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Sample size determination for a binary response in a superiority clinical trial using a hybrid classical and Bayesian procedure
BACKGROUND: When designing studies that have a binary outcome as the primary endpoint, the hypothesized proportion of patients in each population experiencing the endpoint of interest (i.e., π (1),π (2)) plays an important role in sample size and power calculations. Point estimates for π (1) and π (...
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| Udgivet i: | Trials |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5324236/ https://ncbi.nlm.nih.gov/pubmed/28231813 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13063-017-1791-0 |
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