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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01587456
Other study ID # 2011-A00453-38
Secondary ID
Status Recruiting
Phase N/A
First received April 26, 2012
Last updated June 15, 2016
Start date April 2012
Est. completion date April 2017

Study information

Verified date June 2016
Source Central Hospital, Nancy, France
Contact Georges WERYHA, MD, PHD
Phone 33 3 83 15 35 05
Email g.weryha@chu-nancy.fr
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

The investigators planned to study relationship between osteoporosis and arterial rigidity within fractured patients cohort.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

- women and men > 60 years of age

- medical history of low energy fracture

- DXA Tscore -2,5 DS

- FREE AND INFORMED CONSENT SIGNED

Exclusion Criteria:

- women and men < 60 years of age

- Corticoids treatment

- Breast cancer or prostat cancer medical history

- High energy fracture (traumatic fracture)

- No social security affiliation

- Incapacity to informed consent signed.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU de Brabois Endocrinology Vandoeuvre

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

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