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Clinical Trials/NCT06844942
NCT06844942RecruitingNot Applicable

Vessel Imaging Using Optical Coherence Tomography for Plaque Morphology and Vessel Fractional Flow Reserve

Medical University of Warsaw1 site in 1 country200 target enrollmentStarted: September 20, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Correlation between vessel fractional flow reserve (FFR) and minimal lumen area within the coronary stenosis

Study Overview

Brief Summary

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.

Detailed Description

This is a prospective, single center, non-randomized, single-arm, investigator-initiated study evaluating diagnostic accuracy and correlations between morphometric indices: luminal and qualitative parameters evaluated by optical coherence tomography (OCT) including minimal lumen area, plaque stratification into fibrotic, calcific, lipidic plaque, or 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.

The additional objectives encompass assessing the influence of age, sex, diabetes mellitus, renal dysfunction on the relationship between vFFR results and morphometric indices of intermediate coronary stenosis.

We hypothesized that in patients with intermediate grade coronary stenosis in chronic coronary syndrome a positive correlation exists between vFFR and the morphometric parameters associated with coronary stenosis.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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

Exclusion Criteria

  • •Acute coronary syndrome
  • •Proximal left main lesion
  • •Ostial right coronary artery lesion
  • •Bypass of the assessed vessel
  • •Contraindications for adenosine administration
  • •Hemodynamic instability
  • •Heart insufficiency in New York Heart Association (NYHA) class IV scale
  • •Acute renal insufficiency
  • •Pregnancy

Outcomes

Primary Outcomes

Correlation between vessel fractional flow reserve (FFR) and minimal lumen area within the coronary stenosis

Time Frame: 0 days

Correlation between vessel fractional flow reserve (FFR) and minimal lumen area within the coronary stenosis

Secondary Outcomes

  • Major adverse cardiovascular events(36 months)

Investigators

Sponsor
Medical University of Warsaw
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mariusz Tomaniak

Mariusz Tomaniak, MD, PhD, Assoc. Prof.

Medical University of Warsaw

Study Sites (1)

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