None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age =19 years 2) ST-segment elevation myocardial infarction (STEMI) - ST-segment elevation = 0.1 mV in at least two contiguous leads or - New-onset left bundle branch block (LBBB) 3) Primary PCI within 12 h after symptom development 4) At least 1 non-infarct related artery (non-IRA) with diameter = 2.5 mm and 50% stenosis by visual estimation
Exclusion criteria
Exclusion criteria: 1) Cardiogenic shock at initial presentation or after infarct-related artery (IRA) treatment 2) Thrombolysis in myocardial infarction flow at non-IRA = 2 3) Severe procedural complications during primary percutaneous coronary intervention that, in the judgement of the operator, preclude study enrollment 4) Non-IRA lesion unsuitable for percutaneous coronary intervention (PCI) treatment that, in the judgement of the operator, preclude study enrollment 5) Chronic total occlusion in a non-IRA 6) History of anaphylaxis to contrast agent 7) Pregnancy and lactation 8) Life expectancy 2.0 mmol/L.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Composite of all-cause death, nonfatal myocardial infarction, or all unplanned revascularization | — |
Secondary
| Measure | Time frame |
|---|---|
| Composite of all-cause death, nonfatal myocardial infarction, or all unplanned revascularization;All-cause death;Nonfatal myocardial infarction;All unplanned revascularization;Cardiac death;Non-cardiac death;Nonfatal spontaneous myocardial infarction;Nonfatal procedure-related myocardial infarction;Target-lesion revascularization;Target-vessel revascularization;Non-target vessel revascularization;Hospitalization for unstable angina;Hospitalization for heart failure;Stent thrombosis;Stroke;Major bleeding;Contrast-induced nephropathy | — |
Countries
Korea, Republic of
Contacts
Chonnam National University Hospital