Actively Recruiting
Validation of Multi-contrast, High-resolution Cardiac Magnetic Resonance Imaging
Led by University Hospital, Bordeaux · Updated on 2025-04-22
200
Participants Needed
1
Research Sites
258 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Bordeaux
Lead Sponsor
G
Grant Agreement ERC SMHEART
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Validation of Multi-contrast, High-resolution Cardiac Magnetic Resonance Imaging
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chu de Bordeaux
Pessac, France, 33600
Actively Recruiting
Research Team
B
BUSTIN Aurelien, PHD
CONTACT
C
COCHET Hubert, MD, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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