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Rheumatoid Arthritis clinical trials

View clinical trials related to Rheumatoid Arthritis.

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NCT ID: NCT01120366 Completed - Clinical trials for Rheumatoid Arthritis

Success of Tocilizumab in RA Patients With Remission Induction and Sustained Efficacy After Discontinuation

SURPRISE
Start date: October 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to investigate the efficacy and safety of the humanized anti-human IL-6 receptor monoclonal antibody tocilizumab (TCZ) either in monotherapy or in combination therapy with methotrexate (MTX) in patients with an inadequate response to treatment with MTX. Furthermore, in patients who have been able to achieve control of disease activity via the above therapy, we investigate the possibility of stopping TCZ and verify safety when TCZ is restarted after disease recurrence.

NCT ID: NCT01119859 Completed - Clinical trials for Rheumatoid Arthritis

A Study of Tocilizumab (RoActemra/Actemra) Versus Adalimumab in Patients With Rheumatoid Arthritis

Start date: May 2010
Phase: Phase 4
Study type: Interventional

This randomized, blinded, parallel arm study evaluated the efficacy and safety of tocilizumab (RoActemra/Actemra) versus adalimumab as monotherapy in patients with rheumatoid arthritis who are intolerant of methotrexate or where continued treatment with methotrexate was considered inappropriate. Patients were randomized to receive either tocilizumab 8 mg/kg intravenously (iv) every 4 weeks plus placebo subcutaneously (sc) every 2 weeks, or adalimumab 40 mg sc every 2 weeks plus placebo iv every 4 weeks. Treatment was anticipated to last 24 weeks. With regard to the blind, the study nurse was unblinded due to the nature of the treatment administration, but the investigator and the patient remained blinded.

NCT ID: NCT01116141 Completed - Clinical trials for Rheumatoid Arthritis

A Study of CH-4051 in Patients With Rheumatoid Arthritis (RA)

MOTION
Start date: September 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if CH-4051 is a safe and effective treatment for rheumatoid arthritis.

NCT ID: NCT01111357 Completed - Clinical trials for Rheumatoid Arthritis

Study of Human Leukocyte Antigen (HLA) Polymorphisms in Patients With Rheumatoid Arthritis

HLAPRPA
Start date: February 2010
Phase: N/A
Study type: Observational

Rheumatoid arthritis (RA), affects between 0.3% and 1.0% of the population, it can lead to progressive joint destruction and severe disability. To date, two RA genetic susceptibility factors have been identified: HLA-DRB1-SE (Shared epitope) and PTPN22 620W alleles. The predictive value of the alleles for diagnosis of RA was previously investigated in cohorts of caucasians patients with early unclassified arthritis that showed restrained association between RA and HLA-SE. Despite the contribution of HLA to the overall genetic risk has been estimated to range from 30% to 50%, it has never been studied in the French west-Indian population.

NCT ID: NCT01106560 Completed - Clinical trials for Rheumatoid Arthritis

A Randomised Trial Comparing Anterior Versus Posterior Approach in Total Hip Replacement

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

This is a single-centre, randomised, prospective clinical follow-up study to evaluate clinical outcome and gait analysis after total hip arthroplasty using the standard postero-lateral approach or the minimally invasive anterior approach.

NCT ID: NCT01105715 Completed - Clinical trials for Rheumatoid Arthritis

Low Density Lipoprotein Cholesterol (CLDL) as a Cardiovascular Disease Risk Factor in Rheumatoid Arthritis

cLDL in RA
Start date: April 2010
Phase: N/A
Study type: Observational

The investigators hypothesize that cLDL levels are elevated in RA patients and represents an important mechanism for accelerated atherosclerosis leading to excess cardiovascular disease (CVD) in rheumatoid arthritis (RA) patients. The purpose of this study is to improve understanding of the reasons for increased cardiovascular diseases (such as heart attack and stroke) seen in patients with rheumatoid arthritis (RA, an arthritis that causes inflammation and destruction of joints). Specifically, the study plans to determine whether a particular type of change in proteins in LDL cholesterol ("bad cholesterol") known as carbamylation is an important risk factor for cardiovascular diseases in RA patients. The study will utilize a case−control study design. A total of 120 subjects (males and females between the ages of 18 and 80) may be enrolled in order to ensure that 100 subjects (50 RA case subjects and 50 age and sex matched controls) complete the study. Procedures will consist of a single visit for each subject during which a screening evaluation, an enrollment evaluation, and a single blood draw will be performed.

NCT ID: NCT01102829 Completed - Clinical trials for Rheumatoid Arthritis

Early Migration in a High Congruent Rotating Platform Total Knee Prosthesis Design

ROCC
Start date: September 2007
Phase: N/A
Study type: Observational

The aim of this study is to accurately assess the relationship between knee joint kinematics and migration of the tibial component of a high congruent, rotating platform total knee prosthesis by using fluoroscopy synchronised in time and space with a force plate, an external motion registration system and Electromyography (EMG).

NCT ID: NCT01098201 Completed - Clinical trials for Rheumatoid Arthritis

Certolizumab and Lower Extremity Lymph Flow in Rheumatoid Arthritis (RA)

Start date: October 2010
Phase: Phase 4
Study type: Observational

This open-label pilot study will select subjects who are inadequate responders to methotrexate. These subjects will receive certolizumab subcutaneously on a monthly basis for six months. The study is attempting to determine the following: 1. Is lymphatic flow altered in the extremities of RA patients with an inflamed knee? 2. Is resolution of synovitis associated with a restoration of lymphatic flow and lymph node volume following therapy with certolizumab? 3. Can Doppler ultrasound be used to detect and follow alterations of lymph node size?

NCT ID: NCT01095393 Completed - Clinical trials for Rheumatoid Arthritis

National Data Bank for Rheumatic Disease Registry Study of Safety in Patients With Rheumatoid Arthritis Treated With Cimzia® or Disease-modifying Antirheumatic Drugs (DMARDs)

Start date: September 1, 2009
Phase:
Study type: Observational

Observational registry to assess the longer-term risk of serious infections and malignancies reported with TNFα-blocker therapy, as well as the longer-term risk of cardiovascular and thromboembolic events in adult Rheumatoid Arthritis (RA) patients treated with Cimzia® as compared to non-biologic DMARD-treated controls.

NCT ID: NCT01094795 Completed - Clinical trials for Rheumatoid Arthritis

Safety Study of Abatacept in Sweden

Start date: March 31, 2011
Phase:
Study type: Observational

The primary purpose of this study is to assess incidence rates of targeted infections, malignancies and mortality among patients with rheumatoid arthritis who are treated with abatacept.