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NCT06875089Possibly a fitRecruiting

Newborn gene screening study in France

Newborn Screening Programmes for Rare Diseases

Part of Genetic & congenital clinical trials.

This study is testing a new way to screen newborns for certain health conditions by analyzing their DNA from a small blood sample. It aims to see if parents find this type of screening acceptable and helpful.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
5,000 people
Ages
birth to 4 weeks
Study type
Observational

Who can take part

  • Your baby is born in one of the participating maternity centers or your baby's care will be provided there.
  • Your baby is less than 28 days old when the blood sample is taken.
  • At least one biological parent has received information about the study and can give permission for the baby to be tested.
  • You are not under legal guardianship or a court order.
  • Your baby is not born under anonymous birth (French law 'nés sous X').

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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