Public preferences on written informed consent for low‐risk pragmatic clinical trials in Spain

AIMS: Pragmatic randomized clinical trials (pRCTs) collect data that have the potential to improve medical care significantly. However, these trials may be undermined by the requirement to obtain written informed consent, which can decrease accrual and increase selection bias. Recent data suggest th...

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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: John Wiley and Sons Inc. 2017
Materias:
Clinical Trials
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582372/
https://www.ncbi.nlm.nih.gov/pubmed/28419518
http://dx.doi.org/10.1111/bcp.13305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582372/
https://www.ncbi.nlm.nih.gov/pubmed/28419518
http://dx.doi.org/10.1111/bcp.13305

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