Sensitivity Analysis of Per-Protocol Time-to-Event Treatment Efficacy in Randomized Clinical Trials
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Publication:2861792
DOI10.1080/01621459.2013.786649WikidataQ41883968 ScholiaQ41883968MaRDI QIDQ2861792
Michael G. Hudgens, Peter B. Gilbert, Bryan E. Shepherd
Publication date: 11 November 2013
Published in: Journal of the American Statistical Association (Search for Journal in Brave)
Full work available at URL: http://europepmc.org/articles/pmc3811958
selection bias; causal inference; principal stratification; exclusion restriction; ignorance region; intention to treat
62-XX: Statistics
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Cites Work
- Causal proportional hazards models and time-constant exposure in randomized clinical trials
- Inference for the Effect of Treatment on Survival Probability in Randomized Trials with Noncompliance and Administrative Censoring
- Principal Stratification in Causal Inference
- A Causal Proportional Hazards Estimator for the Effect of Treatment Actually Received in a Randomized Trial with All-or-Nothing Compliance
- Sensitivity Analyses Comparing Time-to-Event Outcomes Only Existing in a Subset Selected Postrandomization and Relaxing Monotonicity
- A Global Sensitivity Test for Evaluating Statistical Hypotheses with Nonidentifiable Models
- Sensitivity Analyses Comparing Time-to-Event Outcomes Existing Only in a Subset Selected Postrandomization
- Confidence Intervals for Partially Identified Parameters