Aspirin Mono Therapy 12-months After Drug-eluting Stents Implantation
- Conditions
- Drug-eluting Stent (DES)
- Interventions
- Registration Number
- NCT01557075
- Lead Sponsor
- Yonsei University
- Brief Summary
The purpose of this study is to determine whether high dose statin therapy in patients with aspirin mono antiplatelet therapy who had received drug-eluting stent (DES) previously and were free of the adverse cardiac events during the first 12 months could be superior over pravastatin therapy in the prevention of late adverse cardiac and cerebrovascular events during the additional 12 months.
Study Design.
- Detailed Description
Objective: To determine whether high dose statin therapy in patients with aspirin mono antiplatelet therapy who had received drug-eluting stent (DES) previously and were free of the adverse cardiac events during the first 12 months could be superior over pravastatin therapy in the prevention of late adverse cardiac and cerebrovascular events during the additional 12 months.
Study Design
* Prospective, randomized, multi-center study of each 1000 subjects enrolled.
* Eligible subjects will be randomized 1:1 to a) atorvastatin 40 mg (n=1000) vs. b) pravastatin 20 mg/day (n=1000). All subjects will be followed for 1 year after randomization. Additional long-term follow-up (2- or 3-year) will be preceded in the next plan after 1-year study period.
* Subjects with coronary artery diseases who meet all inclusion and exclusion criteria will be included Clinical and laboratory follow-up should be performed.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 2000
- Patients who had previously received DES at least 12 months(±2month) ago
- Patients who were free of death, MI, stroke, repeat revascularization, or ST within first 12 months after DES implantation
- Patients with mono antiplatelet therapy with only aspirin after
- Age 20 years of older
- Patients with signed informed consent
- History of DES or BMS implantation within 10 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Atorvastatin group Atorvastatin (High dose statin treatment) Atorvastatin 40 mg daily for 12 months after randomization Pravastatin group Pravastatin (High dose statin treatment) Pravastatin 20mg daily for 12 months after randomization
- Primary Outcome Measures
Name Time Method the composite of death from any cause 12 months after randomization Occurrence of the composite of death from any cause, MI, target vessel revascularization (TVR, either by PCI or CABG), non-TVR, stent thrombosis (ST), peripheral artery intervention, deterioration of renal function, stroke or admission for significant clinical cardiac events for 12 months following the randomization to the assigned statin therapy.
- Secondary Outcome Measures
Name Time Method cardiac or non-cardiac death 12month 1. Major determinant for the occurrence of major events(death,MI,TVR,ST)
2. Comparisons of the occurrence of major events according to the attainment of recommended LDL-C goal on current lipid guideline
3. Association between laboratory test and clinical outcomes;
4. Sub-study according to the subsets of disease
5. Association between parameters at index procedure and clinical outcomes
Trial Locations
- Locations (1)
Hong Myeong-Ki
🇰🇷Seoul, Korea, Republic of