Back to resultsEstimation of Osteoporosis' Prevalence in France: Pilot Study in the Department of the Alpes-Maritimes
Primary Purpose
Osteoporosis
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
bone densitometry
Sponsored by
About this trial
This is an interventional screening trial for Osteoporosis focused on measuring osteoporosis
Eligibility Criteria
Inclusion Criteria:
- Patient member of Caisse Primaire d'Assurance Maladie
Exclusion Criteria:
- Patient incapable of understanding the questionary
Sites / Locations
- Department of Rheumatology
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00821925
First Posted
January 12, 2009
Last Updated
December 7, 2011
Sponsor
Centre Hospitalier Universitaire de Nice
1. Study Identification
Unique Protocol Identification Number
NCT00821925
Brief Title
Estimation of Osteoporosis' Prevalence in France: Pilot Study in the Department of the Alpes-Maritimes
Official Title
Estimation of Osteoporosis' Prevalence in France: Pilot Study in the Department of the Alpes-Maritimes
Study Type
Interventional
2. Study Status
Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to estimate Osteoporosis' prevalence in France and is a pilot study in the Department of the Alpes-Maritimes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
osteoporosis
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
800 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
bone densitometry
Intervention Description
All patients do a bone densitometry after the inclusion.
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient member of Caisse Primaire d'Assurance Maladie
Exclusion Criteria:
Patient incapable of understanding the questionary
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liana Euller-Ziegler, PU-PH
Organizational Affiliation
Department of Rheumatology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Rheumatology
City
Nice
ZIP/Postal Code
06002
Country
France
12. IPD Sharing Statement
Learn more about this trial
Estimation of Osteoporosis' Prevalence in France: Pilot Study in the Department of the Alpes-Maritimes
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