Evaluation of the postoperative clinical and fluoroscopical outcome of a kinematic knie endoprosthesis, comparison of operation techniques with and without ligament tensioning against and standard knie endoprosthesis
Not Applicable
Recruiting
- Conditions
- Total Knee ArthroplastyZ96.6Presence of orthopaedic joint implants
- Registration Number
- DRKS00010775
- Lead Sponsor
- Krankenhaus Märkisch-Oderland GmbH Betriebsteil WriezenKlinik für Orthopädie und Unfallchirurgie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
•Indication for a total knee arthroplasty after primary and secondary medial knee osteoarthritis
•Patient agreement to participate in the study
•Implantation of the previously described TKA designs
Exclusion Criteria
Patients with contra indications to total knee arthroplasty
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fluoroscopic examination of the knee joint kinematik in patients with three different knie implant designs at 6 and 12 months postoperative
- Secondary Outcome Measures
Name Time Method Examination of the knee joint Range of motion (RoM) with a goniometer and collection of the clinical data with the questionnaries KSS, High flexion knee score and Forgotten joint score preoperative and after 6 and 12 months postoperative.