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PubMed
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Stroke Interventions in Clinical Trials
Printable Version
CAST
Chinese Acute Stroke Trial



Contact Address
Dr. Zheng-Ming Chen, Clinical Trial Service Unit, Nuffield Department of Clinical Medicine, Radcliffe Infirmary, Oxford OX2 6HE, UK



Trial Phase:Phase III
Study Size Actual:21106
Centers Actual:413
Max Time from onset:48 Hours
Status:
Trial published 1997.

Purpose:
To study the effects on early mortality and major morbidity of early aspirin treatment in a wide range of stroke patients.

Interventions:
Aspirin (acute stroke)
Antiplatelet agent; inhibits thromboxane A2

Year Published: 1997


Design:
Randomized, placebo-controlled trial of 21106 patients at 413 Chinese hospitals.

Inclusion Criteria
Acute ischemic stroke presenting within 48 hours of onset. No clear indications for, or contraindications to aspirin.

Patient Involvement:
10,554 patients were randomized to receive aspirin (160 mg/day) and 10,552 received placebo.

Primary Outcome:
Death from any cause during 4-week treatment period and death or dependence at the time of discharge from hospital.

Secondary Outcome:
Fatal or non-fatal recurrent stroke and death or non-fatal stroke.

Results:
There was a significant (14%, SD 7) proportional reduction in mortality and fewer recurrent ischemic strokes (2p=0.01) in patients receiving aspirin during treatment period. At discharge, 11.4 fewer patients per 1000 were dead or dependent (2p=0.08) in the group receiving aspirin.

Source of Information:
Lancet 1997 Jun 7;349(9066): 1641-9

Web Links and Publications:
The results of CAPRIE, IST and CAST. Clopidogrel vs. Aspirin in Patients at Risk of Ischaemic Events. International Stroke Trial. Chinese Acute Stroke Trial.
Thromb Res. 1998 Sep 15;92(1 Suppl 1):S13-6.

CAST: randomised placebo-controlled trial of early aspirin use in 20,000 patients with acute ischaemic stroke. CAST (Chinese Acute Stroke Trial) Collaborative Group.
Lancet 1997 Jun 7;349(9066):1641-1649

This information last updated on: 7/28/2008

Reviewed on: 07/28/2008.

UID: 88

   

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