The patients on DAPT after PCI who underwent follow-up coronary angiography
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1:The patients on DAPT after PCI who underwent follow-up coronary angiography 2:Patients agreening with this study after informed consent
Exclusion criteria
Exclusion criteria: 1:Ptients who has high risk for bleeding 2:Patients with heart Valve Disease and congenital heart disease 3:Patients with cerebrovascular disease 4:Patients who have infection or Inflammatory disease 5:Patients with malignant neoplasm 6:CKD <G4 eGFR<30(ml/min/1.7m2) 7:Patients with allergy against thienopyridines 8:Patients undergoing anticoagulation therapy 9:Patients who are not suitable for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of change on PRU from baseline to observation point(6M+-3M) between Clopidgrel with Aspirin and Prasugrel with Aspirin | — |
Secondary
| Measure | Time frame |
|---|---|
| 1:The effect of CYP2C19 polymorphism against the PRU from baseline to observation point between Clopidgrel with Aspirin and Prasugrel with Aspirin 2:Quantitative change on FMD from baseline to observation point between Clopidgrel with Aspirin and Prasugrel with Aspirin 3:Quantitative change on RHI from baseline to observation point between Clopidgrel with Aspirin and Prasugrel with Aspirin 4:Quantitative change and rate of change on Inflammatory biomarkers from baseline to observation point between Clopidgrel with Aspirin and Prasugrel with Aspirin 5:Quantitative change on CD34+/CD133+/CD45low cells from baseline to observation point between Clopidgrel with Aspirin and Prasugrel with Aspirin | — |
Countries
Japan
Contacts
Dokkyo Medical University Cardiovascular Medicine