Design and analysis of crossover trials for investigating high-risk medical devices: A review

During evaluation of new investigational medical devices, the FDA recommends that investigators design a crossover clinical trial, in which the patients are arranged to cross over from one treatment arm to another. The FDA annually receives the premarket applications of investigational medical devic...

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Detalles Bibliográficos
Autores principales: Zhang, Bo, Guo, Jing, Zhang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508509/
https://www.ncbi.nlm.nih.gov/pubmed/36164356
http://dx.doi.org/10.1016/j.conctc.2022.101004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508509/
https://www.ncbi.nlm.nih.gov/pubmed/36164356
http://dx.doi.org/10.1016/j.conctc.2022.101004

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