Department of Global Health & Development, London School of Hygiene and Tropical Medicine, London, UK.
Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Trials. 2021 Jun 1;22(1):375. doi: 10.1186/s13063-021-05330-5.
Clinical trial transparency forms the foundation of evidence-based medicine, and trial sponsors, especially publicly funded institutions such as universities, have an ethical and scientific responsibility to make the results of clinical trials publicly available in a timely fashion. We assessed whether the thirty UK universities receiving the most Medical Research Council funding in 2017-2018 complied with World Health Organization best practices for clinical trial reporting on the US Clinical Trial Registry ( ClinicalTrials.gov ). Firstly, we developed and evaluated a novel automated tracking tool ( clinical-trials-tracker.com ) for clinical trials registered on ClinicalTrials.gov . This tracker identifies the number of due trials (whose completion lies more than 395 days in the past) that have not reported results on the registry and can now be used for all sponsors. Secondly, we used the tracker to determine the number of due clinical trials sponsored by the selected UK universities in October 2020. Thirdly, using the FDAAA Trials Tracker, we identified trials sponsored by these universities that are not complying with reporting requirements under the Food and Drug Administration Amendments Act 2007. Finally, we quantified the average and median number of days between primary completion date and results posting. In October 2020, the universities included in our study were sponsoring 1634 due trials, only 1.6% (n = 26) of which had reported results within a year of completion. 89.8% (n = 1468) of trials remained unreported, and 8.6% (n = 140) of trials reported results late. We also identified 687 trials that contained inconsistent data, suggesting that UK universities often fail to update their data adequately on ClinicalTrials.gov . The mean reporting delay after primary completion for trials that posted results was 981 days, the median 728 days. Only four trials by UK universities violated the FDAAA 2007. We suggest a number of reasons for the poor reporting performance of UK universities on ClinicalTrials.gov : (i) efforts to improve clinical trial reporting in the UK have to date focused on the European clinical trial registry (EU CTR), (ii) the absence of a tracking tool for timely reporting on ClinicalTrials.gov has limited the visibility of institutions' reporting performance on the US registry and (iii) there is currently a lack of repercussions for UK sponsors who fail to report results on ClinicalTrials.gov which should be addressed in the future.
临床试验透明度是循证医学的基础,临床试验发起者,尤其是大学等公共资助机构,有责任及时将临床试验结果公开。我们评估了 2017-2018 年获得英国医学研究理事会(MRC)资助最多的 30 所英国大学是否符合世界卫生组织(WHO)在美国临床试验注册中心(ClinicalTrials.gov)上报告临床试验的最佳实践。首先,我们开发并评估了一种用于识别 ClinicalTrials.gov 上注册临床试验的新型自动跟踪工具(clinical-trials-tracker.com)。该跟踪器可识别未在注册中心报告结果的应报试验(完成时间超过 395 天)数量,并可用于所有赞助商。其次,我们使用该跟踪器于 2020 年 10 月确定了选定英国大学赞助的应报临床试验数量。第三,使用 FDAAA Trials Tracker,我们确定了这些大学赞助的不符合 2007 年《食品和药物管理局修正案》报告要求的试验。最后,我们量化了主要完成日期和结果发布之间的平均和中位数天数。2020 年 10 月,我们研究中的大学赞助了 1634 项应报试验,其中只有 1.6%(n=26)在完成后一年内报告了结果。89.8%(n=1468)的试验仍未报告,8.6%(n=140)的试验报告结果延迟。我们还发现了 687 项包含不一致数据的试验,这表明英国大学经常未能在 ClinicalTrials.gov 上充分更新其数据。主要完成后发布结果的试验的平均报告延迟为 981 天,中位数为 728 天。只有 4 项英国大学的试验违反了 2007 年 FDAAA。我们提出了英国大学在 ClinicalTrials.gov 上报告表现不佳的几个原因:(i)迄今为止,改善英国临床试验报告的努力主要集中在欧洲临床试验登记处(EU CTR),(ii)缺乏及时报告的跟踪工具限制了机构在 US 登记处报告表现的可见性,(iii)目前对未能在 ClinicalTrials.gov 上报告结果的英国赞助商缺乏后果,未来应予以解决。