Risk to bystanders in clinical trials: A symposium

被引：7

作者：

Eyal, Nir ^{[1
]}

机构：

[1] Rutgers State Univ, Ctr Populat Level Bioeth, 112 Paterson St, New Brunswick, NJ 08901 USA

来源：

CLINICAL TRIALS | 2019年 / 16卷 / 05期

基金：

英国惠康基金;

关键词：

Clinical trials; research ethics; human research subject protection; third-party consent; informed consent; research subject; bystander; research non-participant;

D O I：

10.1177/1740774519862758

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

This symposium takes a critical look at the ethics of impact on "bystanders" to clinical research. By that we mean study non-participants who nevertheless are at risk of being affected by the study in some way. This introduction suggests some questions to consider while reading through the symposium contributions, and gives a precis of each.

引用

页码：447 / 449

页数：3

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Clarridge, Katherine E. ;

Proschan, Michael A. ;

Kwan, Richard ;

Shi, Victoria ;

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Egan, Michael A. ;

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SCIENCE TRANSLATIONAL MEDICINE, 2017, 9 (419)

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