Coronary Artery Disease Clinical Trial
Objective: To evaluate the early and late prognoses of patients according to platelet
reactivity after clopidogrel administration and determine whether the measurement of
platelet inhibition predicted 1-year clinical outcomes after off-pump coronary bypass
(OPCAB) Study design
- Prospective, observational, single-center study
- Subjects with OPCAB surgery who meet all inclusion and exclusion criteria will be
enrolled.
- Platelet reactivity after 7-days clopidogrel treatment from the day of surgery will be
measured by VerifyNow system.
- Dual antiplatelet therapy including aspirin and clopidogrel will be administered for 1
year after surgery and subjects will be followed-up for 1 year about primary endpoint.
- Cutoff value of P2Y12 reactivity units (PRUs) for primary endpoint will be assessed and
the cohort will be divided by the PRU cutoff value (low/high platelet reactivity
groups).
- The primary and secondary endpoints will be compared between two groups
| Status | Completed |
| Enrollment | 859 |
| Est. completion date | July 2013 |
| Est. primary completion date | June 2013 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 19 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - Patients with indications for surgical myocardial revascularization - Patients who undergo off-pump coronary artery bypass - Age between 19~80 years - Patients with signed informed consent Exclusion Criteria: - Patients with combined surgery with coronary bypass grafting - On-pump conversion - Patients with moderate renal dysfunction (creatinine>2.0mg/dl) or need for dialysis - Patients with chronic treatment with proton pump inhibitors - Patients with preoperative bleeding - Thrombocytopenia (Platelet count 70,000/ml) - Re-do surgery - Early death before the measurement of platelet reactivity |
Observational Model: Case Control, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Korea, Republic of | Division of Cardiovascular Surgery, Severance Cardiovascular Hospital , Yonsei University College of Medicine | Seoul |
| Lead Sponsor | Collaborator |
|---|---|
| Yonsei University |
Korea, Republic of,
Patti G, Nusca A, Mangiacapra F, Gatto L, D'Ambrosio A, Di Sciascio G. Point-of-care measurement of clopidogrel responsiveness predicts clinical outcome in patients undergoing percutaneous coronary intervention results of the ARMYDA-PRO (Antiplatelet therapy for Reduction of MYocardial Damage during Angioplasty-Platelet Reactivity Predicts Outcome) study. J Am Coll Cardiol. 2008 Sep 30;52(14):1128-33. doi: 10.1016/j.jacc.2008.06.038. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Major adverse cardiovascular events (MACEs) | The primary endpoint of the study was the 1-year incidence of MACEs, which included the following: (1) cardiac death, defined as death in the presence of acute coronary syndrome, sudden cardiac arrest with documented cardiac arrhythmia, or refractory congestive heart failure; 2) nonfatal MI; and (3) target vessel revascularization in relation to platelet reactivity as measured by the VerifyNow system. | 1 year after off-pump coronary bypass surgery | No |
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