Robust Bayesian sample size determination for avoiding the range of equivalence in clinical trials-Reference-Cited by-同舟云学术

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Robust Bayesian sample size determination for avoiding the range of equivalence in clinical trials

Published:2008-07 Issue:6 Volume:138 Page:1577-1591
ISSN:0378-3758
Container-title:Journal of Statistical Planning and Inference
language:en
Short-container-title:Journal of Statistical Planning and Inference

Author:

Brutti Pierpaolo,De Santis Fulvio

Publisher

Elsevier BV

Subject

Applied Mathematics,Statistics, Probability and Uncertainty,Statistics and Probability

Reference28 articles.

1. Sample size determination: a review;Adcock;Statistician,1997

2. Statistical Methods in Medical Research;Armitage,2002

3. The robust Bayesian viewpoint (with discussion);Berger,1984

4. Robust Bayesian analysis: sensitivity to the prior;Berger;J. Statist. Plann. Inference,1990

5. Bayesian robustness;Berger,2000

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1. Joint control of consensus and evidence in Bayesian design of clinical trials;Biometrical Journal;2021-12-10

2. Sample Size Requirements for Calibrated Approximate Credible Intervals for Proportions in Clinical Trials;International Journal of Environmental Research and Public Health;2021-01-12

3. A note on the progressive overlap of two alternative Bayesian intervals;Communications in Statistics - Theory and Methods;2019-11-25

4. Bayesian consensus‐based sample size criteria for binomial proportions;Statistics in Medicine;2019-07-11

5. Sample size requirements to estimate key design parameters from external pilot randomised controlled trials: a simulation study;Trials;2014-07-03

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