Actively Recruiting
LUMIERE on the FETUS
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-11-20
1500
Participants Needed
1
Research Sites
390 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
L
LUMIERE Fondation ( fondation-lumiere.org) under the aegis of Fondation de France
Collaborating Sponsor
AI-Summary
What this Trial Is About
Congenital anomalies are a major public health problem. They affect 2-3% of births, around 20,000 new cases per year in France, of which 15% are cared for in Ile de France. These congenital anomalies are a major cause of morbidity, infant mortality and disability. They are also a major cause of death during the infant period (22% of deaths during the first year of life: source CépiDC Inserm 2010). The detection, accurate diagnosis and accurate prognosis, particularly functional, of these congenital anomalies are still difficult in the current monitoring of pregnancy, which is based primarily on ultrasound. The use and development of modern imaging techniques is now essential to enable doctors to better see and better examine the fetus. Alongside ultrasound, Magnetic Resonance Imaging (MRI) is a technique that has undergone significant development in recent years. MRI must allow the effective anatomical and functional evaluation of the main fetal organs and could in particular be interesting in several situations in which it has not yet been sufficiently evaluated and is not yet performed in clinical routine.
CONDITIONS
Official Title
LUMIERE on the FETUS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged 18 years or older
- Single or twin pregnancy
- Gestational age between 16 and 36 weeks based on cranio-caudal length dating
- Patient has given consent to participate
You will not qualify if you...
- Any contraindication to MRI
- More than two fetuses in pregnancy (multiple pregnancies > 2)
- Follow-up impossible after inclusion
- Maternal condition that contraindicates continuation of pregnancy
- Patient requires MRI as part of normal clinical pregnancy care due to identified or suspected fetal abnormalities such as echocardiographic abnormality, diaphragmatic hernia, CMV fetal infection, prior sibling brain abnormality, or surgery for spina bifida (STT)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Necker - Enfants Malades Hospital
Paris, France, 75015
Actively Recruiting
Research Team
D
David Grevent, MD PHD
CONTACT
A
Aminata TRAORE
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
4
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here