S.E.S Shoulder Arthroplasty Data Collection
- Conditions
- Arthritis
- Registration Number
- NCT00754416
- Lead Sponsor
- Zimmer Biomet
- 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, minimising bone resection and restoring the natural anatomy of the patient.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 100
- 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
- Glenohumeral joint infection, osteomyelitis
- Neuro-muscular complications
- Inability to co-operate with and complete the study
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Constance and oxford Scores 6m, 1yr, 2yr, 3yr, 4yr and 5 yr
- Secondary Outcome Measures
Name Time Method Complication Any time Patient Satisfaction 6m,1yr,2yr,3yr,4yr and 5yr
Trial Locations
- Locations (12)
De Dreef Van Zonnebos 13
🇧🇪Schilde, Belgium
Clinique St Joseph
🇫🇷Chambery, France
Clinique Générale
🇫🇷Annecy, France
Clinique Chirurgicale Orthopédique A.D.R.
🇫🇷Maxeville, France
Clinique St Jean
🇫🇷Montpellier, France
Polyclinique de l'Atlantique
🇫🇷Saint Herblain, France
Clinique St Martin
🇫🇷Pessac, France
IRCOS
🇫🇷Paris, France
Institut A. Tzanck
🇫🇷St Laurent du Var, France
Clinique Mutualiste
🇫🇷St Etienne, France
Institut Calot
🇫🇷St Laurent du Var, France
Centre Hospitalier Général
🇫🇷Dax, France