Clinical Trials Logo

Knee Osteoarthritis clinical trials

View clinical trials related to Knee Osteoarthritis.

Filter by:

NCT ID: NCT03545048 Completed - Knee Osteoarthritis Clinical Trials

Effects of Internet / Web-based Exercises on the Population With Knee Arthritis

Knee OA
Start date: October 15, 2018
Phase: N/A
Study type: Interventional

1. To test whether internet-based exercises reduce the pain in knee OA 2. To check whether internet-based exercises improve the physical activity in the patients with knee OA. 3. To explore the correlation between sleep, knee inflammation (effusion, synovial hypertrophy or/and synovial hyper vascularity) and biomarkers of insulin resistance and knee pain.

NCT ID: NCT03541265 Completed - Knee Osteoarthritis Clinical Trials

Liposomal Bupivacaine in Total Knee Arthroplasty

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

Pain management after total knee arthroplasty is essential for optimized clinical outcomes and higher satisfaction. Exparel (Pacira Pharmaceuticals, Parsippany, New Jersey, USA) is a long-acting Bupivacaine extended release liposome compound that is injected peri-articularly or as regional block. The purpose of this study was to compare the analgesic efficacy of single administration of Exparel for local peri-articular infiltration versus adductor canal regional block.

NCT ID: NCT03527849 Completed - Knee Osteoarthritis Clinical Trials

Effects of Mindfulness-Based Stress Reduction on Knee Osteoarthritis

MBSR on KOA
Start date: January 30, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to see if stress reduction can lead to less pain due to knee osteoarthritis. To do this the investigators will compare two types of stress reduction modalities, Mindfulness-Based Stressed Reduction (MBSR) and a Health Enhancement Program (HEP). Both include stress reduction techniques, but MBSR has a mindfulness component that includes meditation. MBSR will be provided either in-person or online and HEP will be in-person. The assignment to the stress reduction program will be determined by the Principal Investigator. In order to assess for stress reduction and pain reduction the investigators will use validated measuring tools before, during, and after the course instructions.

NCT ID: NCT03509025 Completed - Knee Osteoarthritis Clinical Trials

Follow-up Study for Participants Jointstem Clinical Trial

Start date: February 8, 2017
Phase: Phase 2
Study type: Interventional

This study is a long term follow-up study to investigate the safety of autologous transplantation of Adipose Tissue derived Mesenchymal stem cells (MSCs) in patient with Knee Osteoarthritis.

NCT ID: NCT03491397 Completed - Knee Osteoarthritis Clinical Trials

Genicular Artery Embolization for the Treatment of Knee Osteoarthritis

GAE-OA
Start date: February 10, 2019
Phase: N/A
Study type: Interventional

The purpose of this clinical research study is to examine whether Embozene treatment of the genicular artery is a safe and effective way to treat arthritic knee pain. Embozene is a medical device made by Boston Scientific approved in the United States for the treatment of hypervascular tumors and arteriovenous malformations. It consists of thousands of microscopic spheres that are injected into the artery in the knee going to the region of pain. One of the causes of pain in the setting of knee arthritis is increased blood flow going to the specific area of pain. The goal of this procedure is to decrease the blood flow (embolize) to the specific region of the knee that is causing your pain. This is done by infusing Embozene particles into the specific blood vessel (genicular artery) supplying the area of pain in the knee.

NCT ID: NCT03485157 Completed - Knee Osteoarthritis Clinical Trials

Micronized dHACM vs. Saline in the Treatment of Osteoarthritis of the Knee

Start date: March 27, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of micronized dehydrated human amnion chorion membrane as compared to the 0.9% Sodium Chloride Injection, USP placebo control for the treatment of knee osteoarthritis

NCT ID: NCT03473873 Completed - Knee Osteoarthritis Clinical Trials

Protective Role of Muscle Function for Early Features of Knee Osteoarthritis After Anterior Cruciate Ligament Injury

SHIELD
Start date: March 9, 2018
Phase:
Study type: Observational

In this longitudinal prospective cohort study including young people with anterior cruciate ligament reconstruction (ACLR), the aims are to 1) study the association between different measures of muscle function and early future of knee osteoarthritis (OA) assessed as patient-reported pain, 2) explore potential associations between muscle function and features indicative of early radiographic OA measured with MRI, and early detection of OA in biomarker profiles, respectively, 3) monitor the patients' functional status, and early OA development over time and 4) investigate the prevalence of early knee OA in individuals 1 and 3 years post ACLR, respectively, compared to non-injured controls.The main hypothesis is that knee extensor weakness predicts future symptomatic OA of the knee (KOOS pain).

NCT ID: NCT03448198 Completed - Knee Osteoarthritis Clinical Trials

Validation of a New Technique for the Evaluation of the Patello-femoral Joint Kinematics

CINE-FEMORO
Start date: November 16, 2012
Phase: N/A
Study type: Interventional

The objective of this study is to validate a new technique for intraoperative quantification of the patello-femoral joint kinematics in patients undergoing total knee replacement, and for postoperative quantification of implanted knee and general lower limb activity, along with relevant muscle dynamics.

NCT ID: NCT03434600 Completed - Knee Osteoarthritis Clinical Trials

Comparison of Oxford UKA and Sigma UKA With RSA.

Start date: January 2014
Phase: N/A
Study type: Interventional

Comparison of two unicompartmental knee arthroplasties (UKA), to see if Sigma UKA performs equally good as the Oxford UKA. The study focuses on how well the arthroplasty is fixated to the bone and on the difference in wear of the plastic insert. Finally, the functional outcome after surgery is compared between the two arthroplasties. Hypothesis: H1: The Sigma UKA has an equal migration pattern compared to the Oxford UKA with a follow up of two years - that is, no significant difference in migration between 1-2 years follow-up. H2: The Oxford and Sigma UKA's have comparable polyethylene wear with a follow up of 5 years. H3: The Oxford and Sigma UKA's have comparable patient perceived outcome measures (PROM) and leg extension power (LEP) postoperative. H4: BMD of the proximal tibia does not influence migration of the tibial component

NCT ID: NCT03425019 Completed - Chronic Pain Clinical Trials

Self Transcranial Direct Current Stimulation for Pain in Older Adults With Knee Osteoarthritis

Start date: March 14, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility and preliminary efficacy of two weeks of self Transcranial Direct Current Stimulation (tDCS) for pain in older patients with knee osteoarthritis (OA).