494950|NCT00964158|113528|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494951|NCT00964158|113528|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493532|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
2493533|NCT00306696|49653/342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493534|NCT00704405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-009&kw=7009-009&tab=access|
2493535|NCT01602562|116100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493536|NCT01602562|116100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493537|NCT01602562|116100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493538|NCT01602562|116100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493539|NCT01751074|115677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493540|NCT01751074|115677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493541|NCT01751074|115677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493542|NCT01751074|115677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493543|NCT01751074|115677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493544|NCT01751074|115677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493545|NCT01751074|115677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493546|NCT01395888|115247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493547|NCT01395888|115247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493548|NCT01395888|115247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493549|NCT01395888|115247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493550|NCT01395888|115247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493551|NCT01395888|115247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493552|NCT01395888|115247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493553|NCT02549014||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-001&kw=1064-001&tab=access|
2493554|NCT01016977|114566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493555|NCT01016977|114566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493556|NCT01016977|114566|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493557|NCT01016977|114566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493558|NCT01016977|114566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493559|NCT01016977|114566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493560|NCT01016977|114566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493561|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Hand Shape Representation in Parietal Reach Region. The Journal of Neuroscience."
2493562|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Decoding motor imagery from the posterior parietal cortex of a tetraplegic human. Science"
2493563|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.
2493564|NCT00839657||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coag/|
2493565|NCT00839657||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coag/|
2493566|NCT00839657||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coag/|
2493567|NCT01362257|112014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493568|NCT01362257|112014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493569|NCT01362257|112014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493570|NCT01362257|112014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493571|NCT01362257|112014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491290|NCT00263666|444563/022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491291|NCT00263666|444563/022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491292|NCT00355082|LAM30055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491293|NCT00355082|LAM30055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491294|NCT00355082|LAM30055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491295|NCT00355082|LAM30055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491296|NCT00355082|LAM30055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491297|NCT00355082|LAM30055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491298|NCT00355082|LAM30055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491299|NCT04411290||Principal investigator data|https://scholar.google.com.tr/citations?user=6bFlCZwAAAAJ&hl=tr|
2491300|NCT01196975|112963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491301|NCT01196975|112963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491302|NCT01196975|112963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491303|NCT01196975|112963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491304|NCT01196975|112963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491305|NCT01196975|112963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491306|NCT01196975|112963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491307|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
2491308|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."
2491309|NCT00550225|MAB108115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491310|NCT00550225|MAB108115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491311|NCT00550225|MAB108115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491312|NCT00550225|MAB108115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491313|NCT00550225|MAB108115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491314|NCT00550225|MAB108115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491315|NCT00550225|MAB108115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491316|NCT00345904|107507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491317|NCT00345904|107507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491318|NCT00345904|107507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491319|NCT00345904|107507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491320|NCT00345904|107507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491321|NCT06426537||Study Protocol|http://drive.google.com/drive/u/3/folders/15qW39gHRtgwIuP8rGm8ukhXtYnLRCFNO|
2491322|NCT02676479||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/4037016|
2491323|NCT00379613||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2491324|NCT02672631||Study Protocol|http://clinical-mri.com/mr-neurography-diagnostic-criteria-to-determine-lesions-of-peripheral-nerves/|
2491325|NCT00374842|108656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491326|NCT00374842|108656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491327|NCT00374842|108656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491328|NCT00374842|108656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491329|NCT00374842|108656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491330|NCT00354874|B2C101762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491331|NCT00354874|B2C101762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491332|NCT00354874|B2C101762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491333|NCT00354874|B2C101762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491334|NCT00354874|B2C101762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491335|NCT00354874|B2C101762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491336|NCT00354874|B2C101762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491337|NCT00319098|107064|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491338|NCT00319098|107064|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491339|NCT00319098|107064|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491340|NCT00319098|107064|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491341|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.
2491342|NCT00319098|107064|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491343|NCT01217073||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-006&kw=3102-006&tab=access|
2491344|NCT00989287|113866|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491345|NCT00989287|113866|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491346|NCT00989287|113866|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491347|NCT00989287|113866|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491348|NCT00989287|113866|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491349|NCT00989287|113866|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491350|NCT00989287|113866|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491351|NCT00697749|208129/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491352|NCT00697749|208129/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491353|NCT00697749|208129/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491354|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
2491355|NCT00697749|208129/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491356|NCT00697749|208129/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491357|NCT06520111|sice|Study Protocol|https://siceitalia.com/|SICE- Team di ricerca Endocrino-metabolica- crisal
2491358|NCT02322671|200107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491359|NCT02322671|200107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491360|NCT02322671|200107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491361|NCT02322671|200107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491362|NCT02322671|200107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491363|NCT02322671|200107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491364|NCT02322671|200107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491365|NCT01090453|113615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491366|NCT01090453|113615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494952|NCT00964158|113528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494953|NCT00964158|113528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494954|NCT00964158|113528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494955|NCT00964158|113528|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494956|NCT00964158|113528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494957|NCT00989612|113519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494958|NCT00989612|113519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494959|NCT00989612|113519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494960|NCT00989612|113519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494961|NCT00989612|113519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494962|NCT00989612|113519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494963|NCT00989612|113519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494964|NCT00971425|113572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494965|NCT00971425|113572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494966|NCT00971425|113572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494967|NCT00971425|113572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494968|NCT00971425|113572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494969|NCT00971425|113572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494970|NCT00971425|113572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494971|NCT00240539|100449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494972|NCT00240539|100449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494973|NCT00240539|100449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494974|NCT00240539|100449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494975|NCT00240539|100449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494976|NCT04744636||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2494977|NCT04744636||Study Protocol|https://clinicaltrials.servier.com/|
