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Osteoarthritis, Knee clinical trials

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NCT ID: NCT01360281 Recruiting - Knee Osteoarthritis Clinical Trials

Neuromuscular Electrical Stimulation and Strength Training in Patients With Knee Osteoarthritis

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficiency of neuromuscular electrical stimulation and of resisted exercises on increasing quadriceps strength, decreasing pain and on recovering motor function of patients with knee osteoarthritis.

NCT ID: NCT01210742 Recruiting - Knee Osteoarthritis Clinical Trials

The Efficacy of Viscosupplementation for Early Knee Osteoarthritis

EVOKE
Start date: May 2011
Phase: N/A
Study type: Interventional

Treatment for early osteoarthritis (OA) of the knee is an increasing problem yet much of the research into OA, to date, concentrates on predisposition, genetic and cellular aspects and the treatment of late stage disease (arthroplasty). Clinicians reviewing patients with early OA have great difficulty in recommending an appropriate and efficacious intervention. The first line of treatment for patients with early OA is exercise, self-management and weight loss. These tools are suggested to minimize the need for higher risk treatments such as non-steroidal antiinflammatory drugs (NSAIDs) and surgery. Viscosupplementation using intra-articular injections of hyaluronan (Synvisc One) is a relatively new treatment. To date, the ideal patient for viscosupplementation has yet to be defined. It is not known whether incorporation of viscosupplementation into the overall clinical management will have beneficial influence for patients with early OA of the knee. This study will generate rigorous pilot data to assess the need and inform a larger randomized controlled trial (RCT) assessing the efficacy of viscosupplementation. The study will be a single blind randomised RCT. 60 patients with documented early OA will be randomised into one of two groupsÍž Group V will undergo "one shot" viscosupplementation using Synvisc One in addition to routine physiotherapy management for knee OA. Group No V (control) will have no viscosupplementation but will undergo similar routine management including physiotherapy management for knee OA. Outcome measures will include walking pain (The Western Ontario and McMaster Universities Arthritis Index-WOMAC), the overall WOMAC score, Oxford Knee Score (OKS), American Knee Society score (AKS), complications, activity level and patient satisfaction. Health economics will also be evaluated. Measurements will be recorded pre-intervention and at six months following treatment. The risks associated with viscosupplementation are minimal. Considering the limited resources currently available in health care, if the latter is shown to have higher effectiveness than physiotherapy alone, in addition to patient benefit, there will be important health economic implications.

NCT ID: NCT01159899 Recruiting - Osteoarthritis Clinical Trials

Transplantation of Bone Marrow Stem Cells Stimulated by Proteins Scaffold to Heal Defects Articular Cartilage of the Knee

Start date: July 2010
Phase: Phase 0
Study type: Interventional

The purpose of this pilot study is to investigate the efficacy and safety of autologous transplantation, under arthroscopy, of Bone Marrow Mesenchymal stem cells, using, with a cell separator, a fresh non-culture expanded Autologous Bone Marrow derived Mesenchymal Stem, mixed and activated with proteins scaffold in patient with Knee cartilage defects and osteoarthritis. Based on extensive preclinical investigations, the technology of using freshly isolated bone marrow mononuclear cells mixed with proteins seems safe and most effective for a one-step correction of cartilage defect and restoration of the osteochondral complex, because the same mixture can generate cartilage in the vasculature-free knee joint, and bone in the environment of bone defects.

NCT ID: NCT01020591 Recruiting - Knee Osteoarthritis Clinical Trials

The Effect of Osteopathic Manual Therapy on the Vascular Supply to the Lower Extremity, Function and Symptoms of Subjects With Knee Osteoarthritis

Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of osteopathic manual therapy can influence the vascular supply to the knee, knee range of motion, balance and knee pain, in a group of subjects with knee osteoarthritis. It is also the objective of this study to determine if there is a difference between the osteopathic evaluation and the combination of an osteopathic evaluation and treatment.

NCT ID: NCT00991445 Recruiting - Knee Osteoarthritis Clinical Trials

Minimal Versus Conventional Exposure in Unicompartmental Knee Arthroplasty

Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Minimal Invasive Surgery results in less postoperative pain and better mobilization than conventional technique in Unicompartmental Knee Arthroplasty, provided that both groups receive Local Infiltration Analgesia.

NCT ID: NCT00954629 Recruiting - Pain Clinical Trials

A Study of the Efficacy and Safety of 2PX in Patients With Pain Due to Osteoarthritis of the Knee

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The purpose of the study is to demonstrate the superiority of topically administered 2PX versus placebo (vehicle) control in terms of reduction in pain intensity and physical function.

NCT ID: NCT00724139 Recruiting - Knee Osteoarthritis Clinical Trials

The Effect of Training With Custom-Made Biomechanical Perturbation Platform on Kinetics, Kinematics and Electromyography in Knee Osteoarthritis Patients

Start date: January 2008
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the outcome of specific repetitive biomechanical perturbation training on motor patterns. The first hypothesis of this project is that footwear derived biomechanical challenges will convey active and passive matching biomechanical responses (i.e. kinetic, kinematic and electromyographic) trough out the musculoskeletal kinematic chain. The second hypothesis of the project is that repetitive exposure to in-situ (trough out the gait sickle) introduction to a biomechanical stimulus would generate a process of motor learning thus conveying plasticity of existing locomotor patterns and gait strategies.

NCT ID: NCT00599729 Recruiting - Knee Osteoarthritis Clinical Trials

Measurement of Gait Spatio-Temporal Characteristics in Knee Osteoarthritis Patients

Start date: January 2008
Phase: N/A
Study type: Observational

The purpose of the study is to evaluate the gait spatio-temporal parameters of patients with degenerative changes in the knee joint and to relate them with 2 questionares (WOMAC and SF-36).

NCT ID: NCT00393393 Recruiting - Osteoarthritis Clinical Trials

Effectiveness Study of Hylan G-F 20 to Preserve Cartilage in Osteoarthritis of the Knee

Start date: January 2006
Phase: Phase 4
Study type: Interventional

That Hylan G-F 20 may act to protect cartilage from the expected degree of degradation over a 12 month period in subjects with moderate to marked osteoarthritis of the knee

NCT ID: NCT00294528 Recruiting - Clinical trials for Osteoarthritis, Knee

Comparing Clinical Outcome of 2 Different Total Knee Prostheses: Nexgen LPS-Flex Versus AGC

Start date: January 2004
Phase: Phase 4
Study type: Interventional

A randomized blinded study is conducted comparing 2 different knee prostheses. Range of motion (ROM), pain, feel of prosthesis, satisfaction and ability to do daily activities are registered at intervals up to one year postop, where patients are informed on which prosthesis they received. We want to: - determine whether an increased ROM is achieved with a high-flex knee compared to a standard knee - and if so, does it matter