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Point estimation for adaptive trial designs I: A methodological review

Recent FDA guidance on adaptive clinical trial designs defines bias as “a systematic tendency for the estimate of treatment effect to deviate from its true value,” and states that it is desirable to obtain and report estimates of treatment effects that reduce or remove this bias. The conventional en...

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Detalhes bibliográficos
Publicado no:Stat Med
Main Authors: Robertson, David S., Choodari‐Oskooei, Babak, Dimairo, Munya, Flight, Laura, Pallmann, Philip, Jaki, Thomas
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2022
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7613995/
https://ncbi.nlm.nih.gov/pubmed/36451173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/sim.9605
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