Exploration of deferred informed consent in clinical research
10.12026/j.issn.1001-8565.2024.02.05
- VernacularTitle:临床研究中延迟知情同意的探讨
- Author:
Yan WANG
1
;
Xu LI
;
Kuikui WEI
;
Mengdan LIU
;
Qiong WU
;
Pingping DONG
;
Xiaomei CAO
;
Weiqin LI
;
Yuxiu LIU
Author Information
1. 南京医科大学金陵临床医学院重症医学科,江苏 南京 210002
- Keywords:
deferred informed consent;
informed consent;
medical ethics;
clinical research;
emergency medicine
- From:
Chinese Medical Ethics
2024;37(2):152-157
- CountryChina
- Language:Chinese
-
Abstract:
Informed consent is an important ethical symbol in clinical research,and researchers have the responsibility to fully inform participants of the research information before conducting clinical research.However,it is difficult to obtain complete informed consent form participants or their guardians within a narrow treatment time period in clinical research conducted in emergency situations.Currently,in addition to traditional general informed consent,there are also reality-accepted informed consent,including exemption of informed consent,broad informed consent,and deferred informed consent.By introducing the origin and development process of deferred informed consent in clinical research,this paper sorted out the current application status of deferred informed consent,proposed the prerequisites for applying deferred informed consent in emergency situations,and explored the issues that need to be noted during the application process of deferred informed consent.It is hoped to provide an ethical defense and ethical procedure for the application of deferred informed consent in clinical research in emergency situations.