2494978|NCT04744636||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2494979|NCT04744636||Informed Consent Form|https://clinicaltrials.servier.com/|
2494980|NCT04744636||Clinical Study Report|https://clinicaltrials.servier.com/|
2494981|NCT04744636||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2494982|NCT01153841|113151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494983|NCT01153841|113151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494984|NCT01153841|113151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494985|NCT01153841|113151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494986|NCT01153841|113151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494987|NCT01153841|113151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494988|NCT00044486||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494989|NCT00083343||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2494990|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)
2494991|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)
2494992|NCT00866515|112205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494993|NCT00866515|112205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494994|NCT00866515|112205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494995|NCT00866515|112205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494996|NCT00866515|112205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494997|NCT00866515|112205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494998|NCT00866515|112205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2494999|NCT00880763||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-016&kw=7009-016&tab=access|
2495000|NCT01231607|114263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495001|NCT01231607|114263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495002|NCT01231607|114263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495003|NCT01231607|114263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495004|NCT01231607|114263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495005|NCT01231607|114263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495006|NCT01231607|114263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495007|NCT00118729|FFR101816|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495008|NCT00118729|FFR101816|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495009|NCT00118729|FFR101816|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495010|NCT00118729|FFR101816|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495011|NCT00118729|FFR101816|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495012|NCT00118729|FFR101816|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495013|NCT00118729|FFR101816|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491367|NCT01090453|113615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491368|NCT01090453|113615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495014|NCT01293006||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-032&kw=4305-032&tab=access|
2495015|NCT00823940|111497|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495016|NCT00823940|111497|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495017|NCT00823940|111497|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495018|NCT00823940|111497|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495019|NCT00823940|111497|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495020|NCT00823940|111497|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495021|NCT00823940|111497|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495022|NCT05184309|Principle investigator|Statistical Analysis Plan|https://pubmed.ncbi.nlm.nih.gov/28446376/|
2495023|NCT00406211|208136/039|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495024|NCT00406211|208136/039|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495025|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
2495026|NCT00406211|208136/039|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495027|NCT00406211|208136/039|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495028|NCT00406211|208136/039|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491369|NCT01090453|113615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491370|NCT01090453|113615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491371|NCT00515502|AC4108123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491372|NCT00515502|AC4108123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491373|NCT00515502|AC4108123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491374|NCT00515502|AC4108123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491375|NCT00515502|AC4108123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491376|NCT00515502|AC4108123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491377|NCT00515502|AC4108123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491378|NCT03058211|PI16/00486|Study Protocol|http://www.iispv.cat|Protocol in Spanish language
2491379|NCT03058211|PI16/00486|Informed Consent Form|http://www.iispv.cat|Informed consent form in Spanish language
2491380|NCT00695669|111626|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491381|NCT00695669|111626|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491382|NCT00695669|111626|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491383|NCT00695669|111626|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491384|NCT00695669|111626|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491385|NCT00695669|111626|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491386|NCT00695669|111626|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491387|NCT00679939|AVD111179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491388|NCT00679939|AVD111179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491389|NCT00679939|AVD111179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491390|NCT00679939|AVD111179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491391|NCT00679939|AVD111179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491392|NCT00679939|AVD111179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491393|NCT00679939|AVD111179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491394|NCT00493818|AKT106757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491395|NCT00493818|AKT106757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491396|NCT00493818|AKT106757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491397|NCT00493818|AKT106757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491398|NCT00493818|AKT106757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491399|NCT00493818|AKT106757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491400|NCT00493818|AKT106757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491401|NCT01258608|200149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491402|NCT01258608|200149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491403|NCT01258608|200149|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491404|NCT01258608|200149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491405|NCT01258608|200149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491406|NCT01258608|200149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495029|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.
2495030|NCT04392869|clinicaltrialsCRAFT|Human Subjects Review|https://drive.ugr.es/index.php/s/DGKxnBhZfm058DA|Human Subjects Review approval and its translation into English
2495031|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.
2495032|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.
2495033|NCT01376245|113684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495034|NCT01376245|113684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495035|NCT01376245|113684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495036|NCT01376245|113684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495037|NCT01376245|113684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495038|NCT01376245|113684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495039|NCT01376245|113684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495040|NCT01357889|114856|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495041|NCT01357889|114856|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495042|NCT01357889|114856|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495043|NCT01357889|114856|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495044|NCT01357889|114856|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495045|NCT01357889|114856|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495046|NCT01357889|114856|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495047|NCT01021813||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-009&kw=4305-009&tab=access|
2495048|NCT03336827||Study design|http://pdf.lu/YtWd|
2495049|NCT03336827||List of questionnaires|http://pdf.lu/TJ4c|
2495050|NCT03336827||Informed Consent Form|http://pdf.lu/dN2P|
2495051|NCT03336827||Informed Consent Form|http://pdf.lu/07Xz|
2495052|NCT02979366||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2495053|NCT02979366||Study Protocol|https://clinicaltrials.servier.com/|
2495054|NCT02979366||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2495055|NCT02979366||Informed Consent Form|https://clinicaltrials.servier.com/|
2495056|NCT02979366||Clinical Study Report|https://clinicaltrials.servier.com/|
2495057|NCT02979366||Study-level clinical trial data|https://clinicaltrials.servier.com/|
2495058|NCT00533611||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495059|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.
