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提高临床试验报告的透明度。

Improving transparency in clinical trial reporting.

作者信息

Farrell Alison

机构信息

Public Library of Science, San Francisco, California, United States of America.

出版信息

PLoS Med. 2025 Apr 28;22(4):e1004588. doi: 10.1371/journal.pmed.1004588. eCollection 2025 Apr.

Abstract

The power to interpret the results of randomised clinical trial results relies on transparent reporting of the study design, protocol, methods and analyses. Without such clarity, the benefits of the findings, to both healthcare, policy and research, cannot be realized in full. The publication of the updated CONSORT 2025 and SPIRIT 2025 statements for reporting of randomised clinical trials and protocols, respectively, offers the opportunity to reflect on the power that transparent reporting of clinical trial design and data offers to improve the quality of trials and outcomes.

摘要

解读随机临床试验结果的能力取决于对研究设计、方案、方法和分析的透明报告。没有这种清晰度,研究结果在医疗保健、政策和研究方面的益处就无法充分实现。分别用于报告随机临床试验和方案的更新后的CONSORT 2025和SPIRIT 2025声明的发布,为反思临床试验设计和数据的透明报告对提高试验质量和结果的作用提供了契机。

相似文献

1
Improving transparency in clinical trial reporting.提高临床试验报告的透明度。
PLoS Med. 2025 Apr 28;22(4):e1004588. doi: 10.1371/journal.pmed.1004588. eCollection 2025 Apr.
7
SPIRIT 2025 statement: Updated guideline for protocols of randomised trials.《SPIRIT 2025声明:随机试验方案的更新指南》
PLoS Med. 2025 Apr 28;22(4):e1004589. doi: 10.1371/journal.pmed.1004589. eCollection 2025 Apr.

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