Arthroplasty, Replacement, Hip Clinical Trial
— ETODOfficial title:
A Comparison of Alendronate vs. Alfacalcidol Medication for the Preservation of Bone Mineral Density Around the Femoral Implant and in the Lumbar Spine After a Total Hip Arthroplasty
The purpose of this study is to evaluate whether alendronate and alfacalcidol are effective on prosthetic or lumbar spine BMD after total hip arthroplasty.
Status | Active, not recruiting |
Enrollment | 60 |
Est. completion date | |
Est. primary completion date | April 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 44 Years to 82 Years |
Eligibility |
Inclusion Criteria: - osteoarthritis of the hip - patients after total hip arthroplasty Exclusion Criteria: - diseases related to bone metabolism - patients taking drugs which affect bone metabolism |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Japan | Department of orthopaedic surgery, Yokohama City University | Yokohama | Kanagawa |
Lead Sponsor | Collaborator |
---|---|
Yokohama City University Medical Center |
Japan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | DEXA QDR 2000, Hologic Co. | 1, 12, 24 and 48 weeks after operation | Yes |
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