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Patient involvement in clinical research: why, when, and howDo informed consent documents for cancer trials do what they should? A study of manifest and latent functionsThe definition of placebo in the informed consent forms of clinical trials.Placebo-controlled clinical trials: how trial documents justify the use of randomisation and placebo.Participants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis.Health literacy predicts participant understanding of orally-presented informed consent information.Understanding of research, genetics and genetic research in a rapid ethical assessment in north west Cameroon.Therapeutic misconception in research subjects: development and validation of a measure
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Consent in clinical trials: what do patients know?
@en
Consent in clinical trials: what do patients know?
@nl
type
label
Consent in clinical trials: what do patients know?
@en
Consent in clinical trials: what do patients know?
@nl
prefLabel
Consent in clinical trials: what do patients know?
@en
Consent in clinical trials: what do patients know?
@nl
P2093
P1476
Consent in clinical trials: what do patients know?
@en
P2093
Inma Fuentes
Josep Maria Arnau
Pilar Hereu
Pilar Suñé
P304
P356
10.1016/J.CCT.2010.05.004
P407
P577
2010-05-10T00:00:00Z