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Trials / Recruiting

RecruitingNCT06659367

Dedinje FFR/QFR Registry

Institute for Cardiovascular Diseases "Dedinje" Fractional Flow Reserve (FFR) and Quantitative Flow Ratio (QFR) Registry

Status
Recruiting
Phase
Study type
Observational
Enrollment
2,500 (estimated)
Sponsor
Institute for Cardiovascular Diseases Dedinje · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Quantitative Flow Ratio (QFR) has shown good diagnostic performance against Fractional Flow Reserve (FFR) in several meta-analyses, comparable or even superior to nonhyperemic pressure ratios. However, the reproducibility of QFR is modest and there is high inter- and intra-observer variability even when fairly experienced but non-core lab operators (at least 150 QFR procedure experience) are performing the analysis. Although smaller studies have demonstrated that non-core analysis and even paramedical user analysis can have good correlation with FFR, the concern about the diagnostic performance of QFR in real-world clinical practice by inexperienced users remains. The primary objective of "Dedinje FFR/QFR Registry" is to determine the feasibility and diagnostic performance of QFR analysis by vendor-certified inexperienced medical users in a real-world setting using FFR as the gold standard. All patients \>18 years old who present to the Institute for Cardiovascular Diseases "Dedinje" and undergo a planned or ad hoc FFR procedure will be asked to participate in the registry. FFR procedure is performed according to the standardized institutional protocol. QFR analysis will be subsequently performed offline according to a standard operating procedure.

Conditions

Timeline

Start date
2024-10-02
Primary completion
2029-10-02
Completion
2034-10-02
First posted
2024-10-26
Last updated
2024-10-26

Locations

1 site across 1 country: Serbia

Source: ClinicalTrials.gov record NCT06659367. Inclusion in this directory is not an endorsement.