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Low risk pragmatic trials do not always require participants’ informed consent

dc.contributor.authorDal-Re, Rafael
dc.contributor.authorAvendaño-Solà, Cristina
dc.contributor.authorBloechl-Daum, Brigitte
dc.contributor.authorde Boer, Anthonius
dc.contributor.authorEriksson, Stefan
dc.contributor.authorFuhr, Uwe
dc.contributor.authorHolm, Søren
dc.contributor.authorJames, Stefan K.
dc.contributor.authorMentz, Robert J.
dc.contributor.authorPerucca, Emilio
dc.contributor.authorRosendaal, Frits R.
dc.contributor.authorTreweek, Shaun
dc.contributor.institutionUniversity of Aberdeen.Institute of Applied Health Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Aberdeen Centre for Evaluationen
dc.date.accessioned2019-03-28T10:20:05Z
dc.date.available2019-03-28T10:20:05Z
dc.date.issued2019-03-27
dc.descriptionAcknowledgments We thank Cristina Gómez Piqueras (general subdirectorate of data inspection, Spanish Data Protection Agency) and Alessandro Spina (data protection officer, European Medicines Agency) for their comments on our interpretation of the provisions of the GDPR regarding participants’ informed consent in medical research, and Jan P Vandenbroucke (Leiden University) for his advice. We also thank A de longh, N Ivers, M, Zwarenstein, and The BMJ editors for their comments and suggestions.en
dc.description.statusPeer revieweden
dc.format.extent8
dc.format.extent384203
dc.identifier141193958
dc.identifier686513c7-8ca6-4eb2-a8fd-bd7ec524ec6d
dc.identifier85063604396
dc.identifier000463218200003
dc.identifier.citationDal-Re, R, Avendaño-Solà, C, Bloechl-Daum, B, de Boer, A, Eriksson, S, Fuhr, U, Holm, S, James, S K, Mentz, R J, Perucca, E, Rosendaal, F R & Treweek, S 2019, 'Low risk pragmatic trials do not always require participants’ informed consent', BMJ, vol. 364, 1092. https://doi.org/10.1136/bmj.l1092en
dc.identifier.doi10.1136/bmj.l1092
dc.identifier.issn0959-8146
dc.identifier.otherMendeley: 9c0c1533-23ca-3a0e-a663-320c2e89f744
dc.identifier.otherORCID: /0000-0002-7239-7241/work/186968400
dc.identifier.urihttp://hdl.handle.net/2164/12090
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85063604396&partnerID=8YFLogxKen
dc.identifier.urlhttp://www.mendeley.com/research/low-risk-pragmatic-trials-not-always-require-participants-informed-consenten
dc.identifier.vol364en
dc.language.isoeng
dc.relation.ispartofBMJen
dc.subjectCLINICAL-TRIALSen
dc.subjectR Medicine (General)en
dc.subjectGeneral Medicineen
dc.subject.lccR1en
dc.titleLow risk pragmatic trials do not always require participants’ informed consenten
dc.typeJournal articleen

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