Clinical, Biological, Genetic and Functional Characterization of Rare Iron Overload Phenotypes Associated With Hepcidin Deficiency Except C282Y Homozygosity.

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT01541813

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-28T10:35:44.527820+00:00

Published At

2015-03-10T00:00:00+00:00

Record Updated At

2015-03-10

Timestamp Basis

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Date limitation

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Fields recorded by this source

protocolSection.conditionsModule.conditions

["Rare Iron Overloads Except C282Y Homozygosity"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2015-03-10"

protocolSection.identificationModule.nctId

"NCT01541813"

protocolSection.identificationModule.officialTitle

"Clinical, Biological, Genetic and Functional Characterization of Rare Iron Overload Phenotypes Associated With Hepcidin Deficiency Except C282Y Homozygosity."

protocolSection.statusModule.overallStatus

"TERMINATED"

protocolSection.designModule.phases

[]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• Rare Iron Overloads Except C282Y Homozygosity (protocolSection.conditionsModule.conditions)

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