Clinical Trials for Newborn Screening Programmes for Rare Diseases

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A Pilot Study to Assess the Feasibility and Acceptability of Newborn Screening Using in Silico Panel-based Solo Genome Sequencing in France

NCT ID: NCT06875089

This clinical trial, called the PERIGENOMED Project, is looking into a new way to screen newborns for rare diseases using advanced genome sequencing technology. The goal is to see how well this met...

Recruiting

Type: observational Locations: Besançon, , France, Angers, , France +3 more

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