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NCT04761991Recruiting

CMR Versus CT in Coronary Artery Disease

Comparison of Cardiovascular Magnetic Resonance and Computed Tomography With Fractional Flow Reserve in the Diagnosis of Suspected Coronary Artery Disease

Source: ClinicalTrials.gov · Last updated 1 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
17 Dec 2020
Start date
5 Nov 2020
Primary completion date
30 Nov 2025
Lead sponsor
University of Leicester
NCT number
NCT04761991

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 5 Nov 2020 to the primary completion date, 30 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous coronary artery bypass grafting
  • Participation in a research study involving an investigational product in the past 12 weeks

Other illness

  • Recent acute coronary syndrome (\< 6 months)
  • Severe chronic obstructive pulmonary disease

Other

  • Severe claustrophobia
  • Absolute contraindications to CMR - those with MR conditional or safe devices will be included
  • Second-/third-degree atrioventricular block
  • Moderate-severe asthma
  • Estimated glomerular filtration rate \<30 ml/min/1.73m2
  • Women who are pregnant, breast-feeding or of child-bearing potential( premenopausal women)
  • Contraindication to iodinated contrast

Who the study is looking for

  • Patients aged ≥18 years
  • Referred for invasive coronary angiography for investigation of chest pain

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Glenfield Hospital
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LeicesterUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.