Interval estimation of odds ratio in a stratified randomized clinical trial with noncompliance

DOI10.1016/j.csda.2009.02.002zbMath1453.62145OpenAlexW2055315203MaRDI QIDQ961707

Kuang-Chao Chang, Kung-Jong Lui

Publication date: 1 April 2010

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

Full work available at URL: https://doi.org/10.1016/j.csda.2009.02.002

Mathematics Subject Classification ID

Computational methods for problems pertaining to statistics (62-08) Applications of statistics to biology and medical sciences; meta analysis (62P10) Estimation in survival analysis and censored data (62N02)

Uses Software

• SAS

Cites Work

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• Estimation of proportion ratio in non-compliance randomized trials with repeated measurements in binary data
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• Notes on estimation of proportion ratio under a non-compliance randomized trial with missing outcomes
• Compliance Subsampling Designs for Comparative Research: Estimation and Optimal Planning
• Identification of Causal Effects Using Instrumental Variables
• On the use of the ratio or the odds ratio of cure rates in therapeutic equivalence clinical trials with binary endpoints
• Addressing complications of intention-to-treat analysis in the combined presence of all-or-none treatment-noncompliance and subsequent missing outcomes
• Five Interval Estimators for Proportion Ratio under a Stratified Randomized Clinical Trial with Noncompliance
• A Mixed Approach for Proving Non‐Inferiority in Clinical Trials with Binary Endpoints
• Simple maximum likelihood estimates of efficacy in randomized trials and before-and-after studies, with implications for meta-analysis
• Designs in partially controlled studies: messages from a review
• Clinical Trials
• Likelihood Methods for Treatment Noncompliance and Subsequent Nonresponse in Randomized Trials
• Stratified Analysis in Randomized Trials with Noncompliance

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