Followup of Glenoid Fix Utilizing Auto Bone Graft in Shoulder Replacement

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Arthritis Joint Diseases Musculoskeletal Diseases

Age range

19 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Nebraska Medical Center, Dept Orthopaedic Surgery

Omaha, Nebraska, 68198-1080, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients who received a total shoulder replacement with an anchor peg glenoid and autologous bone grafting from the investigator of this study will be recruited for this study.

Exclusion criteria

Patients will be excluded if they are unable to comprehend the consent information.
Pregnant women will be excluded from this study.

Treatment and study plan

X-rays and CT scan

Procedure

CT Scan x-rays

Other names: No names

Primary outcomes

Autologous bone graft, anchor-peg glenoid prosthesis and functional outcomes

Time frame: case study over approximate 3 months time.

To determine if the use of autologous bone graft around the anchor-peg glenoid prosthesis correlate with bony apposition on computed tomography scans, decreased radiolucent lines and component loosening, and functional outcomes.

Sponsors and collaborators

Lead sponsor

University of Nebraska

Other

Registry information

Official study title

Computed Tomographic and Functional Follow-up of Glenoid Anchor Peg Component Fixation Utilizing Autologous Bone Graft in Total Shoulder Arthroplasty

Important dates

Study start: 2008
Primary completion: 2009
Study completion: 2009
First posted: May 2, 2008
Registry last updated: Sep 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed