ACTRN12611000289910
Recruiting
Not Applicable
A multicentre, prospective, consecutive clinical study of the anthropometric dimensions of the Genesis II and Genesis II Slim Total Knee Prostheses in patients with degenerative joint disease requiring knee replacement.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Smith & Nephew
- Enrollment
- 1060
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient presents with non\-inflammatory degenerative joint disease of predominantly the medial compartment requiring knee replacement.
- •Patient, or his/her legal guardian, has given consent to participate in the study.
- •Patient plans to be available for follow\-up through to 2 years postoperative.
Exclusion Criteria
- •Patient is known to have insufficient femoral or tibial bone stock.
- •Patient is immunosuppressed or has an autoimmune disorder.
- •Patient has inflammatory arthritis (e.g. rheumatoid arthritis).
- •Patient has had major, non\-arthroscopic surgery to the study knee.
- •Patient has an active, local infection or systemic infection.
- •Patient has a physical, emotional or neurological condition that would compromise compliance with postoperative rehabilitation and follow\-up.
- •Patient has hip arthritis and/or replacement.
- •Patient has lateral knee compartment disease (e.g. valgus knee).
- •Patient is pregnant or plans to become pregnant during the course of the study.
- •Patient is on workman’s compensation.
Outcomes
Primary Outcomes
Not specified
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