Literature DB >> 9147601

A computationally simpler algorithm for the UMVUE of a normal mean following a group sequential trial.

S S Emerson1, J M Kittelson.   

Abstract

When using data collected in a group sequential clinical trial, the sample mean is no longer the uniform minimum variance unbiased estimator (UMVUE) of the mean of a normal distribution. Emerson (1993, Computers and Biomedical Research, 26, 68-73) described an algorithm for computing the UMVUE in this setting. This algorithm, although computationally expensive, used only the basic software necessary for deriving group sequential boundaries. In this paper, we present an improved algorithm that results in greatly decreased computation times.

Mesh:

Year:  1997        PMID: 9147601

Source DB:  PubMed          Journal:  Biometrics        ISSN: 0006-341X            Impact factor:   2.571


  3 in total

1.  Conditional estimation of sensitivity and specificity from a phase 2 biomarker study allowing early termination for futility.

Authors:  Margaret Sullivan Pepe; Ziding Feng; Gary Longton; Joseph Koopmeiners
Journal:  Stat Med       Date:  2009-02-28       Impact factor: 2.373

Review 2.  An Investigation of the Shortcomings of the CONSORT 2010 Statement for the Reporting of Group Sequential Randomised Controlled Trials: A Methodological Systematic Review.

Authors:  Abigail Stevely; Munyaradzi Dimairo; Susan Todd; Steven A Julious; Jonathan Nicholl; Daniel Hind; Cindy L Cooper
Journal:  PLoS One       Date:  2015-11-03       Impact factor: 3.240

3.  Estimation of treatment effects following a sequential trial of multiple treatments.

Authors:  John Whitehead; Yasin Desai; Thomas Jaki
Journal:  Stat Med       Date:  2020-03-23       Impact factor: 2.373

  3 in total

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