None listed
Conditions
Interventions
Medical Device : The appropriate diameter and length of the stent are selected based on the IVUS measurement for IVUS guidance group and visual inspection for the angiography guidance group.
Angiograp
Sponsors
Gachon University Gil Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: ? Qualified for the DES implantation ? Above the age of 19 ? Signed the consent form for participation in this research study voluntarily and agreed on the procedures to be followed during the clinical trial.
Exclusion criteria
Exclusion criteria: ? Implanted other DES product on the target lesion area ? Restricted from coronary angiography (ex. severe symptoms of heart failure.) ? Allergic reaction or intolerance to dual antiplatelet therapy (DAPT) ? Expected lifespan of less than one year with concurrent disorder/s. ? Pregnancy and lactation (or plan to give birth in near future)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Major Adverse Cardiac Events : Cardiac Death, Myocardial Infarction, Stent Thrombosis, Target lesion revascularization | — |
Secondary
| Measure | Time frame |
|---|---|
| in stent late loss;in segment late loss;TVR(target vessel revasculirization) | — |
Countries
Korea, Republic of
Contacts
Public ContactAHN HOON
Gachon University Gil Medical Center
Outcome results
None listed