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Reporting of noninferiority and equivalence randomized trials: an extension of the CONSORT statement.

机译:非劣效性和等效性随机试验的报告:CONSORT声明的扩展。

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摘要

The CONSORT (Consolidated Standards of Reporting Trials) Statement, including a checklist and a flow diagram, was developed to help authors improve their reporting of randomized controlled trials. Its primary focus was on individually randomized trials with 2 parallel groups that assess the possible superiority of one treatment compared with another but is now being extended to other trial designs. Noninferiority and equivalence trials have methodological features that differ from superiority trials and present particular difficulties in design, conduct, analysis, and interpretation. Although the rationale for such trials occurs frequently, those designed and described specifically as noninferiority or equivalence trials appear less commonly in the medical literature. The quality of reporting of those that are published is often inadequate. In this article, we present an adapted CONSORT checklist for reporting noninferiority and equivalence trials and provide illustrative examples and explanations for those items amended from the original CONSORT checklist. The intent is to improve reporting of noninferiority and equivalence trials, enabling readers to assess the validity of their results and conclusions.
机译:制定CONSORT(报告试验的合并标准)声明,包括清单和流程图,以帮助作者改善对随机对照试验的报告。它的主要重点是与2个平行组的单独随机试验,这些试验评估一种治疗方案与另一种治疗方案相比可能的优越性,但现在正扩展到其他试验设计。非劣效性和等效性试验的方法学特征与优越性试验不同,在设计,行为,分析和解释方面存在特殊困难。尽管此类试验的理由经常出现,但在医学文献中较少专门设计和描述为非劣效性或等效性试验的试验。这些出版物的报告质量常常不足。在本文中,我们提供了经过修改的CONSORT检查表,用于报告非劣效性和等效性试验,并提供了从原始CONSORT检查表中修改的那些项目的说明性示例和解释。目的是改善非劣效性和等效性试验的报告,使读者能够评估其结果和结论的有效性。

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