Clinical results of a subscapularis-preserving access in the treatment by means of inverse shoulder prosthesis

• Conditions: Osteoarthritis, unspecified : shoulder region [clavicle, scapula, acromioclavicular, glenohumeral, sternoclavicular joint].; M75.1; Rotator cuff syndrome

• Registration Number: DRKS00021485
• Lead Sponsor: Medizinische Hochschule Hannover

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-07-27
• Study Completion: 2021-09-22
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 92

Inclusion Criteria

Men and women aged 18 and over
- Primary implantation of an inverse shoulder prosthesis
- Minimum follow-up 2 years to maximum follow-up 6 years

Exclusion Criteria

- Implantation for post-traumatic conditions
- Neurological diseases, which limit the shoulder strength
- Existing damage or reconstruction of the subscapularis muscle

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Assessment of the functional result based on the Constant Score

Secondary Outcome Measures

Name	Time	Method
o Assessment of the functional result based on the range of motion, especially internal rotation<br>o Evaluation of the force, especially in internal rotation<br>o Detection of complications, especially luxations