Validation of Multi-contrast, High-resolution Cardiac Magnetic Resonance Imaging

Recruiting now · Not applicable

Conditions studied: Cardiac Disease

In brief

Cardiovascular disease (CVD) causes at least 1.8 million European deaths annually, exceeding fatalities from cancer, chronic respiratory disease, and diabetes. Consequently, the fight against CVD has become the main priority of the World Health Organization. In the pursuit of understanding and treating CVD, cardiac magnetic resonance imaging (CMR) has remained the only modality capable of providing a comprehensive assessment of the heart's function and structure without harmful radiation. Unfortunately, current CMR systems remain too slow, too complex, require highly trained specialists and, as such, have presented a barrier to a wider adoption of CMR. The aim of CARDIO-IRM is to unleash the full potential of CMR to transform patient trajectories by introducing a fast, one-click, fully automated, and comprehensive imaging pipeline applicable to diagnosis, prognosis, and therapy selection in cardiology.

Key facts

Study ID

NCT05877755

Run by

University Hospital, Bordeaux

People needed

200

Starts

2025-04-15

Expected to finish

2030-03-31

Last updated by the study team

2025-04-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Adult patient (over 18 years of age) requiring an MRI scan as part of their care.
• Male or female.
• Affiliated or beneficiary of a social security scheme
• Having given his/her oral no objection after having read the information note

You may not qualify if…

• Patient unable to give oral consent (guardianship, non-French speaker, etc.)
• Patient deprived of liberty
• Patient who does not meet the specific eligibility criteria for an MRI examination: pregnant women, known pathology that may interfere with acquisition (e.g. Parkinson's disease), absolute or relative contraindication to an MRI examination
• Patient participating in a therapeutic interventional trial or in a period of relative exclusion in relation to another protocol

Where it is running

• Chu de Bordeaux — Pessac, France (enrolling)

Full record on ClinicalTrials.gov

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