NL-OMON34366
Completed
Not Applicable
Feasibility study to evaluate the clinical outcome of the Scorpio knee prosthesis following THE LAZIRUSH CONCEPT - Lazirush study
Stryker SA0 sites50 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Knee arthrosis
- Sponsor
- Stryker SA
- Enrollment
- 50
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A.Patients willing to sign the EC approved, study specific Informed Patient Consent Form.
- •B.Patients willing and able to comply with scheduled postoperative clinical and radiographic evaluations and rehabilitation.
- •C.Patients requiring a primary unilateral total knee replacement.
- •D.Patients with ASA Physical status 1 \&2\.
- •E. Patients having a partner at home for assistence.
Exclusion Criteria
- •A.Patients with Rheumatoid arthritis, insulin dependent diabetes, severe osteoporosis, or an inflammatory cause for osteoarthritis.
- •B.Patients with other lower limb problems than their planned primary unilateral total knee arthroplasty.
- •C.Patients requiring revision knee surgery.
- •D.Patients with ASA physical status more than 2\.
- •E.Patients requiring bilateral total knee replacement
Outcomes
Primary Outcomes
Not specified
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