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Arthritis clinical trials

View clinical trials related to Arthritis.

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NCT ID: NCT01618955 Completed - Clinical trials for Rheumatoid Arthritis (RA)

Actual Human Use of Methotrexate (MTX) Subcutaneously Administered Via the VIBEX™ MTX Auto-Injector Device

Start date: May 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the usability of the VIBEX MTX device for SC self-injection of methotrexate.

NCT ID: NCT01618019 Completed - Clinical trials for Rheumatoid Arthritis

N-3 PUFA and Rheumatoid Arthritis in Korea

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

The purpose of this study is to see if supplementation of n-3 polyunsaturated fatty acid (PUFA) can be beneficial for the patients with rheumatoid arthritis.

NCT ID: NCT01617421 Completed - Clinical trials for Rheumatoid Arthritis

Yoga as Self-Care for Arthritis in Minority Communities

Start date: May 31, 2012
Phase: N/A
Study type: Interventional

Background: - People with arthritis should be active. Regular exercise leads to less pain, more energy, improved sleep, and better day-to-day function. Yet arthritis is one of the most common reasons people give for limiting activities. - Yoga for arthritis has been studied before. However, few studies have included minorities. Making changes to yoga classes based on language and culture may help people use yoga to care for their arthritis symptoms. Researchers want to see if minority populations with arthritis will come to and benefit from yoga classes. Objectives: - To see if yoga classes designed for people with arthritis will be acceptable to minorities with arthritis. Eligibility: - Adults at least 18 years of age who are enrolled in the Natural History of Rheumatic Disease in Minority Communities study. - Participants will have osteoarthritis or rheumatoid arthritis. - Participants will be able to speak and read English or Spanish. Design: - The total study period covers 10 weeks. - The first study visit will include an initial questionnaire about health and arthritis. Participants will also have a physical exam. - Participants will have yoga classes twice a week for 8 weeks. The classes will be 1 hour long each. - After completing the yoga classes, participants will complete another questionnaire about their health. They will have a final physical exam. - Follow-up contact will be made 3 months after the end of the study.

NCT ID: NCT01617005 Completed - Clinical trials for Rheumatoid Arthritis

An Observational Study of RoActemra (Tocilizumab) in Patients With Active Rheumatoid Arthritis and an Inadequate Response to Non-Biological DMARDs

Start date: May 2012
Phase: N/A
Study type: Observational

This observational study will evaluate the safety and efficacy of RoActemra (tocilizumab) in patients with active moderate to severe rheumatoid arthritis and an inadequate response to non-biologic disease-modifying anti-rheumatic drugs (DMARDs). Data will be collected from each eligible patient initiating RoActemra treatment over 6 months.

NCT ID: NCT01616641 Completed - Clinical trials for Rheumatoid Arthritis

Orofacial Evaluation in Women With Rheumatoid Arthritis

Start date: June 2011
Phase: N/A
Study type: Observational

Rheumatoid arthritis (RA) can affect any synovial joint. Unlike the hand, ever so valued in the physical examination of patients with RA, the joints in the area of the jaw and neck may also be affected in this disease and have their involvement usually underdiagnosed. There are few studies evaluating the incidence of orofacial alteration in the examination as well as the correlation between bite force (BF) and clinical and functional parameters in these patients. The aim of our study was to chacacterize the orofacial alterations in RA patients, correlate the results of the orofacial evaluation with clinical and disease activity parameters, and correlate the bite force with the hand strenght.

NCT ID: NCT01616433 Completed - Hypertension Clinical Trials

Arthritis Foundation Exercise Program & "10 Keys" to Healthy Aging--Prevention Research Center

AFEP+10 Keys
Start date: March 2012
Phase: Phase 2
Study type: Interventional

Older adults are at high risk for loss of independence because of age-related chronic health conditions. Of these chronic conditions, arthritis accounts for the largest proportion of the disability in the community. The investigators propose to target older adults who have self-reported arthritis or joint pain for dissemination of a disability prevention program. The program will be a collaborative effort of the Arthritis Foundation, the investigators Prevention Research Center staff and other key partners in the community. The project will develop information needed to provide guidance for implementation of the investigators intervention by other agencies and organizations. As a major thrust of the investigators CDC Prevention Research Center, the investigators have developed a comprehensive program focused on preventing disease and disability in older adults: the "10 Keys to Healthy Aging". Each of the 10 Keys disseminates proven approaches and current recommendations for prevention in older adults, focusing on age 65+ but also addressing age 50-65 years. The overall objective is to determine if an integrated evidence based exercise intervention (AFEP) combined with health education on preventive practices for older adults ("10 Keys") is more effective for improving mobility and risk factors for mobility disability and use of preventive services compared to exercise alone (AFEP). The investigators will also propose to evaluate the impact of geographic location on outcomes and overall sustainability of the program.

NCT ID: NCT01615991 Completed - Arthritis Clinical Trials

Multicentre Canadian Study to Measure the Safety and Efficacy of Radiosynoviorthesis

RSO
Start date: May 31, 2012
Phase: Phase 3
Study type: Interventional

Radiation synovectomy by intra-articular injection of beta-emitting radionuclides is considered a reliable and easy-to-perform therapy without harmful side-effects for the treatment of inflammatory joint disease in many countries. The goal of this study is to demonstrate Yttrium-90 citrate colloid or Rhenium-186 sulfide synovectomy are appropriate therapeutic interventions in patients with persistent active synovitis of a joint (characterized by pain, tenderness, and effusion) which is resistant to systemic therapy and intra-articular corticosteroid injections. The primary objective will be to assess the safety of an intra-articular administration of Yttrium-90 citrate colloid or Rhenium-186 sulfide. The secondary objective will be to assess the efficacy on synovitis.

NCT ID: NCT01615419 Completed - Clinical trials for Rheumatoid Arthritis

An Observational Study of RoActemra/Actemra (Tocilizumab) in Rheumatoid Arthritis Patients

Start date: May 2012
Phase: N/A
Study type: Observational

This multi-center, observational study will evaluate the use in clinical practice and efficacy of RoActemra/Actemra (tocilizumab) in patients with rheumatoid arthritis. Eligible patients initiated on RoActemra/Actemra treatment according to the approved label will be followed for 6 months.

NCT ID: NCT01613378 Completed - Clinical trials for Rheumatoid Arthritis

A Non-Interventional Study in Rheumatoid Arthritis Patients Treated With RoActemra/Actemra (Tocilizumab)

Start date: February 2012
Phase: N/A
Study type: Observational

This multi-center, non-interventional study will evaluate the pattern of usage in clinical practice, efficacy and safety of RoActemra/Actemra (tocilizumab) in patients with rheumatoid arthritis. Patients initiated on treatment with RoActemra/Actemra according to the licensed Canadian product monograph recommendations will be followed for 12 months from the start of treatment.

NCT ID: NCT01613079 Completed - Clinical trials for Arthritis, Rheumatoid

Efficacy and Safety of Tripterygium Wilfordii in Patients With Rheumatoid Arthritis

TRIFRA
Start date: May 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Evaluation of oral T2 (chloroform/methanol extract of Tripterygium wilfordii Hook F) in the treatment of RA patients with clinical efficacy and safety.Open-labeled, randomized, prospective multi-center clinical trial. Observation period of 24 weeks.