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Anticoagulation in Intracerebral Hemorrhage (ICH) Survivors for Stroke Prevention and Recovery

UCI Specialty Area: Neurology
Principal Investigator: Wengui Yu
Official Title: Anticoagulation in Intracerebral Hemorrhage (ICH) Survivors for Stroke Prevention and Recovery (ASPIRE)
A Study On:
Brain - Neurologic/ Psychologic
Stroke

Study Description

ASPIRE is a randomized, double-blinded, phase III clinical trial designed to test the efficacy and safety of anticoagulation, compared with aspirin, in patients with a recent Intracerebral hemmorhage (ICH) and high-risk non-valvular atrial fibrillation (AF) (CHA2DS2-VASc score >/= 2). Seven hundred patients will be enrolled over 3.5 years and followed for study outcomes for a minimum of 12 months and maximum of 36 months. The primary efficacy outcome is any stroke (hemorrhagic or ischemic) or death from any cause. The secondary efficacy outcome is the change in the modified Rankin Scale score. Recruitment will take place at sites coordinated through the NIH/NINDS StrokeNet.

Eligibility

  1. Age at least 18 years
  2. Intracerebral hemorrhage (ICH) (including primary intraventricular hemorrhage) confirmed by brain CT or MRI
  3. Can be randomized within 14-120 days after ICH onset
  4. Non-valvular AF (defined as atrial fibrillation or atrial flutter), documented by electrocardiography or a physician-confirmed history of prior AF
  5. CHA2DS2-VASc score >/= 2
  6. Provision of signed and dated informed consent form by patient or legally authorized representative
  7. Able to comply with all study procedures and available for duration of the study
  8. For females of reproductive potential: use of highly effective contraception
  1. History of ICH before index event
  2. Active infective endocarditis
  3. Lobar ICH with cerebral amyloid angiopathy
  4. Clear indication for anticoagulant drugs (e.g., requires anticoagulation for deep vein thrombosis or pulmonary embolism) or antiplatelet drugs (e.g., requires aspirin or clopidogrel for recent MI).
  5. Previous or planned left atrial appendage closure
  6. Clinically significant bleeding diathesis
  7. Serum creatinine >/= 2.5 mg/dL
  8. Active hepatitis or hepatic insufficiency with Child-Pugh score B or C
  9. Anemia (hemoglobin <8 g/dL) or thrombocytopenia (<100 x 109/L) that is chronic in the judgment of the investigator
  10. Life expectancy <1 year
  11. Pregnant or breastfeeding
  12. Known allergy to aspirin or apixaban
  13. Concomitant participation in a competing therapeutic trial
  14. Considered by the investigator to have a condition that precludes safe participation in the trial
  15. Unwilling to discontinue prohibited medications
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Privacy Policy

University of California, Irvine - Study Information Sheet

UCI Center for Clinical Research Potential Participant Database

Lead Researcher
Maheswari Senthil, MD
UCI Center for Clinical Research

In the instance of parental permission, “You” refers to “Your child.”

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