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Clinical trial

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

NCT01541813 is registered in ClinicalTrials.gov with Rennes University Hospital as lead sponsor.

NCT NCT01541813
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Registry record

As filed in ClinicalTrials.gov.

Title
Clinical, Biological, Genetic and Functional Characterization of Rare Iron Overload Phenotypes Associated With Hepcidin Deficiency Except C282Y Homozygosity.
Lead sponsor
Rennes University Hospital
Phase
Observational
Overall status
Terminated
Start date
March 31, 2011
Completion date
December 31, 2014
Enrollment
62 (actual)
Sites
10

Conditions

As the registry lists them; a condition with its own page is linked.

rare iron overloads except c282y homozygosity