Sarpogrelate-Aspirin Comparative Clinical Study for Efficacy and Safety in Secondary Prevention of Cerebral Infarction (S-ACCESS)
Cerebral Infarction
About this trial
This is an interventional prevention trial for Cerebral Infarction
Eligibility Criteria
Inclusion Criteria: Cerebral infarction except cardiac source of embolism Onset ≧ 1 week to ≦ 6 months before randomization Neurological signs persisting ≧ 1 day from onset Computed tomography (CT) or magnetic resonance imaging (MRI) detection of responsible site Age ≧ 20 years Systolic pressure ≦ 180 mmHg; diastolic pressure ≦ 110 mmHg Exclusion Criteria: Functional outcome at randomization: Modified Rankin Scale = 4, 5 Previous or planned vascular surgery for cerebral infarction History of intracranial hemorrhage History of systemic bleeding, or other history of bleeding diathesis or coagulopathy Severe complications (renal or hepatic insufficiency, heart failure, hemopathy, etc.) Pregnant or possibly pregnant women, or nursing mothers History of sarpogrelate and aspirin sensitivity Treating malignant tumor or treated within 5 years Current peptic ulceration
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
MCI-9042
Aspirin