754416
Last Update Posted: 2017-03-07
Recruiting has ended
All Genders accepted | 18 Years + |
100 Estimated Participants | No Expanded Access |
Observational Study | Does not accept healthy volunteers |
S.E.S Shoulder Arthroplasty Data Collection
This observational study intends to collect efficacy and safety data on S.E.S shoulder system
The S.E.S.® shoulder system has been developed to provide a complete solution for all the indications for Shoulder Arthroplasty, Arthritis, Rotator Cuff Arthropathy, Proximal Humeral Fracture, minimising bone resection and restoring the natural anatomy of the patient.
Eligibility
Relevant conditions:
Arthritis
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the study if you think are close to fitting criteria.
Inclusion criteria
Exclusion criteria
locations
Data sourced from ClinicalTrials.gov