Indobufen versus aspirin in acute ischaemic stroke (INSURE): rationale and design of a multicentre randomised trial

Author:

Pan YuesongORCID,Meng Xia,Chen WeiqiORCID,Jing JingORCID,Lin Jinxi,Jiang Yong,Johnston S ClaiborneORCID,Bath Philip M,Dong Qiang,Xu An-DingORCID,Li HaoORCID,Wang Yongjun

Abstract

BackgroundIndobufen can reversibly inhibit platelet aggregation and showed to be effective in the treatment of ischaemic heart and peripheral vascular diseases. However, it is unclear whether indobufen is an alternative antiplatelet agent for treatment of patients with ischaemic stroke.AimTo test whether indobufen is non-inferior to aspirin in reducing the risk of new stroke at 3 months in patients with moderate to severe ischaemic stroke.DesignThe Indobufen vs Aspirin in Acute Ischaemic Stroke (INSURE) is a randomised, double-blind, double-dummy, positive drug control, non-inferior multicentre clinical trial conducted in 200 hospitals in China. Participants will be randomised at a 1:1 ratio to receive either 100 mg indofufen two times daily or 100 mg aspirin once daily within 72 hours of the onset of symptoms from day 1 to 3 months.Study outcomesThe primary efficacy outcome is a new stroke (ischaemic or haemorrhagic) within 3 months and the primary safety outcome is a severe or moderate bleeding event within 3 months.DiscussionThe INSURE trial will evaluate whether indobufen is non-inferior to aspirin in reducing the risk of new stroke at 3 months in patients with moderate to severe ischaemic stroke.Trial registration numberNCT03871517.

Funder

National Natural Science Foundation of China

Hangzhou Zhongmei Huadong Pharmaceutical Co,Ltd

Capital’s Funds for Health Improvement and Research

Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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