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首页> 外文期刊>Anaesthesia: Journal of the Association of Anaesthetists of Great Britain and Ireland >Adherence to guidance on registration of randomised controlled trials published in Anaesthesia Anaesthesia
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Adherence to guidance on registration of randomised controlled trials published in Anaesthesia Anaesthesia

机译:在麻醉麻醉中发表的随机对照试验注册指导的遵守

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摘要

Summary The International Committee of Medical Journal Editors recommends the prospective registration of interventional clinical trials. We aimed to assess the compliance with these guidelines for manuscripts submitted to and published by a single anaesthetic journal. We examined the rates of prospective trial registration, the incidence of discrepancies in primary outcome measure(s) and sample sizes, and the citation metrics of all randomised controlled trials published in Anaesthesia over a 3‐year period (2014–2016). Of the 422 randomised controlled trials submitted during the study period, 115 (27.3%) were accepted for publication, of which 90 (78.3%) were patient studies, with the remaining 25 comprising manikin, simulation, volunteer, bench, cadaver and other non‐patient intervention studies. Of the accepted patient studies, 64 (71.1%) were prospectively registered with a clinical trials registry, 20 (22.2%) were not registered and 6 (6.7%) were retrospectively registered after manuscript submission. There was no difference in the frequency of registration between accepted and rejected manuscripts (77.8% vs. 84.5%, respectively, p?=?0.143). The median ( IQR [range]) time from registration of accepted manuscripts to journal submission was 701 (331–1341 [99–2436])?days. There was no correlation between number of patients recruited to a study and time to submission. Fifty‐two (81.3%) of the prospectively registered studies reported the same primary outcomes in both registration and submission, and 34 (53.1%) studies were published with the same powered sample size as that described in the registry. Eleven (12.2%) studies recruited more patients and 19 (21.1%) recruited fewer patients than described in the registration protocol. There was no difference in the median ( IQR [range]) number of citations per month since publication between prospectively (0.27 (0.15–0.46 [0.00–1.59]), and retrospectively (0.39 (0.15–0.62 [0.10–0.67]); p?=?0.502) or unregistered (0.33 (0.10–0.52 [0.00–0.67]); p?=?0.867) studies. Our results suggest that prospective clinical trial registration has no influence on acceptance for publication by Anaesthesia or subsequent citation metrics. The international recommendation for prospective trial registration appears to have not been universally incorporated into anaesthetic‐related research practice.
机译:发明内容国际医学期刊编辑委员会建议前瞻性注册介入临床试验。我们旨在评估符合单一麻醉期刊提交和发布的稿件的这些准则。我们审查了前瞻性审判登记的率,主要结果措施的差异发生率和样本规模,以及在3年期间出现麻醉(2014-2016)的麻醉中出版的所有随机对照试验的引文指标。在研究期间提交的422项随机对照试验中,出版物的115例(27.3%),其中90例(78.3%)是患者研究,其余25例包含人体模型,模拟,志愿者,长凳,尸体和其他非 - 病价干预研究。在接受的患者研究中,64(71.1%)预期在临床试验登记处注册,未注册20(22.2%),并在稿件提交后回顾性注册6(6.7%)。接受和拒绝的手稿之间的登记频率没有差异(分别为77.8%,分别为84.5%,p?= 0.143)。从接受的稿件注册到日志提交的中位数(IQR [Range])时间为701(331-1341 [99-2436])?天。招募在研究和提交时间的患者之间没有相关性。五十二(81.3%)的前瞻性注册研究报告了登记和提交的主要成果,34名(53.1%)的研究发表了与注册表中所述相同的动力样本尺寸。十一(12.2%)研究招募了更多患者,19名(21.1%)招募了较少的患者,而不是注册议定书。中位数(IQR [RANGE])每月的引用数量没有差异(0.27(0.27(0.15-0.46 [0.00-1.59])和回顾性(0.39(0.15-0.62 [0.10-0.67]); p?= 0.502)或未注册(0.33(0.10-0.52 [0.00-0.67]); p?= 0.867)研究。我们的研究结果表明,前瞻性临床试验登记对麻醉或随后的引文指标的出版物的接受没有影响。潜在审判登记的国际建议似乎没有普遍纳入与麻醉相关的研究实践。

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