巴西涉及人类的研究中的伦理行为:研究伦理委员会的诊断。

Maria Rita Garbi Novaes, Dirce Guilhem, Fernando Lolas
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引用次数: 0

摘要

目的:诊断巴西涉及人类的研究中的伦理行为,以及联邦地区卫生部人类研究伦理委员会(CEP/SES/DF)过去10年的活动。方法:本研究采用文献研究、描述性和回顾性相结合的方法。它审查了载有提交CEP/SES/DF的案件记录的数据库,该数据库对应于1997年6月至2007年12月期间。结果在Excel程序2007版中生成。结果:CEP/SES/DF提交评估的研究项目数量不断增加(n=1129),其中:90.4%的项目获得批准,1.7%的项目未获得批准,7.4%的项目被删除/提交,0.5%的项目被排除在外。在这些项目中,83%属于第三组,18%属于多中心项目,10%属于外国参与的协议。多年来,审批时间有所减少(30至60天)。经常悬而未决的问题:自由知情同意终止(30%)、封面(25%)、方法(20%)、简历(12%)、预算(9%)和其他(4%)。结论:在十年的时间里,对CEP/SES/DF活动的评估表明,它致力于研究伦理审查和科学生产SES/DF的合法性。存在一些弱点,例如难以监测研究的伴随情况;因药物不良反应而中断工作;研究人员提交的方案中的空白或错误。这些情况是制定具体标准的实现目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ethical Conduct in Research Involving Human Beings In Brazil: Diagnosis of Research Ethics Committee.

OBJECTIVE: Diagnose ethical conduct in research involving human beings in Brazil and the last 10 years of activity by the Human Research Ethics Committee of the Health Department - Federal District - CEP/SES/DF. METHODS: This work was based on a documentary research, descriptive and retrospective. It examined the database containing records of cases brought before the CEP/SES/DF, corresponding the period of June 1997 to December 2007. Results were generated in Excel program, version 2007. RESULTS: CEP/SES/DF has presented increasing number of research projects submitted to appreciation (n = 1129), composing: 90.4% approved 1.7% disapproved, 7.4% removed/filed and 0.5% excluded. Of these projects, 83% belonged to Group III, 18% multi-centered projects and 10% protocols with foreign participation. Time for approval has decreased over the years (30 to 60 days). Frequent pendencies: End of Free and Informed Consent (30%), Cover Sheet (25%), Methodology (20%), Curriculum vitae (12%), Budget (9%), and Others (4%). CONCLUSION: The assessment of the CEP/SES/DF activities, during a ten-year period has shown its commitment to the legitimacy of research ethics review and scientific production SES/DF. There were some weaknesses such as difficulty in monitoring the accompaniment of the research; interruption of works due to adverse drug reaction; gaps or errors in the protocol submitted by the researcher. These situations are the achieving targets for the elaboration of specific criteria.

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