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Study of Post Menopausal Osteoporosis (PMO) Among Gynecology Outpatients in Pakistan

Completed
Conditions
Postmenopausal Osteoporosis
Registration Number
NCT02422069
Lead Sponsor
Hoffmann-La Roche
Brief Summary

This observational study will provide an opportunity to document local patterns of susceptibility, patient profile, and usefulness of screening in postmenopausal patients coming to gynecology outpatient clinics in Pakistan. This will also capture the initial management of PMO in diagnosed patients. The information gathered will serve as a foundation for developing national guidelines on screening and management of PMO in Pakistan.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
624
Inclusion Criteria
  • Postmenopausal women
  • Age 50 years or greater
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Exclusion Criteria
  • Previously diagnosed osteoporosis, or receiving treatment for osteoporosis
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Percentage of patients diagnosed with PMO based upon dual-energy X-ray absorptiometry (DXA) resultsUp to 12 months
Secondary Outcome Measures
NameTimeMethod
Use of various PMO treatment modalitiesUp to 12 months
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