Last updated on February 2018

Optimal Antithrombotic Therapy in Ischemic Stroke Patients With Non-Valvular Atrial Fibrillation and Atherothrombosis


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Ischemic Stroke | Atrial Fibrillation | Atherothrombosis
  • Age: Between 20 - 89 Years
  • Gender: Male or Female

Inclusion Criteria:

  1. Patients with an acute ischemic stroke or TIA from 8 days and up to 360 days from the onset of symptoms
  2. Age: 20-90 years.
  3. Patients with non-valvular atrial fibrillation (chronic or paroxysmal) who start or continue taking an oral anticoagulant
  4. Patients who have one of the following atherothrombotic diseases
  5. A past history of ischemic heart disease (myocardial infarction, angina pectoris, coronary artery bypass graft (CABG), percutaneous coronary intervention (PCI)
  6. A past history of peripheral artery disease (symptomatic peripheral arterial occlusive disease, lower extremity bypass surgery/angioplasty/stenting)
  7. Carotid artery stenosis (symptomatic or asymptomatic (=>50% diameter), a history of carotid artery stenting (CAS) or carotid endarterectomy (CEA))
  8. Intracranial artery stenosis (=>50% stenosis of the diameter of a major intracranial artery: intracranial internal carotid artery, anterior cerebral artery (ACA)-A1 and A2, middle cerebral artery (MCA)-M1 and M2, posterior cerebral artery (PCA)-P1 and P2, vertebral artery, and basilar artery; a history of intracranial stent placement or intracranial bypass surgery)
  9. A past history of atherothrombotic brain infarction, lacunar infarction, or branch atheromatous disease
  10. Patients who can walk independently (modified Rankin Scale score =<3)
  11. Patients who can take oral medications
  12. Patients who can receive follow-up survey
  13. Provision of written informed consent either directly or by a suitable surrogate

Exclusion Criteria:

  1. History of myocardial infarction or acute coronary syndrome within the past 12 months
  2. Patients who underwent PCI with drug-eluting stents within the past 12 months or PCI with bare-metal stents within the past 3 months
  3. Patients who underwent carotid artery stent placement, intracranial stent placement, or lower extremity stent placement within the past 3 months
  4. History of symptomatic intracranial hemorrhage or gastrointestinal bleeding within the past 6 months
  5. Hemorrhagic diathesis or blood coagulation disorders
  6. Platelet counts <100,000 /mm3 at enrollment.
  7. Severe anemia (hemoglobin <7 g/dL)
  8. Severe renal failure (creatinine clearance =<15 mL/min) or undergoing chronic hemodialysis.
  9. Severe liver dysfunction (Grade B or C of the Child-Pugh classification)
  10. Patients who are unable to walk independently (modified Rankin Scale score =>4)
  11. Pregnant or possibly pregnant women
  12. Active cancer
  13. Expectation of survival less than 2 years
  14. Anticoagulant or antiplatelet is scheduled to be discontinued for more than 4 weeks during the follow-up period
  15. Planned revascularization procedure during the follow-up period
  16. Patients who are enrolled in other trials
  17. Patients judged as inappropriate for this study by investigators

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


Volunteer Sign-up

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.