M17
Conditions
Interventions
Group 1: Patients who will receiving a TKA will be treated with medial stabilizing prosthesis design (MS design)
Group 2: Patients who will receiving a TKA will be treated with a Cruciate Retaining (C
Sponsors
Labor für Biomechanik & Experimentelle OrthopädieKlinik und Poliklinik für Orthopädie, Physikalische Medizin und Rehabilitation, Klinikum der Universität München, LMU München
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Planned total knee arthroplasty
Exclusion criteria
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)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement of knee stability/instability using EMG, gait parameters and knee stability scale (1-10) The data are measured pre-operatively and 6, 12 and 24 weeks postoperatively according to the following tasks: - 100 meter walk - direction change during walking - go upstairs - go downstairs - get up from the chair Used muscle groups: - lateral quadrizeps (vastus lateralis) - medial quadrizeps (vastus medialis) - lateral hamstrings (biceps femoris) - lateral gastrocnemius - medial hamstrings (semitendinosus) - medial gastrocnemius - glutaeus maximus | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Germany
Contacts
Public ContactMatthias Woiczinski
Labor für Biomechanik & Experimentelle OrthopädieKlinik und Poliklinik für Orthopädie, Physikalische Medizin und Rehabilitation, Klinikum der Universität München, LMU München
Outcome results
None listed