NAVIGATE-ESUS: Secondary Prevention of Stroke in Patients with a Recent ESUS
Phase 3: Multicenter, randomized, double-blind study of secondary prevention of stroke & prevention of systemic embolism in patients with a recent Embolic Stroke of Undetermined Source (ESUS)
Supported by: BAYER
Principal Investigator at BMC: Viken Babikian, MD
Study drugs: Rivaroxaban 15mg vs aspirin 100mg QD
Enrollment Criteria
Inclusion Criteria:
Recent ESUS (between 7 days and 6 months), defined as:
- Recent ischemic stroke (including transient ischemic attack with positive neuroimaging) visualized by brain imaging that is not lacunar, and
- Absence of cervical carotid atherosclerotic stenosis > 50% or occlusion, and
- No atrial fibrillation after ≥ 24-hour cardiac rhythm monitoring (at least 20 hrs acceptable), and
- No intra-cardiac thrombus on either transesophageal or transthoracic echocardiography, and
- No other specific cause of stroke (i.e. arteritis, dissection, migraine/vasospasm, drug abuse)
Exclusion criteria:
- Severely disabling stroke (modified Rankin score ≥4 at screening)
- If imaging of intracranial arteries is performed by CT or MR angiography or transcranial Doppler: > 50% luminal stenosis or occlusion in arteries supplying the area of ischemia
- Patent foramen ovale with plans for closure
- Known serious infection or inflammatory disease that may be the cause of stroke
- Patient has or is intended to receive an implantable ECG loop recorder
- Indication for chronic anticoagulation (e.g., patient with prosthetic mechanical valve, venous thromboembolism, hypercoagulable state)
- Indication for chronic antiplatelet therapy or chronic therapy with NSAID for a non-stroke indication
- Hypersensitivity or other contraindication for ASA or rivaroxaban
- Active bleeding, major bleeding within last 6 months, high risk for serious bleeding contraindicating anticoagulant or antiplatelet therapy or history of primary intracranial hemorrhage
- Hepatic disease associated with coagulopathy (PTT>normal range) and clinically relevant bleeding risk including cirrhotic patients with Child Pugh B and C
- Estimated GFR< 30 mL/min/1.73 m2 as assessed at local laboratory within 1 month of screening
- Life expectancy less than 6 months
- Concomitant use of strong inhibitors of both cytochrome P450 isoenzyme 3A4 (CYP3A4) and P-glycoprotein (P-gp), i.e., human immunodeficiency virus protease inhibitors and the following azole-antimycotics agents: ketoconazole, itraconazole, voriconazole, or posaconazole, if used systemically
- Female of childbearing potential who are not surgically sterile, or, if sexually active not willing to use adequate contraceptive measures, and pregnant or breast feeding women