CLINICAL_TRIALS ClinicalTrials.gov record update

Evaluation of the Diagnostic Performance of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT06147414
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-25T22:29:03.795190+00:00
Published At: 2026-04-23T00:00:00+00:00
Record Updated At: 2026-04-23
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Invasive PreNatal Diagnosis in a Context of Family History of Single-gene Disorders, Including", "Sickle Cell Disease", "Cystic Fibrosis", "Fragile X Syndrome", "Proximal Spinal Muscular Atrophy", "Myotonic Dystrophy", "Muscular Dystrophy, Duchenne", "Muscular Dystrophy, Becker", "Neurofibromatosis-Noonan Syndrome", "Huntington Disease", "Hemophilia A", "Hemophilia B", "MODY2 Diabetes", "X-Linked Hydrocephalus", "Autosomal Recessive Polycystic Kidney Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2026-04-23"
protocolSection.identificationModule.nctId: "NCT06147414"
protocolSection.identificationModule.officialTitle: "Evaluation of the Diagnostic Performance of Non-Invasive Prenatal Diagnosis for Single Gene Disorders"
protocolSection.statusModule.overallStatus: "RECRUITING"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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