Trials / Terminated
TerminatedNCT00751673
TESS Shoulder Arthroplasty Data Collection
A Prospective, Multicentre Study Evaluating the Clinical Performance of the T.E.S.S Anatomic and Reverse Shoulder Prostheses
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 600 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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, minimising bone resection and restoring the natural anatomy of the patient.
Conditions
Timeline
- Start date
- 2006-01-01
- Primary completion
- 2019-10-01
- Completion
- 2019-10-01
- First posted
- 2008-09-12
- Last updated
- 2019-10-08
Locations
13 sites across 2 countries: Belgium, France
Source: ClinicalTrials.gov record NCT00751673. Inclusion in this directory is not an endorsement.