Literature DB >> 8444028

Computation of the uniform minimum variance unbiased estimator of a normal mean following a group sequential trial.

S S Emerson1.   

Abstract

The sampling distribution of data collected in a group sequential trial is such that the usual fixed-sample estimates of treatment effect are biased. Improved estimates can be obtained by taking the group sequential stopping rule into account. In particular, in the case of inference about the mean of a normal distribution, the sample mean is no longer the uniform minimum variance unbiased estimator (UMVUE). In this paper, I present a way in which the UMVUE for a normal mean can be calculated using software capable of determining the operating characteristics of a group-sequential test.

Mesh:

Year:  1993        PMID: 8444028     DOI: 10.1006/cbmr.1993.1004

Source DB:  PubMed          Journal:  Comput Biomed Res        ISSN: 0010-4809


  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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