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Estimation of Number of Subjects Required for Comparison of Drug versus Control in Adaptive Designs

  • F. F. Hu
  • , J. H. Hu

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Adaptive designs have often been proposed as a way of using accruing data to affect future allocation scheme in clinical trials. The goal is to assign more patients to the better treatment. To implement clinical trials efficiently, sample size must be estimated in advance. In adaptive design, it is difficult to calculate the required sample size, because the allocation probabilities keep changing during the course of the trials. Methods: We focus on the sample size of two-arm (drug versus control) clinical trials. Based on its asymptotic properties, a formula of calculating sample size is derived for the randomised play-the-winner rule. We also compare sample size and power between the randomised play-the-winner rule and equal allocation. Some simulation studies illustrate the operating characteristics of the designs. Results and Discussion: The required sample size of the randomised play-the-winner rule is slightly larger than that of the equal allocation design in most cases. The randomised play-the-winner rule is recommended for ethical reasons.

Original languageEnglish (US)
Pages (from-to)565-569
Number of pages5
JournalAnnals of the Academy of Medicine Singapore
Volume29
Issue number5
StatePublished - Sep 2000

Keywords

  • Power
  • Randomised play-the-winner rule
  • Sample size
  • Sequential design

ASJC Scopus subject areas

  • General Medicine

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