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Arthritis clinical trials

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NCT ID: NCT01123070 Completed - Clinical trials for Rheumatoid Arthritis

TL011 in Severe, Active Rheumatoid Arthritis Patients

Start date: February 5, 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and pharmacology of TL011 in patients with severe rheumatoid arthritis.

NCT ID: NCT01121874 Completed - Clinical trials for Thumb Carpometacarpal Arthritis

Suture Fixation System Versus Tendonous Reconstruction in Carpometacarpal (CMC) Arthroplasty

Start date: April 12, 2010
Phase: N/A
Study type: Interventional

Thumb carpometacarpal (CMC) arthritis affect 1 in 4 females and 1 in 12 males. Patients who fail to respond to conservative treatment may benefit from surgery; however, controversy exists over the most effective surgical technique. A popular technique, ligament reconstruction with tendon interposition (LRTI) involves a trapeziectomy, followed by reconstruction of the palmar oblique ligament using a harvested flexor tendon from the wrist. We believe that use of a suture fixation system to reconstruct the palmar oblique ligament, instead of harvesting a wrist tendon, may provide a superior repair. The objective of this study is to compare functional outcome measurements among patients who receive CMC arthroplasty using a suture fixation system (investigational group) to those who receive LRTI surgery (control group). We hypothesize that patients in the investigational group will demonstrate superior functionality, compared to patients in the control group.

NCT ID: NCT01121146 Completed - Osteoarthritis Clinical Trials

Study Comparing Marathon Polyethylene and Enduron Polyethylene Acetabular Liners Used in Total Hip Arthroplasty

Start date: December 1998
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether crosslinked Marathon and standard Enduron polyethylene liners show differences in bone loss around the hip implant.

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: NCT01117480 Completed - Clinical trials for Moderate-to-severe Rheumatoid Arthritis

Real Life Evaluation of Rheumatoid Arthritis in Canadians Taking HUMIRA

REACH
Start date: July 2005
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the clinical effectiveness and safety of adalimumab as used in routine clinical practice in adult participants with moderate to severe rheumatoid arthritis (RA) in Canada.

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: NCT01111240 Completed - Psoriatic Arthritis Clinical Trials

Efficacy and Safety of Humira® in Patients With Psoriatic Arthritis in Normal Medical Practice

Start date: August 2005
Phase: N/A
Study type: Observational

This study is a documentation of effectiveness and safety of Humira in patients with psoriatic arthritis.

NCT ID: NCT01106079 Completed - Psoriatic Arthritis Clinical Trials

TIght COntrol of Psoriatic Arthritis

TICOPA
Start date: May 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate whether tight control of patients with newly diagnosed psoriatic arthritis (consisting of regular 4 weekly objective assessment of disease activity and protocol-led intensive treatment) can improve outcome as opposed to standard care (usually 3 monthly reviews with no objective outcome measures and no protocol for treatment). The principle hypothesis of this study is that tight control of inflammation in psoriatic arthritis using a treatment protocol and pre-defined objective targets for treatment will lead to an improvement in patients' disease activity and a reduction in radiological joint damage.

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.