CLINICAL_TRIALS ClinicalTrials.gov record update

Identification and Functional Characterization of Genetic Variants Associated With Specific Clinical Phenotypes in Hereditary Angioedema Due to C1 Inhibitor Deficiency: An Unbiased Approach

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT05833620
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:39:12.226105+00:00
Published At: 2023-04-27T00:00:00+00:00
Record Updated At: 2023-04-27
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: ["Hereditary Angioedema With C1 Esterase Inhibitor Deficiency"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2023-04-27"
protocolSection.identificationModule.nctId: "NCT05833620"
protocolSection.identificationModule.officialTitle: "Identification and Functional Characterization of Genetic Variants Associated With Specific Clinical Phenotypes in Hereditary Angioedema Due to C1 Inhibitor Deficiency: An Unbiased Approach"
protocolSection.statusModule.overallStatus: "NOT_YET_RECRUITING"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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