Clinical Outcomes Study of the Nexel Total Elbow
NCT02469662
This study is recruiting at 4 US sites in 4 states, according to its ClinicalTrials.gov record last updated .
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.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Elbow Joint Destruction
- Post-traumatic Lesions
- Ankylosed Joints
- Advanced Rheumatoid Arthritis
- Joint Instability or Loss of Motion
- Acute Comminuted Articular Fracture of Elbow Joint Surfaces
- Bone Loss Contributing to Elbow Instability
- Bilateral Ankylosis From Causes Other Than Active Sepsis
- Post-traumatic Arthritis
- Degenerative Arthritis
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Zimmer Biomet
- Last updated on ClinicalTrials.gov
- July 9, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Colorado · 1
- Panorama Orthopedics and Spine Center · Golden, CO
North Carolina · 1
- OrthoCarolina Research Institute · Charlotte, NC
Pennsylvania · 1
- Rothman Institute · Philadelphia, PA
Tennessee · 1
- Campbell Clinic · Germantown, TN
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.