Clinical Trials Directory

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

TypeNameDescription
DRUGalendronate, alfacalcidolAlendronate: 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.