Effect of posterior condyle resection volume in unicompartmental knee arthroplasty: a randomized controlled trial
Not Applicable
- Conditions
- knee osteoarthritisspontaneous osteonecrosis of the knee
- Registration Number
- JPRN-UMIN000040018
- Lead Sponsor
- Ogaki Tokushukai Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with implant loosening or infection Patients with knee contracture more than 15 degrees Patients with restricted flexion more than 120 degrees
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method