New clinical trials for rheumatoid arthritis


















Study is a double-blind, randomized, placebo controlled, dose escalating study. The purpose of this post-marketing study is to compare the safety of tofacitinib versus tumor necrosis factor inhibitor with respect to major cardiovascular adverse events and malignancies, excluding non-melanoma skin cancers, when given to subjects with rheumatoid arthritis.

Other safety events, including non-melanoma skin cancers, hepatic events, infections, and effectiveness parameters will be collected and evaluated in the study. Corticosteroid injections are commonly used for the symptomatic treatment of knee osteoarthritis. Common practice is to inject the joint with a combination of corticosteroid and local anesthetic, with the rationale of providing longer duration pain relief with the corticosteroid and immediate, though short duration relief with the anesthetic.

However, multiple in vitro and animal studies have shown that local anesthetic may be harmful to chondrocytes. Despite this data, use of intra-articular anesthetic remains widespread. Many clinicians believe incorporating the anesthetic is important because it can provide immediate pain relief and facilitate patient confidence in the treatment program.

However, there is The purpose of this study is to assess and compare regenerative injection therapies such as bone marrow aspiration and concentration BMAC and platelet rich plasma PRP for osteoarthritis. The purpose of this study is to determine if a treatment based on the combination of platelet rich plasma and HA obtained with the A-CP HA Kit is statistically superior to a saline placebo or HA alone in terms of Improvement of OA-related symptoms between baseline D0 and Month 6, and reduction of pain at walking between baseline D0 and Month 6.

Continuation of the CARRA Registry as described in the protocol will support data collection on patients with pediatric-onset rheumatic diseases. In particular, this observational registry will be used to answer pressing questions about therapeutics used to treat pediatric rheumatic diseases, including safety questions. This study aims to compare postoperative pain levels between three 3 treatment groups, using the Numerical Rating Scale NRS.

Patients with active Axial Spondyloarthritis without x-ray evidence of Ankylosing Spondylitis and with signs of inflammation will be randomly assigned to receive certolizumab pegol CZP mg every two weeks or placebo. The primary objective is to demonstrate the efficacy of CZP in these patients. The purpose of this study is to establish a comparator cohort of patients with rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, and other spondyloarthropathies.

We will collect demographic information, historical information about diagnosis and past treatment, and clinical, radiographic, and laboratory data on each patient using standardized data collection forms. We will also collect blood and synovial tissue samples from each patient. This will provide data and material for clinical and translational research to address questions related to the fundamental differences between the spondyloarthropathies and inflammatory arthritis relating to the response of bone to chronic inflammation.

We intend to enroll sequential The purpose of this study is to understand the extent of routine cardiovascular screening in patients with rheumatoid arthritis to improve management of their cardiovascular disease and optimize cardiovascular preventive strategies for this group of patients.

This is a prospective, randomized, multicenter comparison study examining the outcomes of subjects with osteoarthritis and knee pain undergoing a procedure to create a radiofrequency lesion of the genicular nerves with the Cooled Radiofrequency Ablation CRFA system compared to subjects receiving Hyaluronic Acid HA. Approximately subjects will be enrolled into this study, with subjects undergoing either CRFA or HA injection in a randomization scheme.

Follow-up will be conducted for 12 months post-CRFA, with the primary endpoint being completed at month 6. Subjects randomized to the comparison HA group will have the option to cross-over to the neurotomy group The positive impact of this award is anticipated to be the development of a clinical framework and approach to managing the various causes of inadequate clinical improvement, ultimately improving patient-physician communication and Study objective: Define pharmacogenomics markers and clinical phenotype features associated with response to RA treatments.

The anticipated time on study drug is up to 5 years. Study is a double-blind, randomized, placebo controlled, dose escalating study. The purpose of this post-marketing study is to compare the safety of tofacitinib versus tumor necrosis factor inhibitor with respect to major cardiovascular adverse events and malignancies, excluding non-melanoma skin cancers, when given to subjects with rheumatoid arthritis.

Other safety events, including non-melanoma skin cancers, hepatic events, infections, and effectiveness parameters will be collected and evaluated in the study. Objective : Identify a microbial biomarker signature that is predictive of treatment response in patients with rheumatoid arthritis RA. The purpose of this study is to assess the efficacy of sirukumab as measured by the reduction of the signs and symptoms of rheumatoid arthritis RA in patients with active RA who are unresponsive or intolerant to treatment with anti-TNF-alpha agents.

Rheumatoid arthritis RA patients have a higher prevalence of subclinical atherosclerosis than the general population. In addition, they experience higher rates of heart failure with preserved ejection fraction HFpEF. There is evidence that myocardial mechanics and left ventricular diastolic function are more abnormal in the RA population and these changes occur earlier than in the general population. Recently a study suggested that RA patient have abnormal myocardial inflammation during a disease flare and that this is improved with anti-inflammatory treatment.

Our study is aimed at describing the prevalence of myocardial inflammation in patients during active RA disease flares and comparing A few participants experienced adverse events during treatment, but none of the reported events were serious or permanent. In addition to taking your prescribed medications, studies suggest that adding an omega-3 supplement to your daily routine might help limit RA symptoms. Omega-3 fatty acid consumption has been linked to reduced inflammation in the body.

When investigators from the University of Houston reviewed the research on omega-3 supplementation, they found 20 clinical trials that focused on RA in particular. In 16 out of 20 trials, omega-3 supplementation was linked to significant improvements in RA symptoms.

Recent observational research has also found a link between omega-3 supplementation and reduced disease activity in people with RA. Certain RA medications may have benefits for your heart, as well as your joints. In one study , investigators followed 2, veterans with RA from to They found that participants who received treatment with methotrexate were less likely to experience cardiovascular events, such as heart attack or stroke.

Participants who received methotrexate were also less likely to be hospitalized for heart failure. In another study , Canadian researchers analyzed registry data collected from three groups: people with RA, people with systemic lupus erythematosus SLE , and healthy controls with neither condition. People with RA or SLE who were treated with hydroxychloroquine had a reduced risk of cardiovascular events, such as heart attack or stroke.

Breakthroughs in medical science can also help researchers optimize existing treatments and develop new treatment approaches for managing RA. To learn more about the latest treatment options for RA, talk to your doctor. They can help you understand the potential benefits and risks of adjusting your treatment plan. They may also recommend lifestyle changes, such as not smoking or vaping, to help you enjoy the best possible health and quality of life with this condition.

Patient advocate and blogger Leslie Rott shares why the invisibleillnessawareness campaign matters to people living with rheumatoid arthritis. One of the goals of rheumatoid arthritis is remission, or freedom from disease activity. Learn more about the definition of remission, why early…. Some RA triggers are well-known, but others can be surprising. Patient advocate Leslie Rott shares the triggers that surprised her the most.



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