France launches major genetic screening test for 5,000 newborns
NCT ID NCT06875089
Summary
This study is testing a new method of screening newborns for rare genetic diseases using advanced DNA sequencing. It will enroll 5,000 newborns across five French hospitals to see if this screening process is practical, fast, and acceptable to parents. The goal is to gather information to help decide if this type of genetic screening should be used more widely in the future.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for NEWBORN SCREENING PROGRAMMES FOR RARE DISEASES are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
-
CHU Besançon
NOT_YET_RECRUITINGBesançon, 25000, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
-
CHU Dijon Bourgogne
RECRUITINGDijon, 21000, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
-
CHU Hôtel Dieu
NOT_YET_RECRUITINGNantes, 44093, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
-
CHU Rennes - Hôpital Sud
NOT_YET_RECRUITINGRennes, 35203, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
-
CHU d'Angers
NOT_YET_RECRUITINGAngers, 49933, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.