France launches major pilot to screen Newborns' genes for rare diseases
NCT ID NCT06875089
First seen Nov 21, 2025 · Last updated May 13, 2026 · Updated 26 times
Summary
This study tests whether it is practical and acceptable to screen newborns' entire genome for rare diseases that appear in early childhood. Researchers will offer the screening to parents of 5000 newborns in five French hospitals. The goal is to see how many families agree and whether results can be returned within 4 weeks, helping to decide if this approach could be used nationwide.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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CHU Besançon
NOT_YET_RECRUITINGBesançon, 25000, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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CHU Dijon Bourgogne
RECRUITINGDijon, 21000, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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CHU Hôtel Dieu
NOT_YET_RECRUITINGNantes, 44093, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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CHU Rennes - Hôpital Sud
NOT_YET_RECRUITINGRennes, 35203, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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CHU d'Angers
NOT_YET_RECRUITINGAngers, 49933, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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