Trials / Completed
CompletedNCT01359540
Femoral Remodeling Following Total Hip Arthroplasty With OMNI Apex Modular™ and OMNI Apex ARC™ Stem Compared to Competitive Designs
A Dual Energy X-Ray Absorptiometry (DXA) Evaluation Of Bone Density Changes After Hip Replacement. Performance Of The OMNI Apex Modular™ Hip Stem And The OMNI Apex ARC™ Hip Stem In Primary Total Hip Arthroplasty, Five-Year Clinical And DXA Analysis
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 73 (actual)
- Sponsor
- Spokane Joint Replacement Center · Academic / Other
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
This study compares the change in bone density which occurs after hip replacement with different femoral stem devices.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | OMNI Apex Modular™ Hip Device | |
| DEVICE | OMNI Apex ARC™ Hip Device |
Timeline
- Start date
- 2009-11-01
- Primary completion
- 2018-04-01
- Completion
- 2018-04-01
- First posted
- 2011-05-24
- Last updated
- 2019-04-26
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01359540. Inclusion in this directory is not an endorsement.