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Knee Osteoarthritis clinical trials

View clinical trials related to Knee Osteoarthritis.

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NCT ID: NCT04017403 Recruiting - Knee Osteoarthritis Clinical Trials

Probiotics Attenuate Postoperative Cognition Decline

Start date: December 15, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate whether perioperative probiotics can reduce the incidence of postoperative cognitive dysfunction and postoperative delirium.

NCT ID: NCT04015323 Completed - Knee Osteoarthritis Clinical Trials

The Efficacy of Interferential Current Treatment on Knee Osteoarthritis

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The effects of different carrier frequencies of interferential current on pain and function in patients with knee arthrosis will be compared

NCT ID: NCT04011553 Completed - Knee Osteoarthritis Clinical Trials

The Effectiveness of Virtual Reality Based Rehabilitation in Patients With Knee Osteoarthritis

Start date: April 21, 2018
Phase: N/A
Study type: Interventional

We aimed to investigate the effects of virtual reality based rehabilitation program on patients with knee osteoarthritis.

NCT ID: NCT04011488 Terminated - Knee Osteoarthritis Clinical Trials

Shared Decision Making and How It Impacts the Patient Understanding

Start date: June 2016
Phase: N/A
Study type: Interventional

Shared Decision Making (SDM) supports patient centered care and improves patient outcomes and satisfaction. Movement is Life (MIL) created an innovative SDM tool to provide a personalized framework for discussion of the projected impact to patients of their decisions regarding treatment options for knee osteoarthritis. 1. Did use of the MIL SDM tool for knee osteoarthritis result in an increased level of self-reported physical activity at one month in African American and Hispanic women? 2. Did use of the MIL SMD tool increase subject likeliness to recommend the physician? 3. What is the qualitative feedback from subjects on ease of use of the MIL SDM tool?

NCT ID: NCT04006314 Recruiting - Knee Osteoarthritis Clinical Trials

Platelet Rich Plasma and Neural Prolotherapy Injections in Treating Knee Osteoarthritis

Start date: September 4, 2018
Phase: N/A
Study type: Interventional

Osteoarthritis (OA) of the knees is the most common degenerative disorder seen in a rehabilitation outpatient clinic. It is characterized by metabolic, biochemical, and structural changes in the articular cartilage and the surrounding tissues. Knee OA patients are often troubled with knee pain and functional disturbance. Several studies have shown that the earlier the injection of autologous platelet rich plasma (a PRP) to treat early stages of knee OA, the better the treatment outcome. However, no consensus has been reached as to whether PRP injection is beneficial for patients with moderate to severe degrees of knee OA. Studies have also shown that the application of neural prolotherapy (NPT) to the genicular nerves may have beneficial effects in treating patients with severe knee OA. However, patients may start to walk for a longer period of time due to reduced knee pain after NPT. If the regenerative effect of PRP is not yet obvious on the knee cartilage, this excess walking may result in further destruction of the knee joints. No studies have examined the combined treatment effect of a PRP and NPT on patients with moderate to severe degrees of knee OA. NPT is the injection of low percentage dextrose water (5%) with the rationale to repair and reduce pain caused by the nerves. We would like to bring our PRP study to a higher level by conducting a two-year study to recruit patients with moderate to severe degrees of knee OA. PRP will be injected into the knee joint and the pes anserine tendons. Simultaneous NPT will also be performed to the genicular nerves. The effectiveness will be examined using proteomics, isokinetic measurements and functional scale evaluations. Synovial fluid (SF) is in direct contact with the cartilage and synovium, protein biomarkers related to the disease pathophysiology of knee OA are contained within the SF and will be used for proteomic analysis. Patients will receive monthly injections for a total of 3 months. In short, if inflammatory proteins in the SF are not reduced after PRP injections, this indicates that PRP is not a good treatment choice for patients with moderate to severe degrees of knee OA. If inflammatory protein concentrations are further increased after NPT as patients may start strenuous exercises with reduced knee pain, more knee joint destruction may result.

NCT ID: NCT04001361 Not yet recruiting - Knee Osteoarthritis Clinical Trials

Laser Cell Therapy for Knee Cartilage Repair

Start date: July 15, 2019
Phase: N/A
Study type: Interventional

Laser pulsed energy will be delivered over an optical fiber to create channels into damaged cartilage of the knee or knees. The channels have a diameter of approximately 100 microns or less and an approximate depth of 1 millimeter or less. Bone marrow aspirate will then be delivered into the damaged joint.

NCT ID: NCT03998943 Recruiting - Knee Osteoarthritis Clinical Trials

NOCTURNAL PAIN After Knee Arthroplasty : Incidence and Risk Factor: an Observational Study

NOCTURN-PAIN
Start date: May 6, 2019
Phase:
Study type: Observational

In prosthetic knee surgery, there is a certain number of patients with post-operative nocturnal pain. The purpose of our study is to determine the impact of this problem and to better understand its risk factors.

NCT ID: NCT03990805 Completed - Knee Osteoarthritis Clinical Trials

A Phase 3 Study to Evaluate the Efficacy and Safety of JointStem in Treatment of Osteoarthritis

Start date: June 11, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the efficacy and safety of autologous Adipose Tissue derived Mesenchymal stem cells (JOINTSTEM®) in patient with severe Knee Osteoarthritis.

NCT ID: NCT03987932 Terminated - Knee Osteoarthritis Clinical Trials

NEAT!2 Sedentary Behavior Reduction for Individuals With Past or Present Knee Symptoms, Injuries, or Surgeries

Start date: June 22, 2019
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of an mHealth sedentary reduction program over a 6-month period of time in adults with past or present knee symptoms, injuries, or surgeries.

NCT ID: NCT03984942 Completed - Surgery Clinical Trials

Bypass PACU in Knee and Hip Arthroplasty

Start date: October 1, 2019
Phase:
Study type: Observational [Patient Registry]

A Quality Study in the use of Post-Anaesthesia Care Unit(PACU) in Hip and Knee Arthroplasty, and the ability to bypass this unit. The investigators wish to investigate the amount of patients who is required to be secondary admitted to the PACU, after primary discharge from the operating room to the surgical ward, thereby bypassing the PACU.