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Osteoarthritis, Knee clinical trials

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NCT ID: NCT00435773 Completed - Osteoarthritis Clinical Trials

Leeches for the Treatment of Knee Osteoarthritis

Start date: February 2004
Phase: Phase 2
Study type: Interventional

Previous studies have not addressed the question, whether or not a repeated leeching can supply symptomatic relief of osteoarthritic pain for extended periods of time. We present a randomized study to the effectiveness of single and repeated leech therapy in cases with advanced osteoarthritis of the knee using a large patient group compared to a control group, who were both blinded to the actual treatment modality.

NCT ID: NCT00435292 Completed - Osteoarthritis Clinical Trials

Study of Flavocoxid (Limbrel) vs Naproxen in Subjects With Mod-Severe Osteoarthritis of the Knee

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

Randomized, double-blind, placebo controlled parallel group, multi center study in subjects with moderate-severe osteoarthritis.

NCT ID: NCT00433290 Completed - Clinical trials for Osteoarthritis Knee Pain

Duloxetine vs. Placebo in the Treatment of Osteoarthritis Knee Pain

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

The primary purpose of this study is to determine if duloxetine reduces pain severity in patients with osteoarthritis knee pain.

NCT ID: NCT00427843 Completed - Clinical trials for Osteoarthritis, Knee

The Influence of Hip Strengthening Exercises on Walking Patterns and Muscle Strength in Persons With Knee Osteoarthritis

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the influence of a home program of exercises for the hip muscles which support the pelvis on walking patterns and hip muscle strength in people with knee osteoarthritis. Following a hip muscle strengthening program, we hypothesize that participants with knee osteoarthritis will demonstrate decreased loading at the knee joint during walking and greater strength of the hip muscles.

NCT ID: NCT00426907 Completed - Clinical trials for Osteoarthritis, Knee

Weightbearing After High Tibial Osteotomy

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

In this project we want investigate the clinical results after different rehabilitation regimens(Limited or unlimited weightbearing after surgery) in Open-wedge High Tibial Osteotomies. The hypothesis is that unlimited weightbearing is beneficial for the healing and rehabilitation.

NCT ID: NCT00426621 Completed - Clinical trials for Osteoarthritis of the Knee

Efficacy and Safety of Diclofenac Sodium Gel (DSG) in Knee Osteoarthritis

Start date: November 2006
Phase: Phase 3
Study type: Interventional

This study will test the efficacy and safety of topical diclofenac sodium gel in the treatment of knee osteoarthritis.

NCT ID: NCT00422643 Not yet recruiting - Clinical trials for Osteoarthritis of the Knee

The Effect of Intraaricular Knee Injections of Hyaluronic Acid (HA) on Bone and Cartilaginous Debris, as a Therapeutic Indicator

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

Osteoarthritis is the most common disease effecting human beings with incidence of about 20% and prevalence close to 80% of the adult population. It is most common after the age of 60 years and more in females with the ratio 4:1 F:M. Osteoarthritis Can be present in every hyaline joint, but is mostly damaging to the weight bearing joints, the knees and hips. At the final stage of cartilage destruction (from wear and tear) joint replacement is the solution. Since these operations were introduced about 50 years ago, the indications and the number of yearly procedures has been increasing with alarming speed. Last year in the united states, about 500,000 Total Knee procedures were done, exceeding Total Hip replacements. By 2030, close to 4.5 million joint replacement procedures are expected in the United States, the majority of which will be knee replacements. Joint replacement is the solution for the final stage of damaged cartilage. In early and advanced stages of cartilage wear and specifically in the knee H.A. acts as an anti inflammatory and lubricant agent, reducing the knee pain and improving knee motion and function. The biological effect of H.A. is well documented in clinical studies and less with scientific evidence derived from patients themselves. Our study proposal briefly is, as follows: 60 patients with evidence of osteoarthritis of the knees will join the study after I.R.B. (Helsinki Committee) approval. All of them will be examined, x-rays will be performed and blood tests will exclude patients with infections or inflammatory disease. A V.A.S. (Visual Analog Score) and SF-36 evaluation form will be completed prior to each intraarticular injection, in addition to a complete medical examination. The enrolled patients will receive the usual three intraarticular knee injections of H.A.(Arthrease), but prior to each injection, the joint will be aspirated and the joint fluid will be analyzed for Chondroitin sulfate type I and type II as described further in this project. Three and six months after the third initial injections, the patients will recalled and joint fluid will be aspirated again, followed by an H.A. injections, if symptomatic. This study is the only one ever proposed, for evaluating joint debris qualitatively and quantitatively. It will provide clinical information as well as objective data on the preservation of the joint cartilage. Hopefully, this study will provide additional information such as the relationship between the presence of debris and symptomatic vs. asymptomatic patients. It may help in determining how long the injected H.A. has an effect and whether serial and periodical injections are indicated. Inclusion criteria: 1. patients with the diagnosis of Osteoarhtritis of the knee, graded according to Kellgren as grade 1-4 Exclusion criteria: 1. Patients that suffer from acute septic arthritis. 2. Patients that treated with coumadin and/or other anti-coagulant drugs 3. Patients that show mental or physical conditions, which preclude compliance with study and/or device.

NCT ID: NCT00421928 Completed - Pain Clinical Trials

Tapentadol (CG5503)

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

The purpose of this trial is to evaluate the effectiveness (level of pain control) and safety of orally administered tapentadol (CG5503) Extended Release (ER) (base) at doses of 100-250 mg twice daily in patients with moderate to severe chronic pain due to osteoarthritis of the knee, in comparison with placebo and Oxycodone Controlled Release (CR).

NCT ID: NCT00420147 Completed - Knee Osteoarthritis Clinical Trials

Wedged Orthoses and Knee Osteoarthritis

Start date: February 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The five-year goal of this project is to investigate the effect of in-shoe wedged orthoses on lower extremity function in patients with knee osteoarthritis. In general, our aims address the immediate effects of orthoses, the long-term effects of orthoses, and the immediate and long-term treatment effects comparing medial versus lateral wedged orthoses. The investigators hypothesize the wedged orthosis will result in altered gait mechanics that reflect a reduction in knee joint forces, reduced knee joint pain and increased function during weight bearing activities.

NCT ID: NCT00417859 Completed - Knee Osteoarthritis Clinical Trials

Total Knee Arthroplasty: Comparison of Fixed and Mobile Bearings

Start date: February 2004
Phase: N/A
Study type: Interventional

The goal of this study is to provide gait parameters as a new objective method to assess total knee arthroplasty outcome between patients with fixed- and mobile-bearing, using an ambulatory device with minimal sensor configuration.