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Clinical Trials (London, England)|August 10, 2006
Problems in comprehension of informed consent in rural and peri-urban Mali, West AfricaMichael T Krosin, Robert Klitzman, Bruce Levin, et al.Clinical Trials (London, England)|November 29, 2007
Monitoring rare serious adverse events from a new treatment and testing for a difference from historical controlsMichael P Fay, Chiung-Yu Huang, Nana A Y Twum-DansoClinical Trials (London, England)|November 29, 2007
A comparison of methods for fixed effects meta-analysis of individual patient data with time to event outcomesCatrin Tudur Smith, Paula Ruth WilliamsonClinical Trials (London, England)|April 1, 2008
Building community partnerships: case studies of Community Advisory Boards at research sites in Peru, Zimbabwe, and ThailandStephen F Morin, Simon Morfit, Andre Maiorana, et al.Clinical Trials (London, England)|April 1, 2008
Maintaining confidentiality of interim data to enhance trial integrity and credibilityThomas R Fleming, Katrina Sharples, John McCall, et al.Clinical Trials (London, England)|June 19, 2008
Designing phase II studies in cancer with time-to-event endpointsKouros Owzar, Sin-Ho JungClinical Trials (London, England)|April 11, 2025
Consent to recontact for future research using linked primary healthcare data: Outcomes and general practice perceptions from the ATHENA COVID-19 studyKim Greaves, Amanda King, Zoltan Bourne, et al.Clinical Trials (London, England)|May 26, 2025
Comparison of adaptive seamless Phase 2/3 designs for dose selection in clinical trials with multiple endpointsMan JinClinical Trials (London, England)|May 22, 2013
Adaptive adjustment of the randomization ratio using historical control dataBrian P Hobbs, Bradley P Carlin, Daniel J SargentClinical Trials (London, England)|July 9, 2013
Inference following designs which adjust for imbalances in prognostic factorsYolanda Barbáchano, D Stephen CoadPageof 146