CLINICAL_TRIALS ClinicalTrials.gov record update

The Primordial Dwarfisms: Diagnosis, Identification of the Molecular Basis of Seckel Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPDII).

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT03139903
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:45.241036+00:00
Published At: 2017-11-20T00:00:00+00:00
Record Updated At: 2017-11-20
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: ["Microcephalic Osteodysplastic Primordial Dwarfism Type II", "Seckel Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2017-11-20"
protocolSection.identificationModule.nctId: "NCT03139903"
protocolSection.identificationModule.officialTitle: "The Primordial Dwarfisms: Diagnosis, Identification of the Molecular Basis of Seckel Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPDII)."
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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