Boonchana Pongcharoen
Pathum Thani, Changwat Pathum Thani, 12120, Thailand
NCT Number: NCT02557763
The aims of this study is to compare the results between patients without severe patellofemoral arthritis and patients with severe patellofemoral arthritis after mobile bearing UKA.
The investigators prospective compute the results including anterior knee pain, knee society score, pain score, functional score, range of motion, operative time, blood loss, and component alignment.
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Notify Me40 year and older
All sexes
Interventional
Not applicable
Pathum Thani, Changwat Pathum Thani, 12120, Thailand
The patients were performed surgery. The Oxford UKA was applied for all patient.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The patients with medial osteoarthritis knee with patellofemoral arthritis were performed surgery and applied Oxford unicompartmental knee arthroplasty.
Other names: Oxford UKA
Time frame: 1 year
The 10-point visual analog scale is 0 representing no pain and 10 representing maximum pain experience.
Time frame: 1year
The standard clinical evaluation system for reporting results for patients undergoing unicompartmental knee arthroplasty
Thammasat University
Other
Study of Oxford Unicompartmental Knee Arthroplasty to Determine Anterior Knee Pain, Pain Score, Knee Score and Functional Score Between Patients Without Severe Patellofemoral Arthritis and Patients With Severe Patellofemoral Arthritis
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