CLINICAL_TRIALS ClinicalTrials.gov record update

Identification of The Novel Mutations and A Comprehensive Analysis of The Phenotype and Genetic Etiology Underlying Unclassifiable Inherited Bone Marrow Failure Syndromes With Bone Fragility Fractures

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT05436587
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:38:36.212309+00:00
Published At: 2022-07-01T00:00:00+00:00
Record Updated At: 2022-07-01
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: ["Inherited BMF Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2022-07-01"
protocolSection.identificationModule.nctId: "NCT05436587"
protocolSection.identificationModule.officialTitle: "Identification of The Novel Mutations and A Comprehensive Analysis of The Phenotype and Genetic Etiology Underlying Unclassifiable Inherited Bone Marrow Failure Syndromes With Bone Fragility Fractures"
protocolSection.statusModule.overallStatus: "RECRUITING"
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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