About this trial

The aim of this prospective, investigator-initiated study is to evaluate the diagnostic accuracy and correlations between mopphometric indices: luminal and qualitative parameters assessed by optical coherence tomography (OCT) including minimal lumen area, plaque type, presence of thin cap fibroatheroma and a functional index - angiography based vessel fractional flow reserve (vFFR) among patients with chronic coronary syndrome identified with intermediate grade coronary stenosis.

Eligibility criteria

Qualifiers

18 years or older

Chronic coronary syndrome defined as presence of chest pain ranked 2-3 in the Canadian Cardiovascular Society classification or positive ischemia test (exercise test, single photon emission tomography (SPECT)

Intermediate grade coronary stenosis of 40-80% assessed visually in coronary angiography and OCT examination The patient is willing to participate in the study and has provided a written informed consent

Disqualifiers

Acute coronary syndrome

Proximal left main lesion

Ostial right coronary artery lesion

Bypass of the assessed vessel

Trial design

Treatments tested in this trial

  • vessel Fractional Flow Reserve

Treatment groups

200 Participants
are divided into 1 treatment group

Locations

1
1st Department and Clinic of Cardiology, Medical University of Warsaw02-097, WarsawMazowieckie Voivodenship, Poland

Sponsors and collaborators

Medical University of Warsaw

Lead sponsor