Clinical Outcomes Study of the Nexel Total Elbow

Status Recruiting

Clinical Trial Summary

The objectives of the study are to confirm safety and performance of the Zimmer Nexel Total Elbow when used in primary or revision total elbow replacement.

Clinical Trial Description

The objectives of the study are to confirm safety and performance of the Zimmer® Nexel™ Total Elbow when used in primary or revision total elbow replacement by analysis of standard scoring systems, radiographs, and adverse event records. The safety of the device will be monitored using the frequency and incidence of reporting adverse events. The performance of the device will be evaluated by assessing the pain and functional performance, survival of the device, patient health status, and radiographic success of the implant. ;

Study Design

Related Conditions & MeSH terms

Acute Comminuted Articular Fracture of Elbow Joint Surfaces
Advanced Rheumatoid Arthritis
Ankylosed Joints
Ankylosis
Arthritis
Arthritis, Rheumatoid
Bilateral Ankylosis From Causes Other Than Active Sepsis
Bone Loss Contributing to Elbow Instability
Degenerative Arthritis
Elbow Joint Destruction
Fractures, Comminuted
Intra-Articular Fractures
Joint Instability
Joint Instability or Loss of Motion
Osteoarthritis
Post-traumatic Arthritis
Post-traumatic Lesions

Clinical Trial Details

NCT number	NCT02469662
Study type	Interventional
Source	Zimmer Biomet
Contact	Richard Marek
Phone	574-453-7567
Email	richard.marek@zimmerbiomet.com
Status	Recruiting
Phase	N/A
Start date	June 2015
Completion date	December 2032

View Details

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