Causal proportional hazards models and time-constant exposure in randomized clinical trials
DOI10.1007/S10985-005-5233-ZzbMATH Open1121.62097OpenAlexW2003283626WikidataQ49097967 ScholiaQ49097967MaRDI QIDQ995964FDOQ995964
Authors: A. Vandebosch, Tom Loeys, Els Goetghebeur 
Publication date: 10 September 2007
Published in: Lifetime Data Analysis (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1007/s10985-005-5233-z
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Cites Work
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- Correcting for Noncompliance and Dependent Censoring in an AIDS Clinical Trial with Inverse Probability of Censoring Weighted (IPCW) Log‐Rank Tests
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- Correcting for non-compliance in randomized trials using rank preserving structural failure time models
- A class of rank test procedures for censored survival data
- Addressing complications of intention-to-treat analysis in the combined presence of all-or-none treatment-noncompliance and subsequent missing outcomes
- On the Effect of Treatment among Would-Be Treatment Compliers: An Analysis of the Multiple Risk Factor Intervention Trial
- A causal proportional hazards estimator for the effect of treatment actually received in a randomized trial with all-or-nothing compliance
Cited In (10)
- Estimating the causal effects in randomized trials for survival data with a cure fraction and non compliance
- Sensitivity Analysis of Per-Protocol Time-to-Event Treatment Efficacy in Randomized Clinical Trials
- Instrumental variable analysis for cost outcome: Application to the effect of primary care visit on medical cost among low‐income adults
- A semiparametric linear transformation model to estimate causal effects for survival data
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- A causal proportional hazards estimator for the effect of treatment actually received in a randomized trial with all-or-nothing compliance
- Instrumental variable estimation of early treatment effect in randomized screening trials
- Semiparametric transformation models for causal inference in time-to-event studies with all-or-nothing compliance
- A causal proportional hazards estimator under homogeneous or heterogeneous selection in an IV setting
- Distribution-based causal inference models for the estimation of therapy effects in randomized and controled clinic studies.
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