Status:
TERMINATED
S.E.S Shoulder Arthroplasty Data Collection
Lead Sponsor:
Zimmer Biomet
Collaborating Sponsors:
Biomet France SARL
Conditions:
Arthritis
Eligibility:
All Genders
18+ years
Brief Summary
This observational study intends to collect efficacy and safety data on S.E.S shoulder system
Detailed Description
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, minimis...
Eligibility Criteria
Inclusion
- A pre-operative level of pain and function the same as for conventional joint replacement
- A likelihood of obtaining relief of pain and improved function
- Full skeletal maturity
- Ability to follow instructions
- Good general health for age
- Willing to return for follow-up evaluations
Exclusion
- Glenohumeral joint infection, osteomyelitis
- Neuro-muscular complications
- Inability to co-operate with and complete the study
Key Trial Info
Start Date :
March 1 2003
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2016
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00754416
Start Date
March 1 2003
End Date
September 1 2016
Last Update
March 7 2017
Active Locations (12)
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1
De Dreef Van Zonnebos 13
Schilde, Belgium
2
Clinique Générale
Annecy, France
3
Clinique St Joseph
Chambéry, France
4
Centre Hospitalier Général
Dax, France