CLINICAL_TRIALS ClinicalTrials.gov record update

Validation of Optical Genome Mapping for the Identification of Constitutional Genomic Variants in a Postnatal Cohort

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT05295277
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:39:38.802312+00:00
Published At: 2023-08-07T00:00:00+00:00
Record Updated At: 2023-08-07
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: ["Developmental Disability", "Intellectual Disability", "Autism Spectrum Disorder", "Congenital Anomaly", "Fragile X Syndrome", "Facioscapulohumeral Muscular Dystrophy 1"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2023-08-07"
protocolSection.identificationModule.nctId: "NCT05295277"
protocolSection.identificationModule.officialTitle: "Validation of Optical Genome Mapping for the Identification of Constitutional Genomic Variants in a Postnatal Cohort"
protocolSection.statusModule.overallStatus: "UNKNOWN"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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