A simple procedure to estimate the optimal sample size in case of conjunctive coprimary endpoints

DOI10.1002/BIMJ.201500231zbMATH Open1369.62308OpenAlexW2475258578WikidataQ47293720 ScholiaQ47293720MaRDI QIDQ5280177FDOQ5280177

Authors: Z. Varga, Yu C. Tsang, Júlia Singer 

Publication date: 20 July 2017

Published in: Biometrical Journal (Search for Journal in Brave)

Full work available at URL: https://doi.org/10.1002/bimj.201500231

Recommendations

• Sample size determination in clinical trials with multiple co-primary endpoints including mixed continuous and binary variables
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• Sample size optimization and initial allocation of the significance levels in group sequential trials with multiple endpoints
• Sample Sizes Based on the Log-Rank Statistic in Complex Clinical Trials
• Sample size determination for controlling the upper confidence limit of incidence rate of a binomial endpoint

zbMATH Keywords

sample size estimationmultiple coprimary endpointstype-II error rate

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10) Sampling theory, sample surveys (62D05)

Cites Work

• Sources for McVittie’s mass particle in an expanding universe

Cited In (3)

• Assessing the Impact of Endpoint Shopping on Power in Confirmatory Clinical Trials
• Efficient calculation of the joint distribution of order statistics
• Power Analysis for Cluster Randomized Trials with Continuous Coprimary Endpoints

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