stable angina pectoris
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)patients whose glucose fluctuation was assessed by continuous glucose monitoring before percutaneous coronary intervention (PCI) 2)patients treated with everolimus-eluting stent at PCI 3)LDL-chol < 100mg/dl in patients without statin. LDL-chol < 120mg/dl in patients with statin. 4)patients between 20 and 80 years old 5)written consent for participation in the study
Exclusion criteria
Exclusion criteria: Patients meeting one of the following conditions will be excluded: 1) treated with other kind of stent 2) unsuitable anatomy for OCT analysis in stented segment 3) severe renal dysfunction 4) any change of medical interventions for the control of diabetes, lipids, and hypertension during this study 5) judged as ineligible by clinical investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Association between glucose variability and neointimal proliferation nine (six to twelve) months after stenting assessed continuous glucose monitoring (CGM) and coronary imaging device (optical coherence tomography; OCT) | — |
Secondary
| Measure | Time frame |
|---|---|
| Major cardiovascular adverse events (target lesion revascularization, myocardial infarction and cardiac death) at nine (six to twelve) months after percutaneous coronary intervention. | — |
Countries
Japan
Contacts
Kobe University Graduate School of Medicine Division of Cardiovascular Medicine