2495060|NCT02800720||Embedded Qualitative Study|http://link.springer.com/article/10.1007/s12671-015-0458-8|
2495061|NCT00092482||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495062|NCT01315847||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-067&kw=0974-067&tab=access|
2495063|NCT02141217|117044|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495064|NCT02141217|117044|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495065|NCT02141217|117044|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495066|NCT02141217|117044|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491407|NCT05154279||Study Protocol|https://www.ijrcog.org/index.php/ijrcog/article/view/3925|
2495067|NCT02141217|117044|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495068|NCT02141217|117044|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495069|NCT03909672||Study Protocol|http://facisa.ufrn.br|
2495070|NCT00546286||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495071|NCT07091838||Study Protocol|https://pubmed.ncbi.nlm.nih.gov/28179436/|
2495072|NCT05464472||BECK DEPRESSION INVENTORY|https://www.ismanet.org/doctoryourspirit/pdfs/Beck-Depression-Inventory-BDI.pdf|
2495073|NCT05464472||SF-36 QUESTIONNAIRE|https://clinmedjournals.org/articles/jmdt/jmdt-2-023-figure-1.pdf|
2487152|NCT01453478|115550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487153|NCT01453478|115550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487154|NCT01453478|115550|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487155|NCT01453478|115550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487156|NCT01453478|115550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487157|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.
2487158|NCT00005276||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/access|
2487159|NCT00005276||Study Forms|http://biolincc.nhlbi.nih.gov/studies/access|
2487160|NCT00005276||Procedures Manual|http://biolincc.nhlbi.nih.gov/studies/access|
2493572|NCT01362257|112014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493573|NCT01362257|112014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493574|NCT01636960||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08556&kw=P08556&tab=access|
2493575|NCT01055379|2009-011144-19|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2009-011144-19/results|
2493576|NCT06727760|Survey in efficacy of probioti|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
2493577|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|
2493578|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|
2493579|NCT06727760|0-1 Yaş Arası Bebekler|rewiev|https://dergipark.org.tr/tr/pub/firattip/issue/6338/84544|
2493580|NCT06727760|kangroo care guide|Guide|https://www.who.int/publications/i/item/9241590351|
2493581|NCT06727760|The Effects of Kangaroo Mother|article|https://ijn.mums.ac.ir/article_4152.html|
2493582|NCT06727760|efficacy of probiotic|article|https://pejouhesh.sbmu.ac.ir/article-1-1582-en.html|
2493583|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|
2493584|NCT06727760|The Effect of Aromatherapy|doctora thesis|https://tez.yok.gov.tr/UlusalTezMerkezi/tezSorguSonucYeni.jsp|
2493585|NCT00675090|H3B109689|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493586|NCT00675090|H3B109689|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493587|NCT00675090|H3B109689|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493588|NCT00675090|H3B109689|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493589|NCT00675090|H3B109689|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493590|NCT00675090|H3B109689|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493591|NCT00675090|H3B109689|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493592|NCT01498653|113714|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493593|NCT01498653|113714|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493594|NCT01498653|113714|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493595|NCT01498653|113714|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493596|NCT01498653|113714|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493597|NCT01498653|113714|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493598|NCT01498653|113714|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493599|NCT01457547|217744/094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493600|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
2493601|NCT01457547|217744/094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493602|NCT01457547|217744/094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493603|NCT01457547|217744/094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2493604|NCT01457547|217744/094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495074|NCT01319019|115032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495075|NCT01319019|115032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495076|NCT01319019|115032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495077|NCT01319019|115032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495078|NCT01319019|115032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495079|NCT01319019|115032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495080|NCT01319019|115032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495081|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.
2495082|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.
2495083|NCT00290303|100478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495084|NCT00290303|100478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495085|NCT00290303|100478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495086|NCT00290303|100478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495087|NCT00290303|100478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495088|NCT00290303|100478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495089|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
2495090|NCT01527110|115215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495091|NCT01527110|115215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495092|NCT01527110|115215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495093|NCT01527110|115215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495094|NCT01527110|115215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495095|NCT01527110|115215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495096|NCT01235728||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-022&kw=0873-022&tab=access|
2495097|NCT05752786||Study Protocol|https://osf.io/3gts8/|
2495098|NCT05752786||Statistical Analysis Plan|https://osf.io/3gts8/|
2495099|NCT05752786||Individual Participant Data Set|https://osf.io/3gts8/|
2495100|NCT00306241|106001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495101|NCT00306241|106001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495102|NCT00306241|106001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495103|NCT00306241|106001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495104|NCT00306241|106001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495105|NCT00306241|106001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495106|NCT02542813|201558|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495107|NCT02542813|201558|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495108|NCT02542813|201558|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495109|NCT02542813|201558|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495110|NCT02542813|201558|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495111|NCT02542813|201558|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495112|NCT02542813|201558|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495113|NCT00704431|LPL111814|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495114|NCT00704431|LPL111814|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495115|NCT00704431|LPL111814|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495116|NCT00704431|LPL111814|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495117|NCT00704431|LPL111814|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495118|NCT00704431|LPL111814|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495119|NCT00334152|NKT102552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495120|NCT00334152|NKT102552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495121|NCT00334152|NKT102552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495122|NCT00334152|NKT102552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495123|NCT00334152|NKT102552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495124|NCT00334152|NKT102552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495125|NCT00334152|NKT102552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495126|NCT03427138|C2495|Individual Participant Data Set|http://ndar.nih.gov|
2495127|NCT00092404||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495128|NCT00702910|B2C111401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495129|NCT00702910|B2C111401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495130|NCT00702910|B2C111401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495131|NCT00702910|B2C111401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495132|NCT00702910|B2C111401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495133|NCT00702910|B2C111401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495134|NCT00702910|B2C111401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495135|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.
