Estimation of proportion ratio in non-compliance randomized trials with repeated measurements in binary data

DOI10.1016/J.STAMET.2007.06.003zbMath1248.62217OpenAlexW2048414071MaRDI QIDQ713821

Kung-Jong Lui

Publication date: 19 October 2012

Published in: Statistical Methodology (Search for Journal in Brave)

Full work available at URL: https://doi.org/10.1016/j.stamet.2007.06.003

zbMATH Keywords

interval estimation

Mathematics Subject Classification ID

Asymptotic properties of parametric estimators (62F12) Parametric tolerance and confidence regions (62F25) Applications of statistics to biology and medical sciences; meta analysis (62P10) Monte Carlo methods (65C05) Medical applications (general) (92C50) Estimation in survival analysis and censored data (62N02)

Related Items (4)

Notes on odds ratio estimation for a randomized clinical trial with noncompliance and missing outcomes ⋮ Interval estimation of odds ratio in a stratified randomized clinical trial with noncompliance ⋮ Notes on estimation of proportion ratio under a non-compliance randomized trial with missing outcomes ⋮ Testing and estimation of proportion (or risk) ratio under the matched-pair design with multiple binary endpoints

Uses Software

• SAS

Cites Work

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• Sample size calculation for non-compliance randomized trials with repeated measurements in binary data
• Identification of Causal Effects Using Instrumental Variables
• Estimation of a Common Effect Parameter from Sparse Follow-Up Data
• Stratified Analysis in Randomized Trials with Noncompliance

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