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Inclusion of Clinical Trial Registration Numbers in Conference Abstracts and Conformance of Abstracts to CONSORT Guidelines

机译:在会议上纳入临床试验登记号码,摘要摘要和摘要的摘要指南

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摘要

Clinical trial registration facilitates identification, tracking, and assessment of clinical trials and limits publication bias caused by the selective reporting of trial results. Inclusion of trial registration numbers in conference abstracts, as recommended by the Consolidated Standards of Reporting Trials (CONSORT) guidelines for abstracts is particularly important because many conference presentations of trials remain unpublished. In the present study, we reviewed abstracts presented at 8 major medical and surgical conferences held in 2017 to assess the extent to which conference abstracts reporting randomized clinical trial (RCT) results cite trial registration numbers and conform to other key CONSORT guidelines. Methods I For this cross-sectional study, 8 major conferences held in 2017 in the fields of cardiology, endocrinology, gastro-enterology, hepatology, nephrology, and urology (medical specialties of special interest to the authors) and with readily available abstracts were selected for review (Table). Abstracts were identified by searching for the word randomized (or randomised). Abstracts that reported primary results of an RCT were then examined for inclusion of a trial registration number, and the following 5 additional key elements of the CONSORT guidelines for abstracts: the word randomized or randomised or RCT in the title, statement of a primary outcome, number of participants randomized in each group, and number of participants analyzed in each group, and dates of recruitment and follow-up. Inclusion of a trial registration number and the additional 5 CONSORT reporting items in the abstract were each given a score of 1 if present and 0 if absent and then combined to obtain a summary score with a range of 0 to 6.
机译:临床试验注册有助于鉴定,跟踪和评估临床试验,并限制由试验结果的选择性报告引起的出版物偏见。纳入会议摘要中的试验登记号码,按照摘要试验(Consort)摘要标准的建议尤为重要,因为许多会议审判仍未发表。在本研究中,我们审查了2017年举行的8个主要医疗和外科会议的摘要,以评估会议摘要报告随机临床试验(RCT)结果引用试验登记号码并符合其他关键联合指南。方法我对这一横断面研究的方法,在2017年举行的8个主要会议,在2017年在心脏病学,内分泌,胃肠学,肝脏,肾病和泌尿外科(作者特别兴趣的医学专业)中,选择了摘要审查(表)。通过搜索随机(或随机)的单词来识别摘要。摘要然后审查了RCT的主要结果以列入审判登记号码,以及以下5个摘要指南的另外5个额外关键要素:标题中随机或随机或RCT的单词,主要结果的声明,在每组中随机分配的参与者的数量,以及在每组中分析的参与者数量,以及招聘和随访的日期。包含试验登记号码和摘要中的其他5个联合报告项目每个都给出1,如果存在,如果缺席,则为0,然后组合以获得0到6的摘要得分。

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