M17.1
Conditions
Interventions
Group 1: Patients of the University Hospital for Orthopedics and Trauma Surgery Pius-Hospital, Medical Campus University of Oldenburg, who were provided with a medial unicompartmental knee arthroplast
Sponsors
Universitätsklinik für Orthopädie und Unfallchirurgie Pius-Hospital; Medizinischer Campus Uni Oldenburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients provided with a unicompartmental knee arthroplasty in Pius-Hospital between 2014 to 2016. 2. Age >18 3. signed informed consent form
Exclusion criteria
Exclusion criteria: Inability to properly understand, read, and/or write German.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Differences between navigated and conventional operated knees regarding clinical outcome and patient satisfaction. The following parameters will be evaluated: active and passive range of motion as well as anterior, medial, and lateral knee stability. All clinical tests will be done in a side-to-side comparison manner between the operated and non-operated knee. Knee range of motion will be assessed utilizing a goniometer. Stability assessment will include the Lachmann-test for anterior stability as well as valgus/varus tests for medial/lateral knee stability. Additionally, knee function will be objectively assessed utilizing the Timed up and Go-Test and subjectively with the Oxford Knee Score and Knee Osteoarthritis Outcome Score - Physical Function Short Form. Patient satisfaction will be assessed with the EQ-5D-3L. | — |
Countries
Germany
Contacts
Public ContactGesine Seeber
Universitätsklinik für Orthopädie und Unfallchirurgie Pius-Hospital; Medizinischer Campus Uni Oldenburg
Outcome results
None listed