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Meta-Analysis of Rare Adverse Events in Randomized Clinical Trials: Bayesian and Frequentist Methods

BACKGROUND/AIMS: Regulatory approval of a drug or device involves an assessment of not only the benefits but also the risks of adverse events associated with the therapeutic agent. Although randomized controlled trials (RCTs) are the gold standard for evaluating effectiveness, the number of treated...

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Bibliografske podrobnosti
izdano v:Clin Trials
Main Authors: Hong, Hwanhee, Wang, Chenguang, Rosner, Gary L.
Format: Artigo
Jezik:Inglês
Izdano: 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8041270/
https://ncbi.nlm.nih.gov/pubmed/33258698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774520969136
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