KCT0007441
Recruiting
未知
ProspeCtive evaluatiOn of long-terM clinical outcomes after resting Full-cycle ratiO (RFR)-guided percutaneous coronary RevascularizaTion; A multi-center, international, Single arm interventional, Comparing study (COMFORT study)
BUCHEON SEJONG HOSPITA0 sites1,167 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- BUCHEON SEJONG HOSPITA
- Enrollment
- 1167
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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).
Outcomes
Primary Outcomes
Not specified
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