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Lupus Erythematosus, Systemic clinical trials

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NCT ID: NCT01863641 Recruiting - Clinical trials for Systemic Lupus Erythematosus

The Effect of Calcitriol on Progress and Activity of Lupus Nephritis

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether calcitriol is effective in the treatment of lupus nephritis.

NCT ID: NCT01741857 Recruiting - Clinical trials for Systemic Lupus Erythematosus

Umbilical Cord Derived Mesenchymal Stem Cells Transplantation for Active and Refractory Systemic Lupus Erythematosus

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

This study will explore safety and efficacy of allogeneic umbilical cord (UC) derived mesenchymal stem cells transplantation (MSCT) to treat patients with active and refractory systemic lupus erythematosus (SLE) who have been resistant to multiple standard treatments. The underlying hypothesis is that the active SLE condition is caused by an abnormal immune homeostasis that can be restored by MSCT.

NCT ID: NCT01642706 Recruiting - Clinical trials for Rheumatoid Arthritis

Regulatory B Cells in Inflammatory Rheumatisms and Biomarkers of Response to Biologic Treatments

Start date: July 2, 2012
Phase:
Study type: Observational

B cells are known to play an important role in auto-immune diseases by activating T cells, secreting inflammatory cytokines and autoreactive antibodies. However, a sub-type of B cells named regulatory B cells or Bregs has recently shown capacities to prevent or cure arthritis in mouse models. Bregs have also been identified in humans.

NCT ID: NCT01510067 Recruiting - Clinical trials for Cutaneous Lupus Erythematosus (CLE)

Prevalence and Clinical Severity of Cutaneous Lupus Erythematosus

Start date: December 2006
Phase:
Study type: Observational

The Cutaneous Lupus Erythematosus (CLE) database, established in 2006, is a multi-site database between the University of Pennsylvania and the University of Texas Southwestern (UTSW).

NCT ID: NCT01471301 Recruiting - Clinical trials for Arthritis, Rheumatoid

Ultrasound Evaluation of Hands in Patients With Systemic Lupus Erythematosus

Start date: June 2011
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate ultrasound hands in patients with systemic lupus erythematosus.

NCT ID: NCT01217320 Recruiting - Clinical trials for Juvenile Dermatomyositis

Creatine Supplementation in Pediatric Rheumatology

Start date: January 2011
Phase: N/A
Study type: Interventional

Creatine supplementation may improve strength, muscle mass, bone mass and muscle function in healthy and elderly people. The investigators speculate that creatine supplementation could have therapeutic effects in pediatric rheumatic (i.e., juvenile systemic lupus erythematosus and juvenile dermatomyositis) patients who usually present muscle weakness, muscle wasting and bone mass loss.

NCT ID: NCT00866229 Recruiting - Clinical trials for Systemic Lupus Erythematosus

Efficacy and Adverse Effect of Simvastatin Compare to Rosuvastatin in Systemic Lupus Erythematosus (SLE) Patients With Corticosteroid Therapy and High Low-Density Lipoprotein (LDL) Cholesterol Level

Start date: April 2008
Phase: Phase 4
Study type: Interventional

Early statin therapy in SLE patients that have high cholesterol level and other atherosclerosis risk should reduce atherosclerosis and coronary artery events in later course of disease. By the way, statin is used in restricted groups of rheumatologists due to awareness of side effects; myositis and hepatitis, that are frequently found in SLE patients more so than other groups of atherosclerosis patients and reporting data of autoimmune diseases that occur after statin use.

NCT ID: NCT00797784 Recruiting - Clinical trials for Discoid Lupus Erythematosus (DLE)

The Safety and Efficacy of Etanercept (Enbrel®) for the Treatment of Discoid Lupus Erythematosus

DISCLUP2008
Start date: October 2008
Phase: Phase 2
Study type: Interventional

A 20 week study to assess the safety and efficacy of etanercept(Enbrel®)for the treatment of Discoid Lupus Erythematosus

NCT ID: NCT00775476 Recruiting - Clinical trials for Systemic Lupus Erythematosus

Treatment of Systemic Lupus Erythematosus (SLE) With N-acetylcysteine

NAC
Start date: March 31, 2022
Phase: Phase 2
Study type: Interventional

Systemic lupus erythematosus (SLE) is a chronic inflammatory disease which often has debilitating and potentially life-threatening consequences. The cause of SLE is unknown and current therapies lack specificity and carry significant side-effects. We previously discovered the depletion of glutathione in lymphocytes of patients with SLE and associated this metabolic change with the elevation of the mitochondrial transmembrane potential. This study will titrate to tolerance during an initial 3 month open label period and then subjects will be randomized to one of 2 arms. It was determined by statistical analysis that each group must have 105 subjects. All subjects will be enrolled and evaluated for tolerance of NAC between dosages of 2.4 g/day and 4.8 g/day for 3 months. After A 3-month open-label dose-titration phase, SLE subjects will be randomized into 2 groups of 105 subjects either to continue the tolerated dosage of NAC or switched to equal number of placebo capsules. There will be up to seven study visits per SLE subject, including the screening and wash out visits. Visits 2-6 will be scheduled three months apart. The study will last 13 months with the wash-out visit. Each subject will donate approximately 100 ml of blood for biomarker studies at each visit. Healthy control subjects will donate blood at the same time. They will be matched to the SLE subjects by gender, age within 10 years, and ethnicity. Their blood will be used as reference for biomarker assays. There is a consent form required to participate in the phase II study.

NCT ID: NCT00756769 Recruiting - Clinical trials for Systemic Lupus Erythematosus

Systemic Lupus Erythematosus in Gullah Health

SLEIGH
Start date: April 2003
Phase:
Study type: Observational

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by the production of autoantibodies, multiple organ involvement, and diverse clinical symptoms and immunologic manifestations. African Americans are at a disproportionately higher risk of developing SLE, develop SLE at an earlier age, and have increased morbidity and mortality compared with European Americans. Our central study hypothesis is that there are specific genetic factors that interact with environmental exposures leading to the development of SLE. The African American Gullah population from the Sea Islands of South Carolina and Georgia are unique in their genetic homogeneity with minimal non-African genetic admixture, making them an ideal cohort to address questions of environmental and genetic influence on the development and progression of SLE.