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NCT07469657Possibly a fitRecruiting

Cost-effectiveness of a non-invasive prenatal test for genetic disorders

Monogenic DiseasesGenetic Diseases, Inborn

Part of Genetic & congenital clinical trials.

This study is testing a non-invasive prenatal blood test (NIPD) that can check for certain serious genetic disorders in your baby, instead of using more invasive methods like amniocentesis. If you are at risk of passing on a severe genetic condition, this test may help you get answers safely.

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

Phase
N/A
Enrollment
300 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You and your partner are both over 18 and your pregnancy is at least 7 weeks along.
  • Your doctor has recommended a prenatal test (like amniocentesis or a special blood test) for a serious genetic condition, and a special prenatal center (CPDPN) has approved it.
  • The condition's gene can be found with a specific genetic test (called the Agilent V8 exome capture kit).
  • You (the pregnant woman) do NOT carry the disease gene yourself.
  • You and your partner have French social security and both agree to join the study.
  • Neither you nor your partner is in prison, under guardianship, or under curatorship.

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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