2495136|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.
2495137|NCT00383227|208129/032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495138|NCT00383227|208129/032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495139|NCT00383227|208129/032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495140|NCT00383227|208129/032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495141|NCT00383227|208129/032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495142|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
2495143|NCT05885048||Study Protocol|https://www.researchprotocols.org/2024/1/e51145|
2495144|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
2495145|NCT06120192|10.6084/m9.figshare.23994768|Informed Consent Form|https://doi.org/10.6084/m9.figshare.23994768|
2491408|NCT05154279||Study Protocol|https://ebwhj.journals.ekb.eg/article_125772.html|
2495146|NCT06120192|10.6084/m9.figshare.23994768|Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.23994768|
2495147|NCT02697058||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2495148|NCT02697058||Study Protocol|https://clinicaltrials.servier.com/|
2495149|NCT02697058||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2495150|NCT02697058||Informed Consent Form|https://clinicaltrials.servier.com/|
2495151|NCT02697058||Clinical Study Report|https://clinicaltrials.servier.com/|
2495152|NCT02697058||study-level clinical trial data|https://clinicaltrials.servier.com/|
2495153|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.
2495154|NCT00005306||Study Forms|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|
2495155|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
2495156|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
2495157|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
2495158|NCT00996593|104507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495159|NCT00996593|104507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495160|NCT00996593|104507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495161|NCT00996593|104507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495162|NCT00996593|104507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495163|NCT00996593|104507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495164|NCT00996593|104507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495165|NCT02197598|2014-000413-31|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-000413-31/results|
2495166|NCT00750178||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495167|NCT00937326|113160|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495168|NCT00937326|113160|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495169|NCT00937326|113160|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495170|NCT00937326|113160|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495171|NCT00937326|113160|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495172|NCT00937326|113160|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495173|NCT00937326|113160|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495174|NCT01366534|114460|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495175|NCT01366534|114460|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495176|NCT01366534|114460|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495177|NCT01366534|114460|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495178|NCT01366534|114460|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495179|NCT01366534|114460|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495180|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.
2495181|NCT02798640||Informed Consent Form|https://mega.nz/#!C5U1HZwI!7XB2jar-JDElrnYOZTbwg0RD5T1WPQEv3HkzT0XPXz8|
2495182|NCT02798640||Clinical Investigation plan|https://mega.nz/#!3gEnFCDK!DK911mpjGBw_bAKdfsR4F2RgzCQG7mYR3oBqrVkRtpA|
2495183|NCT02798640||Clinical Study Report|https://mega.nz/#!S1tThKrL!gaWPII28P3I0BLBrLD9iZJYRqb2R1x-uZT5djgV4ML8|
2495184|NCT01376388|115362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495185|NCT01376388|115362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495186|NCT01376388|115362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495187|NCT01376388|115362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495188|NCT00329784|SDY660|Individual Participant Data Set|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
2495189|NCT00329784|SDY660|Study summary, -design, -adverse event(s), -demographics, -study files|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
2495190|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)
2495191|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)
2495192|NCT00654420||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0646-007&kw=0646-007&tab=access|
2495193|NCT00264667|ADG103440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495194|NCT00264667|ADG103440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495195|NCT00264667|ADG103440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495196|NCT00264667|ADG103440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495197|NCT00264667|ADG103440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495198|NCT00264667|ADG103440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495199|NCT00264667|ADG103440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495200|NCT01594749||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-031&kw=0517-031&tab=access|
2495201|NCT05837000|MKSU 51- 2 _ 16|Study Protocol|http://kfs.edu.eg/engkfs/|
2495202|NCT00076856||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495203|NCT00911144|112933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495204|NCT00911144|112933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495205|NCT00911144|112933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495206|NCT00911144|112933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495207|NCT00911144|112933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495208|NCT00911144|112933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495209|NCT00911144|112933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495210|NCT00964249|112017|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495211|NCT00964249|112017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495212|NCT00964249|112017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495213|NCT00964249|112017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495214|NCT00964249|112017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495215|NCT00783549|111596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495216|NCT00783549|111596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495217|NCT00783549|111596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495218|NCT00783549|111596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495219|NCT00783549|111596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495220|NCT00783549|111596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495221|NCT00783549|111596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495222|NCT03612674||Analytic Code|http://www.epiclin.it|
2495223|NCT00111891||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495224|NCT01031108|114089|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495225|NCT01031108|114089|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495226|NCT01031108|114089|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495227|NCT01031108|114089|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495228|NCT01031108|114089|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495229|NCT01031108|114089|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495230|NCT01031108|114089|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495231|NCT01722903||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25807199|
2495232|NCT01177826|111426|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495233|NCT01177826|111426|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495234|NCT01177826|111426|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495235|NCT01177826|111426|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495236|NCT01177826|111426|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495237|NCT01177826|111426|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495238|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
2495239|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
2495240|NCT01160224|114312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495241|NCT01160224|114312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495242|NCT01160224|114312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495243|NCT01160224|114312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495244|NCT01160224|114312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495245|NCT01160224|114312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495246|NCT01160224|114312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495247|NCT01899768|117270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495248|NCT01899768|117270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495249|NCT01899768|117270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495250|NCT01899768|117270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495251|NCT01899768|117270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495252|NCT01899768|117270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495253|NCT01899768|117270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495254|NCT03582969||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
2495255|NCT00684463||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495256|NCT00469040|B2C108784|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495257|NCT00469040|B2C108784|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495258|NCT00469040|B2C108784|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495259|NCT00469040|B2C108784|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495260|NCT00469040|B2C108784|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495261|NCT00469040|B2C108784|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495262|NCT00469040|B2C108784|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495263|NCT01962467|200284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495264|NCT01962467|200284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495265|NCT01962467|200284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495266|NCT01962467|200284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495267|NCT01962467|200284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495268|NCT01962467|200284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495269|NCT01962467|200284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495270|NCT01431521||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4074-008&kw=4074-008&tab=access|
2495271|NCT05859906||Clinical Study Report|http://doi.org/10.1093/bjaceaccp/mkh037|
2495272|NCT01808365|114991|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495273|NCT01808365|114991|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495274|NCT01808365|114991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495275|NCT01808365|114991|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495276|NCT01808365|114991|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495277|NCT01808365|114991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495278|NCT01808365|114991|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495279|NCT00345956|105722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495280|NCT00345956|105722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495281|NCT00345956|105722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495282|NCT00345956|105722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495283|NCT00345956|105722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495284|NCT00345956|105722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495285|NCT01086449|113819|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495286|NCT01086449|113819|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495287|NCT01086449|113819|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495288|NCT01086449|113819|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495289|NCT01086449|113819|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495290|NCT01086449|113819|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495291|NCT01086449|113819|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495292|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).
