Current Index to Statistics
Controlled Clinical Trials
Estimating sample sizes for repeated measurement designs
Overall, John E.
Doyle, Suzanne R.
Extension of one-sided test to multiple treatment trials
Chen, T. Timothy
Simon, Richard M.
A comparison of two methods of estimating a common risk difference in a stratified analysis of a multicenter clinical trial
O'Gorman, Thomas W.
Woolson, Robert F.
Jones, Michael P.
Sample size estimation using repeated measurements on biomarkers as outcomes
Kirby, Alison J.
An optimal rule for screening subjects for clinical trials in the presence of within-person variability
Cook, Nancy R.
Rosner, Bernard A.
Interim monitoring of bivariate responses using repeated confidence intervals
Cook, Richard John
Power function arguments in support of an alternative approach for analyzing management trials
Willan, Andrew R.
An efficient multiple-stage procedure for phase II clinical trials that have high response rate objectives
Wheeler, Richard H.
A new proposal for benefit-less-risk analysis in clinical trials
Simple Bayesian analysis in clinical trials: A tutorial
Decision making during a phase III randomized controlled trial
Berry, Donald A.
Wolff, Mark C.
The case for confidence intervals in controlled clinical trials
A Bayesian approach to establishing sample size and monitoring criteria for phase II clinical trials
Thall, Peter F.
Power considerations for testing an interaction in a $2 × k$ factorial design with a failure time outcome
Xiang, Anny H.
Sather, Harland N.
Azen, Stanley P.