The purpose of this study is to evaluate whether a higher dosage of clopidogrel with aspirin (two doses) will decrease the risk of ischemic complications (cardiac death, stroke, myocardial infarction) after a percutaneous coronary intervention.

Official Title

CURRENT/OASIS 7: Clopidogrel Optimal Loading Dose Usage to Reduce Recurrent EveNTs/Optimal Antiplatelet Strategy for InterventionS

Conditions

Acute Coronary DiseaseAngina Unstable

Study Type

Interventional

Study Design

Treatment, Randomized, Double-Blind, Dose Comparison, Factorial Assignment, Efficacy Study

Further Details

  • Primary Outcome Measures: At Day 30, first occurrence of cardiovascular death, myocardial infarction and stroke; second co-primary outcome: first occurrence of cardiovascular death, stroke, myocardial infarction and recurrent ischemia
  • Secondary Outcome Measures: At Day 30, rate of major bleeding

Study Start

June 2006

Eligibility & Criteria

  • Ages Eligible for Study: 18 Years and above
  • Genders Eligible for Study: Both

Inclusion Criteria:

  • Diagnosed with acute coronary disease with clinical symptoms and at least electrocardiogram changes or aged > 60 years and documented previous coronary artery disease or cardiac enzymes elevated

Exclusion Criteria:

  • Use of anticoagulants within 10 days with an international normalized ratio (INR) > 1.5 or planned use during the hospitalisation period
  • Administration of clopidogrel > 300 mg prior to randomization
  • Contraindication to clopidogrel or aspirin
  • Active bleeding or significant risk of bleeding

Total Enrolment

14000

Contact Details

  • Macquarie Park, Australia; Recruiting
  • Cove, New South Wales, Australia; Recruiting
  • GV-Contact-us@sanofi-aventis.com

Sanofi-Aventis

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