Stability, functional and clinical outcomes following Reverse Total Shoulder Arthroplasty (RSA); Repair versus Non-Repair of the Subscapularis

Not Applicable

Completed

• Conditions: Management of the subscapularis following reverse total shoulder arthroplasty; arthritis; Musculoskeletal - Osteoarthritis; Surgery - Surgical techniques

• Registration Number: ACTRN12616000864426
• Lead Sponsor: Professor Jeganath Krishnan

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-07-01
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 56

Inclusion Criteria

Patient has provided written, informed consent and is willing to participant.
Participant is a male or non-pregnant female, at least 40 years old, and preferably at least 50 years of age.
Patient has received a Reverse Total Shoulder Replacement implanted within the previous 5 years.

Exclusion Criteria

Patient has undergone Revision reverse shoulder arthroplasty (i.e. previous resurfacing, hemi, total or reverse).

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To assess the difference in the function, as measured by the self-reported ASES score, between two RSA treatment groups up to 5 years post-surgery.[Single time-point between 0 and 5 years post reverse total shoulder replacement.]