Planning and Monitoring of Equivalence Studies

DOI10.2307/2531438zbMath0718.62223OpenAlexW2312665876WikidataQ37938413 ScholiaQ37938413MaRDI QIDQ5750254

Sylvain Durrleman, Richard M. Simon

Publication date: 1990

Published in: Biometrics (Search for Journal in Brave)

Full work available at URL: https://doi.org/10.2307/2531438

zbMATH Keywords

equivalenceconfidence intervalsclinical trialsgroup sequential methods

Mathematics Subject Classification ID

Parametric tolerance and confidence regions (62F25) Applications of statistics to biology and medical sciences; meta analysis (62P10)

Related Items (8)

Statistical Issues On Objective, Design, And Analysis Of Noninferiority Active-controlled Clinical Trial ⋮ Equivalence of normal means compared with a control ⋮ Sequential type nonparametric tests for ordered bivariate alterenatives ⋮ Bayesian Design and Analysis of Active Control Clinical Trials ⋮ Complementary hypotheses in safety surveillance ⋮ Determining equivalence and the impact of sample size in anti-infective studies: a point to consider ⋮ A group sequential approach to crossover trials for average bioequivalence ⋮ CLINICAL EQUIVALENCE

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