试验的前瞻性注册:我们的现状、原因以及如何改进

Denis Mongin, Diana Buitrago-Garcia, Sami Capderou, Thomas Agoritsas, Delphine Shophie Courvoisier, Michele Iudici
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引用次数: 0

摘要

目标:透明的试验行为要求随机对照试验在招收第一名参与者之前进行前瞻性注册。登记的目的是尽量减少因对试验设计进行不合理或隐蔽的修改而可能造成的偏差。我们的目标是:(1)估算前瞻性登记的随机对照试验的比例,并确定与前瞻性登记相关的时间趋势和因素;(2)评估未坚持前瞻性登记的原因,并探索加强坚持前瞻性登记的潜在机制。我们将风湿病学上发表的试验作为案例进行研究:我们使用MEDLINE-PubMed检索了2009年1月至2022年12月期间发表的风湿病学试验报告。我们使用元数据检索了试验注册号,并查阅了全文。我们进行了多变量逻辑回归,以确定与前瞻性试验注册相关的因素。我们向未进行前瞻性注册的试验的作者发送了一份在线调查。我们询问了未进行前瞻性注册的可能原因,并询问了潜在的解决方案。结果我们确定了 1093 项随机对照试验的主要报告,其中 453 项(41.4%)未进行前瞻性注册。其中,130 项(11.9%)未登记,323 项(29.5%)进行了回顾性登记。随着时间的推移,前瞻性注册以每年3%的速度增加(p<0.001),2009年只有13.3%(2/15)的试验进行了前瞻性注册,到2022年则达到73.2%(112/153)。即使在公开支持ICMJE建议的期刊中,2022年发表的试验中也有16%未进行前瞻性注册。在多变量模型中,前瞻性注册与样本量较大、跨国招募以及发表在影响因子较高的期刊上有关。评估非药物干预(尤其是教育、医疗保健或健康)的试验的前瞻性注册率较低。研究者称,缺乏知识或组织问题是导致回顾性注册的主要原因。作者还建议,将伦理审批与试验登记挂钩是确保前瞻性登记的最佳选择。结论:尽管风湿病学在前瞻性注册方面取得了重大进展,但其遵守情况仍不能令人满意。针对期刊编辑、医护人员和研究人员的不同策略可能会改善试验注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prospective Registration of Trials: Where we are, why, and how we could get better
Objectives: Transparent trial conduct requires prospective registration of a randomized controlled trial before the enrolment of the first participant. Registration aims to minimize potential biases through unjustified or hidden modification of trial design. We aimed to (1) estimate the proportion of randomized controlled trials that are prospectively registered and determine the time trends and the factors associated with prospective registration; (2) evaluate the reasons for non-adherence with prospective registration and explore potential mechanisms to enhance adherence with prospective registration. We studied trials published in rheumatology as a case study. Design and setting: We searched for reports of trials in rheumatology published between January 2009 and December 2022 using MEDLINE-PubMed. We retrieved trial registration numbers using metadata and reviewed full texts. We conducted a multivariable logistic regression to identify factors associated with prospective trial registration. We sent an online survey to authors of trials that were not prospectively registered. We inquired about possible reasons for non-adherence with prospective registration and asked about potential solutions. Results: We identified 1093 primary reports of randomized controlled trials; 453 (41.4%) were not prospectively registered. Of these, 130 (11.9%) were not registered, and 323 (29.5%) were retrospectively registered. Prospective registration increased over time at a rate of 3% per year (p<0.001), with only 13.3% (2/15) trials prospectively registered in 2009 to 73.2% (112/153) trials in 2022. Even among journals publicly supporting ICMJE recommendation, 16% of the trials published in 2022 were not prospectively registered. In the multivariable model, prospective registration was associated with a larger sample size, recruitment conducted across countries, and publication in a journal with a higher impact factor. Trial evaluating non pharmaceutical intervention, especially education, delivery of health care or wellness, had a lower rate of prospective registration. Investigators reported lack of knowledge, or organizational problems as the main reasons for retrospective registration. Authors also suggested linking ethical approval to trial registration as the best option to ensure prospective registration. Conclusions: Despite significant improvement, adherence to prospective registration remains unsatisfactory in rheumatology. Different strategies targeting journal editors, healthcare professionals, and researchers may improve trial registration.
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