CLINICAL_TRIALS ClinicalTrials.gov record update

Piloting an Early Intervention Program for Infants With Rare Neurogenetic Disorders

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT03836300
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-25T22:27:31.979428+00:00
Published At: 2025-07-31T00:00:00+00:00
Record Updated At: 2025-07-31
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: ["Fragile X Syndrome", "Angelman Syndrome", "Prader-Willi Syndrome", "Dup15Q Syndrome", "Duchenne Muscular Dystrophy", "Phelan-McDermid Syndrome", "Rett Syndrome", "Smith Magenis Syndrome", "Williams Syndrome", "Turner Syndrome", "Klinefelter Syndrome", "Chromosome 22q11.2 Deletion Syndrome", "Tuberous Sclerosis", "Down Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2025-07-31"
protocolSection.identificationModule.nctId: "NCT03836300"
protocolSection.identificationModule.officialTitle: "Piloting an Early Intervention Program for Infants With Rare Neurogenetic Disorders"
protocolSection.statusModule.overallStatus: "ENROLLING_BY_INVITATION"
protocolSection.designModule.phases: ["NA"]
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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