None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Patient diagnosed with acute coronary syndrome at the age of 19 or older, performing coronary angioplasty with BioMimeTM stent (2) Patients who voluntarily decide to participate in this research and agree to the consent form (3) De novo target lesion
Exclusion criteria
Exclusion criteria: (1) Patients with a taboo or hypersensitivity to anti-diagetic treatment (2) If the life expectancy is less than two years (3) Women who are feeding, pregnant, or hoping to conceive
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of failure of target lesions (combination of cardiac death, target vascular myocardial infarction, and ischemia - induced target lesion reconstruction) | — |
Secondary
| Measure | Time frame |
|---|---|
| Major cardiac event(death,myocardial infartion,Complex variables in target lesion reconstruction);The incidence of death (cardiac or non-cardiac);Rate of myocardial infarctin(target or non-representative vessels);Rate of target lesion reconstruction (ischemia or non-ischemia);Incidence of target vessel reconstruction;Stroke (ischemia or hemorrhagic) incidence;The incidence of acute stent thrombosis, subacute stent thrombosis, and stent thrombosis after one year. | — |
Countries
Korea, Republic of
Contacts
Chonnam National University Hospital