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Osteoarthritis, Knee clinical trials

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NCT ID: NCT05728827 Recruiting - Knee Osteoarthritis Clinical Trials

A Study to Compare Two Rehabilitation Protocols for Knee Osteoarthritis

Start date: March 15, 2023
Phase: N/A
Study type: Interventional

The aim of this randomized controlled study is to investigate whether the implementation of Blood Flow Restriction, in which the de-loading factor is delivered by the combined progressive de-loaded walking to running activity on an antigravity treadmill (treatment group), is more effective than the same antigravity protocol alone (control group). Participants will be divided as follows: Intervention group: anti-gravity treadmill combined with blood flow restriction Control group: anti-gravity treadmill Both groups will also undergo a standardized knee Osteoarthritis management through an aerobic and strength program.

NCT ID: NCT05727371 Recruiting - Knee Osteoarthritis Clinical Trials

Combination of PRP and XLHA Prepared With RegenMatrix Medical Device To Treat Moderate to Severe Knee Osteoarthritis

Start date: August 21, 2023
Phase: N/A
Study type: Interventional

In this clinical trial the investigator assess the safety and efficacy of a single injection of a combination of cross-linked hyaluronic acid (HA) with autologous platelet-rich plasma (PRP) obtained with the RegenMatrix medical device to improve symptoms of moderate to severe knee osteoarthitis (grade III-IV Kellgren-Lawrence).

NCT ID: NCT05723458 Not yet recruiting - Knee Osteoarthritis Clinical Trials

Turmeric, Black Seeds, Flaxseed and Medicago Sativa in Knee Osteoarthritis

Start date: July 1, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

This study investigates the safety and combined effect of Turmeric, Black Seeds, Flaxseed, and Medicago Sativa for relieving symptoms of knee osteoarthritis compared to the placebo group.

NCT ID: NCT05723029 Completed - Knee Osteoarthritis Clinical Trials

Bowen Technique and Post Isometric Relaxation in Knee Osteoarthritis Patients

Start date: January 18, 2023
Phase: N/A
Study type: Interventional

The Hamstring muscles are present at the posterior surface of the thigh. The muscles start in the gluteal region and run back of the thigh and insert into the popliteal fossa. The function of hamstring muscles flexes the knee and extension of the thigh. In degenerative joint disease, muscles tightness of the lower extremity leads to a decrease in joint flexibility. In knee joint osteoarthritis, hamstring muscles are more prone to tightness. The objective of this study is to compare the effects of the Bowen technique and Post Isometric Relaxation on pain, range of motion, and hamstring flexibility in knee osteoarthritis patients.

NCT ID: NCT05722626 Completed - Clinical trials for Osteoarthritis, Knee

The Effects of Intra-articular Platelet-Rich Plasma Injection on The Severity of Knee Osteoarthritis

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

This is a single-center, randomized control trial The aim of this study is to compare PRP with placebo as the treatment of knee OA Conducted at Puri Raharja Hospital Bali in January-June 2022 Sample consisted of 106 patients with knee OA grades 2-3 Kellgren-Lawrence, randomized into PRP group and placebo group Samples were injected with 2 ml PRP or normal saline twice at one-week interval The severity of knee OA was assessed by Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) before injection and two weeks after the first injection.

NCT ID: NCT05715645 Recruiting - Clinical trials for Unilateral Primary Osteoarthritis of Knee

Assessment of Recovery After Adductor Canal Block Analgesia in Unilateral Prosthetic Knee Surgery

IPACKNEE
Start date: April 5, 2023
Phase: N/A
Study type: Interventional

The purpose of the study is post-operative recovery from prosthetic knee surgery will be assessed by the proportion of patients entering the Accelerated Rehabilitation After Surgery program eligible for discharge from hospital at 2 days according to the following definition: Chung score ≥ 9 with no intravenous (IV) infusion, solid food, transit restored, no signs of infection and Cumulated Ambulation Score D1 ≥ 5 (if discharged on Day 1), Cumulated Ambulation Score Day 2 ≥ 10 (if discharged on Day 2), or Cumulated Ambulation Score Day 3 ≥ 11/18.

NCT ID: NCT05714267 Enrolling by invitation - Knee Osteoarthritis Clinical Trials

Effect of Noise Control During Total Knee Arthroplasty

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Music has emerged as a well-received medical intervention. Patients may be uncomfortable during total joint replacement, which can result in high sedation requirements. These requirements put patients at risk of surgical stress. This study compares the effect of passive noise-cancellation versus active noise cancellation with music on pain, vital signs and anxiety during elective total knee replacement.

NCT ID: NCT05712291 Recruiting - Knee Osteoarthritis Clinical Trials

Optimization of Total Knee Arthroplasty Using Robotic Systems

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT05707000 Completed - Knee Osteoarthritis Clinical Trials

Comparison of Quadriceps Strengthening and Kinesiotaping on Gait in Knee Osteoarthritis

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The aim of this research is to determine the Effects of facilitatory Kinesio-taping and concentric quadriceps strengthening on gait parameters in knee osteoarthritis. Randomized clinical trials will be done at Physio Experts Clinic, Islamabad. The sample size is 38. The subjects were divided in two groups, with 19 subjects in Group A and 19 in Group B. Study duration was of 6 months. Sampling technique applied was Non probability Convenience Sampling technique. Both males and females of aged 50-60 years with Knee OA grade 2 or 3 were included. Tools used in the study are Numeric Pain Rating Score (NPRS), dynamometer, WOMAC questionnaire and Mobile app for measuring Temporospatial gait parameters.

NCT ID: NCT05706844 Recruiting - Clinical trials for Osteoarthritis, Knee

Spinal Anaesthesia vs. General Anaesthesia for THA, TKA and UKA

RCT SAGA
Start date: March 6, 2023
Phase: Phase 4
Study type: Interventional

The goal of this randomized clinical trial is to investigate the postoperative recovery following hip and knee arthroplasty procedures depending on the use of either spinal anaesthesia (SA) or general anaesthesia (GA). The main questions are: - Are more patients able to be safely mobilized within 6 hours postoperatively when using GA compared to SA? - Does postoperative pain, nausea and vomiting, dizzyness, occurence of delirium and urinary retention differ between the anaesthetic methods? Participants, scheduled for total hip, total knee and unicomartmental knee arthroplasty, will be randomized to recieve spinal anaesthesia or general anaesthesia in relation to surgery. At 6 hours postoperatively a physiotherapist will conduct a 5-meter walking test to evaluate whether the participant can be safely mobilized.