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Study identifier: NCT06147414 Synced from ClinicalTrials.gov · July 28, 2026
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Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

Condition: Invasive PreNatal Diagnosis in a Context of Family History of Single-gene Disorders, Including · Sickle Cell Disease · Cystic Fibrosis  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseN/A
Planned participants550
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cell-free fetal DNA (cffDNA) is present in the maternal blood from the early first trimester of gestation and makes up 5%-20% of the total circulating cell-free DNA (cfDNA) in maternal plasma. Its presence in maternal plasma has allowed development of noninvasive prenatal diagnosis for single-gene disorders (SGD-NIPD). This can be performed from 9 weeks of amenorrhea and offers an early, safe and accurate definitive diagnosis without the miscarriage risk associated with invasive procedures. One of the major difficulties is distinguishing fetal genotype in the high background of maternal cfDNA, which leads to several technical and analytical challenges. Besides, unlike noninvasive prenatal testing for aneuploidy, NIPD for monogenic diseases represent a smaller market opportunity, and many cases must be provided on a bespoke, patient- or disease-specific basis. As a result, implementation of SGD-NIPD remained sparse, with most testing being delivered in a research setting. The present project aims to take advantage of the unique French collaborative network to make SGD-NIPD possible for theoretically any monogenic disorder and any family.

This description comes directly from the study's public registry record.

Talk to the study team

Juliette NECTOUX, MD,PhD  ·  01 58 41 11 86  ·  juliette.nectoux@aphp.fr

Christelle AUGER  ·  01 71 76 07 53  ·  christelle.auger@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Hôpital Cochin, Maternité Port-Royal, service de Gynécologie obstétriqueParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06147414