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ClinicalTrials.gov registration can supplement information in abstracts for systematic reviews: a comparison study

机译:ClinicalTrials.gov注册可以补充摘要中的信息以进行系统评价:一项比较研究

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摘要

BackgroundThe inclusion of randomized controlled trials (RCTs) reported in conference abstracts in systematic reviews is controversial, partly because study design information and risk of bias is often not fully reported in the abstract. The Association for Research in Vision and Ophthalmology (ARVO) requires trial registration of abstracts submitted for their annual conference as of 2007. Our goal was to assess the feasibility of obtaining study design information critical to systematic reviews, but not typically included in conference abstracts, from the trial registration record.
机译:背景技术会议摘要中报告的随机对照试验(RCT)是否包含在系统评价中是有争议的,部分原因是摘要中的研究设计信息和偏倚风险通常未得到充分报道。视觉与眼科研究协会(ARVO)要求对提交至2007年年会的摘要进行试验注册。我们的目标是评估获取对于系统评价至关重要的研究设计信息的可行性,但通常不包括在会议摘要中,从试用注册记录中。

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