2495293|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.
2495294|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.
2495295|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.
2495296|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/|
2495297|NCT05394363||Current GenV collaborations|https://www.genv.org.au/for-researchers/current-genv-collaborations/|
2495298|NCT05394363||Working Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/working-papers/|
2495299|NCT05394363||Published Papers relevant to GenV design, data sharing and researchers working with GenV|https://genv.org.au/for-researchers/published-papers/|
2495300|NCT00748306|111834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495301|NCT00748306|111834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495302|NCT00748306|111834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495303|NCT00748306|111834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495304|NCT00748306|111834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495305|NCT00748306|111834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495306|NCT00748306|111834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495307|NCT00419237|FFA10013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495308|NCT00419237|FFA10013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495309|NCT00419237|FFA10013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495310|NCT00419237|FFA10013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495311|NCT00419237|FFA10013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495312|NCT00419237|FFA10013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495313|NCT00419237|FFA10013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495314|NCT00067444|29060/874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495315|NCT00067444|29060/874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495316|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
2495317|NCT00067444|29060/874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495318|NCT00067444|29060/874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495319|NCT00067444|29060/874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495320|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.
2495321|NCT00732472|105211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495322|NCT00732472|105211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495323|NCT00732472|105211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495324|NCT00732472|105211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495325|NCT00732472|105211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495326|NCT00732472|105211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495327|NCT00732472|105211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495328|NCT07135388|MBarone|Study Protocol|https://www.sanita.puglia.it/web/ospedalegiovannixxiii/comitato-etico|Dataset can be obtained on request by sending an email to the following address: michele.barone@uniba.it
2495329|NCT04704206|Registration platform REBEC|Study Protocol|https://ensaiosclinicos.gov.br/rg/RBR-8j3tzw|Project registered at REBEC
2495330|NCT02968966||Synopsis|http://www.medizin.uni-tuebingen.de/kinder/de/abteilungen/cpcs/projekte/|
2495331|NCT00772889|111738|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495332|NCT00772889|111738|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491409|NCT00464815|109069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491410|NCT00464815|109069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491411|NCT00464815|109069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491412|NCT00464815|109069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491413|NCT00464815|109069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495333|NCT00772889|111738|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491414|NCT00464815|109069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491415|NCT00464815|109069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491416|NCT06485817||Analytic Code|https://osf.io/3jvw8/|Project directory where study relevant documentation can be found and data will be uploaded.
2495334|NCT00772889|111738|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495335|NCT00772889|111738|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495336|NCT00772889|111738|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495337|NCT00772889|111738|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495338|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
2495339|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
2495340|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
2495341|NCT00329459|TRX105850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495342|NCT00329459|TRX105850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495343|NCT00329459|TRX105850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495344|NCT00329459|TRX105850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495345|NCT00329459|TRX105850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495346|NCT00329459|TRX105850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495347|NCT00329459|TRX105850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495348|NCT05399836||Study Protocol|https://osf.io/hx75k/|Protocol on the Open Science Framework (OSF)
2495349|NCT05399836||Statistical Analysis Plan|https://osf.io/hx75k/|
2495350|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.
2495351|NCT02202161|201351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495352|NCT02202161|201351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495353|NCT02202161|201351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495354|NCT02202161|201351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495355|NCT02202161|201351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495356|NCT02202161|201351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495357|NCT02202161|201351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495358|NCT00518336|109616 (Y7)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495359|NCT00518336|109616 (Y7)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495360|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.
2495361|NCT00518336|109616 (Y7)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495362|NCT00518336|109616 (Y7)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495363|NCT00518336|109616 (Y7)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495364|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
2495365|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
2495366|NCT00034697||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495367|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.
