Actively Recruiting

Age: 18Years +
All Genders
NCT06261866

Multimodality Imaging and Functional Lesion Assessment in Intermediate Coronary Stenosis in Chronic Coronary Syndrome

Led by Medical University of Warsaw · Updated on 2024-02-15

200

Participants Needed

1

Research Sites

925 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Multimodality Imaging and Functional Lesion Assessment in Intermediate Coronary Stenosis in Chronic Coronary Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Chronic coronary syndrome defined as chest pain ranked 2-3 in the Canadian Cardiovascular Society classification or positive ischemia test (exercise test, SPECT)
  • Intermediate grade coronary stenosis of 40-80% assessed visually in coronary angiography
  • FFR and OCT examination of the same lesion
  • Willing to participate and provided written informed consent
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University of Warsaw

Warsaw, Poland

Actively Recruiting

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Research Team

M

Mariusz Tomaniak

CONTACT

P

Piotr Baruś

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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