Trials / Unknown
UnknownNCT01020253
The Effectiveness of Two Osteoporosis Drugs on Prosthetic Bone Mineral Density (BMD) Loss After Total Hip Arthroplasty(THA)
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
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Yokohama City University Medical Center · Academic / Other
- Sex
- All
- Age
- 44 Years – 82 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate whether alendronate and alfacalcidol are effective on prosthetic or lumbar spine BMD after total hip arthroplasty.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | alendronate, alfacalcidol | Alendronate: 5mg per day, Tablet, Duration is 48 weeks. Alfacalcidol: 1μg per day, Tablet, Duration is 48 weeks. |
Timeline
- Start date
- 2006-01-01
- Primary completion
- 2008-04-01
- First posted
- 2009-11-25
- Last updated
- 2009-12-03
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT01020253. Inclusion in this directory is not an endorsement.