Registration of phase 3 crossover trials on ClinicalTrials.gov

被引:0
作者
Lijuan Zeng
Riaz Qureshi
Shilpa Viswanathan
Lea Drye
Tianjing Li
机构
[1] Statistics Collaborative,Center for Clinical Trials and Evidence Synthesis, Department of Epidemiology
[2] Inc,Department of Ophthalmology
[3] Johns Hopkins Bloomberg School of Public Heath,undefined
[4] IQVIA,undefined
[5] Blue Cross Blue Shield Association,undefined
[6] School of Medicine,undefined
[7] University of Colorado Denver,undefined
来源
Trials | / 21卷
关键词
Crossover trials; Trial registration; ClinicalTrials.gov; Longitudinal trial; Data sharing; Trial reporting;
D O I
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[1]  
Zarin DA(2008)Moving toward transparency of clinical trials Science 319 1340-1342
[2]  
Tse T(2012)Characteristics of clinical trials registered in ClinicalTrials.gov, 2007–2010 JAMA 307 1838-1847
[3]  
Califf RM(2019)Robustness of crossover trials against subject drop-out – examples of perpetually connected designs Stat Methods Med Res 28 788-800
[4]  
Zarin DA(2015)Design, analysis, and reporting of crossover trials for inclusion in a meta-analysis PLoS One 10 1-12
[5]  
Kramer JM(2015)The method quality of cross-over studies involved in Cochrane Systematic Reviews PLoS One 10 1-8
[6]  
Sherman RE(2014)Reporting discrepancies between the ClinicalTrials.gov results database and peer-reviewed publications Ann Intern Med 160 477-483
[7]  
Aberle LH(2015)Compliance with results reporting at ClinicalTrial N Engl J Med 372 1031-1039
[8]  
Tasneem A(2011)The ClinicalTrials.gov results database – update and key issues N Engl J Med 364 852-860
[9]  
Godolphin PJ(2020)Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study Lancet. 395 361-369
[10]  
Godolphin EJ(2019)CONSORT 2010 statement: extension to randomised crossover trials BMJ. 366 l4378-undefined