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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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Détails bibliographiques
Publié dans:Br J Clin Pharmacol
Auteurs principaux: Dal‐Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2017
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5582372/
https://ncbi.nlm.nih.gov/pubmed/28419518
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.13305
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