...
首页> 外文期刊>British Medical Journal >Registering clinical trials
【24h】

Registering clinical trials

机译:注册临床试验

获取原文
获取原文并翻译 | 示例
           

摘要

Clinical trials should be registered so that essential details are made public from a trial's inception, rather than from publication many years later. Openness about trials in progress reduces the impact of publication bias, prevents duplication of effort, promotes collaboration, and can save lives. Hundreds of trial registers already exist, but the information on them is not standardised and is incomplete; most contain only a subset of trials, often in high profile areas such as cancer or AIDS; and there are few incentives for researchers to register trials. Initiatives have begun to unify the existing web of registers, but they are at an early stage. Registration of clinical trials should be compulsory, either by law or by linking it to ethical approval of research.
机译:应该注册临床试验,以便从试验开始就公开关键细节,而不是在多年以后公开。对正在进行中的试验的公开态度可减少出版偏见的影响,防止重复工作,促进协作并可以挽救生命。已经有成百上千的试验登记册,但有关登记册的信息尚未标准化且不完整;大多数只包含一部分试验,通常在癌症或艾滋病等知名领域进行;研究人员注册试验的动机很少。倡议已经开始统一现有的登记册网络,但是它们处于早期阶段。依法或将其与研究的伦理批准相关联,应该强制性地进行临床试验的注册。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号