Iron Overload's hidden toll on bones revealed in new study
NCT ID NCT01556360
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 100 adults with genetic hemochromatosis (a condition causing too much iron in the body) for 3 years to see how their bone health changed. Researchers measured bone density and checked for fractures and joint problems. The goal was to understand if iron overload weakens bones over time, even with treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better predict and manage bone problems in people with genetic hemochromatosis.
- What could go wrong
- This is an observational study, not a treatment trial. It only describes what happens, so it won't directly improve bone health. Results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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100 people
The number who actually took part.
- Started
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Jul 2008
- Finished
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Jun 2014
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patient with genetic hemochromatosis diagnosed in western France hospitals
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients between 18 and 80 years * C282 homozygosity Exclusion Criteria: * corticosteroids during the last 3 months * following treatments during the last 6 months : anabolic steroids, growth hormone, hormone therapy for menopause, tibolone, raloxifene. * following treatments during inclusion or in the last 6 month : teriparatide, parathormone, fluor, strontium ranelate, biphosphonate. * cancer or evolutionary hemopathy (including monoclonal gammopathy) * pregnancy at inclusion time * treated osteoporosis * patient in wich follow up seems hard * inclusion in another study incompatible with this one
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Angers University Hospital
Angers, 49933, France
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Brest University Hospital
Brest, 29609, France
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Nantes University Hospital
Nantes, 44093, France
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Orleans Regional Hospital
Orléans, 45100, France
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Poitiers University Hospital
Poitiers, 86021, France
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Rennes University Hospital
Rennes, 35033, France
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