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Searching ClinicalTrials.gov and the International Clinical Trials Registry Platform to inform systematic reviews: What are the optimal search approaches?

机译:搜索ClinicalTrials.gov和国际临床试验注册平台以告知系统评价:最佳搜索方法是什么?

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Background:Since 2005, International Committee of Medical Journal Editors (ICMJE) member journals have required that clinical trials be registered in publicly available trials registers before they are considered for publication. Objectives:The research explores whether it is adequate, when searching to inform systematic reviews, to search for relevant clinical trials using only public trials registers and to identify the optimal search approaches in trials registers. Methods:Asearchwasconductedin Clinical Trials.gov and the International Clinical Trials Registry Platform (ICTRP) for research studies that had been included in eight systematic reviews. Four search approaches (highly sensitive, sensitive, precise, and highly precise) were performed using the basic and advanced interfaces in both resources. Results:On average, 84% of studies were not listed in either resource. The largest number of included studies was retrieved in Clinical Trials.gov and ICTRP when a sensitive search approach was used in the basic interface. The use of the advanced interface maintained or improved sensitivity in 16 of 19 strategies for Clinicaltrials.gov and 8 of 18 for ICTRP. No single search approach was sensitive enough to identify all studies included in the 6 reviews. Conclusions:Trials registers cannot yet be relied upon as the sole means to locate trials for systematic reviews. Trials registers lag behind the major bibliographic databases in terms of their search interfaces. Implications:For systematic reviews, trials registers and major bibliographic databases should be searched. Trials registers should be searched using sensitive approaches, and both the registers consulted in this study should be searched.
机译:背景:自2005年以来,国际医学期刊编辑委员会(ICMJE)成员期刊要求临床试验必须先在公开的试验注册簿中进行注册,然后再考虑发表。目的:本研究探讨了在进行检索以提供系统评价时,仅使用公共试验注册簿进行相关的临床试验并在试验注册簿中确定最佳检索方法是否足够。方法:Asearchwasconducted在Clinical Trials.gov和国际临床试验注册平台(ICTRP)中进行了八项系统评价中的研究。使用这两种资源中的基本和高级界面执行了四种搜索方法(高度敏感,敏感,精确和高度精确)。结果:平均而言,这两种资源中都没有列出84%的研究。当在基本界面中使用敏感的搜索方法时,在Clinical Trials.gov和ICTRP中检索到最多的纳入研究。在Clinicaltrials.gov的19种策略中的16种和在ICTRP中的18种策略中的8种,使用高级界面可以保持或提高敏感性。没有任何一种搜索方法能够足够敏感地识别出6条评论中包括的所有研究。结论:尚不能依靠试验注册作为唯一定位系统评价的试验方法。从搜索界面的角度来看,试验记录的数量落后于主要的书目数据库。启示:要进行系统评价,应搜索试验登记簿和主要书目数据库。应该使用敏感的方法来搜索试验注册簿,并且应该搜索本研究中参考的两个注册簿。

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