Comparison of the early clinical and radiological results and patient satisfaction of the mobile and fixed insert unicondylar knee prostheses routinely used in the clinic.
Unicondylar knee prosthesis operation will be performed on patients with unicompartmental knee arthrosis who apply to our clinic. Patients will be randomized to use mobile or fixed inserts. After 1 year of follow-up, SF-36, KOOS and HSS scores will be taken to examine the clinical satisfaction of the patients. In addition, radiological evaluation will be made for the presence of osteolysis at the tibial implant interface between both groups.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
Patients with unicondylar knee replacement using the mobile insert option
Patients with unicondylar knee replacement using the fixed insert option
Volkan Ezici
Istanbul, Fatih, Turkey (Türkiye)
RECRUITINGShort Form Health Survey (SF-36)
SF-36 Score (0-100) to assess patient satisfaction at postoperative 1st year
Time frame: 0-1 year
Knee injury and osteoarthritis outcome score (KOOS)
Knee injury and osteoarthritis outcome score (0-100)
Time frame: 0-1 year
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