Ischemic heart disease
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients those who have obtained the informed consent of the research subject
Exclusion criteria
Exclusion criteria: Patients with contraindications to antithrombotic therapy, Pregnant women, lactating women, women who may be pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Major adverse cardiac or cerebrovascuar events: all cause death, non-fatal myocardial infarct, stent thrombosis, revascularization, stroke | — |
Secondary
| Measure | Time frame |
|---|---|
| Major and minor bleeding event | — |
Countries
Japan
Contacts
Nihon University School of Medicine Division of Cardiology, Department of Internal Medicine