Easytech Reversed Shoulder System Clinical Study

Status Active, not recruiting

Clinical Trial Summary

The purpose of the study is to collect data to demonstrate the safety and effectiveness of the Easytech Reversed Shoulder System for the treatment of patients who require a reverse total shoulder arthroplasty.

Clinical Trial Description

The clinical study will enroll patient who require a reverse total shoulder arthroplasty as a result of osteoarthritis, post-traumatic arthritis, avascular necrosis and have a massive and non-repairable rotator cuff tear and a functional deltoid muscle. If patients meet the eligibility criteria, evaluations and x-rays will be completed pre-operatively and post-operatively out to 24 months. ;

Study Design

Related Conditions & MeSH terms

Avascular Necrosis of the Head of Humerus
Necrosis
Osteo Arthritis Shoulders
Osteoarthritis
Rotator Cuff Injuries
Rotator Cuff Tear

Clinical Trial Details

NCT number	NCT03806842
Study type	Interventional
Source	FX Shoulder Solutions
Contact
Status	Active, not recruiting
Phase	N/A
Start date	November 28, 2018
Completion date	December 28, 2024

View Details

See also
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