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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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Dettagli Bibliografici
Autori principali: Lynöe, N, Sandlund, M, Dahlqvist, G, Jacobsson, L
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1991
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1671066/
https://ncbi.nlm.nih.gov/pubmed/1932901
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