Clinical Trials Directory

Trials / Completed

CompletedNCT01353326

Bone Mineral Density (BMD) in Cemented Versus Cementless Hip Resurfacing

Randomized Clinical Trial of a Cemented Versus Cementless Femoral Component for Metal on Metal Hip Resurfacing Assessing Bone Mineral Density

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Ottawa Hospital Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the bone mineral density of patients who have undergone either cemented or cementless hip resurfacing.

Detailed description

Recent research is inconclusive regarding the degree to which the density or strength of the bone around the hip implant is preserved following a hip resurfacing system. Certainly, there are many factors which contribute to the preservation of bone mineral density - we are studying the role of cement. More specifically, we are trying to compare outcomes between patients who receive the cementless Cormet Hip Resurfacing System to those who receive the cemented CONSERVE® Plus Total Resurfacing Hip System. Therefore, the primary purpose of the current study is to compare the bone mineral density between the cementless and cemented hip resurfacing systems. We are also comparing patients who receive these two different hip systems in terms of their x-rays and how they are managing with their hip.

Conditions

Interventions

TypeNameDescription
DEVICECormetCementless hip resurfacing system
DEVICEConserveCemented hip resurfacing system

Timeline

Start date
2009-05-15
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2011-05-13
Last updated
2018-04-02

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01353326. Inclusion in this directory is not an endorsement.