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Clinical Trials/KCT0007441
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
BUCHEON SEJONG HOSPITA

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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