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Arthritis clinical trials

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NCT ID: NCT00555542 Completed - Clinical trials for Rheumatoid Arthritis

An Analysis of Peripheral Blood T Cell Subsets on Rheumatoid Arthritis

Start date: July 2006
Phase: Phase 2
Study type: Interventional

To study the effects of T cell in peripheral blood of patients with RA undergoing selective B cell depletion have not been studied. We analyze the B and T cell subsets in patients with active RA treated undergoing this form of treatment with rituximab.

NCT ID: NCT00555230 Completed - Clinical trials for Rheumatoid Arthritis

Effects of HMG-coA Reductase Inhibitor on Rheumatoid Arthritis

Start date: July 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is: 1. To evaluate the prevalence of preclinical atherosclerosis in Chinese patients with RA compared to healthy controls. 2. To determine those clinical and biological measures that best predict the presence of plaque and increased arterial stiffness. 3. To ascertain the efficacy and safety of rosuvastatin in the prevention of atherosclerosis in patients with RA measured by carotid intima-media thickness (IMT) and pulse wave velocity (PWV).

NCT ID: NCT00554853 Completed - Clinical trials for Rheumatoid Arthritis

PPAR-gamma Agonists, Rheumatoid Arthritis and Cardiovascular Disease

RA PPAR
Start date: November 2007
Phase: Phase 3
Study type: Interventional

Patients with rheumatoid arthritis have a significantly higher risk to develop heart attacks and other complications of their blood vessels. New therapies are needed to prevent this complication. The purpose of this study is to establish the role of the medication pioglitazone in improving the function of the blood vessels and heart and decreasing the risk of future atherosclerosis development in individuals with rheumatoid arthritis. As a secondary aim-point, we will evaluate the efficacy of pioglitazone in improving rheumatoid arthritis disease activity and markers of inflammation.

NCT ID: NCT00554606 Completed - Clinical trials for Rheumatoid Arthritis

Long-term Efficacy, Safety and Tolerability of ACZ885 in Patients With Rheumatoid Arthritis

Start date: October 11, 2007
Phase: Phase 2
Study type: Interventional

This study will assess the long-term safety and tolerability of ACZ885 in patients with rheumatoid arthritis, as well as long-term efficacy, long-term preservation and/or improvement of joint structure and bone mineral density, and long term maintenance of health-related quality of life.

NCT ID: NCT00552136 Recruiting - Ankle Arthritis Clinical Trials

Canadian Orthopaedic Foot and Ankle Society Surgical Treatment of Ankle Arthritis Outcome Study

Start date: February 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see if the clinical outcome success rate of Total Ankle Arthroplasty is similar to that of Ankle Arthrodesis over a period of 10 years. This will include looking at whether Total ankle arthroplasty results in a lower rate of hindfoot arthrosis and arthritis after surgery compared to ankle joint arthrodesis and if the rate of complications and revision surgery is acceptable when compared to Ankle Arthrodesis over a period of 10 years.

NCT ID: NCT00551707 Completed - Clinical trials for Rheumatoid Arthritis

Multicenter Study to Evaluate CRx-102 vs. Each of Its Components to Treat Active Rheumatoid Arthritis

MARS-1
Start date: October 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 Osteoarthritis (OA) and Rheumatoid Arthritis (RA). In this trial, CRx-102 will be given to subjects with active RA as an add-on therapy to existing stable doses of Disease Modifying Anti-Rheumatic Drugs (DMARDs) including methotrexate (MTX), sulfasalazine, hydroxychloroquine, leflunomide or azathioprine. MTX in combination with other DMARDs (e.g., sulfasalazine or hydroxychloroquine) will be permitted to reflect the current standard of care practices within rheumatology.

NCT ID: NCT00550446 Completed - Clinical trials for Arthritis, Rheumatoid

A Phase 2 Study For Patients With A Physician's Diagnosis Of Rheumatoid Arthritis

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effectiveness and safety, over 6 months, of 5 doses of CP-690,550 for the treatment of adults with active rheumatoid arthritis. Five out of seven subjects will receive CP-690,550. One out of seven will receive adalimumab (Humira®) and one out of seven will only receive inactive substances (placebo.)

NCT ID: NCT00550355 Completed - Clinical trials for Arthritis, Rheumatoid

Dose-Escalating Multiple Dose Study of PD-0360324 in Combination With Methotrexate in Patients With Rheumatoid Arthritis

Start date: August 2007
Phase: Phase 1
Study type: Interventional

This study is designed to evaluate the safety and tolerability of multiple intravenously administered doses of PD 0360324 in patients with rheumatoid arthritis receiving methotrexate.

NCT ID: NCT00550043 Completed - Clinical trials for Rheumatoid Arthritis

A Study Exploring the Safety, Tolerability and Efficacy of a 4 Week Course of INCB018424 in Subjects With Active Rheumatoid Arthritis

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to understand the safety and tolerability of INCB018424 in patients with rheumatoid arthritis

NCT ID: NCT00549549 Completed - Arthritis, Gouty Clinical Trials

Celebrex In Acute Gouty Arthritis Study

Start date: February 2008
Phase: Phase 3
Study type: Interventional

This is a multicenter, double-blind, double-dummy, randomized, active-controlled study that will include an 8-day treatment period followed by a 1-week follow-up period in patients experiencing symptoms of an acute exacerbation of gouty arthritis.