Patients’ beliefs regarding informed consent for low-risk pragmatic trials

BACKGROUND: The requirement to obtain written informed consent may undermine the potential of pragmatic randomized clinical trials (pRCTs) to improve evidence-based care. This requirement could compromise trials statistical power or even force it to close them down prematurely. However, recent data...

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Detalles Bibliográficos
Autores principales: Dal-Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604493/
https://www.ncbi.nlm.nih.gov/pubmed/28923007
http://dx.doi.org/10.1186/s12874-017-0424-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604493/
https://www.ncbi.nlm.nih.gov/pubmed/28923007
http://dx.doi.org/10.1186/s12874-017-0424-3

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