Primary objective: * Comparison of efficacy of the combination therapy (clopidogrel plus aspirin) and the aspirin alone (main comparison) to prevent any recurrent ischemic lesion . Secondary objectives: * Comparison of Modified Rankin scale (mRS) scores; * Comparison of the Incidence of all kinds of stroke and vascular death; * Comparison of the Incidence of bleeding episodes (major and minor) and symptomatic intracerebral hemorrhages during the follow-up period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
358
75mg tablet, oral administration once daily
Matching tablet, oral administration once daily
100mg tablet, oral administration once daily
Sanofi-Aventis Administrative Office
Seoul, South Korea
Number of participants with new ischemic lesions after the onset of acute atherothrombotic stroke
Time frame: Within 30 days following the onset of acute atherothrombotic stroke
Distribution of Modified Rankin Scale (mRS) scores
Time frame: Day 30 after the onset of acute atherothrombotic stroke
Number of participants with non-fatal stroke, myocardial infarction (MI) or cardiovascular death (composite endpoint, first-ever)
Time frame: Within 30 days following the onset of acute atherothrombotic stroke
Number of participants with stroke (all kinds)
Time frame: Within 30 days following the onset of acute atherothrombotic stroke
Number of participants with bleeding episode (major or minor)
Time frame: Within 30 days following the onset of acute atherothrombotic stroke
Number of participants with symptomatic intracerebral hemorrhage (ICH)
Time frame: Within 30 days following the onset of acute atherothrombotic stroke
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