Treatment of Hemochromatosis

Recruitment Status
ACTIVE, NOT RECRUITING
(See Contacts and Locations)Verified February 2026 by National Institutes of Health Clinical Center (CC)
Sponsor
National Institutes of Health Clinical Center (CC)
Information Provided by (Responsible Party)
National Institutes of Health Clinical Center (CC)
Clinicaltrials.gov Identifier
NCT00007150
Other Study ID Numbers:
010045
First Submitted
December 8, 2000
First Posted
December 10, 2000
Last Update Posted
April 23, 2026
Last Verified
February 2026

ClinicalTrials.gov processed this data on April 2026Link to the current ClinicalTrials.gov record .

History of Changes

Study Details

Study Description

Hereditary hemochromatosis (HH) occurs in 1 in every 200-250 individuals of northern European descent, and is the most common inherited disease in this population. Although the molecular pathophysiology remains incompletely understood, a homozygous mutation in the HFE gene (Cys282Tyr) is observed in nearly 100% of clinically confirmed cases. The clinical manifestations of HH are due to inappropriately increased iron absorption with excessive iron deposition in the liver, heart, endocrine organs, and joints.

Phlebotomy treatment, with removal of iron contained in the hemoglobin of red cells, is the only effective therapy for HH. Phlebotomy therapy relieves many of the symptoms of iron-mediated tissue damage and prevents progression to cirrhosis. However, published laboratory guidelines for monitoring phlebotomy therapy are based on retrospective data, and in general allow a moderate level of iron overload to persist during maintenance therapy. Since 1987, the DTM has piloted the use of the red cell mean corpuscular volume (MCV), in conjunction with the hemoglobin, as a prospective guide to phlebotomy therapy in a small cohort of HH patients. In contrast to other retrospectively-derived guidelines, this simple, inexpensive, physiologic method was found to be a precise indicator of iron-limited erythropoiesis, and could be easily applied to adjust the pace of phlebotomy and prevent excess iron reaccumulation.

Although the majority of persons with HH meet eligibility criteria for allogeneic blood donation, until recently regulatory guidelines restricted the use of therapeutically withdrawn blood for transfusion. New regulations now permit increased flexibility in the use of such units for this purpose. The purposes of this protocol are: (1) to prospectively study the genotypic and phenotypic response to phlebotomy therapy in HH patients using the MCV/hemoglobin monitoring guide, and to validate the use of this guide in a large study cohort; (2) to evaluate the course of severe hepatic disease and rheumatologic symptoms following sustained iron depletion; and (3) to establish the safety and efficacy and document the operational issues inherent in a program to collect therapeutically withdrawn blood for use in allogeneic transfusion. These goals have as their combined target the establishment of the simplest, safest system for donor processing, phlebotomy management, and transfusion of blood drawn from HH subjects.

Condition or DiseaseIntervention/Treatment
Hemochromatosis
Procedure: Phlebotomy

Study Design

Study TypeInterventional
Actual Enrollment622 participants
Design AllocationN/A
Interventional ModelSingle Group Assignment
MaskingNone (Open Label)
Primary PurposeDiagnostic
Official TitleStudies of Phlebotomy Therapy in Hereditary Hemochromatosis
Study Start DateDecember 31, 2000
Actual Primary Completion Date7mos 1w from now
Actual Study Completion Date7mos 1w from now

Groups and Cohorts

Group/CohortIntervention/Treatment
1/HH patients
HH patients
Procedure: Phlebotomy
Therapeutic phlebotomy, the periodic, frequent removal of the iron contained in the hemoglobin of red blood cells.

Outcome Measures

Primary Outcome Measures
  1. MCV drops 1-3% below baseline
    Response to phlebotomy therapy in HH patients, as evidenced by iron-depletion

Eligibility Criteria

Ages Eligible for Study(Adult, Older Adult)
Sexes Eligible for StudyAll
Accepts Healthy VolunteersNo
Inclusion Criteria
INCLUSION CRITERIA: Confirmed diagnosis of HH, defined by the following HFE genotypes: C282Y/C282 or C282Y/H63D. Up to 50 percent of the total study population may have received prior phlebotomy therapy. Elevated transferrin saturation and/or ferritin level, but diagnosis of HH not yet confirmed by genotype or liver biopsy. Elevated transferrin saturation and/or ferritin level without genotype findings listed above, but with elevated hepatic iron index on liver biopsy. Family member screening (unknown HH phenotype or genotype) EXCLUSION CRITERIA: Age less than 15 years. Pregnancy. Patients requiring therapeutic phlebotomy for reasons other than iron overload (polycythemia vera). Patients with iron overload not due to HH (e.g. hepatitis C infection, porphyria cutanea tarda, Wilson s disease, alpha-1-antitrypsin deficiency, alcohol abuse). Other medical illness or condition which, in the opinion of the Investigators, may contraindicate participation due to risk to patient or to Donor Center.
Exclusion Criteria
INCLUSION CRITERIA: Confirmed diagnosis of HH, defined by the following HFE genotypes: C282Y/C282 or C282Y/H63D. Up to 50 percent of the total study population may have received prior phlebotomy therapy. Elevated transferrin saturation and/or ferritin level, but diagnosis of HH not yet confirmed by genotype or liver biopsy. Elevated transferrin saturation and/or ferritin level without genotype findings listed above, but with elevated hepatic iron index on liver biopsy. Family member screening (unknown HH phenotype or genotype) EXCLUSION CRITERIA: Age less than 15 years. Pregnancy. Patients requiring therapeutic phlebotomy for reasons other than iron overload (polycythemia vera). Patients with iron overload not due to HH (e.g. hepatitis C infection, porphyria cutanea tarda, Wilson s disease, alpha-1-antitrypsin deficiency, alcohol abuse). Other medical illness or condition which, in the opinion of the Investigators, may contraindicate participation due to risk to patient or to Donor Center.

Contacts and Locations

Sponsors and CollaboratorsNational Institutes of Health Clinical Center (CC)
Locations
National Institutes of Health Clinical Center | Bethesda Maryland, United States, 20892
Investigators
Principal Investigator: Leonard N Chen, M.D., National Institutes of Health Clinical Center (CC)