Clinical trial

Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

NCT06147414

StatusRECRUITING

Study typeOBSERVATIONAL

Start date2024-10-23

PhaseN/A

Study timeline

Study start (actual)2024-10-23Date precision: day

Registry last updated2026-04-23

Observed by CureCurrent2026-10-07

Recorded dates are source observations, not predictions. Missing milestones are not estimated.

Conditions

Invasive PreNatal Diagnosis in a Context of Family History of Single-gene Disorders, Includingunresolved

Sickle Cell Diseaseunresolved

Cystic Fibrosisunresolved

Fragile X Syndromeunresolved

Proximal Spinal Muscular Atrophyunresolved

Myotonic Dystrophyunresolved

Muscular Dystrophy, Duchenneunresolved

Muscular Dystrophy, Beckerunresolved

Neurofibromatosis-Noonan Syndromeunresolved

Huntington Diseaseunresolved

Hemophilia Aunresolved

Hemophilia Bunresolved

MODY2 Diabetesunresolved

X-Linked Hydrocephalusunresolved

Autosomal Recessive Polycystic Kidney Diseaseunresolved

Interventions

Blood sampleBIOLOGICAL

Sponsors & collaborators

Assistance Publique - Hôpitaux de Parislead sponsor

URC-CIC Paris Descartes Necker Cochincollaborator

Mapped research locations

Registry source

Open the source record to verify current eligibility, contacts, locations and registry updates.

Open NCT06147414 on ClinicalTrials.gov ↗

Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.