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Informed consent: study of quality of information given to participants in a clinical trial.

OBJECTIVE--To determine whether the participants in a clinical trial had perceived adequate information about the trial according to the guidelines of the Declaration of Helsinki. DESIGN--About 18 months after the end of a gynaecological clinical trial the participants received a questionnaire by po...

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Detalhes bibliográficos
Main Authors: Lynöe, N, Sandlund, M, Dahlqvist, G, Jacobsson, L
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1671066/
https://ncbi.nlm.nih.gov/pubmed/1932901
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