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Rheumatoid Arthritis clinical trials

View clinical trials related to Rheumatoid Arthritis.

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NCT ID: NCT00867256 Terminated - Clinical trials for Rheumatoid Arthritis

Cormet Large Diameter Metal on Metal (LDMOM) Total Hip System (G030265)

Start date: March 31, 2004
Phase: N/A
Study type: Interventional

To demonstrate the safety and efficacy of the Cormet Large Diameter Metal on Metal (LDMOM) Total Hip System using a composite clinical success (CCS) primary endpoint.

NCT ID: NCT00859859 Terminated - Clinical trials for Rheumatoid Arthritis

Vagus Nerve Stimulation in Rheumatoid Arthritis

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine the short-term effects of vagus nerve stimulation (VNS) by auricular stimulation (stimulation of the auricular branch of the vagus nerve which innervates the ear) in rheumatoid arthritis (RA). RA is characterized by a chronic systemic inflammation affecting the joints but also carries an increased risk for extra-articular manifestations as well as other organ manifestations such as cardiovascular disease (CVD), which significantly contributes to morbidity and mortality in this disorder.

NCT ID: NCT00845832 Terminated - Clinical trials for Rheumatoid Arthritis

A Study of Combination Treatment With MabThera (Rituximab) and RoActemra (Tocilizumab) Versus RoActemra in Patients With Rheumatoid Arthritis With an Incomplete Response to Methotrexate

Start date: March 2009
Phase: Phase 2
Study type: Interventional

This 2 part study will investigate the safety, tolerability and efficacy of MabT hera in combination with RoActemra in patients with active rheumatoid arthritis despite a stable dose of methotrexate. In Part 1 of the study, patients will be randomized to receive either MabThera 0.5g iv or placebo on days 1 and 15, follo wed by RoActemra at one of the ascending doses between 2mg/kg and 8mg/kg at week s 4, 8 and 12 (MabThera arm) or 8mg/kg (placebo arm). In Part 2, additional pati ents will be randomized to one of 2 groups to receive MabThera 0.5g on days 1 an d 15 followed by the selected dose (from Part 1)of RoActemra at weeks 4, 8 and 1 2, or placebo on days 1 and 15 followed by RoActemra 8mg/kg at weeks 4,8 and 12. All patients will then be eligible to receive extension treatment withRoActemra every 4 weeks. The anticipated time on study treatment is 12 months, and the tar get sample size is <100 individuals.

NCT ID: NCT00839020 Terminated - Clinical trials for Rheumatoid Arthritis

Minimally Invasive Versus Conventional Approaches in Navigated Total Knee Arthroplasty (TKA)

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

50 patients are randomized to two groups who receive a navigated knee prosthesis. Aim of the study is a comparison between a minimally invasive and a conventional approach. In both groups OrthoPilot computer assisted-navigation will be used. Pain intensity as well as concomitant pain medication are monitored during the first 20 postoperative days and will be compared for the two groups. Various scores are surveyed.

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: NCT00808210 Terminated - Clinical trials for Rheumatoid Arthritis

A Study to Evaluate Ocrelizumab in Combination With Methotrexate Compared With Infliximab Plus Methotrexate in Patients With Active Rheumatoid Arthritis Currently Responding Inadequately to Etanercept or Adalimumab

Start date: March 5, 2009
Phase: Phase 2
Study type: Interventional

This is a Phase II, randomized, active-controlled, double-blind, double-dummy, parallel-group, multicenter study in the United States enrolling patients with active RA. The study will enroll approximately 290 patients at approximately 130 sites.

NCT ID: NCT00805467 Terminated - Clinical trials for Rheumatoid Arthritis

Open-Label, Multicenter Extension Study for Patients Completing Treatment Phase of a Rigel-Sponsored R935788 Studies

Start date: August 2008
Phase: Phase 2
Study type: Interventional

The purpose of this new research study is to gain additional information about how safe and effective R935788 is over a longer period of time.

NCT ID: NCT00805116 Terminated - Clinical trials for Rheumatoid Arthritis

Marine Oils and Arthritis

Start date: December 2008
Phase: N/A
Study type: Interventional

NSAIDS are associated with adverse GI effects and COX-2 inhibitors have cardiovascular risk. Long-term oral supplementation with fish oil reduce e.g. joint pain in rheumatoid arthritis (R.A) patients, with reduced need for NSAIDS, in addition to being cardioprotective. The aim is to investigate if 4 month supplementation of 15 ml/day of whale blubber oil compared with cod liver oil reduce the intensity of joint pain in patients with R.A (primary outcome). Patients are assessed at inclusion and after study (4 months) during routine polyclinical visit. Patients are called for interview after 6 and 12 weeks. Secondary outcomes are e.g. morning stiffness, quality of life and functional level

NCT ID: NCT00796705 Terminated - Clinical trials for Rheumatoid Arthritis

Switching Anti-TNF-Alpha Agents in Rheumatoid Arthritis (RA)

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

Rheumatoid Arthritis (RA) is a systemic inflammatory autoimmune disorder that leads to inflammation and progressive joint damage affecting 2.5 million people in the United States. The primary purpose of this study is to determine the effectiveness of switching to an alternative Tumor Necrosis Factor (TNF) alpha inhibitor in comparison to continuing treatment with an existing TNF-alpha inhibitor in adults suffering from RA in a setting of inadequate clinical response to etanercept or adalimumab.

NCT ID: NCT00781469 Terminated - Clinical trials for Rheumatoid Arthritis

A Study to Evaluate the RNA Signature of Rheumatoid Arthritis From Synovium and Whole Blood

Start date: November 2008
Phase:
Study type: Observational

Rheumatoid arthritis is a systemic disease, it is not clear whether the gene expression profile exhibited by circulated peripheral blood cells and that expressed by the inflamed synovium mirror one another. Understanding this relationship would be useful not only in potentially having a relatively non-invasive means to predict response to therapy but it might be useful in better understanding differences in RA expression amongst patients with this disease, thus perhaps assisting in target identification through a better understanding of disease processes.