The fast assessment of stroke and transient ischemic attack to prevent early recurrence (FASTER) trial

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Abstract

New evidence has shown that the highest risk of stroke is in the 48 to 72 hours immediately after a transient ischemic attack. No evidence currently exists to guide the optimal management of these patients. The Fast Assessment of Stroke and Transient Ischemic Attack to Prevent Early Recurrence (FASTER) trial aims to enroll this group of patients. The trial has a 2×2 factorial design. All patients will be on aspirin. Patients will be randomized to clopidogrel or placebo, and to simvastatin or placebo to ensure that these are both safe and effective treatments. Patients will be followed for 90 days.

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