2495368|NCT00998985||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-004&kw=5172-004&tab=access|
2495369|NCT00686699||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04628&kw=P04628&tab=access|
2495370|NCT00290355|249553/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495371|NCT00290355|249553/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495372|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
2495373|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
2495374|NCT00290355|249553/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495375|NCT00290355|249553/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495376|NCT00290355|249553/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495377|NCT00829010|111634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495378|NCT00829010|111634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495379|NCT00829010|111634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495380|NCT00829010|111634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495381|NCT00829010|111634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495382|NCT00829010|111634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495383|NCT00829010|111634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495384|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)
2495385|NCT07100288||preprint|https://www.researchsquare.com/article/rs-283444/v1|
2495386|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
2495387|NCT01021553|109059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495388|NCT01021553|109059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495389|NCT01021553|109059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495390|NCT01021553|109059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495391|NCT01021553|109059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495392|NCT01021553|109059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495393|NCT01021553|109059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495394|NCT05327309||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/22456397/|
2495395|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
2495396|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
2495397|NCT01371799|113746|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495398|NCT01371799|113746|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495399|NCT01371799|113746|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495400|NCT01371799|113746|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495401|NCT01371799|113746|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495402|NCT01371799|113746|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495403|NCT04746027||Study Protocol|https://www.stmarys.ac.uk/staff-directory/jonathan-nixon|
2495404|NCT02685839||Clinical Study Report|http://goo.gl/FilVtL|
2495405|NCT04340804||Study Protocol|https://osf.io/k369t/|
2495406|NCT04340804||Statistical Analysis Plan|https://osf.io/k369t/|
2495407|NCT04340804||Informed Consent Form|https://osf.io/k369t/|
2495408|NCT04340804||Individual Participant Data Set|https://osf.io/k369t/|When results will be published
2495409|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.
2495410|NCT00005128||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrcps/|
2495411|NCT01619176|GSE59526|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/geo|
2495412|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.
2495413|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.
2495414|NCT01428479|115070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495415|NCT01428479|115070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495416|NCT01428479|115070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495417|NCT01428479|115070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495418|NCT01428479|115070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495419|NCT01428479|115070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495420|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
2495421|NCT00381472|101468/169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495422|NCT00381472|101468/169|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495423|NCT00381472|101468/169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495424|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
2495425|NCT00381472|101468/169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495426|NCT00381472|101468/169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495427|NCT01021293|112679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495428|NCT01021293|112679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495429|NCT01021293|112679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495430|NCT01021293|112679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495431|NCT01021293|112679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495432|NCT01021293|112679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495433|NCT02084316|CTN0056|Study Protocol|http://ctndisseminationlibrary.org/protocols/ctn0056.htm|
2495434|NCT05386641|18192154|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2495435|NCT05386641|25977305|Individual Participant Data Set|https://pubmed.ncbi.nlm.nih.gov/|
2495436|NCT05386641|26079868|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2495437|NCT05386641|29332760|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2495438|NCT05386641|32031629|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2495439|NCT05386641|32767329|Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2495440|NCT05386641||Individual Participant Data Set|http://pubmed.ncbi.nlm.nih.gov/|
2495441|NCT00989664|104504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495442|NCT00989664|104504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495443|NCT00989664|104504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495444|NCT00989664|104504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495445|NCT00989664|104504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495446|NCT00989664|104504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495447|NCT00989664|104504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495448|NCT00750360|218352/054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495449|NCT00750360|218352/054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495450|NCT00750360|218352/054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495451|NCT00750360|218352/054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495452|NCT00750360|218352/054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495453|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
2495454|NCT01979250||Manuscript|http://www.ncbi.nlm.nih.gov/pubmed/27273977|To acces the results, please go to the above mentioned manuscript.
2495455|NCT02135848|114272|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495456|NCT02135848|114272|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495457|NCT02135848|114272|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495458|NCT02135848|114272|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495459|NCT02135848|114272|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495460|NCT02135848|114272|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495461|NCT02135848|114272|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495462|NCT01213849|102932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495463|NCT01213849|102932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495464|NCT01213849|102932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495465|NCT01213849|102932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495466|NCT01213849|102932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495467|NCT01213849|102932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495468|NCT01213849|102932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491417|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
2491418|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
2491419|NCT00951041|113574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491420|NCT00951041|113574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495469|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.
2495470|NCT02356770|PMID: 28107560|2. publicaton|https://www.ncbi.nlm.nih.gov/pubmed/28107560|2\. publication concerning the volumetric changes of the soft tissue
2495471|NCT02896686||Study Protocol|https://cirurgiahj23.wordpress.com|
2495472|NCT00104299|ITN021AI|Individual Participant Data Set|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
2491421|NCT00951041|113574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491422|NCT00951041|113574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495473|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.
2495474|NCT02671786||Pilot Study Research Paper|http://www.worldwidejournals.com/ijar/file.php?val=April_2015_1427896145__152.pdf|
2495475|NCT00090246||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495476|NCT00539825|AC6108697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495477|NCT00539825|AC6108697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495478|NCT00539825|AC6108697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495479|NCT00539825|AC6108697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495480|NCT00539825|AC6108697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495481|NCT00539825|AC6108697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495482|NCT00539825|AC6108697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495483|NCT00517634|HZA109912|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495484|NCT00517634|HZA109912|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495485|NCT00517634|HZA109912|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495486|NCT00517634|HZA109912|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495487|NCT00517634|HZA109912|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495488|NCT00517634|HZA109912|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495489|NCT00517634|HZA109912|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495490|NCT00354991||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495491|NCT02250586|awtg7|Individual Participant Data Set|https://osf.io|The trial's outcome data and scripts are available for download: https://osf.io/awtg7/
2495492|NCT00115622|FFR30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495493|NCT00115622|FFR30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495494|NCT00115622|FFR30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495495|NCT00115622|FFR30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495496|NCT00115622|FFR30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495497|NCT00115622|FFR30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495498|NCT00115622|FFR30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491423|NCT00951041|113574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491424|NCT00951041|113574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491425|NCT00951041|113574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491426|NCT00137930|104480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491427|NCT00137930|104480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491428|NCT00137930|104480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495499|NCT00591786||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
2495500|NCT01681004|INSITE|Individual Participant Data Set|http://yoda.yale.edu/|
2495501|NCT02619942||Study Protocol|http://www.trialsjournal.com/content/17/1/582|
2495502|NCT00955682|112036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495503|NCT00955682|112036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495504|NCT00955682|112036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495505|NCT00955682|112036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495506|NCT00955682|112036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495507|NCT00955682|112036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495508|NCT01733758|113121|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495509|NCT01733758|113121|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495510|NCT01733758|113121|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495511|NCT01733758|113121|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495512|NCT01733758|113121|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495513|NCT01733758|113121|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495514|NCT01733758|113121|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495515|NCT00965458|T1DAL ITN045AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
2495516|NCT00965458|T1DAL ITN045AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
2495517|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.
