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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
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| Materias: | |
| 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 |