Estimation of the proportion ratio under a simple crossover trial

DOI10.1016/J.CSDA.2011.08.013MaRDI QIDQ425644zbMATHOpenAlexFDO

Authors Kung-Jong Lui, Kuang-Chao Chang

Publication date 8 June 2012

Published in Computational Statistics and Data Analysis (Search for Journal in Brave)

Full work available at URL https://doi.org/10.1016/j.csda.2011.08.013

zbMATH Keywords

biasbinary datacoverage probabilitypoint estimationprecisioninterval estimator

Mathematics Subject Classification ID

Point estimation (62F10) Applications of statistics to biology and medical sciences; meta analysis (62P10) Monte Carlo methods (65C05) Parametric tolerance and confidence regions (62F25)

Recommendations

• Notes on interval estimation of the proportion ratio under a three-treatment three-period crossover trial
• Notes on estimation of the proportion ratio in the presence of carryover effects under the AB/BA crossover trial
• Testing and estimation of proportion (or risk) ratio under the matched-pair design with multiple binary endpoints
• Estimation of proportion ratio in non-compliance randomized trials with repeated measurements in binary data
• Five Interval Estimators for Proportion Ratio under a Stratified Randomized Clinical Trial with Noncompliance

Cites work

• scientific article; zbMATH DE number 3144846 (Why is no real title available?)
• scientific article; zbMATH DE number 3866350 (Why is no real title available?)
• scientific article; zbMATH DE number 4088796 (Why is no real title available?)
• scientific article; zbMATH DE number 45786 (Why is no real title available?)
• scientific article; zbMATH DE number 46578 (Why is no real title available?)
• A Random Effects Model for Binary Data from Crossover Clinical Trials
• Ethical considerations concerning treatment allocation in drug development trials
• Statistical Methods for Rates and Proportions
• Testing Hypotheses in the Two-period Change-over with Binary Data

Cited in

(8)

• Notes on estimation of the proportion ratio in the presence of carryover effects under the AB/BA crossover trial
• Testing and estimation of proportion (or risk) ratio under the matched-pair design with multiple binary endpoints
• Notes on interval estimation of the proportion ratio under a three-treatment three-period crossover trial
• Notes on estimation in Poisson frequency data under an incomplete block crossover design
• Estimation of proportion ratio in non-compliance randomized trials with repeated measurements in binary data
• Sample size determination for testing equality in frequency data under an incomplete block crossover design
• Cross-product ratio calculation under different sampling schemes in clinical trials -- case study of the CYP-GUIDES trial
• An IM-based efficient test for non inferiority of the odds ratio between two independent binomial proportions

Describes a project that uses

Uses Software

• SAS

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