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Clinical Trials/NL-OMON34366
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.

Registry
who.int
Start Date
TBD
End Date
October 16, 2012
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Stryker SA

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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