2495518|NCT00635804||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3281-002&kw=3281-002&tab=access|
2495519|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.
2495520|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.
2495521|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
2495522|NCT00422955|49653/376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495523|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
2495524|NCT00422955|49653/376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495525|NCT00422955|49653/376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495526|NCT00422955|49653/376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495527|NCT00422955|49653/376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495528|NCT00540228|110794|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495529|NCT00540228|110794|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495530|NCT00540228|110794|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495531|NCT00540228|110794|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495532|NCT00540228|110794|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491429|NCT00137930|104480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495533|NCT00540228|110794|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495534|NCT00950755|104505|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495535|NCT00950755|104505|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495536|NCT00950755|104505|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495537|NCT00950755|104505|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495538|NCT00950755|104505|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495539|NCT00950755|104505|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495540|NCT00950755|104505|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495541|NCT04308668||Individual Participant Data Set|http://www.covidpep.umn.edu/data|
2491430|NCT00137930|104480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491431|NCT00137930|104480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491432|NCT01627327|115805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491433|NCT01627327|115805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491434|NCT01627327|115805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491435|NCT01627327|115805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491436|NCT01627327|115805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491437|NCT01627327|115805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491438|NCT01627327|115805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491439|NCT01825213|PMID: 25181365|Peer reviewed article|http://ieeexplore.ieee.org/document/6887313/?arnumber=6887313|
2491440|NCT00518115|GLP110125|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491441|NCT00518115|GLP110125|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491442|NCT00518115|GLP110125|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491443|NCT00518115|GLP110125|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491444|NCT00518115|GLP110125|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491445|NCT00518115|GLP110125|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491446|NCT00518115|GLP110125|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2491447|NCT01377480||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05267&kw=P05267&tab=access|
2491448|NCT04605978||Individual Participant Data Set|https://clinicaltrials.servier.com/|
2491449|NCT04605978||Study Protocol|https://clinicaltrials.servier.com/|
2495542|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
2495543|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.
2495544|NCT00000565||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ippb/|
2495545|NCT00000565||Study Forms|http://biolincc.nhlbi.nih.gov/studies/ippb/|
2495546|NCT00000565||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/ippb/|
2491450|NCT04605978||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
2491451|NCT04605978||Informed Consent Form|https://clinicaltrials.servier.com/|
2491452|NCT04605978||Clinical Study Report|https://clinicaltrials.servier.com/|
2491453|NCT04605978||study-level clinical trial data|https://clinicaltrials.servier.com/|
2495547|NCT00346775|FFR105693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495548|NCT00346775|FFR105693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495549|NCT00346775|FFR105693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495550|NCT00346775|FFR105693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495551|NCT00346775|FFR105693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495552|NCT00346775|FFR105693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495553|NCT00346775|FFR105693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495554|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.
2495555|NCT00000610||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/magic/|
2495556|NCT00000610||Study Forms|http://biolincc.nhlbi.nih.gov/studies/magic/|
2495557|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.
2495558|NCT01231620|114373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495559|NCT01231620|114373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495560|NCT01231620|114373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495561|NCT01231620|114373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495562|NCT01231620|114373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495563|NCT01231620|114373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495564|NCT01231620|114373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495565|NCT06047886||Prodigy technical sheet|https://www.miltenyibiotec.com/US-en/products/clinimacs-prodigy.html|
2495566|NCT01590810||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-001&kw=8150-001&tab=access|
2495567|NCT00403962|NKP103401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495568|NCT00403962|NKP103401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495569|NCT00403962|NKP103401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495570|NCT00403962|NKP103401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495571|NCT00403962|NKP103401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495572|NCT00403962|NKP103401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495573|NCT00403962|NKP103401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495574|NCT01852565|115679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495575|NCT01852565|115679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495576|NCT01852565|115679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495577|NCT01852565|115679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495578|NCT01852565|115679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487161|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
2487162|NCT00325156|100917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487163|NCT00325156|100917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487164|NCT00325156|100917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2487165|NCT00325156|100917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495579|NCT01852565|115679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495580|NCT01852565|115679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495581|NCT01439308|111925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495582|NCT01439308|111925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495583|NCT01439308|111925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495584|NCT01439308|111925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495585|NCT01439308|111925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495586|NCT01439308|111925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495587|NCT01439308|111925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495588|NCT00570492|FFR101782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495589|NCT00570492|FFR101782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495590|NCT00570492|FFR101782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495591|NCT00570492|FFR101782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495592|NCT00570492|FFR101782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495593|NCT00570492|FFR101782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495594|NCT00570492|FFR101782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495595|NCT06724874||Individual Participant Data Set|https://www.stat.ubc.ca/~rollin/stats/ssize/n2.html|
