None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) over 19 year 2) Acute coronary syndrome-Percutaneous Coronary Intervention patients treated with prasugrel according to the labeled indication 3) Patients who initiate or switch to prasugrel within 6 months after Percutaneous Coronary Intervention 4) Patients who gie voluntary written informed consent to participate in the study
Exclusion criteria
Exclusion criteria: 1) Patients who are not simultaneously participating in interventional study administering of antiplatelet agents except prasugrel/antithrombotic agents
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Net clinical events: Death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, non-CABG related TIMI major bleeding | — |
Secondary
| Measure | Time frame |
|---|---|
| Individual incidence: Death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, non-CABG related TIMI major bleeding | — |
Countries
Korea, Republic of
Contacts
Seoul National University Hospital