Trials / Completed
CompletedNCT00670852
Followup of Glenoid Fix Utilizing Auto Bone Graft in Shoulder Replacement
Computed Tomographic and Functional Follow-up of Glenoid Anchor Peg Component Fixation Utilizing Autologous Bone Graft in Total Shoulder Arthroplasty
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 29 (actual)
- Sponsor
- University of Nebraska · Academic / Other
- Sex
- All
- Age
- 19 Years – 90 Years
- Healthy volunteers
- Accepted
Summary
This is a case study to evaluate the adequacy of fixation and functional outcome of the glenoid anchor peg following autologous bone grafting around the prosthesis at the time of implant.
Detailed description
To investigate if the use of autologous bone graft around the anchor-peg glenoid prosthesis correlates with bony apposition on computed tomography scans, decreased radiolucent lines and component loosening, and functional outcomes. We hypothesize that by utilizing autologous bone graft from the resected humeral head, placed around the anchor peg glenoid prosthesis at implantation, there is a low incidence of glenoid loosening. We suggest that the absence of radiolucent lines correlated with excellent shoulder function.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | X-rays and CT scan | CT Scan x-rays |
Timeline
- Start date
- 2008-04-01
- Primary completion
- 2009-06-10
- Completion
- 2009-06-10
- First posted
- 2008-05-02
- Last updated
- 2023-09-26
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00670852. Inclusion in this directory is not an endorsement.