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Clinical Trials (London, England)|September 17, 2015
The Food and Drug Administration and pragmatic clinical trials of marketed medical productsMonique L Anderson, Joseph Griffin, Sara F Goldkind, et al.Clinical Trials (London, England)|September 17, 2015
Ethical responsibilities toward indirect and collateral participants in pragmatic clinical trialsJaye Bea Smalley, Maria W Merritt, Sana M Al-Khatib, et al.Clinical Trials (London, England)|March 24, 2016
Did death certificates and a death review process agree on lung cancer cause of death in the National Lung Screening Trial?Pamela M Marcus, Vincent Paul Doria-Rose, Ilana F Gareen, et al.Clinical Trials (London, England)|May 15, 2016
Statistical lessons learned for designing cluster randomized pragmatic clinical trials from the NIH Health Care Systems Collaboratory Biostatistics and Design CoreAndrea J Cook, Elizabeth Delong, David M Murray, et al.Clinical Trials (London, England)|August 11, 2017
Evaluating biomarkers for prognostic enrichment of clinical trialsKathleen F Kerr, Jeremy Roth, Kehao Zhu, et al.Clinical Trials (London, England)|August 12, 2017
The optimal design of stepped wedge trials with equal allocation to sequences and a comparison to other trial designsJennifer A Thompson, Katherine Fielding, James Hargreaves, et al.Clinical Trials (London, England)|August 5, 2017
Power estimation in biomarker studies where events are already observedMei-Yin C PolleyClinical Trials (London, England)|September 2, 2017
PrEP Chicago: A randomized controlled peer change agent intervention to promote the adoption of pre-exposure prophylaxis for HIV prevention among young Black men who have sex with menLindsay E Young, Phil Schumm, Leigh Alon, et al.Clinical Trials (London, England)|April 21, 2016
A post hoc evaluation of a sample size re-estimation in the Secondary Prevention of Small Subcortical Strokes studyLeslie A McClure, Jeff M Szychowski, Oscar Benavente, et al.Clinical Trials (London, England)|April 22, 2016
Enhancing clinical evidence by proactively building quality into clinical trialsAnn Meeker-O'Connell, Coleen Glessner, Mark Behm, et al.Pageof 146