Colchicine in High-risk Patients with Acute Minor-to-moderate Ischemic Stroke or Transient Ischemic Attack (CHANCE-3): Rationale and design of a multicenter randomized placebo-controlled trial

被引:14
作者
Wang, Yongjun [1 ,2 ,3 ,7 ,8 ]
Li, Jiejie [1 ,2 ]
Johnston, S. Claiborne [4 ]
Hankey, Graeme J. [5 ,6 ]
Easton, J. Donald [4 ]
Meng, Xia [1 ,2 ]
Shi, Fu-Dong [1 ,2 ]
Wang, Yilong [1 ,2 ]
Zhao, Xingquan [1 ,2 ]
Li, Zixiao [1 ,2 ]
Liu, Liping [1 ,2 ]
Gu, Hongqiu [1 ,2 ]
Jiang, Yong [1 ,2 ]
Wang, Anxin [1 ,2 ]
Pan, Yuesong [1 ,2 ]
Jing, Jing [1 ,2 ]
Niu, Siying [1 ,2 ]
Li, Hao [1 ,2 ]
机构
[1] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Beijing, Peoples R China
[2] China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China
[3] Capital Med Univ, Clin Ctr Precis Med Stroke, Beijing, Peoples R China
[4] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[5] Univ Western Australia, Med Sch, Perth, WA, Australia
[6] Perron Inst Neurol & Translat Sci, Perth, WA, Australia
[7] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, 119 Rd Nansihuanxi, Beijing 100075, Peoples R China
[8] China Natl Clin Res Ctr Neurol Dis, 119 Rd Nansihuanxi, Beijing 100075, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Ischemic stroke; inflammation; colchicine; randomized controlled trial; CORONARY-HEART-DISEASE; INTERLEUKIN-6; RECEPTOR; INFLAMMATION; METAANALYSIS; CLOPIDOGREL; MYOTOXICITY; PREVENTION; PATHWAYS; ASPIRIN; EVENTS;
D O I
10.1177/17474930231172312
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Anti-inflammatory therapy using colchicine has reduced recurrent vascular events in patients with coronary heart disease. Design: Colchicine in High-risk Patients with Acute Minor-to-moderate Ischemic Stroke or Transient Ischemic Attack (CHANCE-3) is a randomized, double-blind, placebo-controlled multicenter trial, in which 8,238 patients with acute minor-to-moderate ischemic stroke (NIHSS <= 5) or high-risk transient ischemic attack (TIA) (ABCD(2) score >= 4) and a high-sensitivity CRP (hsCRP) level of >= 2 mg/L will be randomly assigned within 24 h of symptom onset to colchicine (1 mg daily on days 1-3, followed by 0.5 mg daily for a total of 90 days) or matching placebo, on a background of optimal medical therapy. The study will have 90% power to detect a 25% reduction in the primary efficacy outcome of any stroke within 3 months of randomization. Adverse events potentially related to the use of colchicine will also be analyzed. The primary analysis will be by intention to treat.
引用
收藏
页码:873 / 878
页数:6
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