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Knee Osteoarthritis clinical trials

View clinical trials related to Knee Osteoarthritis.

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NCT ID: NCT01478386 Terminated - Knee Osteoarthritis Clinical Trials

Effectiveness of a Knee Brace When Combined With Viscosupplementation in the Treatment of Knee Osteoarthritis

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

Hypothesis: Viscosupplementation when combined with an off-loading knee brace is more effective in treating the symptoms of knee OA then treating with viscosupplementation alone

NCT ID: NCT01457742 Terminated - Knee Osteoarthritis Clinical Trials

Effectiveness Study of the Ivivi SofPulse for Pain Amelioration in Adults With Mild to Moderate Knee Osteoarthritis

Start date: October 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effectiveness of non-thermal Pulsed Radio Frequency (PRF) treatment with the Ivivi SofPulse for amelioration of knee pain in patients with mild to moderate Osteoarthritis and to determine the duration of clinical benefit following discontinuation of treatment.

NCT ID: NCT01447303 Terminated - Knee Osteoarthritis Clinical Trials

Functional and Quality of Life Outcomes Following Viscosupplementation for Knee Osteoarthritis

Start date: August 2009
Phase: N/A
Study type: Observational

This study will compare changes in outcomes following viscosupplementation for knee osteoarthritis.

NCT ID: NCT01382173 Terminated - Knee Osteoarthritis Clinical Trials

Monitoring Of Helsingborg Acute Knee Injuries (MOHAK)

Start date: March 2012
Phase:
Study type: Observational

Using magnetic resonance imaging (MRI), laboratory analyses and patient reported outcomes, the overall aim of this study is to investigate structural injuries and biochemical alterations in the acutely injured knee and to relate these findings to clinical outcomes at various time points.

NCT ID: NCT00988468 Terminated - Knee Osteoarthritis Clinical Trials

Manual Therapy Versus Exercise on Knee Osteoarthritis

Start date: October 2009
Phase: Phase 2
Study type: Interventional

Earlier research has shown that exercising while receiving manual therapy improves function and reduces pain in people with knee osteoarthritis. However, very little is known about the mechanisms by which manual therapy and exercise reduce pain and improve function. This study will ask subjects with knee osteoarthritis to receive one of the following interventions: (1) no treatment, (2) exercise only, or (3) manual therapy only. Measures will be taken of the patient's knee range of motion, knee swelling and pain before and after receiving the intervention. These measures will be analyzed to determine what effect exercise and manual therapy applied to the knee have on improving knee range of motion and reducing knee pain and swelling. Swelling will be measured using an ultrasound device which is used to take pictures inside the knee. This type of ultrasound measurement is painless and harmless.

NCT ID: NCT00983762 Terminated - Knee Osteoarthritis Clinical Trials

Comparison of Functional Outcomes of Three Surgical Approaches in Knee Arthroplasty

Start date: June 2009
Phase: N/A
Study type: Observational

A functional outcomes comparison study of three surgical techniques using minimally invasive surgery mini-incision (MIS) for total knee arthroplasty (TKA), standard para-patellar TKA and the unicompartmental knee arthroplasty performed over a 2+ year post-op period.

NCT ID: NCT00771082 Terminated - Knee Osteoarthritis Clinical Trials

Osteoarthritis and Body Composition: Evaluation of Systematic Mediators

Start date: January 2003
Phase: N/A
Study type: Observational

The purpose of this study is to examine the relationship between body composition and knee osteoarthritis, and effects of inflammatory, metabolic, and hormonal factors.

NCT ID: NCT00734110 Terminated - Knee Osteoarthritis Clinical Trials

Long-term Study of The Press Fit Condylar (P.F.C.) Sigma Total Knee Replacement System

Start date: July 2000
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to record information from clinical and radiographic examinations and patient assessment questionnaires before surgery and at suitable postoperative intervals to assess the functioning and symptomology of each knee following surgery. In addition, any adverse events or complications are to be recorded, and any device failures or early revisions are to be recorded and reported directly to the Sponsor. The data are to be used in an evaluation of the performance of the P.F.C. Sigma knee implants over a minimum of 5 years.

NCT ID: NCT00733369 Terminated - Knee Osteoarthritis Clinical Trials

A Study to Compare the Press Fit Condylar (P.F.C.) Sigma Rotating-platform High-flexion (RP-F) Versus The Press Fit Condylar (P.F.C.) Sigma Rotating-platform (RP) Knee Implants

Start date: November 2007
Phase: Phase 4
Study type: Interventional

The main objective of this study is to determine if the P.F.C. Sigma RP-F Knee delivers a greater post-operative range of motion (ROM) compared with the P.F.C. Sigma RP Knee in primary TKA. The secondary objectives of this investigation are to evaluate the clinical and patient outcomes and survivorship associated with the DePuy P.F.C. Sigma RP-F and RP Posterior Stabilised (PS) Knee over 5 years.

NCT ID: NCT00521989 Terminated - Knee Osteoarthritis Clinical Trials

CRx-102 Osteoarthritis Multicenter Evaluation Trial

COMET-1
Start date: August 2007
Phase: Phase 2
Study type: Interventional

CRx-102 is a synergistic combination drug candidate containing the cardiovascular drug dipyridamole and a very low dose of the glucocorticoid prednisolone. CRx-102 is believed to work through a novel mechanism of action in which dipyridamole selectively amplifies the anti-inflammatory and immunomodulatory activities of the glucocorticoid without replicating the dose-dependent adverse effects. CRx-102 has been associated with clinical benefit in proof of concept studies in subjects with hand OA and RA. This is the first study to explore the efficacy of CRx-102 in knee OA. It is considered a dose-finding study and will also compare the potential benefits of CRx-102 treatment to both prednisolone administered alone and to placebo in this indication.