Trial of Unicompartmental Versus Total Knee Arthroplasty
Not Applicable
Active, not recruiting
- Conditions
- Osteo Arthritis Knee
- Interventions
- Procedure: Total knee arthroplastyProcedure: Unicompartmental knee arthroplasty
- Registration Number
- NCT03385759
- Lead Sponsor
- Anderson Orthopaedic Research Institute
- Brief Summary
This study is a prospective, randomized trial to compare patient outcomes of unicompartmental knee arthroplasty (UKA) and total knee arthroplasty (TKA) for the treatment of medial compartment osteoarthritis.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 112
Inclusion Criteria
- medial compartment osteoarthritis of the knee
- knee flexion greater than greater than 90 degrees
- flexion contracture of less than 10 degrees
- varus deformity < 20 degrees
- grade IV degeneration of the medial compartment
Exclusion Criteria
- lateral compartment degenerative changes
- previous lateral meniscectomy
- anterior cruciate ligament deficiency
- body mass index > 40
- inflammatory arthritis
- history of septic arthritis
- hemoglobin A1c > 8.0
- chronic liver disease
- stage 3A or greater chronic renal disease
- active IV drug abuse
- patients requiring thromboembolic prophylaxis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description TKA Total knee arthroplasty Total knee arthroplasty UKA Unicompartmental knee arthroplasty Medial unicompartmental knee arthroplasty
- Primary Outcome Measures
Name Time Method Knee Society Score 2 years Functional knee outcome questionnaire ranging from 0-100, with 100 being best
- Secondary Outcome Measures
Name Time Method Revision 2 years complication requiring revision surgery
Trial Locations
- Locations (2)
Rush University Medical Center
🇺🇸Chicago, Illinois, United States
Anderson Orthopaedic Research Institute
🇺🇸Alexandria, Virginia, United States