Actively Recruiting
CMR Versus CT in Coronary Artery Disease
Led by University of Leicester · Updated on 2025-07-01
300
Participants Needed
1
Research Sites
264 weeks
Total Duration
On this page
Sponsors
U
University of Leicester
Lead Sponsor
H
HeartFlow, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
CONCORD is a prospective observational study evaluating the diagnostic accuracy of cardiovascular magnetic resonance (CMR) and computed tomography with fractional flow reserve (CT-FFR) in patients with suspected coronary artery disease, using invasive fractional flow reserve (FFR) as the reference standard.
CONDITIONS
Official Title
CMR Versus CT in Coronary Artery Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 6518 years
- Referred for invasive coronary angiography for investigation of chest pain
You will not qualify if you...
- Recent acute coronary syndrome (less than 6 months)
- Previous coronary artery bypass grafting
- Severe claustrophobia
- Absolute contraindications to CMR (patients with MR conditional or safe devices will be included)
- Second- or third-degree atrioventricular block
- Severe chronic obstructive pulmonary disease
- Moderate to severe asthma
- Estimated glomerular filtration rate less than 30 ml/min/1.73m2
- Women who are pregnant, breast-feeding, or of child-bearing potential (premenopausal women)
- Contraindication to iodinated contrast
- Participation in another research study involving an investigational product within the past 12 weeks
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Glenfield Hospital
Leicester, Leics, United Kingdom, LE3 (QP
Actively Recruiting
Research Team
J
Jayanth Arnold
CONTACT
M
Mo Elshibly
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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