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Osteoarthritis, Knee clinical trials

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NCT ID: NCT02063542 Completed - Knee Osteoarthritis Clinical Trials

CSF Cholinergic Biomarkers and Postoperative Cognitive Change

Start date: July 2014
Phase:
Study type: Observational

Previous study demonstrated that the condition of central cholinergic nerve is important for the postoperative cognitive dysfunction. In present study investigators hypothesized that the acetylcholine concentration in the cerebral spinal fluid is associated to the postoperative cognitive changes in aged patients undergoing osteopathic surgery.

NCT ID: NCT02063373 Completed - Clinical trials for Bilateral Knee Osteoarthritis

Gait, Stair Climbing and Postural Stability in Knee Osteoarthritis Patients After Hyaluronic Acid Injection

Start date: September 2012
Phase: Phase 3
Study type: Interventional

Treatment: five intro-articular Hyaluronic Acid injection Assessment has two parts, that are as follow: 1. Postural stability and risk of fall assessment using Biodex stability index and "Timed up and Go" test 2. Gait and stair climbing assessment using Vicon motion capture system synchronized with four force plates. For knee OA subjects, assessment was done in week one or before injection; and for healthy controls one assessment was performed.

NCT ID: NCT02061410 Completed - Knee Osteoarthritis Clinical Trials

Effects of Neuromuscular Electrical Stimulation (NMES) in Patients With Knee Osteoarthritis

Start date: January 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of neuromuscular electrical stimulation (NMES) on neuromuscular and functional parameters in elderly with knee osteoarthritis. The hypothesis is that NAMES is able to strengthen the quadriceps muscle and to improve healthy status of elderly with knee osteoarthritis.

NCT ID: NCT02050438 Completed - Clinical trials for Total Knee Replacement

How Total Knee Prosthesis Dessigns Influence in Quality of Live

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

The purpose of this study is to determine whether different kind of prostesis designs influences in the quality of life of patients

NCT ID: NCT02049879 Completed - Knee Osteoarthritis Clinical Trials

Daily Activity After Corticosteroids Injection Among Knee Osteoarthritis Patients

Start date: November 2008
Phase: Phase 4
Study type: Interventional

The objective of this study was to objectively measure daily physical activity and spatiotemporal gait pattern, as well as improvements in self reported symptoms and quality of life, before and six weeks after an intra-articular corticosteroids injection in patients suffering from knee osteoarthritis. Fourteen patients with unilateral knee osteoarthritis were recruited. The intra-articular corticosteroid injection was given at the end of the second week. Physical activity was objectively measured by an accelerometer worn by the participants for eight weeks. In addition, the Western Ontario and McMaster Universities Arthritis Index (WOMAC), the Medical Outcome Study Short Form-36 (MOS-SF36) and gait trials were completed every two weeks to assess symptoms, quality of life and spatiotemporal parameters of gait.

NCT ID: NCT02049606 Completed - Clinical trials for Osteoarthritis of the Knee

To Compare the Efficacy and Safety of LAYLA in Osteoarthritis Patients of the Knee

Start date: February 24, 2014
Phase: Phase 4
Study type: Interventional

This is a randomized, double-blind study to compare the efficacy and safety of LAYLA tablet and CENATONE tablet in the treatment of osteoarthritis of the knee.

NCT ID: NCT02049216 Completed - Osteoarthritis Clinical Trials

The Effect of Flexible Tape in Knee Osteoarthritis

FTKOA
Start date: August 2014
Phase: N/A
Study type: Interventional

People with osteoarthritis (OA) of the knee attending The Alfred hospital will be invited to participate in a randomised controlled trial comparing two different types of knee taping. Both groups will also be prescribed an exercise program to assist in management of their knee OA. Hypothesis are as follows: 1. Participants treated with flexible tape with have greater reductions in pain and improvements on timed performance based measures when compared to those treated with a placebo tape. 2. Participants in both groups will have clinically significant improvements in pain and timed performance based measures compared to their baseline scores.

NCT ID: NCT02048956 Completed - Knee Osteoarthritis Clinical Trials

Hydrotherapy Intervention in Elderly With Knee Osteoarthritis

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

Knee osteoarthritis is a common condition characterized by pain and functional disability in older people. Prevalence increases with age and is more frequent in older women. The aim of this study was to assess the effects of an 8-weeks hydrotherapy training with elastic bands on pain and functional disability in old people with knee osteoarthritis.

NCT ID: NCT02046668 Completed - Clinical trials for Osteoarthritis, Knee

The Effect of Spironolactone on Pain in Older People With Osteoarthritis

SPIR-OA
Start date: November 2013
Phase: Phase 4
Study type: Interventional

This pilot study will obtain preliminary evidence on which to base sample size calculations for a future trial of whether spironolactone (an aldosterone blocker) reduces knee pain in older people with symptomatic OA knee when given in addition to usual analgesia. Aldosterone is known to be pro-inflammatory, and spironolactone suppresses cytokine production in chronic arthritis. This application builds on previous work by the applicants showing that spironolactone significantly improved quality of life (particularly pain) in frail older people. The investigators will recruit 86 people (aged 70 years or over) with well-defined OA knee to 25mg spironolactone daily or to matching placebo for 12 weeks. The primary outcome is the between group difference in change in WOMAC pain sub-score at 12 weeks. Secondary outcomes are the WOMAC stiffness and physical function subscales and health related quality of life (EQ-5D). Morning cortisol levels will be measured to assess the effect of mineralocorticoid receptor blockade on glucocorticoid levels, which may mediate the anti-inflammatory effect of spironolactone; and urinary CTX-II, and serum matrix metalloproteinase-3 (MMP-3) will be measured as biomarkers as both are sensitive to the effects of pharmacological interventions for osteoarthritis.

NCT ID: NCT02043613 Completed - Clinical trials for Osteoarthritis, Knee

Context Effects in Exercise Therapy for Knee and/or Hip Pain

CONEX
Start date: February 2014
Phase: N/A
Study type: Interventional

The study is designed to investigate the effect of physical surroundings on the effect of exercise therapy for knee and hip pain.