Outcome Analysis of the Oxford Partial Knee Arthroplasty
Not Applicable
Completed
- Conditions
- Knee Arthroplasty
- Registration Number
- NCT00759616
- Lead Sponsor
- Zimmer Biomet
- Brief Summary
Prospectively monitor the patients receiving the Oxford Partial knee arthroplasty
- Detailed Description
Utilization of systematic outcome measurements and specific designated time frames to monitor patient satisfactions will assist in analysing this type of prosthesis and the post operative period. Data collected will be added to the compiled information from previous studies in relation to the Oxford knee.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 156
Inclusion Criteria
- Patient Suitable for Knee Replacement
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method WOMAC, SF12, oxford Knee,KSCRS 3weeks, 3months,6months, yearly
- Secondary Outcome Measures
Name Time Method Length of Hospital Stay Postop
Trial Locations
- Locations (1)
Dartmouth General Hospital
🇨🇦Dartmouth, Canada
Dartmouth General Hospital🇨🇦Dartmouth, Canada