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Clinical Trials/ACTRN12606000325505
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.

Registry
who.int
Start Date
July 31, 2006
End Date
December 31, 2008
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Mater Health Services

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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