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Combination Effects of High-dose Statin and Trimetazidine on Patients With Aspirin Mono Antiplatelet Therapy 12-months After Coronary Artery Bypass Surgery

Registration Number
NCT01857921
Lead Sponsor
Yonsei University
Brief Summary

Trimetazidine is a metabolic agent without any negative inotropic or vasodilatory properties. In addition, previous reports showed that trimetazidine was effective in reducing intracoronary platelet aggregation and preventing platelet thrombogenesis. Therefore, for the evaluation of these combination effects of statin and trimetazidine on patients with aspirin monotherapy who had previously received CABG and were free of the major adverse cardiac events such as death, MI, TLR, or TVR for 12 months, the investigators hypothesize that atorvastatin 40mg/day would be more effective in the prevention of the further late adverse cardiac and cerebrovascular events than other statin. To test this hypothesis, the investigators will perform a multi-center, randomized, prospective trial aimed at demonstrating the superiority of combination of high dose atorvastatin therapy and trimetazidine to pravastatin in patients with aspirin monotherapy 12 months after CABG surgery in real world practice.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
290
Inclusion Criteria
  • Patients who had previously received CABG 12 months ago
  • Patients who were free of death, MI or repeat revascularization within first 12 months after CABG
  • Patients with mono antiplatelet therapy with aspirin alone
  • Age of 20 years or older
  • Patients with signed informed consent
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Exclusion Criteria
  • History of DES or BMS implantation within 12 months
  • Patients who required the continuing dual antiplatelet therapy or additional other types of antithrombotics or antiplatelets such as cilostazol or ticlopidine, etc besides aspirin after DES implantation
  • Patients who could not be prescribed aspirin or statins due to contraindication or severe side effects
  • Pregnant women or women with potential childbearing
  • Life expectancy ≤ 2 year
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Pravastatin groupPravastatin 20mg/day for 12 months after randomization-
Combination of Atorvastatin and trimetazidine groupAtorvastatin 40 mg and trimetazidine MR 70 mg/day for 12 months after randomization-
Primary Outcome Measures
NameTimeMethod
Occurrence of the composite of death from any cause12 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Severance Hospital

🇰🇷

Seoul, Korea, Republic of

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