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The Comparison of Anterior Knee Pain in Patella With or Without Denervation in Medial Unicompartmental Knee Arthroplasty

Not Applicable
Completed
Conditions
Osteoarthritis, Knee
Interventions
Procedure: patella denervation
Procedure: patella non-denervation
Registration Number
NCT03676179
Lead Sponsor
Ramathibodi Hospital
Brief Summary

the present study will conduct to assess anterior knee pain and complications after medial UKA with or without patella denervation in medial compartment arthritis and severe lateral facet patellofemoral arthritis patients.

Detailed Description

In this prospective cohort study, the investigators will conduct to compare the clinical result of 70 patients of unicompartment knee arthroplasty with and without patella denervation between April, 2018 and April, 2019 for the patients with osteoarthritis.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
66
Inclusion Criteria
  • Patients who diagnose with medial osteoarthritis (OA) of the knee with an Alhback score of 2, 3 and 4 (Ahlback 1968) and with any Kujala score for pre-operative anterior knee pain.
  • Older than 40 years of age.
  • pain on the medial joint line.
  • primary medial compartment osteoarthritis with a well preserved lateral compartment with competent cruciate ligaments with correctable intraarticular varus deformity.
  • ROM flexion up to 110° under anesthesia.
Exclusion Criteria
  • Patients with fixed varus deformity > 15°
  • Inflammatory arthritis
  • Previous high tibial osteotomy or ACL reconstruction

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
unicompartment knee arthroplasty and patella denervationpatella denervationUKA and patella denervation
unicompartment knee arthroplasty and patella non-denervationpatella non-denervationUKA and patella non-denervation
Primary Outcome Measures
NameTimeMethod
Kujala score6 months

Kujala score including 13 parameters with the score of 0-100, the higher the score the better the function.

Secondary Outcome Measures
NameTimeMethod
complication6 months

number of participant with DVT, infections, loosening of implants, fractures, lateral compartment arthritis, and dislocations of the polyethylene

Trial Locations

Locations (1)

Pranungkraw General Hospital

🇹🇭

Bangkok, Thailand

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