This is a prospective observational analysis of consecutive CABG surgery patients in a number of hospitals across Canada. The aim of the study is to assess the rate of re-operations, incidence of major bleeding and inpatient length of stay in patients who received clopidogrel pre-operatively compared to patients who have not received clopidogrel before the time of their surgery.
Study Design: Observational Study.
Intervention: Clopidogrel Plavix®.
Length of Study: 18 months
# of Patients: 500
Patient Populations: CABG surgery patients.
Publications (for a full listing of publications, please visit the 'Media and Publications' section)
Available upon study completion.