Could genome sequencing at birth spot rare diseases sooner? french study launches
NCT ID NCT06875089
First seen Nov 21, 2025 · Last updated May 01, 2026 · Updated 24 times
Summary
This study will test if it's possible and acceptable to screen newborns for rare diseases using genome sequencing. About 5,000 newborns in France will take part. The goal is to see if this method can quickly find treatable or actionable rare diseases, helping doctors start care earlier.
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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
Explore the condition pages connected to this study.