ong-term clinical outcomes after resting full-cycle ratio (RFR)-guided PCI
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0007441
- Lead Sponsor
- BUCHEON SEJONG HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1167
Age > 19 years of age
Patients with intermediate coronary artery stenosis (visually 50-90% diameter stenosis) who decided to undergoing a RFR guided coronary intervention according to clinical necessity
Patients who voluntarily decided to participate in this study and signed informed consent
1) Severe LV systolic dysfunction (LVEF <30%)
2) Cardiogenic shock
3) Culprit vessel in acute coronary syndrome
4) Donor vessel to supply chronic total occlusion lesion of non-target vessel
5) Symptomatic valvular heart disease or cardiomyopathy
6) Hemodynamic instability at the time of intervention (heart rate <50 beats per minute, systolic blood pressure <90mmHg)
7) Previous CABG with patent grafts to the interrogated vessel
8) Pregnancy or breastfeeding
9) Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment).
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A composite of death from any cause, non-fatal myocardial infarction, or unplanned revascularization
- Secondary Outcome Measures
Name Time Method Target lesion failure: cardiac death, target vessel MI, or target lesion revascularization;Target vessel failure: cardiac death, target vessel MI, or target vessel revascularization;Death from any cause ;Cardiovascular death;Cardiac death or non-fatal MI;Non-fatal MI ;Any unplanned revascularization;Target vessel revascularization ;Target lesion revascularization