4.6 Article

Dual antiplatelet Use for extended period taRgeted to AcuTe ischemic stroke with presumed atherosclerotic OrigiN (DURATION) trial: Rationale and design

期刊

INTERNATIONAL JOURNAL OF STROKE
卷 -, 期 -, 页码 -

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/17474930231168742

关键词

Dual antiplatelet therapy; ischemic stroke; large artery atherosclerosis; treatment duration

向作者/读者索取更多资源

The goal of this study is to determine whether a longer duration of dual antiplatelet therapy with clopidogrel-aspirin can reduce the risk of recurrent vascular events in patients with large artery atherosclerotic (LAA) stroke subtype. This is a multicenter, prospective, randomized study comparing the efficacy and safety of a 12-month duration of DAPT versus a 3-month duration of DAPT in LAA stroke subtype patients. The results of this study will help stroke physicians determine the appropriate duration of dual therapy for LAA stroke subtype patients.
Rationale: The optimal duration of dual antiplatelet therapy (DAPT) with clopidogrel-aspirin for the large artery atherosclerotic (LAA) stroke subtype has been debated.Aims: To determine whether the 1-year risk of recurrent vascular events could be reduced by a longer duration of DAPT in patients with the LAA stroke subtype.Methods and study design: A total of 4806 participants will be recruited to detect a statistically significant relative risk reduction of 22% with 80% power and a two-sided alpha error of 0.05, including a 10% loss to follow-up. This is a registry-based, multicenter, prospective, randomized, open-label, blinded end point study designed to evaluate the efficacy and safety of a 12-month duration of DAPT compared with a 3-month duration of DAPT in the LAA stroke subtype. Patients will be randomized (1:1) to either DAPT for 12 months or DAPT for 3 months, followed by monotherapy (either aspirin or clopidogrel) for the remaining 9 months.Study outcomes: The primary efficacy outcome of the study is a composite of stroke (ischemic or hemorrhagic), myocardial infarction, and all-cause mortality for 1 year after the index stroke. The secondary efficacy outcomes are (1) stroke, (2) ischemic stroke or transient ischemic attack, (3) hemorrhagic stroke, and (4) all-cause mortality. The primary safety outcome is major bleeding.Discussion: This study will help stroke physicians determine the appropriate duration of dual therapy with clopidogrel-aspirin for patients with the LAA stroke subtype.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据