Bone Status on Patients With Genetic Hemochromatosis: a 3 Years Descriptive and Evolutionary Study

NCT ID: NCT01556360

Last Updated: 2015-05-27

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-07-31

Brief Summary

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The purpose of this study is to describe bone status on patients with genetic hemochromatosis, at diagnostic time and his evolution under treatment.

Detailed Description

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Bone diseases have been recognized recently as complications of genetic hemochromatosis. Further studies are needed to describe the role of iron in bone injuries. The purpose of this study is to describe bone status on patients with genetical hemochromatosis, at diagnostic time and his evolution under treatment.

Conditions

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Genetic Hemochromatosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ministry of Health, France

OTHER_GOV

Sponsor Role collaborator

Rennes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Brest University Hospital

Brest, , France

Site Status

Nantes University Hospital

Nantes, , France

Site Status

Orleans Regional Hospital

Orléans, , France

Site Status

Poitiers University Hospital

Poitiers, , France

Site Status

Rennes University Hospital

Rennes, , France

Site Status

Countries

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France

Other Identifiers

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2008-A000386-47

Identifier Type: -

Identifier Source: org_study_id

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