The Heartflow Coronary Disease Progression Evaluation Study
NCT ID: NCT04052256
Last Updated: 2022-07-27
Study Results
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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UNKNOWN
250 participants
OBSERVATIONAL
2018-10-05
2023-10-01
Brief Summary
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FFRCT can also effectively guide revascularization safely deferring patient with FFRCT \>0.80 from invasive angiography. In functionally non-significant lesions, computational fluid dynamic models in addition to CT plaque characteristics (low attenuation, positive remodelling, spotty calcification and napkin-ring sign) may be able to predict which lesions will become flow-limiting, causing clinical events in the future.
This study will evaluate disease progression in intermediate lesions (invasive FFR 0.81-0.90 at baseline) using FFRCT at 2 years and determine whether CT characteristics may help to identify lesions that are more susceptible for FFR decline. Additionally, we will correlate CT characteristics with coronary events (a composite endpoint consisting of all-cause mortality, target-vessel myocardial infarction and clinically driven target-vessel revascularization) up to 5 years after the baseline invasive FFR.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with intermediate coronary lesions
Patients (age ≥ 18 years) who have undergone invasive coronary angiography and have a minimum of one non-treated coronary artery with a measured invasive FFR of 0.81-0.90.
Coronary computed tomography angiography
Computational fluid dynamic model information derived from CT
Interventions
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Coronary computed tomography angiography
Computational fluid dynamic model information derived from CT
Eligibility Criteria
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Inclusion Criteria
2. Minimum of one non-treated coronary artery with an intermediate lesion and invasive FFR 0.81-0.90 to serve as the target vessel for FFRCT.
Exclusion Criteria
2. Previous CABG.
3. Target vessel for FFR measurement \< 2.0 mm in diameter.
4. Contraindications to contrast agents, beta-blocking agents, nitroglycerin or adenosine.
5. Life expectancy less than 3 years.
6. Creatinine clearance \< 30 ml/min\*1.73m2.
18 Years
ALL
No
Sponsors
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Erasmus Medical Center
OTHER
Responsible Party
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Nicolas van Mieghem
Director of Interventional Cardiology
Principal Investigators
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Jonathan A Leipsic, MD, PhD
Role: STUDY_CHAIR
University of British Columbia
Locations
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Erasmus MC
Rotterdam, , Netherlands
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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THRONE1
Identifier Type: -
Identifier Source: org_study_id
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