ACTRN12606000325505
Completed
N/A
A randomised controlled trial to evaluate knee range of motion (ROM), pain and functional outcomes of patients after primary total knee arthroplasty (TKA) for knee osteoarthritis with the Increased Flexion Profix Total Knee System (Smith & Nephew, Inc.).
Mater Health Services0 sites40 target enrollmentJuly 31, 2006
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Osteoarthritis of the knee
- Sponsor
- Mater Health Services
- Enrollment
- 40
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Adults listed for total knee replacement at the Mater Adult Hospital, with a diagnosis of non\-inflammatory degenerative joint disease, who will be available for follow\-up evaluations for 2 years.
Exclusion Criteria
- •Active local or systemic infection, patients undergoing revision knee or complex primary arthroplasty, patients who are to have bilateral knee arthroplasty or those who have had knee arthroplasty in the previous 12 months. Pre\-existing severe osteoporosis, or any other systemic or metabolic disorders causing progressive deterioration of bone.
Outcomes
Primary Outcomes
Not specified
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