Could a simple DNA test at birth detect rare diseases? france launches major pilot study
NCT ID NCT06875089
First seen Nov 21, 2025 · Last updated May 24, 2026 · Updated 27 times
Summary
This study is testing whether it is possible and acceptable to use genome sequencing to screen newborns for rare diseases in France. Researchers will offer the test to parents of 5000 newborns across five hospitals. The goal is to see how many families agree to the screening and whether results can be delivered within four weeks. This is a first step toward potentially expanding the national newborn screening program.
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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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Genom att skicka in godkänner du våra Användarvillkor
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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