Knee Osteoarthritis Clinical Trial
Official title:
Optimization of Total Knee Arthroplasty Using Robotic Systems
For the first time, it is planned to create algorithms for working with a robotic system at different patient flow rates, optimize the use of computed tomography to assess bone density and pronounced osteophytes, develop an algorithm and tactics for treating bilateral osteoarthrosis of the knee joint using an active robotic system. Aim: optimization of total knee arthroplasty using robotic systems and improvement of treatment outcomes. Objectives: to develop algorithms for preoperative planning, surgical intervention using an active robotic system; to improve the technique of active robotic total knee arthroplasty in osteoporosis, osteosclerosis and pronounced osteophytes; to develop a tactic for the treatment of patients with bilateral osteoarthrosis of the knee joint using an active robotic system. It is planned to conduct an open-label retrospective and prospective clinical study in parallel observations.The study is planned to include 250 patients with osteoarthritis of the knee joint stage 3-4 (according to Kellgren-Lawrence). The methodology developed and improved in the dissertation will be introduced into the work of the clinical Departments of Traumatology, Orthopedics and Disaster Surgery, studying the learning curve.
Status | Recruiting |
Enrollment | 250 |
Est. completion date | August 31, 2025 |
Est. primary completion date | August 31, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years to 90 Years |
Eligibility | Inclusion Criteria: 1. Availability of written informed consent of the patient to participate in the study; 2. Patients with stage 3-4 osteoarthritis of the knee joint (according to Kellgren-Lawrence). 3. Men and women from 21 to 90 years old. 4. Pain in the knee joint above 3 points according to VAS 5. Opportunity for observations during the entire study period (12 months); 6. Mental adequacy, ability, willingness to cooperate and to fulfill the doctor's recommendations. Exclusion Criteria: 1. Refusal of the patient from surgical treatment; 2. Presence of contraindications to surgical treatment; 3. Severe forms of diabetes mellitus (glycosylated hemoglobin> 9%); 4. Diseases of the blood (thrombopenia, thrombocytopenia, anemia with Hb <90 g / l); 5. The patient's unwillingness to conscious cooperation. 6. Refusal of the patient to participate in the study; 7. 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; 8. The impossibility of observing the patient within the control period after the operation. |
Country | Name | City | State |
---|---|---|---|
Russian Federation | University clinical hospital ?1 I.M.Sechenov First Moscow State Medical University. The Department of Traumatology, Orthopedics and Disaster Surgery | Moscow |
Lead Sponsor | Collaborator |
---|---|
I.M. Sechenov First Moscow State Medical University |
Russian Federation,
LYCHAGIN A.V. 1, a, RUKIN Y.A. 1, b, GRITSYUK A.A. 1, c, ELIZAROV M.P. 1, d, FIRST EXPERIENCE OF USING AN ACTIVE ROBOTIC SURGICAL SYSTEM IN TOTAL KNEE ARTHROPLASTY. 2019; 4 (38) 2019: 10.17238/issn2226-2016.2019.4.27-33
LYCHAGIN A.V.1, a, GRITSYUK A.A.1, b, RUKIN Y.A.1, c, ELIZAROV M.P.1, d, THE HISTORY OF THE DEVELOPMENT OF ROBOTICS IN SURGERY AND ORTHOPEDICS (LITERATURE REVIEW). 2020; 1 (39)2020: 10.17238/issn2226-2016.2020.1.13-19
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Implant position assessment | CT scanning; these diagnostic methods assess the position of the implant, analysis of deformation, assessment of the angles in the knee joint (LDFA, MPTA, MA, these diagnostic methods assess the position of the implant, analysis of deformation, assessment of the angles in the knee joint, analyze the rotation of implant) | 2 months after surgery | |
Primary | Implant position assessment | CT scanning | 6 months after surgery | |
Primary | Implant position assessment | CT scanning | 12 months after surgery | |
Secondary | Quality of life and knee function assessment | Knee Society Score(KSS score), which combines subjective and objective information and separates the knee score (pain, stability, range of motion etc.) from the functional score of the patient (ability to walk, go up and down stairs) | 2,6,12 months after surgery | |
Secondary | Quality of life assessment (joint awareness after surgery) | FJS-12, measures the clinical outcomes focusing on joint awareness after surgery | 2,6,12 months after surgery | |
Secondary | Quality of life assessment (the condition of patients) | WOMAC score is a widely used, proprietary set of standardized questionnaires used by health professionals to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain, stiffness, and physical functioning of the joints | 2,6,12 months after surgery | |
Secondary | Pain assessment | Visual Analog Score (VAS) for pain - dynamics pain assessment | 2,6,12 months after surgery | |
Secondary | Quality of life assessment (an individual's activities of daily living) | OKS score. The OKS is a patient reported outcome measure that consists of 12 questions about an individual's activities of daily living and how they have been affected by pain over the preceding four weeks. | 2,6,12 months after surgery |
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