非劣效性试验的关键见解和挑战。

IF 6.3 4区 医学 Q1 ANESTHESIOLOGY Korean Journal of Anesthesiology Pub Date : 2024-08-01 Epub Date: 2024-07-30 DOI:10.4097/kja.23534
Boohwi Hong, Dong-Kyu Lee
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引用次数: 0

摘要

非劣效性临床试验对于评估新干预措施与标准干预措施相比的有效性至关重要。通过建立统计和临床可比性,这些试验可以证明新的干预措施并不明显劣于标准干预措施。然而,选择适当的非劣效边际和研究设计对于确保结果的有效性和可靠性至关重要。此外,采用《试验报告统一标准》(CONSORT)声明报告非劣效性临床试验可提高研究结果的质量和透明度。本文探讨了研究者在计划、开展和解释非劣效性临床试验结果时所面临的主要考虑因素和挑战。
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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Key insights and challeneges in noninferiority trials.

Noninferiority clinical trials are crucial for evaluating the effectiveness of new interventions compared to standard interventions. By establishing statistical and clinical comparability, these trials can be conducted to demonstrate that a new intervention is not significantly inferior to the standard intervention. However, selecting appropriate noninferiority margins and study designs are essential to ensuring valid and reliable results. Moreover, employing the Consolidated Standards of Reporting Trials (CONSORT) statement for reporting noninferiority clinical trials enhances the quality and transparency of research findings. This article addresses key considerations and challenges faced by investigators in planning, conducting, and interpreting the results of noninferiority clinical trials.

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来源期刊
CiteScore
6.20
自引率
6.90%
发文量
84
审稿时长
16 weeks
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