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Blinded continuous monitoring in clinical trials with recurrent event endpoints

In studies with recurrent event endpoints, misspecified assumptions of event rates or dispersion can lead to underpowered trials or overexposure of patients. Specification of overdispersion is often a particular problem as it is usually not reported in clinical trial publications. Changing event rat...

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Detalles Bibliográficos
Autores principales: Friede, Tim, Häring, Dieter A., Schmidli, Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587844/
https://www.ncbi.nlm.nih.gov/pubmed/30345693
http://dx.doi.org/10.1002/pst.1907