世界中医药Issue(10)：1269-1271,3.DOI:10.3969/j.issn.1673-7202.2014.10.004
临床研究中知情同意实施过程的要点及建议
The key points and suggestions for implementing informed consent in clinical research
摘要
Abstract
With the widely development of Chinese medicine clinical research,the ethic issue has been gradually concerned.Although the ethical review has been implemented according to some rules,there are still many problems and challenges on proceeding informed consent.According to the relevant laws and regulations,this article incorporates the characteristics of Chinese medicine clinical research and the findings from an expert panel interview,to come up with some suggestions about how to proceed informed consent in Chinese clin-ical research.关键词
知情同意/临床研究/伦理/中医药Key words
Informed consent/Clinical study/TCM/Ethic分类
医药卫生引用本文复制引用
柴倩云,费宇彤,王聪聪,夏芸,韩梅,刘建平..临床研究中知情同意实施过程的要点及建议[J].世界中医药,2014,(10):1269-1271,3.基金项目
国家自然科学基金（编号30901929）；新世纪人才计划（NCET－10－0271）；北京市科技新星项目（2011071）；国家重大新药创制“临床评价研究标准化操作规程（SOP）”项目［编号2011ZX09302－006－01－03（5）］ （）
