Effect of Kinesio® Taping in Total Knee Replacement Surgery
Knee Osteoarthritis, Post-Surgical Complication
About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Kinesiotape, Post-Surgical Functional Outcomes, Total Knee Replacement Surgery
Eligibility Criteria
Inclusion Criteria:
- to be volunteered to participate in the study.
- It will be performed in patients who have stage 3-4 osteoarthritis according to the "Kellgren-Lawrence" classification and therefore undergo total knee replacement surgery in a ligament-cutting design in the Department of Orthopedics and Traumatology of Baskent University Ankara Hospital.
Exclusion Criteria:
- Patients who underwent total knee prosthesis surgery in a hinge-preserving and hinged design
- Patients who underwent simultaneous bilateral total knee prosthesis surgery
- Patients with lymphedema
- Skin lesions at the place where the taping will be applied
- Local sensitivity in the skin sensitivity test to be performed the day before the application
- Chronic kidney failure patients
- Patients with congestive heart failure
- Patients with a body mass index of 30 and above
- Patients who underwent surgery for pathological fractures
- Patients who underwent total knee replacement revision surgery
- Patients who had previously undergone high tibial osteotomy or unicondylar knee replacement surgery
- Patients who underwent surgery due to traumatic arthrosis
Sites / Locations
- Baskent University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Group 1: Sterile Kinesio tape application
Group 2: Control group
The standard post-surgical protocol and sterile EDF kinesio-taping will be applied to this group. The clinical evaluation will be made on the 15th, 45th and 90th days; functional measurements will be taken. The follow-up period was determined as 3 months.
The standard post-surgical protocol applied in our clinic will be applied to Group 2. The clinical evaluation will be made on the 15th, 45th and 90th days; functional measurements will be taken. The follow-up period was determined as 3 months.