In vivo study of a medial stabilizing total knee replacement for analysis of postoperative knee stability and patient satisfactio
Not Applicable
- Conditions
- M17Gonarthrosis [arthrosis of knee]
- Registration Number
- DRKS00013308
- Lead Sponsor
- abor für Biomechanik & Experimentelle OrthopädieKlinik und Poliklinik für Orthopädie, Physikalische Medizin und Rehabilitation, Klinikum der Universität München, LMU München
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting stopped after recruiting started
- Sex
- All
- Target Recruitment
- 12
Inclusion Criteria
Planned total knee arthroplasty
Exclusion Criteria
- 10 ° varus / valgus deformity
- Strong knee osteoarthritis on the healthy leg
- Disruption of the gait pattern
- Low fitness status (treadmill study)
- Language skills (German questionnaires)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measurement of knee stability/instability using EMG, gait parameters and knee stability scale (1-10)<br>The data are measured pre-operatively and 6, 12 and 24 weeks postoperatively according to the following tasks:<br>- 100 meter walk<br>- direction change during walking<br>- go upstairs<br>- go downstairs <br>- get up from the chair<br><br>Used muscle groups:<br>- lateral quadrizeps (vastus lateralis)<br>- medial quadrizeps (vastus medialis)<br>- lateral hamstrings (biceps femoris)<br>- lateral gastrocnemius<br>- medial hamstrings (semitendinosus)<br>- medial gastrocnemius<br>- glutaeus maximus<br>
- Secondary Outcome Measures
Name Time Method Patient satisfaction with three questionnaires, the Western Ontario and McMaster Universities Arthritis Index (WOMAC), the Forgotten Knee Joint Score (FJs-12), and the UCLA Activity Score.