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随机对照试验中方案的发表率以及文章、注册信息与方案之间的比较。

Protocol publication rate and comparison between article, registry and protocol in RCTs.

作者信息

Mathieu Sylvain, Bouillon-Minois Jean-Baptiste, Renard Triché Laurent, Coudeyre Emmanuel, Ingrid De Chazeron, Thomas Finotto, Laporte Catherine, Moisset Xavier, Samalin Ludovic, Villatte Guillaume, Pereira Bruno

机构信息

Rheumatology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.

CHU Clermont-Ferrand, Neuro-Dol, Université Clermont Auvergne, Inserm, Clermont- Ferrand, France.

出版信息

BMC Med Res Methodol. 2025 Feb 1;25(1):31. doi: 10.1186/s12874-025-02471-y.

Abstract

BACKGROUND

Increasing transparency in clinical research is crucial to avoid misleading conclusions. Registering clinical trials prior to participant enrolment is mandatory, and the publication of trial protocols could further enhance transparency. However, the impact of protocol publication on primary outcomes (PO) and sample sizes (SS) remains unclear. This study aimed to determine the rates of trial protocol publication and registration for a sample of randomized controlled trials (RCTs) and to compare the consistency of published and registered PO and SS.

METHODS

A search was conducted in MEDLINE via PubMed for RCT reports indexed in May and June 2023 across various medical specialties, focusing on general and high-impact factor journals. Data were extracted regarding trial registration, protocol publication, and comparisons were made between PO and SS in articles, registries, and published protocols.

RESULTS

Out of 1119 references, 589 (52.6%) were RCTs. The corresponding protocol was published for 146 RCTs (24.8%) including 40 over 140 (28.6%) (6 without end date available) after the trial had ended. Sixty-two (42.4%) protocols were published before the trial conclusion, with no significant differences between PO and SS in published protocols and their corresponding articles. Five hundred and twenty-eight (89.6%) RCTs were registered, 225 over 510 (44%) were registered before the study start with no differences in PO and SS between article and registry. Articles published in generalist or high impact factor journals were associated with higher frequencies of published protocols and trial registration and a lower frequency of difference in PO and SS between articles, registries, and published protocols.

CONCLUSIONS

While publishing trial protocols may enhance transparency in peer-review process, the initial registered protocol alone appears sufficient for ensuring consistency in primary outcomes and sample sizes. Protocol publication does not seem to provide additional significant benefits in terms of outcome reporting.

摘要

背景

提高临床研究的透明度对于避免得出误导性结论至关重要。在招募参与者之前注册临床试验是强制性的,而试验方案的发表可以进一步提高透明度。然而,方案发表对主要结局(PO)和样本量(SS)的影响仍不明确。本研究旨在确定随机对照试验(RCT)样本的试验方案发表率和注册率,并比较已发表和注册的PO及SS的一致性。

方法

通过PubMed在MEDLINE中检索2023年5月和6月索引的各医学专科的RCT报告,重点关注综合类和高影响因子期刊。提取有关试验注册、方案发表的数据,并对文章、注册库和已发表方案中的PO和SS进行比较。

结果

在1119篇参考文献中,589篇(52.6%)为RCT。146项RCT(24.8%)发表了相应方案,其中40项(28.6%)(6项无可用结束日期)在试验结束后发表。62项(42.4%)方案在试验结束前发表,已发表方案及其相应文章中的PO和SS无显著差异。528项(89.6%)RCT进行了注册,510项中有225项(44%)在研究开始前注册,文章与注册库之间的PO和SS无差异。在综合类或高影响因子期刊上发表的文章与更高的方案发表频率和试验注册频率以及文章、注册库和已发表方案之间PO和SS差异的更低频率相关。

结论

虽然发表试验方案可能会提高同行评审过程的透明度,但仅最初注册的方案似乎就足以确保主要结局和样本量的一致性。方案发表在结局报告方面似乎并未提供额外的显著益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fd4/11786558/696aba95ff3a/12874_2025_2471_Fig1_HTML.jpg

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