Literature DB >> 12413240

Strategies for changing the test statistic during a clinical trial.

John Lawrence1.   

Abstract

This article discusses the design of a clinical trial where a new treatment will be compared to a control. For a specific type of endpoint, there are a wide variety of test statistics that can be used. Also, the investigator must decide how many patients to accrue in each arm as well as the duration of the study. After an interim look at the data, the investigator may decide that a different test statistic would be more powerful or that more patients or longer follow-up is needed. In this article, we discuss a strategy for making these types of changes. This strategy controls the probability of making a type I error and can result in a procedure that has higher power than the test without adaptation.

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Year:  2002        PMID: 12413240     DOI: 10.1081/bip-120015743

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  1 in total

1.  A Bayesian adaptive design for two-stage clinical trials with survival data.

Authors:  Uttam Bandyopadhyay; Atanu Biswas; Rahul Bhattacharya
Journal:  Lifetime Data Anal       Date:  2009-11-04       Impact factor: 1.588

  1 in total

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