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NCT04102917

Diagnostic Performance and Prognostic Ability of the QFR

Completed Last updated 25 September 2019
What this trial tests

trial testing QFR assessment in Ischemic Heart Disease in 915 participants. Completed in 14 June 2019.

Timeline
1 January 2012
Primary endpoint
31 May 2018
14 June 2019

Quick facts

Lead sponsorSeoul St. Mary's Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment915
Start date1 January 2012
Primary completion31 May 2018
Estimated completion14 June 2019
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Seoul St. Mary's Hospital

Who can join

18 and older, any sex, with Ischemic Heart Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

1. The primary technical endpoint was the diagnostic performance of the QFR against the FFR. 2. The primary clinical endpoint was target vessel failure (TVF) between two groups distributed by a QFR cut-off value of 0.8

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Influence of lesion and disease subsets on the diagnostic performance of the quantitative flow ratio in real-world patients.
    Lee KY, Hwang BH, Kim MJ, Choo EH, et al · · 2021 · cited 17× · PMID 33542310 · DOI 10.1038/s41598-021-82235-y

Verify or expand the search:

Other trials of QFR assessment

Trials testing the same drug.

Other recruiting trials for Ischemic Heart Disease

Currently open trials in the same condition.

Other Seoul St. Mary's Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04102917.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing