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 个研究点目标入组 1,167 人开始时间: 待定最近更新: 2023年1月10日

试验速览

暂无简介。

•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).

发起方

BUCHEON SEJONG HOSPITA