Reverse Shoulder Arthroplasty with Augments to Restore Joint Line Anatomy in Patients with Glenoid Bone Loss

Not Applicable

• Conditions: Glenoid bone loss in patients undergoing reverse shoulder arthroplasty; Surgery - Other surgery; Musculoskeletal - Osteoarthritis

• Registration Number: ACTRN12621000451808
• Lead Sponsor: orthland District Health Board

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-04-19
• Last Update Posted: 26 April 2021

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

primary reverse shoulder arthroplasty, metallic augments, patients with glenoid bone loss

Exclusion Criteria

previous shoulder surgery, concurrent use of bone graft, CT scan follow up less than 3 months from initial surgery

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Glenohumeral joint line position post-surgery based on CT scans (pre and post-operative)[The primary timepoint is dependent on how long ago the patient had their metallic augment implant inserted. This is variable from patient to patient. The timepoint is measured from date of surgery to date of post-operative CT scan. We have excluded all patients within 3 months of their surgery, as we feel this is too soon to provide any meaningful results. ]