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Study identifier: NCT06255678 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Angio-based Final Functional Effect of PCI

Condition: Acute Coronary Syndrome · Non ST Segment Elevation Acute Coronary Syndrome · Chronic Coronary Syndrome  ·  Sponsor: Medical University of Warsaw

PhaseN/A
Planned participants2005
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Fractional flow reserve (FFR) has revolutionized the diagnosis and treatment of coronary artery disease (CAD), and more recently, post percutaneous coronary intervention (post-PCI) FFR has emerged as an independent predictor of cardiovascular events, enabling the identification of cases requiring additional optimization of the implanted stent. Modern technologies allow less invasive alternatives to traditional FFR measurement - angiography-based vessel fractional flow reserve (vFFR) and derivative ΔvFFR, which is calculated by a difference between the post-PCI vFFR and pre-PCI vFFR. In large clinical studies, the good accuracy between vFFR and FFR - measured before and after PCI - has been confirmed. However, insufficient data is available about the value of post-vFFR and ΔvFFR as prognostic values and indicators of patient health. This is a prospective multicenter register study analyzing the association between the value of ΔvFFR, vFFR after PCI and adverse clinical outcomes, residual angina and quality of life using the validated Seattle Angina Questionnaire (SAQ) and EuroQol 5-level 5-dimensional questionnaire (EQ-5D-5L). Patients undergoing PCI for chronic coronary syndromes (CCS), non-ST-segment elevation acute coronary syndromes (NST-ACS) or ST-Segment Elevation Myocardial Infarction (STEMI) will be enrolled in this study.

This description comes directly from the study's public registry record.

Talk to the study team

Mariusz Tomaniak, MD PhD  ·  +48 22 5991951  ·  mariusz.tomaniak@wum.edu.pl

Karol Sadowski  ·  karol.sadowski@wum.edu.pl

Always discuss trial participation with your own doctor first.

Locations (1)

Medical University of WarsawWarsaw, PolandRecruiting

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Source record: clinicaltrials.gov/study/NCT06255678