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Rheumatic Diseases clinical trials

View clinical trials related to Rheumatic Diseases.

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NCT ID: NCT02263638 Terminated - Clinical trials for Refractory Hemochromatosis Rheumatism

Treatment of Refractory Hemochromatosis Rheumatism by Anakinra: a Preliminary Phase II Study

THERA
Start date: February 4, 2015
Phase: Phase 2
Study type: Interventional

Treatment of refractory hemochromatosis rheumatism by Anakinra. Prospective, multicenter, non-randomised, single-arm, open-label, phase II trial.

NCT ID: NCT02260336 Enrolling by invitation - Rheumatic Pain Clinical Trials

The Effect of Panax Notoginseng Powders on Rheumatic Pain

Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of Panax Notoginseng Powders on Rheumatic Pain.

NCT ID: NCT02260323 Enrolling by invitation - Clinical trials for Chronic Rheumatic Diseases

Compliance of Traditional Chinese Medicine in Young Patients With Rheumatic Diseases

Start date: October 2014
Phase: N/A
Study type: Interventional

To evaluate the compliance of traditional Chinese medicine (TCM) in young people with Chronic rheumatic disease

NCT ID: NCT02256098 Completed - Clinical trials for Musculoskeletal Diseases

RSA RCT: ATTUNE™ TKA Versus PFC Sigma TKA

APKnee
Start date: September 2014
Phase: N/A
Study type: Interventional

The PFC Sigma Knee by DePuy Synthes is an excellent knee replacement with an excellent clinical track record, good survival rates (98% 10 years survival in patients aged < 55 years)(Keenan et al., 2012) and minimal early migration as measured with RSA (0.5mm MTPM at two years follow-up)(von et al., 2009). The ATTUNE™ Knee by DePuy Synthes is an advancement in knee replacement options. It is designed to provide better range of motion and address the unstable feeling some patients experience during everyday activities, such as stair descent and bending. To date (March 2013), more than 3,500 patients have received an ATTUNE Knee as part of a limited launch and positive feedback was received regarding patient recovery, stability and motion. The objective of this study is to accurately assess and compare migration, clinical and radiological outcome and patient reported outcomes of two TKR prostheses: the Cemented ATTUNE™ Fixed Bearing Cruciate Retaining Knee System and the Cemented PFC Sigma Fixed Bearing Cruciate Retaining Knee System, both by DePuy Synthes, Warsaw, Indiana, USA. The primary objective of this study is to compare the magnitude and pattern of migration of the prostheses (Femoral and Tibial component). The secondary objective of this study is to compare clinical and radiological outcome of the prostheses and PROMS. The tertiary objective of this study is to compare clinical and radiological outcome and PROMS of the prostheses with migration data. This study is designed as a single-blind, randomized trial between the ATTUNE™ Knee System and PFC Sigma Knee System. 32 patients with the ATTUNE™ Knee System and 32 patients with PFC Sigma Knee System will be included in this study. The study population will consist of patients with symptomatic osteoarthritis of the knee scheduled for TKR surgery at the Department of Orthopaedics, Medisch Centrum Haaglanden, The Hague, The Netherlands. Annually 300 TKA procedures are performed in this department, of which about 90% is Osteo Arthritis (OA) and 10% Rheumatoid Arthritis (RA) and other indications. We anticipate that inclusion can be accomplished within a 1 year period and that the total study duration is 3 years. Main study parameters/endpoints are: - Migration of the prosthesis with respect to the host bone measured by means of roentgen stereophotogrammetric analysis (RSA). - Patient Reported Outcome Measures by means of questionnaires.

NCT ID: NCT02219191 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Puerarin Versus Atorvastatin in Treating Metabolism Syndrome in Patients With Chronic Rheumatic Diseases

Start date: August 2014
Phase: N/A
Study type: Interventional

To evaluate the Effect of Puerarin tablets versus statins in treating metabolism syndrome in patients with chronic rheumatic diseases

NCT ID: NCT02188862 Completed - Clinical trials for Rheumatic Heart Disease

Genetic Susceptibility to Rheumatic Heart Disease in the Pacific Region

Start date: September 2012
Phase: N/A
Study type: Observational

The purpose of this study is to investigate whether there are genetic differences between patients with rheumatic heart disease and members of the general population.

NCT ID: NCT02184065 Completed - Clinical trials for Arthritis, Rheumatoid

Observational Study of Meloxicam in Mexican Patients With Rheumatic Diseases

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

Observational study to evaluate the efficacy and safety of meloxicam (Mobicox®) in Mexican population with rheumatic diseases

NCT ID: NCT02184039 Completed - Osteoarthritis Clinical Trials

Efficacy and Safety of Meloxicam (Mobicox®) in Mexican Population With Rheumatic Diseases

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

Study to evaluate the efficacy and safety of meloxicam (Mobicox®) in Mexican population with rheumatic diseases.

NCT ID: NCT02164214 Completed - Clinical trials for Rheumatoid Arthritis

Does Etanercept Influence Tweak Modulation of Inflammation During Inflammatory Rheumatisms (Psoriatic Arthritis and Rheumatoid Arthritis)?

Start date: September 2011
Phase: Phase 3
Study type: Interventional

TWEAK (TNF weakly inducer of apoptosis) is a type II-transmembrane protein, member of the TNF ligand superfamily that can be cleaved to function as a soluble cytokine. Depending on target cell type, TWEAK triggers multiple cellular responses ranging from modulation of inflammation to cell death when it binds to its main receptor, Fn 14. Our team has been the first to describe pro-inflammatory effects of TWEAK during central nervous system inflammation. Various data support the possibility that TWEAK produced by synovial macrophages may contribute to chronic synovitis in animal models and in humans. In psoriatic arthritis (PsoA), anti-TNF therapy has been successful concording with the key role of TNF in the pathogenesis of this disease and the generation by psoriatic patients of neutralizing anti-TNF autoantibodies referred as "beneficial autoimmunity to pro-inflammatory mediators". In 2010, Van Kuijk et al. have described a high expression of TWEAK in the inflammatory synovial of PsoA and rheumatoid arthritis (RA) patients before and after anti-TNF therapy. The role of TNF-alpha in the regulation of TWEAK expression remains unclear.

NCT ID: NCT02128503 Terminated - Ulcerative Colitis Clinical Trials

Prevalence and Clinical Course of Chronic Hep B Infection in IBD and Rheumatologic Disease

Start date: February 2013
Phase: N/A
Study type: Interventional

This study aims to determine the prevalence of HBV infection in patients with IBD and rheumatologic disease, and to assess the impact of immunosuppressive therapy on viral load and clinical course of IBD patients.