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Rheumatoid Arthritis clinical trials

View clinical trials related to Rheumatoid Arthritis.

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NCT ID: NCT00837434 Completed - Clinical trials for Rheumatoid Arthritis

Anti-TNF Agents for the Treatment of Rheumatoid Arthritis

Start date: March 2009
Phase: Phase 4
Study type: Interventional

Rheumatoid arthritis (RA) is a chronic disease that leads to inflammation and progressive joint damage. RA is a systemic inflammatory autoimmune disorder affecting almost 1% of the United States population. Current therapies target the immune system early in the disease process before joint damage occurs, and include drugs such as methotrexate (MTX) and tumor necrosis factor (TNF)-blocking agents. The primary purpose of this study is to determine the effectiveness of two TNF inhibitors, etanercept and adalimumab, on memory B lymphocytes (B-cells) in the peripheral blood of participants with RA. Additionally, there are 4 optional sub-studies as part of the trial: - B-Cell Kinetic Sub-Study to look at changes in B-cell subsets over time and how quickly reductions in B-cell memory occur - Vaccine Response Sub-Study to assess B cell memory in response to immunization with hepatitis B,-hepatitis A, and diphtheria/tetanus vaccines, and to determine whether T-cell vaccine responses are altered with TNF blockade - Tonsil Biopsy Sub-Study to evaluate how TNF blockade affects memory B-cells in the tonsil dendritic cells and germinal cells - Synovial Biopsy Sub-Study to evaluate how TNF blockade affects changes in memory B-cells in lymphoid tissue.

NCT ID: NCT00832910 Completed - Clinical trials for Rheumatoid Arthritis

Assessment of Body Image in Patients With Rheumatoid Arthritis

BIRA
Start date: June 2007
Phase: N/A
Study type: Observational

Investigate body image of patients with rheumatoid arthritis, correlating with self-esteem, function and quality of life.

NCT ID: NCT00831922 Completed - Clinical trials for Rheumatoid Arthritis

Efficacy of Oral AB1010 in Adult Patients With Active Rheumatoid Arthritis

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

The objective of this study is to evaluate the activity of 2 oral doses of AB1010 in subjects suffering from active RA who have shown an inadequate response to one DMARD including MTX or anti-TNF, after 3 months (12 weeks) of treatment. The safety and efficacy will be evaluated on: Rate of patients achieving ACR 20, 50, 70 and 90 DAS (disease activity score) after 3 months treatment ACRn after 3 months treatment Therapeutic maintenance of AB1010 at 3 months Quality of Life assessed by SF12 Health Assessment Questionnaire (HAQ) Clinical and biological safety Pharmacokinetic profile of AB1010

NCT ID: NCT00831649 Terminated - Clinical trials for Rheumatoid Arthritis

A Phase II, Multicenter, Open-Label, Long-Term Study of the Safety, Tolerability, and Efficacy of Intravenous Natalizumab in Subjects With Rheumatoid Arthritis Who Have Previously Participated in Study ELN100226-RA201

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

The purpose of this study is to evaluate the long-term safety, tolerability, and efficacy of natalizumab in subjects with active rheumatoid arthritis (RA) receiving concomitant methotrexate (MTX)

NCT ID: NCT00828997 Completed - Clinical trials for Rheumatoid Arthritis

Effects of Different Antirheumatic Treatments of Arthritis on Antibody Response Following Vaccination Using Prevenar®

PVA
Start date: August 2008
Phase: Phase 4
Study type: Interventional

Previous studies have analyzed serological responses following pneumococcal vaccination using 23-valent vaccination (Pneumovax) in Rheumatoid Arthritis (RA) patients that were on different therapeutic modalities including TNF-blockers and methotrexate. The results have shown that serological response was significantly reduced in RA patients receiving methotrexate compared to those receiving TNF-blockers. In contrast when using polypeptide immunisation (influenza vaccine) we found that anti-TNF significantly impaired the serological response compared to the methotrexate treated RA patients. The aim of this study is to analyze serological responses after Prevenar vaccination in patients with chronic arthritis and to study the impact of different treatment modalities on serological responses. It will be of interest to see if the result is different compared to the one seen after immunizing with 23-valent nonconjugated pneumococcal polysaccharide vaccine.

NCT ID: NCT00822640 Completed - Clinical trials for Rheumatoid Arthritis

Comparison of Rotating vs. Fixed Platform of the COLUMBUS Knee Prosthesis

Start date: March 2004
Phase: Phase 4
Study type: Interventional

A population of 100 patients randomised to rotating and fixed PE inlays in the Columbus knee prosthesis received a navigated TKR. Knee Society Score as primary endpoint, Oxford Score, and postoperative ROM after one year will be compared.

NCT ID: NCT00819481 Completed - Clinical trials for Rheumatoid Arthritis

Post-Market Study of the 3DKnee™ System

Start date: February 2009
Phase:
Study type: Observational

The purpose of this study is to evaluate the use and efficacy of the 3DKnee™ System for total knee replacement surgery.

NCT ID: NCT00818064 Completed - Healthy Clinical Trials

Safety and Tolerability of Anti-IL-20 in Healthy Volunteers and Patients With Rheumatoid Arthritis

Start date: December 2008
Phase: Phase 1
Study type: Interventional

This trial is conducted in Europe. The aim of this clinical trial is to investigate the safety and tolerability of single doses of Anti-IL-20 in healthy volunteers (HV) and patients with rheumatoid arthritis (RA).

NCT ID: NCT00815425 Completed - Clinical trials for Rheumatoid Arthritis

Consortium for the Longitudinal Evaluation of African Americans With Early Rheumatoid Arthritis (The CLEAR Registry)

CLEAR
Start date: September 2000
Phase: N/A
Study type: Observational

Rheumatoid arthritis (RA) is a long-term autoimmune disease that is characterized by pain, stiffness, inflammation, swelling, and sometimes destruction of joints. RA usually requires lifelong treatment, including medications, physical therapy, exercise, education, and possibly surgery, but the course and severity of the disease can differ significantly from person to person. The purpose of this study is to identify genetic and other factors that determine the severity of RA in African Americans.

NCT ID: NCT00814866 Completed - Clinical trials for Rheumatoid Arthritis

Bone Resorption, Osteoclastogenesis and Adalimumab

BROCA
Start date: September 2008
Phase: N/A
Study type: Interventional

Osteoclastic bone resorption depends on both the capacity to generate osteoclasts (osteoclastogenesis) and on individual osteoclast activity. The investigators objective is to study the effect of anti-TNF therapy on the number of osteoclast precursors in the peripheral blood of patients with Rheumatoid Arthritis, on in vitro osteoclastogenesis and on osteoclast activity before and during the treatment of patients with Rheumatoid Arthritis with Adalimumab.