QIMERA-I: Validation Of Quantitative Flow Ratio (QFR) - Derived Virtual Angioplasty

Sponsor
Hospital Clínico Universitario de Valladolid (Other)
Overall Status
Recruiting
CT.gov ID
NCT04200469
Collaborator
(none)
100
5
1
25
20
0.8

Study Details

Study Description

Brief Summary

Prospective intervention study to assess the accuracy of the predicted QFR-derived virtual angioplasty compared to hyperaemic and non-hyperaemic pressure-wire derived indexes after PCI, as well as with QFR post-PCI.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Quantitative Flow Ratio (QFR) measurement
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Validation Of Quantitative Flow Ratio (QFR) - Derived Virtual Angioplasty
Actual Study Start Date :
Jan 1, 2020
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Jan 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: QFR Intervention

Patients submitted to a coronary angiogram with at least one non-left main stable coronary stenosis between 50 and 90% and PCI indication with paired assessment of QFR, dFR, RFR and FFR, before and after PCI once informed consent is provided.

Diagnostic Test: Quantitative Flow Ratio (QFR) measurement
Quantitative flow ratio (QFR) is a novel approach enabling rapid computation of FFR pullbacks from three-dimensional quantitative coronary angiography (3D-QCA) without using a pressure wire.

Outcome Measures

Primary Outcome Measures

  1. Numerical agreement between predicted post PCI QFR (residual QFR) and post PCI dPR RFR-FFR, as well as direct QFR post-PCI mesurement. [1 hour]

Secondary Outcome Measures

  1. Sensitivity [1 hour]

  2. Specificity [1 hour]

  3. Summary of the receiver-operator characteristics curve (sROC) [1 hour]

  4. Negative predictive value [1 hour]

  5. Positive predictive value [1 hour]

  6. Positive likelihood ratio [1 hour]

  7. Negative likelihood ratio [1 hour]

  8. Identification of independent predictors for increased predicted postPCI QFR (residual QFR) and post PCI dPR-RFR-FFR. [1 hour]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients submitted to a coronary angiogram with at least one non-left main stable coronary stenosis with PCI indication.
Exclusion Criteria:
  • Severe stenosis of the left main coronary artery.

  • Patients admitted with ST-elevation myocardial infarction.

  • Culprit lesions in Non-ST-Elevation Acute Coronary Syndromes (NSTEACS) patients.

  • Unability to identify the culprit lesion in NSTE-ACS patients.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Complejo Hospitalario Universitario, Santiago de Compostela Santiago De Compostela La Coruña Spain
2 Hospital de Lugo Lugo Spain
3 Hospital Clínico San Carlos Madrid Spain
4 Hospital Clínico Universitario Virgen de la Arrixaca Murcia Spain
5 Hospital Clínico Universitario de Valladolid Valladolid Spain 47003

Sponsors and Collaborators

  • Hospital Clínico Universitario de Valladolid

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Carlos Baladron, PhD, Research Coordinator, Cardiology, Hospital Clínico Universitario de Valladolid
ClinicalTrials.gov Identifier:
NCT04200469
Other Study ID Numbers:
  • CASVE-PI-19-1515
First Posted:
Dec 16, 2019
Last Update Posted:
Sep 24, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Carlos Baladron, PhD, Research Coordinator, Cardiology, Hospital Clínico Universitario de Valladolid
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 24, 2021