Patient representatives’ views on patient information in clinical cancer trials

BACKGROUND: Patient enrolment into clinical trials is based on oral information and informed consent, which includes an information sheet and a consent certificate. The written information should be complete, but at the same time risks being so complex that it may be questioned if a fully informed c...

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Detalles Bibliográficos
Autores principales: Dellson, Pia, Nilbert, Mef, Carlsson, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736467/
https://www.ncbi.nlm.nih.gov/pubmed/26831330
http://dx.doi.org/10.1186/s12913-016-1272-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736467/
https://www.ncbi.nlm.nih.gov/pubmed/26831330
http://dx.doi.org/10.1186/s12913-016-1272-2

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