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Iron Overload

Clinical trial condition

Iron Overload

Explore clinical trials studying Iron Overload. Study availability and eligibility vary by location and protocol.

30 public trials 4 recruiting studies

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Iron Overload trial results

Completed

Mi-iron - Moderately Increased Iron - is Reducing Iron Overload Necessary?

NCT01631708

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +7 more
Locations: Royal Brisbane and Woman's Hospital Brisbane, Queensland, Australia

Austin Health Melbourne, Victoria, Australia

Royal Melbourne Hospital Melbourne, Victoria, Australia

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Completed

Statistical Basis for Hemochromatosis Screening

NCT00005559

Conditions: Blood Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +9 more
Locations: Not specified

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Completed

Evaluation of a New MR Pulse Sequence to Quantify Liver Iron Concentration

NCT00587535

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Fibrosis, +12 more
Locations: Mayo Clinic Rochester, Minnesota, United States

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Completed

Hemochromatosis--Genetic Prevalence and Penetrance

NCT00006312

Conditions: Blood Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +9 more
Locations: Not specified

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Completed

Pharmacogenetic Study in Patients Received Iron Chelating Agent

NCT01623895

Conditions: Hemosiderosis, Iron Metabolism Disorders, Iron Overload, +2 more
Locations: Seoul National University Hospital Seoul, Chongno-gu, South Korea

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Completed

Screening of Hepatocellular Carcinoma in Patients With Compensated Cirrhosis

NCT00190385

Conditions: Adenocarcinoma, Carcinoma, Carcinoma, Hepatocellular, +21 more
Locations: Hopital Jean Verdier Paris, Île-de-France Region, France

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Completed

Haemochromatosis:Phlebotomy Versus Erythrocytapheresis Therapy

NCT00202436

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +6 more
Locations: Sanquin Blood Bank Southeast Region Maastricht, Netherlands

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Completed

Clinical Management of Hereditary Hemochromatosis: Phlebotomy vs. Erythrocytoapheresis

NCT00440986

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +7 more
Locations: Department of Transfusion Medicine-San Filippo Neri General Hospital Rome, Italy

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Completed

Risk Factors of Porphyria Cutanea Tarda (PCT)

NCT00213772

Conditions: Blood-Borne Infections, Communicable Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +23 more
Locations: Not specified

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Active, Not Recruiting

Impact of Transferrin Saturation Guided Maintenance Treatment on Quality of Life in HFE Haemochromatosis

NCT04779593

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Haemochromatosis, +7 more
Locations: Hopital Avicenne Bobigny, France

CHU Dupuytren Limoges, France

GHBS site du Scorff Lorient, France

GHRMSA - Hôpital Emile Muller Mulhouse, France

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