Effect of high-intensity Statin with ezetimibe COmbination theRapy versus high-intensity sTatin monotherapy after percutaneous coronary intervention with drug-eluting stents; the ESCORT trial
Not Applicable
- Conditions
- Diseases of the circulatory system
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 4310
Inclusion Criteria
1. Age 19-85 years
2. Patients who underwent coronary revascularization with newer generation DES implantation
Exclusion Criteria
1. Allergy or hypersensitive to ezetimibe or statin
2. Active liver disease or persistent unexplained serum AST/ALT elevation more than 2 times the upper limit of normal range
3. History of any adverse drug reaction requiring discontinuation of statin
4. Pregnant women, women with potential childbearing, or lactating women
5. Life expectancy less than 3 years
6. Inability to follow the patient over the period of 1 year after enrollment, as assessed by the investigator
7. Inability to understand or read the informed content
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Composite of all-cause death, myocardial infarction (MI), any coronary revascularization, hospitalization for unstable angina, or nonfatal stroke
- Secondary Outcome Measures
Name Time Method