Bone Status on Patients With Genetic Hemochromatosis: a 3 Years Descriptive and Evolutionary Study
NCT ID: NCT01556360
Last Updated: 2015-05-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
100 participants
OBSERVATIONAL
2008-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* C282 homozygosity
Exclusion Criteria
* 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
18 Years
80 Years
ALL
No
Sponsors
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Ministry of Health, France
OTHER_GOV
Rennes University Hospital
OTHER
Responsible Party
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Principal Investigators
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Guggenbuhl Pascal, MD
Role: PRINCIPAL_INVESTIGATOR
Rennes University Hospital
Locations
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Angers University Hospital
Angers, , France
Brest University Hospital
Brest, , France
Nantes University Hospital
Nantes, , France
Orleans Regional Hospital
Orléans, , France
Poitiers University Hospital
Poitiers, , France
Rennes University Hospital
Rennes, , France
Countries
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Other Identifiers
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2008-A000386-47
Identifier Type: -
Identifier Source: org_study_id
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