Status:
TERMINATED
TESS 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 TESS shoulder system
Detailed Description
The T.E.S.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, minim...
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 :
January 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2019
Estimated Enrollment :
600 Patients enrolled
Trial Details
Trial ID
NCT00751673
Start Date
January 1 2006
End Date
October 1 2019
Last Update
October 8 2019
Active Locations (13)
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1
De Dreef Van Zonnebos 13
Schilde, Belgium
2
Clinique Générale
Annecy, France
3
Institut Calot
Berck, France, 59
4
Polyclinique Jean Villar
Bruges, France