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Principles of Good Clinical Trial Design.
An, Ming-Wen; Duong, Quyen; Le-Rademacher, Jennifer; Mandrekar, Sumithra J.
Afiliación
  • An MW; Department of Mathematics and Statistics, Vassar College, Poughkeepsie, New York. Electronic address: mian@vassar.edu.
  • Duong Q; Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
  • Le-Rademacher J; Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
  • Mandrekar SJ; Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
J Thorac Oncol ; 15(8): 1277-1280, 2020 08.
Article en En | MEDLINE | ID: mdl-32417343
ABSTRACT
Clinical trials are a fundamental component of medical research and serve as the main route to obtain evidence of the safety and efficacy of treatment before its approval. A trial's ability to provide the intended evidence hinges on appropriate design, background knowledge, trial rationale to sample size, and interim monitoring rules. In this article, we present some general design principles for investigators and their research teams to consider when planning to conduct a trial.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Investigación Biomédica / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: J Thorac Oncol Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Investigación Biomédica / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: J Thorac Oncol Año: 2020 Tipo del documento: Article