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Osteoarthritis, Knee clinical trials

View clinical trials related to Osteoarthritis, Knee.

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NCT ID: NCT01331174 Completed - Knee Osteoarthritis Clinical Trials

Pulsed Short Wave in Females With Knee Osteoarthritis

PSW
Start date: August 2006
Phase: N/A
Study type: Interventional

Study design: Randomized clinical trial. Objective: To evaluate the effect of PSW treatment in different doses and to compare to the control and placebo group. Background: Several forms of conservative treatment have been the focus of many recent studies in knee osteoarthritis (OA). Among these techniques, the application of pulsed short wave has been widely used, but the optimal dose and application time still have not been well established.

NCT ID: NCT01328340 Completed - Knee Osteoarthritis Clinical Trials

High-speed Power Training in Older Adults With Knee Osteoarthritis (OA)

Start date: June 2005
Phase: N/A
Study type: Interventional

We are exploring a unique weight-training program for men and women 55 years or older with knee osteoarthritis (OA) that emphasizes high-speed movements. We believe that the speed at which muscles move may be more important to the improvement of muscle performance, function and pain than how strong the muscles are. We are comparing high-speed power training with traditional strength training to determine which method has the greatest effects on muscle strength, muscle power, speed of movement, functional performance and pain. We believe that high-speed training will improve these measures to a greater extent than simply training for increased muscle strength.

NCT ID: NCT01326156 Active, not recruiting - Clinical trials for Osteoarthritis, Knee

Study of Knee Replacements for Patellofemoral Osteoarthritis

PFA/TKR
Start date: June 2007
Phase: N/A
Study type: Interventional

This is a randomized comparison of PFA and TKR in treatment of isolated patellofemoral osteoarthritis.

NCT ID: NCT01320904 Completed - Clinical trials for Osteoarthritis, Knee

Exercise and Muscle Stimulation in Patients With Knee Osteoarthritis

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

Objective: To evaluate the effectiveness of neuromuscular electrical stimulation (NMES) combined with closed kinetic chain (CKC) exercises in patients with knee OA.

NCT ID: NCT01319929 Completed - Clinical trials for Osteoarthritis, Knee

A Study of LY2828360 in Patients With Osteoarthritic Knee Pain

Start date: March 2011
Phase: Phase 2
Study type: Interventional

To investigate the safety, efficacy and pharmacokinetics of single daily oral dose of LY2828360 in male and female subjects with osteoarthritic knee pain

NCT ID: NCT01319461 Completed - Osteoarthritis Clinical Trials

Efficacy and Safety of Intraarticular Injections of Hyalgan in the Treatment of Osteoarthritis of the Knee

Start date: May 2001
Phase: Phase 3
Study type: Interventional

Evaluate the efficacy and safety of Hyalgan, at a dose of 20mg/2ml administered as 5 intraarticular injections at weekly intervals, for the sustained relief of pain and amelioration of joint dysfunction in patients of OA of the knee.

NCT ID: NCT01314820 Completed - Knee Osteoarthritis Clinical Trials

Effects of Joint Effusion on Quadriceps Muscle

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

The present study investigated whether the presence of fluid in the joint affected peak torque and the root mean square (RMS) values of surface electromyography (EMG) in patients symptomatic for osteoarthritis (OA).

NCT ID: NCT01311804 Not yet recruiting - Clinical trials for Unilateral Primary Osteoarthritis of Knee

An Efficacy and Safety Study of Periarticular Parecoxib Sodium for Pain Management in Total Knee Arthroplasty

Start date: April 2011
Phase: Phase 3
Study type: Interventional

Primary Research Objective: The primary objective of this study is to determine efficacy of periarticular parecoxib sodium in a multimodal cocktail versus intravenous parecoxib injections for pain management in total knee arthroplasty Secondary Research Objective: - To determine if perioperative use of parecoxib sodium was associated with improved clinical outcomes - To evaluate the safety, in terms of adverse events; serious adverse events and tolerability of parecoxib sodium in periarticular injections in a multimodal cocktail

NCT ID: NCT01311206 Completed - Knee Osteoarthritis Clinical Trials

Low Intensity Resistance Training With Partial Blood Flow Restriction for Quadriceps Strengthening

PBFR
Start date: February 2011
Phase: N/A
Study type: Interventional

The objective of the proposed research is to assess the efficacy of an eight-week, efficient and tolerable, low-intensity resistance-training program with concurrent application of partial blood flow restriction (PBFR) for improving quadriceps strength and volume in women with risk factors for incident symptomatic or progressive knee OA. This specific aim will be achieved through a randomized, controlled trial, comparing low intensity training with and without PBFR. There have been numerous reports of exercise interventions in people with knee osteoarthritis. However, this research is novel in that it will be the first to use a low intensity regimen that will minimize forces on the knee while still having the potential to lead to clinically meaningful strength gains in older adults with risk factors for incident symptomatic or progressive knee OA.

NCT ID: NCT01310257 Completed - Clinical trials for Osteoarthritis of the Knee

Measures of Pain Relevant to Knee Osteoarthritis

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

The aim is to improve understanding of the assessment of pain experience in patients with osteoarthritis (OA) of the knee. The current study will be divided into two parts. In Study 1, the investigators will analyse existing questionnaires relevant to the mechanisms and therapeutic targets of knee OA to establish discrete dimensions that discriminate between the different mechanisms of pain. On the basis of this analysis, the investigators will refine the questionnaires to maximise their sensitivity to knee OA. In Study 2, the investigators will seek to confirm the factor structure identified in the questionnaires in Study 1 and explore potential mediator and moderator variables between pain and quality of life using the refined measures. The investigators will also evaluate Quantitative Sensory Testing as a predictor of OA knee pain.