Clinical Trials Directory

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

TypeNameDescription
PROCEDUREX-rays and CT scanCT 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.