None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients of acute coronary syndrome (unstable angina or myocardial infarction) who are over 19 years of age Patients participating voluntarily in the study and who have signed the consent form Patients who have undergone an interventional procedure using Centum stents in the last one month
Exclusion criteria
Exclusion criteria: Subjects with restrictions or hypersensitivity to the following drugs or materials: contrast agent, heparin, aspirin, clopidogrel, everolimus, etc. (Subjects with hypersensitivity to contrast agents may enroll in the study if such reaction can be controlled with steroid or pheniramine. Subjects with a history of anaphylaxis should be excluded.) Subjects who are breast-feeding, pregnant or hoping to become pregnant Subjects with life expectancy of less than 1 year Subjects determined unfit by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Target vessek failure | — |
Secondary
| Measure | Time frame |
|---|---|
| Major adverse cardiac events | — |
Countries
Korea, Republic of
Contacts
Wonkwang University Hospital