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

NCT ID: NCT04200469

Last Updated: 2021-09-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-01

Study Completion Date

2022-01-31

Brief Summary

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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.

Detailed Description

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Conditions

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Coronary Occlusion

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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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.

Group Type EXPERIMENTAL

Quantitative Flow Ratio (QFR) measurement

Intervention Type DIAGNOSTIC_TEST

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.

Interventions

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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.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospital Clínico Universitario de Valladolid

OTHER

Sponsor Role lead

Responsible Party

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Carlos Baladron, PhD

Research Coordinator, Cardiology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Complejo Hospitalario Universitario, Santiago de Compostela

Santiago de Compostela, La Coruña, Spain

Site Status RECRUITING

Hospital de Lugo

Lugo, , Spain

Site Status RECRUITING

Hospital Clínico San Carlos

Madrid, , Spain

Site Status RECRUITING

Hospital Clínico Universitario Virgen de la Arrixaca

Murcia, , Spain

Site Status RECRUITING

Hospital Clínico Universitario de Valladolid

Valladolid, , Spain

Site Status RECRUITING

Countries

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Spain

Central Contacts

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Carlos Baladron, PhD

Role: CONTACT

+34983420000

Facility Contacts

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José R Rumoroso, MD

Role: primary

Raymundo Ocaranza-Sanchez, PhD, MD

Role: primary

Javier Escaned, PhD, MD

Role: primary

Eduardo Pinar, PhD

Role: primary

Carlos Baladron, Dr.

Role: primary

983420000

References

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Other Identifiers

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CASVE-PI-19-1515

Identifier Type: -

Identifier Source: org_study_id

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