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Arthritis clinical trials

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NCT ID: NCT00245934 Completed - Clinical trials for Rheumatoid Arthritis

Study Evaluating Enbrel in Patients With Rheumatoid Arthritis

Start date: June 2003
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the incidence of adverse events for patients with rheumatoid arthritis treated with Enbrel under usual care settings. In addition, differences in injection site reactions based on whether health care professionals or patients administer Enbrel will be assessed and evaluated.

NCT ID: NCT00244556 Completed - Clinical trials for Rheumatoid Arthritis

Study Comparing Enbrel (Etanercept) Plus Methotrexate Versus Enbrel Alone in Active Rheumatoid Arthritis Despite Current Methotrexate Therapy

Start date: March 2003
Phase: Phase 4
Study type: Interventional

To investigate the changes in MRI-derived markers of joint inflammation and destruction and in biochemical markers of connective tissue metabolism and angiogenesis in rheumatoid arthritis patients treated with Enbrel and Enbrel+methotrexate.

NCT ID: NCT00244179 Recruiting - Reactive Arthritis Clinical Trials

New Immunomodulatory Therapy Strategies in Chronic Reactive Arthritis

Start date: January 2003
Phase: Phase 2
Study type: Interventional

1. to investigate, whether one of the two alternative therapy strategies (antibiotic plus immunostimulation versus antibiotic plus immunosuppression) in chronic reactive arthritis is therapeutical superior to conventionel standardtherapy (DMARD). 2. to investigate, whether one or more of the different therapy strategies cause an altered detection of bacterial DNA in the joint or colon. 3. to measure the antigen-specific and -unspecific immune response (predominantly t-cell response) during therapy and correlate it with the clinical course. 4. to gain knowledge from these analyses and the clinical course concerning the pathogenesis and the point of attack for possible therapies in chronic reactive arthritis. 5. to compare cytokine-profiles of CD4- and CD8-positive T-cells from patients treated with infliximab to those treated with etanercept.

NCT ID: NCT00243412 Completed - Clinical trials for Rheumatoid Arthritis

A Study of the Safety and Efficacy of Rituximab in Patients With Moderate to Severe Rheumatoid Arthritis Receiving Methotrexate

RUMBA
Start date: August 2005
Phase: Phase 2
Study type: Interventional

This was a Phase II, randomized, double-blind, multicenter study designed to evaluate the safety and efficacy of rituximab, administered at two different regimens for 2 years, in patients with moderate to severe active rheumatoid arthritis (RA) receiving stable doses of methotrexate (MTX).

NCT ID: NCT00242853 Completed - Clinical trials for Rheumatoid Arthritis

A Study To Investigate Markers Of Inflammation In Rheumatoid Arthritis

Start date: October 2004
Phase: N/A
Study type: Observational

This study is being conducted to validate various biomarkers in patients with RA with varying levels of disease severity. Subjects with a diagnosis of rheumatoid arthritis (RA) will be included as controls. The sudy will measure the baseline levels and the intra- and inter-subject variability of exhaled nitric oxide (NO) in patients with inactive/mild and moderate/severe RA on stable therapy or during a course glucocorticoids. In addition exhaled NO levels will be correlated with intra-articular inflammation (power Doppler ultrasonography) as well as markers of systemic inflammation (CRP, ESR).

NCT ID: NCT00241982 Completed - Clinical trials for Rheumatoid Arthritis

Long-Circulating Liposomal Prednisolone Versus Pulse Intramuscular Methylprednisolone in Patients With Active Rheumatoid Arthritis

Start date: October 2005
Phase: Phase 2
Study type: Interventional

Trial to study the safety of a single, intravenous administration of long-circulating liposomal prednisolone disodium phosphate in patients with active rheumatoid arthritis.

NCT ID: NCT00240136 Completed - Clinical trials for Rheumatoid Arthritis

Long-term Observation of Patients With Early Rheumatoid Arthritis

Start date: January 1993
Phase:
Study type: Observational

The purpose of this research is to observe the effects of RA over a long period in order to learn which of the early characteristics of patients' early RA predict future joint damage and disability. We also investigate whether certain treatments can prevent or slow the development of joint damage and disability. Additionally, the costs and effects of RA on the patient are studied in order to improve the methods used to measure these effects. Clinical, demographic, radiographic, and laboratory measures are taken by the rheumatologist in the office. In addition, patient questionnaires are mailed & completed by the patient and returned to the coordinating center at UCLA. All information obtained by these means will be studied in their effects on early, severe RA.

NCT ID: NCT00239720 Terminated - Clinical trials for Arthritis, Psoriatic

hOKT3gamma1 (Ala-Ala) for the Treatment of Psoriatic Arthritis

PART
Start date: March 2006
Phase: Phase 2
Study type: Interventional

hOKT3gamma1 (Ala-Ala) is a man-made antibody that is commonly used to prevent organ rejection. The purpose of this study is to determine whether hOKT3gamma1 (Ala-Ala) is safe and effective in psoriatic arthritis patients who are unable to control their arthritis with methotrexate or azathioprine.

NCT ID: NCT00239382 Completed - Clinical trials for Arthritis, Rheumatoid

A Study to Compare Meloxicam IM Once Daily Versus Meloxicam Orally Once Daily in Patients With Rheumatoid Arthritis

Start date: July 1, 2004
Phase: Phase 3
Study type: Interventional

The objective of this trial was to assess the efficacy and safety of 15 mg meloxicam i.m. once daily compared with 15 mg meloxicam tablets once daily p.o. in patients with Rheumatoid arthritis over a time period of 7 days.

NCT ID: NCT00236678 Terminated - Clinical trials for Rheumatoid Arthritis

Randomized, Double-blind, Placebo-controlled Study to Assess Fatigue in Patients With ACD Due to RA Receiving PROCRIT

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

The purpose of this research study is to determine fatigue (tiredness) in subjects with chronic Rheumatoid Arthritis with chronic anemia. Fatigue in subjects who get PROCRIT will be compared to fatigue in subjects who get placebo (a medically inactive substance). The study will also evaluate hemoglobin levels (oxygen-carrying protein in red blood cells), safety, anemia related health concerns, vitality, arthritis related function and work productivity.