AETOS Shoulder System
AETOS Shoulder System Post Market Clinical Investigation
Smith & Nephew, Inc.
220 participants
Mar 5, 2024
OBSERVATIONAL
Conditions
Summary
The goal of this study is to confirm the safety and performance of the AETOS Shoulder System for USA adoption. This is a prospective, open, adaptive, non-comparative, multi-centre investigation enrolling a maximum of 220 subjects in 2 cohorts (anatomic and reverse) at up to 15 sites. No intra-study comparator group will be included, and there will be no randomization
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
The AETOS Shoulder System will be implanted into the right or left shoulder in the anatomic or reverse configuration
Locations(5)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06319911