Robust Bayesian monitoring of sequential trials

DOI10.1007/S40300-013-0008-XMaRDI QIDQ478376zbMATH OpenOpenAlexFDO

Authors Pierpaolo Brutti, Fulvio de Santis, Stefania Gubbiotti

Publication date 3 December 2014

Published in Metron (Search for Journal in Brave)

Full work available at URL https://doi.org/10.1007/s40300-013-0008-x

zbMATH Keywords

clinical trialsrobustnesssample sizesequential analysis\(\epsilon\)-contamination priors

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10) Sequential statistical analysis (62L10)

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• scientific article; zbMATH DE number 1522737

Cites work

• scientific article; zbMATH DE number 3903818 (Why is no real title available?)
• scientific article; zbMATH DE number 1348603 (Why is no real title available?)
• A simulation-based approach to Bayesian sample size determination for performance under a given model and for separating models
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• Interim Analysis in Clinical Trials: The Role of the Likelihood Principle
• Optimal Experimental Design for Another's Analysis
• Ranges of posterior measures for priors with unimodal contaminations
• Robust Bayes and empirical Bayes analysis with \(\epsilon\)-contaminated priors
• Robust Bayesian analysis in medical and epidemiological settings
• Robust Bayesian analysis: sensitivity to the prior
• Robust Bayesian sample size determination for avoiding the range of equivalence in clinical trials
• Sample Size Determination for Robust Bayesian Analysis

Cited in

(1)

• Sequential monitoring of clinical trials with correlated responses

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