Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02136251

Total Shoulder Replacement Outcomes With Autologous Bone Graft as Fixator for Glenoid Anchor Peg.

Five Year Outcome Follow-up of Glenoid Anchor Peg Component Fixation Utilizing Autologous Bone Graft in Total Shoulder Arthroplasty.

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
University of Nebraska · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

We hypothesize that there will be a low incidence of glenoid loosening with a total shoulder arthroplasty using an anchor peg glenoid and autologous bone grafting. In addition, we suggest that the absence of radiolucent lines will correlate with excellent shoulder function.

Detailed description

This will be five year follow-up of glenoid anchor peg component fixation utilizing autologous bone graft in total shoulder arthroplasty. The purpose of this study is to investigate if the use of autologous bone graft around the anchor peg glenoid prosthesis correlates with better shoulder function. Subjects having had this surgery who are five years or more out from surgery will have computed tomography and three plain radiographs to monitor for bony apposition, radiolucent lines and component loosening. These testings are not a study intervention and are for monitoring purposes.

Conditions

Timeline

Start date
2014-09-01
Primary completion
2015-02-13
Completion
2015-02-13
First posted
2014-05-12
Last updated
2023-08-14

Source: ClinicalTrials.gov record NCT02136251. Inclusion in this directory is not an endorsement.