None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: · Acute ischemic stroke within 48 hours of onset or lesion-positive transient ischemic attack · Adults aged 19 years or older · History of or newly diagnosed non-valvular atrial fibrillation · Imaging-confirmed relevant atherosclerotic large-artery steno-occlusion/occlusion (rLASO) related to the index infarct lesion · Eligible to start anticoagulation within 4 days of onset (within 7 days in major stroke) · Signed informed consent within 7 days of admission
Exclusion criteria
Exclusion criteria: · Contraindications to direct oral anticoagulants (e.g., mechanical valve or valvular atrial fibrillation) · Clinically mandated use of antiplatelet therapy during the study period · Patients for whom study medication is considered inappropriate due to bleeding risk or clinical status at the investigator’s discretion · Hypersensitivity to apixaban, aspirin, or clopidogrel · Any other condition judged by the treating investigator to preclude participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A composite of stroke, myocardial infarction, or death from any cause within 1 year after randomization. | — |
Secondary
| Measure | Time frame |
|---|---|
| All stroke (ischemic and hemorrhagic);Ischemic stroke or transient cerebral ischemia;Myocardial infarction;All-cause death;Vascular death;Ischemic stroke in the territory of rLASO;Composite vascular events (stroke, myocardial infarction, or all-cause death);Recurrent stroke;Major bleeding (BARC Type 3A, 3B, 3C, 4, 5A, 5B);Symptomatic intracerebral hemorrhage;Intracranial hemorrhage | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital