KNEE ARTHROPLASTY USING DIGITAL TEMPLATING:A PROSPECTIVE RANDOMISED CONTROLLED SINGLE-BLIND TRIA
Not Applicable
- Conditions
- Gonarthrosis [arthrosis of knee]M17
- Registration Number
- DRKS00021590
- Lead Sponsor
- Hospital of Traumatology and Orthopaedics
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 99
Inclusion Criteria
elective knee arthroplasty and the consent of the patient and surgeon to participate in the study
Exclusion Criteria
prior femur or tibia fracture, previous hip, knee or ankle bony surgery in anamnesis, knee joint varus or valgus deformity = 15° or flexion contracture > 10°, BMI = 40, and incorrect positioning on radiographs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method femoral component absolute coronal angular deviation (FAD) and knee joint absolute coronal deformity (KAD) after the operation
- Secondary Outcome Measures
Name Time Method Changes in clinical scores (pain NRS, KSS, KOOS) one year after the operation