Estimation of the proportion ratio under a simple crossover trial
DOI10.1016/J.CSDA.2011.08.013zbMATH Open1239.62136OpenAlexW2064143498MaRDI QIDQ425644FDOQ425644
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
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- Testing and estimation of proportion (or risk) ratio under the matched-pair design with multiple binary endpoints
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Point estimation (62F10) Applications of statistics to biology and medical sciences; meta analysis (62P10) Monte Carlo methods (65C05) Parametric tolerance and confidence regions (62F25)
Cites Work
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- Ethical considerations concerning treatment allocation in drug development trials
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- Testing Hypotheses in the Two-period Change-over with Binary Data
- A Random Effects Model for Binary Data from Crossover Clinical Trials
Cited In (8)
- Notes on interval estimation of the proportion ratio under a three-treatment three-period crossover trial
- Estimation of proportion ratio in non-compliance randomized trials with repeated measurements in binary data
- An IM-based efficient test for non inferiority of the odds ratio between two independent binomial proportions
- Notes on estimation of the proportion ratio in the presence of carryover effects under the AB/BA crossover trial
- 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
- Testing and estimation of proportion (or risk) ratio under the matched-pair design with multiple binary endpoints
- Notes on estimation in Poisson frequency data under an incomplete block crossover design
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