[Time for assessing a clinical research project by one of 39 French ethic committees: A retrospective study between 2019 and 2023].

S Roriz, C Michel, M Mezzarobba, M Grit, G Baville Valade, E Cabrera, L ElotmanI, A Ambert, J-Y Lefrant, S Granier, N Boulet, Y Gricourt
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Abstract

Introduction: The study reported the time (from the initial submission to the final decision) to evaluate a clinical research project by one of the 39 French national ethics committees. The times from this final decision to the first participant inclusion and study achievement (first patient inclusion to the end of the last patient's follow-up) were also reported.

Methods: Clinical research projects submitted between January 1st 2019 and June 30th 2023 were analyzed according to their type (research on drugs, clinical investigations, performance studies, research implying human person), and the promotor (industry, university hospital, general hospital, private medical institution, others). The times of assessment of the project by the ethic committee (from the initial submission to the final decision), of the first participant inclusion (from the approval of the project) and of study achievement (first patient inclusion to the end of the last patient's follow-up) were calculated.

Results: Among 467 submitted clinical research projects, 424 were approved (90.8 %). The median time [Q1-Q3] to evaluate a project was 73 days [51-98] whatever the types of projects and promotors. In 307 accepted projects, the first patient inclusion occurred after 134 days [61-237] and was being waited for 347 days [306-510] in 39 other ones. In 122 projects, the time for study achievement was 446 days [230-731]. In 185 other projects, the inclusions were still in progress for 699 days [397-1098].

Conclusion: In this concerned ethic committee, a final decision was edited after a median assessment time of 73 days (with >90 % approvals), shorter than the times to include the first patient and for achieving the study.

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[法国 39 个伦理委员会之一对临床研究项目进行评估的时间:2019年至2023年的回顾性研究]。
简介该研究报告了法国 39 个国家伦理委员会之一对临床研究项目进行评估的时间(从最初提交到最终决定)。此外,还报告了从最终决定到第一名参与者入选的时间以及研究成果(第一名患者入选到最后一名患者随访结束):方法:对 2019 年 1 月 1 日至 2023 年 6 月 30 日期间提交的临床研究项目进行了分析,根据其类型(药物研究、临床调查、绩效研究、涉及人体的研究)和发起方(工业界、大学医院、综合医院、私立医疗机构及其他)进行了分类。我们计算了伦理委员会对项目进行评估的时间(从最初提交到最终决定)、首次纳入受试者的时间(从项目批准开始)和研究成果的时间(首次纳入患者到最后一名患者随访结束):在提交的 467 个临床研究项目中,424 个获得批准(90.8%)。无论项目类型和发起人如何,项目评估的中位时间[Q1-Q3]为 73 天[51-98]。在 307 个已获批准的项目中,首次纳入患者的时间为 134 天[61-237],其他 39 个项目的等待时间为 347 天[306-510]。在 122 个项目中,完成研究的时间为 446 天[230-731]。结论:在这个相关的伦理委员会中,最终决定是在中位评估时间为 73 天后编辑的(批准率大于 90%),比纳入首例患者和完成研究的时间更短。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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