Is there difference of the pre operative planning of the total knee arthroplasty between orthopedic surgeons?
- Conditions
- This case control study will review a cohort (n= 899 cases) of patients operated for unilateral total knee arthroplasty (TKA) with the use of patient specific matched instruments (PSMISignature, Biomet, Warsaw INC).
- Registration Number
- NL-OMON19968
- Lead Sponsor
- Orthopedie Orbis MC, Sittard-Geleen, the Netherlands
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 75
Inclusion Criteria
Pre operative planned TKA of patients with PSMI
Exclusion Criteria
N/A
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes to the plan, the surgeon can modify the settings for femur and tibia alignment.
- Secondary Outcome Measures
Name Time Method The surgeon is also able to change the size for femur or tibia implant.<br>