Interim analyses in clinical trials: Classical vs. bayesian approaches
- 12 October 1985
- journal article
- research article
- Published by Wiley in Statistics in Medicine
- Vol. 4 (4), 521-526
- https://doi.org/10.1002/sim.4780040412
Abstract
This paper concerns interim analysis in clinical trials involving two treatments from the points of view of both classical and Bayesian inference. I criticize classical hypothesis testing in this setting and describe and recommend a Bayesian approach in which sampling stops when the probability that one treatment is the better exceeds a specified value. I consider application to normal sampling analysed in stages and evaluate the gain in average sample number as a function of the number of interim analyses.This publication has 14 references indexed in Scilit:
- Comment on “statistical inference from clinical trials: Choosing the right P value”Controlled Clinical Trials, 1983
- Comments on the Dupont manuscriptControlled Clinical Trials, 1983
- Clinical Trials and Statistical Verdicts: Probable Grounds for AppealAnnals of Internal Medicine, 1983
- Sequential stopping rules and sequentially adjusted P values: Does one require the other?Controlled Clinical Trials, 1983
- On choosing the number of interim analyses in clinical trialsStatistics in Medicine, 1982
- Group sequential methods in the design and analysis of clinical trialsBiometrika, 1977
- Sequential Trials, Sequential Analysis and the Likelihood PrincipleThe American Statistician, 1966
- Sequential Medical TrialsJournal of the American Statistical Association, 1963