Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/39741
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dc.contributor.authorDal-Ré, Rafael
dc.contributor.authorCarcas, Antonio J
dc.contributor.authorCarné, Xavier
dc.contributor.authorWendler, David
dc.date.accessioned2019-07-01T06:22:46Z-
dc.date.available2019-07-01T06:22:46Z-
dc.date.issued2017-09
dc.identifier.citationBr J Clin Pharmacol.2017 Sep;(83)9:1921-1931
dc.identifier.urihttps://hdl.handle.net/20.500.12530/39741-
dc.description.abstractPragmatic 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 that the majority of the US public endorses written consent for low-risk pRCTs. The present study was designed to assess whether this view is specific to the US.
dc.language.isoeng
dc.rightsopenAccess-
dc.subjectclinical trial regulation
dc.subjectgeneral notification
dc.subjectlow-risk
dc.subjectpragmatic trials
dc.subjectverbal informed consent
dc.subjectwritten informed consent
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshCross-Sectional Studies
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInformed Consent
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPragmatic Clinical Trials as Topic
dc.subject.meshSpain
dc.subject.meshYoung Adult
dc.subject.meshPatient Preference
dc.titlePublic preferences on written informed consent for low-risk pragmatic clinical trials in Spain.
dc.typeArtículo
dc.identifier.pubmedID28419518
dc.format.volume83
dc.format.page1921-1931
dc.identifier.e-issn1365-2125
dc.identifier.journalBritish journal of clinical pharmacology
dc.identifier.doi10.1111/bcp.13305
dc.format.number9
dc.identifier.pmcPMC5582372
dc.pubmedtypeJournal Article
Appears in Collections:Fundaciones e Institutos de Investigación > IIS H. U. La Paz > Artículos

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