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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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Dettagli Bibliografici
Pubblicato in:Br J Clin Pharmacol
Autori principali: Dal‐Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2017
Soggetti:
Accesso online: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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