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Clinical Trials/NCT00139438
NCT00139438
Completed
N/A

Improving Management of Patients at High Risk for Osteoporotic Fractures

Merck Sharp & Dohme LLC0 sites4,266 target enrollmentSeptember 2004
ConditionsOsteoporosis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Osteoporosis
Sponsor
Merck Sharp & Dohme LLC
Enrollment
4266
Primary Endpoint
A composite measure of bone mineral density (BMD) testing and/or osteoporosis medications prescriptions.
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to assess the impact of disease management interventions on percent receiving a bone densitometry test and percent appropriately prescribed a medication for osteoporosis.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
June 2005
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Members of the Horizon Blue Cross Blue Shield of New Jersey who are at risk for osteoporosis based on age (women age 65 or older, men and women age 45 or older who have a history of fragility fracture or have a history of taking oral glucocorticoids over 3 months).

Exclusion Criteria

  • Individuals who are not members of Horizon Blue Cross Blue Shield of New Jersey and who otherwise do not meet the inclusion criteria.

Outcomes

Primary Outcomes

A composite measure of bone mineral density (BMD) testing and/or osteoporosis medications prescriptions.

Secondary Outcomes

  • BMD testing, osteoporosis medication prescriptions, fracture

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