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  4. The efficacy and safety of cilostazol in ischemic stroke patients with peripheral arterial disease (SPAD): Protocol of a randomized, double-blind, placebo-controlled multicenter trial
 
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The efficacy and safety of cilostazol in ischemic stroke patients with peripheral arterial disease (SPAD): Protocol of a randomized, double-blind, placebo-controlled multicenter trial

Journal
International Journal of Stroke
Journal Volume
10
Journal Issue
1
Pages
123-127
Date Issued
2015
Author(s)
JIANN-SHING JENG  
Sun Y.
Lee J.-T.
Lin R.-T.
Chen C.-H.
Po H.L.
Lin H.-J.
Liu C.-H.
Sun M.-H.
Sun M.-C.
Chern C.-M.
Lien L.-M.
Chiu H.-C.
Hu H.-H.
Chiou H.-Y.
Chen S.-T.
Ma H.
Hsu C.Y.
SPAD Study Investigators
DOI
10.1111/ijs.12384
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84916238893&doi=10.1111%2fijs.12384&partnerID=40&md5=aea5f75d3b25a9a8d2b8e02aa8770850
https://scholars.lib.ntu.edu.tw/handle/123456789/590495
Abstract
Rationale: It is not uncommon for patients with ischemic stroke to have peripheral arterial disease (PAD). Patients with polyvascular diseases carry greater burden of atherosclerosis and higher risks of developing vascular events and death. More effective regimens, such as dual antiplatelet agents, may be more effective for controlling progression of atherosclerosis in secondary prevention. Aim: This study aims to evaluate whether cilostazol plus aspirin is more efficacious than aspirin alone for preventing progression of atherosclerosis in patients with ischemic stroke or transient ischemic attack (TIA) who also have peripheral arterial disease. Design: The Safety and Efficacy of Cilostazol in Ischemic Stroke Patients with Peripheral Arterial Disease (SPAD) study is a randomized double-blinded placebo-controlled trial. Patients with previous ischemic stroke or TIA who had been taking aspirin (100mg per day), aged 50 years or older, with PAD in the lower limbs based on ankle-brachial index (ABI) <1·0 will be randomized into the treatment group with cilostazol (200mg/day) or the placebo group on 1:1 basis. Study outcomes: Patients will be evaluated at 1, 3, 6, 9 and 12 months after randomization. The primary endpoint is difference in change in ABI between groups. The secondary and tertiary endpoints are the difference between groups in change in carotid intima-media thickness (IMT) and incidence rate of major cardiovascular events, including recurrent stroke, myocardial infarction, unstable angina, other vascular events, and death; and the safety measures, including major bleeding events, hemorrhagic stroke and death of any cause. Conclusion: The SPAD trial is the first study to evaluate the safety and efficacy of dual antiplatelet agents, aspirin plus cilostazol, in comparison with aspirin alone in patients with both ischemic stroke or TIA and PAD. Results from this trial will provide important information on the merit of adding cilostazol to aspirin for slowing down progression of atherosclerosis in patients with ischemic stroke and PAD. ? 2014 World Stroke Organization.
SDGs

[SDGs]SDG3

Other Subjects
acetylsalicylic acid; cilostazol; placebo; acetylsalicylic acid; cilostazol; fibrinolytic agent; tetrazole derivative; adult; ankle brachial index; arterial wall thickness; Article; atherosclerosis; bleeding; brain hemorrhage; brain ischemia; controlled study; death; disease course; double blind procedure; drug efficacy; drug safety; heart infarction; human; major clinical study; middle aged; monotherapy; morbidity; multicenter study; peripheral occlusive artery disease; priority journal; randomized controlled trial; recurrent disease; transient ischemic attack; unstable angina pectoris; clinical trial; complication; drug combination; female; male; methodology; peripheral occlusive artery disease; Stroke; Aspirin; Double-Blind Method; Drug Therapy, Combination; Female; Fibrinolytic Agents; Humans; Male; Middle Aged; Peripheral Arterial Disease; Research Design; Stroke; Tetrazoles
Type
journal article

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