M17.1
Conditions
Interventions
Group 1: There will be a single group of patients who will receive the same monitoring with the use of wearable inertial movement units, as well as the intervention will be a Total-Knee Arthroplasty,
Sponsors
Universitätsklinikum Brandenburg an der Havel
Eligibility
Sex/Gender
All
Age
50 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria includes meeting the requirements for a Total Knee Arthroplasty in the DGOU-Leitlinien, no comorbidities that would negatively affect participants knee function, completing the pre-operative examination in the ambulatory facilities of Oberlinklinik Potsdam, and informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: Exclusion criteria will include previous operations changing the leg axis and comorbidities that decrease the expected knee function or activity level.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient's performance based knee function, using wearable inertial movement units (IMUs) determined 2 weeks before a Total-Knee Arthroplasty and after 6 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patients' subjective knee function, using PROMs (WOMAC and OKS), determined 2 weeks before a Total-Knee Arthroplasty and after 6 weeks. Patients' degree of leg axis correction, using pre and postoperative X-ray imaging, determined 2 weeks before a Total-Knee Arthroplasty and after 6 weeks. | — |
Countries
Germany
Contacts
Public ContactRoland Becker
Universitätsklinikum Brandenburg an der Havel
Outcome results
None listed