2495596|NCT00455572|107240|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495597|NCT00455572|107240|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495598|NCT00455572|107240|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495599|NCT00455572|107240|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495600|NCT00455572|107240|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495601|NCT00455572|107240|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495602|NCT00455572|107240|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495603|NCT00329225|49653/347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495604|NCT00329225|49653/347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495605|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
2495606|NCT00329225|49653/347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495607|NCT00329225|49653/347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495608|NCT00329225|49653/347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495609|NCT03473821||Statistical Analysis Plan|https://lucris.lub.lu.se/admin/files/138815992/MOTIFS_Data_Management_Protocol_1.6_2023_02_24.pdf|
2495610|NCT06934421||Study Protocol|https://osf.io/8ywq6/|
2495611|NCT06934421||Statistical Analysis Plan|https://osf.io/8ywq6/|
2495612|NCT06934421||Informed Consent Form|https://osf.io/8ywq6/|
2495613|NCT06934421||Analytic Code|https://osf.io/8ywq6/|
2495614|NCT06934421||Individual Participant Data Set|https://osf.io/8ywq6/|
2495615|NCT01366846|LEAP-On (ITN049AD)|Individual Participant Data Set|https://www.itntrialshare.org/|
2495616|NCT01366846|LEAP-On (ITN049AD)|Study protocol synopsis; datasets and figures from published NEJM 2016 article|https://www.itntrialshare.org/|
2495617|NCT01587716|115658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495618|NCT01587716|115658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495619|NCT01587716|115658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495620|NCT01587716|115658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495621|NCT01587716|115658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495622|NCT01587716|115658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495623|NCT01587716|115658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495624|NCT05814744||Individual Participant Data Set|https://drive.google.com/file/d/12gNVWYJj8dyy6Bh-6G59rFn2AQzjHycS/view?usp=share_link|
2495625|NCT05814744||Informed Consent Form|https://drive.google.com/file/d/1qPpYheG63CcWJqwWAD3ma3jFmmqCPWgm/view?usp=share_link|
2495626|NCT05814744||Study Protocol|https://drive.google.com/file/d/16x_dHL6GsO6V-K3p13T9EluZi20l4WtN/view?usp=share_link|
2495627|NCT01711736|116926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495628|NCT01711736|116926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495629|NCT01711736|116926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495630|NCT01711736|116926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495631|NCT01711736|116926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495632|NCT01711736|116926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495633|NCT01867996|116073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495634|NCT01867996|116073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495635|NCT01867996|116073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495636|NCT01867996|116073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495637|NCT01867996|116073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495638|NCT01867996|116073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495639|NCT01867996|116073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495640|NCT03626337||Statistical Analysis Plan|https://osf.io/jfke3/|
2495641|NCT01453296|112776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495642|NCT01453296|112776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495643|NCT01453296|112776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495644|NCT01453296|112776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495645|NCT01453296|112776|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495646|NCT01453296|112776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495647|NCT01453296|112776|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495648|NCT06107348|10.17605/OSF.IO/2MGJK|Individual Participant Data Set|http://doi.org/10.17605/OSF.IO/2MGJK|
2495649|NCT00968539|113456|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495650|NCT00968539|113456|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495651|NCT00968539|113456|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495652|NCT00968539|113456|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495653|NCT00968539|113456|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495654|NCT00968539|113456|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495655|NCT00968539|113456|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495656|NCT00326118|106445|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495657|NCT00326118|106445|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495658|NCT00326118|106445|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495659|NCT00326118|106445|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495660|NCT00326118|106445|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495661|NCT00326118|106445|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495662|NCT04631432||Statistical Analysis Plan|https://docs.google.com/document/d/16IlMPOgJMoh8tLIhB4JK5yeHI-0MfJVvRnQ8PdNp8-o/edit?usp=sharing|
2495663|NCT04631432||Study Protocol|https://drive.google.com/file/d/1YoXgB4ifoeu2Z8OnG6_hVWP4sBLRp9wP/view?usp=sharing|
2495664|NCT04631432||Informed Consent Form|https://drive.google.com/file/d/1WHJz01_y_b-gO4ZpZNAQsnqNf_SwdwNX/view?usp=sharing|
2495665|NCT00938392|112662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495666|NCT00938392|112662|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495667|NCT00938392|112662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495668|NCT00938392|112662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495669|NCT00938392|112662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495670|NCT00938392|112662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495671|NCT00938392|112662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495672|NCT03350880||Clinical Study Report|https://periodicos.unicesumar.edu.br/index.php/saudpesq/article/view/9938|
2495673|NCT01817764|114930|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495674|NCT01817764|114930|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495675|NCT01817764|114930|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495676|NCT01817764|114930|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495677|NCT01817764|114930|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495678|NCT01817764|114930|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495679|NCT01817764|114930|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495680|NCT00938275|113261|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495681|NCT00938275|113261|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495682|NCT00938275|113261|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495683|NCT00938275|113261|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495684|NCT00938275|113261|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495685|NCT00938275|113261|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495686|NCT00938275|113261|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495687|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."
2495688|NCT00471237|CR9108963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495689|NCT00471237|CR9108963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495690|NCT00471237|CR9108963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495691|NCT00471237|CR9108963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495692|NCT00471237|CR9108963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495693|NCT00471237|CR9108963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495694|NCT00471237|CR9108963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495695|NCT01016366|2008-003662-25|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-003662-25/results|
2495696|NCT00297063|AVD104742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
2495697|NCT00297063|AVD104742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
