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Knee Osteoarthritis clinical trials

View clinical trials related to Knee Osteoarthritis.

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NCT ID: NCT01245283 Completed - Knee Osteoarthritis Clinical Trials

Resistance Exercise and Knee Osteoarthritis Pain, Functional Impairment and Cartilage Turnover

Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a 4 month resistance exercise program can reduce knee osteoarthritis pain functional impairment and cartilage turnover.

NCT ID: NCT01241812 Completed - Knee Osteoarthritis Clinical Trials

Biomarkers and Knee Osteoarthritis

Start date: October 2010
Phase: N/A
Study type: Interventional

High joint load during walking has been linked to cartilage degradation. Biomarkers, found in the blood and urine, are protein fragments released after cartilage degradation characteristic of OA. They have the potential to enable direct and immediate disease state monitoring and identification of early cartilage changes. Little is known about the association of biomarkers with joint load or if exercise aimed at reducing joint load changes biomarker levels, thus reducing the risk of OA progression. This study will provide novel information on these relationships and will guide future intervention studies. The investigators hypothesize that certain biomarkers will be highly correlated with joint loading during walking and that the levels of these biomarkers in the blood and urine will decrease following an exercise intervention aimed at cartilage unloading.

NCT ID: NCT01239823 Completed - Knee Osteoarthritis Clinical Trials

Platform Exercise Training

Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this randomized, controlled trial is to determine whether a vibration platform exercise program will be more effective than a standard platform exercise program in improving quadriceps strength in women age 45-60 who have risk factors for knee osteoarthritis. Each platform exercise program will be conducted 2 times a week for 12 weeks. The sessions will consist of a series of exercises on a Wave Pro-elite vibration platform (with 1-3 minute rests between sets) and stretches with the platform vibration either turned on (intervention group) or off (control group.) Quadriceps strength (primary outcome), leg press power, and vibration sense will be assessed at baseline and 12 weeks, and changed scores will be compared between groups.

NCT ID: NCT01237405 Completed - Knee Osteoarthritis Clinical Trials

A Study of FolateScan in Patients With Knee Osteoarthritis

Start date: October 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate 99mTc - EC20 imaging (FolateScan), a Nuclear Medicine imaging technology that enables localization of activated macrophages in the joints of participants with knee osteoarthritis (OA). Twenty five participants with symptomatic unilateral or bilateral knee OA will undergo a one-time evaluation of the knee as follows: knee radiography, FolateScan of the knees and whole body, musculoskeletal exam, questionnaires, sampling of blood, urine and synovial fluid for analysis of inflammatory markers. Data analysis will be cross-sectional and include a comparison of the location and intensity of EC20 uptake with the following: radiographic knee OA severity, clinical measures of disease severity, cytokine expression, and synovial fluid cell count.

NCT ID: NCT01226615 Unknown status - Knee Osteoarthritis Clinical Trials

Assessment of the Effects of Chondroitin Sulphate in Patients With Knee Osteoarthritis With Functional Magnetic Resonance Imaging (fMRI)

Start date: October 2010
Phase: Phase 4
Study type: Interventional

The main purposes of this study are: - to determine the effects of chondroitin sulphate on brain response to pain assessed through fMRI in patients with knee osteoarthritis. - to investigate the relationship between treatment response detected by fMRI and the results of the different parameters of clinical assessment.

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: NCT01210183 Completed - Knee Osteoarthritis Clinical Trials

Biological Response of Stage IV Knee Osteoarthritis to Serial 12.5% Dextrose

Start date: July 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Dextrose injection in end-stage knee arthritis will cause growth of cartilage cells in a particular area of complete cartilage loss. Dextrose concentration will be 12.5%. Cartilage status will be monitored by pre and post treatment arthroscopy views with specialized (methylene blue) staining for cartilage.

NCT ID: NCT01209364 Completed - Knee Osteoarthritis Clinical Trials

Durolane Versus Methylprednisolone in Knee Osteoarthritis

Start date: March 2007
Phase: Phase 3
Study type: Interventional

The primary objective is to determine whether Durolane is non-inferior to methylprednisolone, as assessed by level of pain, when each are given as single intra-articular injections for the relief of pain, in the treatment of symptomatic osteoarthritis of the knee at 12 weeks.

NCT ID: NCT01194817 Active, not recruiting - Knee Osteoarthritis Clinical Trials

A Prospective, Randomized Study Comparing Cemented and Cementless Total Knee Replacement

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the the Nexgen knee replacement system using cementless fixation with the same system using cemented fixation. At minimum 2-year follow-up, the hypothesis is that NexGen total knee arthroplasties using cementless and cemented fixation will demonstrate no differences in clinical outcome based on Oxford and Knee Society scores, patient-assessed visual analog pain, clinical complications, radiographic fixation and implant survivorship.

NCT ID: NCT01192334 Completed - Knee Osteoarthritis Clinical Trials

Changes of the Single Limb Standing Balance After Total Knee Arthroplasty in Degenerative Osteoarthritis

Start date: September 2010
Phase: N/A
Study type: Observational

It was well known that total knee arthroplasty could improve the previously impaired proprioception in degenerative osteoarthritis. Most current researches have been focused on the change of the proprioception. However, the evaluation of the proprioception is based on the surrogated end. Double or single limb standing balance is considered functional scale. It is very important view for the prevention of slipping down injury in evidence-based approaches for knee osteoarthritis. Unfortunately, few study have been performed for figuring proprioceptive change after surgery out. Considering the similarity between the proprioception and the standing balance and reported positive result in proprioception after total knee arthroplasty, the investigators supposed that total knee arthroplasty might give an influence on the recovery of single limb standing balance.