Optimization of Total Knee Arthroplasty Using Robotic Systems
Knee Osteoarthritis
About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring total knee arthroplasty, robotic total knee arthroplasty, the active robotic surgical system, robotic system in orthopedic
Eligibility Criteria
Inclusion Criteria: Availability of written informed consent of the patient to participate in the study; Patients with stage 3-4 osteoarthritis of the knee joint (according to Kellgren-Lawrence). Men and women from 21 to 90 years old. Pain in the knee joint above 3 points according to VAS Opportunity for observations during the entire study period (12 months); Mental adequacy, ability, willingness to cooperate and to fulfill the doctor's recommendations. Exclusion Criteria: Refusal of the patient from surgical treatment; Presence of contraindications to surgical treatment; Severe forms of diabetes mellitus (glycosylated hemoglobin> 9%); Diseases of the blood (thrombopenia, thrombocytopenia, anemia with Hb <90 g / l); The patient's unwillingness to conscious cooperation. Refusal of the patient to participate in the study; Non-compliance with the hospital regimen, according to the order of the Ministry of Health and Social Development of Russia dated 01.08.07, No. 514; The impossibility of observing the patient within the control period after the operation.
Sites / Locations
- University clinical hospital №1 I.M.Sechenov First Moscow State Medical University. The Department of Traumatology, Orthopedics and Disaster SurgeryRecruiting
Arms of the Study
Arm 1
Arm 2
Other
Other
total knee arthroplasty using the active robotic system
total knee arthroplasty using the standard manual technic
Total knee arthroplasty using the active robotic surgical system TSolution One TCAT, and system for planning TPlan
Primary total knee arthroplasty using the standard recommended set of instruments