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Juvenile Rheumatoid Arthritis clinical trials

View clinical trials related to Juvenile Rheumatoid Arthritis.

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NCT ID: NCT00443430 Completed - Clinical trials for Juvenile Idiopathic Arthritis

Trial of Early Aggressive Drug Therapy in Juvenile Idiopathic Arthritis

Start date: May 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare two aggressive drug regimens for children with poly-juvenile idiopathic arthritis (JIA) and extended oligo JIA.

NCT ID: NCT00289107 Completed - Clinical trials for Rheumatoid Arthritis

Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA

Start date: April 1, 2001
Phase: N/A
Study type: Interventional

The study will evaluate the clinical performance of the rotating platform and fixed bearing implants through patient questionnaires, outcomes scoring and radiographic assessment.

NCT ID: NCT00289094 Completed - Clinical trials for Rheumatoid Arthritis

Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA

Start date: March 1, 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical performance of the rotating platform and fixed bearing implants in patients undergoing primary total knee replacement. Outcome scoring and radiographic assessment will be the methods used to evaluate performance.

NCT ID: NCT00286689 Withdrawn - HIV Infections Clinical Trials

Effects of Growth Hormone in Chronically Ill Children

Start date: February 3, 2006
Phase: N/A
Study type: Interventional

The specific aims for this study are - 1. To determine the effect of GH on height, height velocity, body weight and lean body mass. This specific aim tests the hypothesis that GH significantly improves height, height velocity, weight, weight velocity and lean body mass in chronically ill children who have grown poorly despite adequate nutritional rehabilitation. 2. To determine the effect of GH on whole body protein turnover (WBPT), IGF-1 levels and on cytokines. This specific aim tests the hypothesis that chronically ill children have increased catabolism, caused by high levels of circulating cytokines and low levels of IGF-1, and that these abnormalities improve with GH treatment. 3. Evaluation of bone mineral density and bone turnover. This specific aim tests the hypothesis that bone density is low in chronically ill children secondary to increased osteoclast activity correlating with elevated cytokine levels. We hypothesize that the anabolic effects of growth hormone (GH) will improve the height and weight of chronically ill children who have failed to grow despite receiving adequate nutrition via gastrostomy tube or oral supplementation.

NCT ID: NCT00095173 Completed - Clinical trials for Juvenile Rheumatoid Arthritis

BMS-188667 in Children and Adolescents With Juvenile Rheumatoid Arthritis

Start date: February 2004
Phase: Phase 3
Study type: Interventional

The primary purpose of the clinical research study is to assess the safety of treating children and juvenile subjects with BMS-188667 (Abatacept). In addition, the study will assess the effectiveness of BMS-188667 in reducing disease activity of Juvenile Rheumatoid Arthritis (JRA) or Juvenile Idiopathic Arthritis (JIA) as measured by the time to occurrence of disease flare.

NCT ID: NCT00090571 Completed - Clinical trials for Juvenile Rheumatoid Arthritis

Juvenile Rheumatoid Arthritis Research Registry

Start date: October 1994
Phase:
Study type: Observational

Juvenile rheumatoid arthritis (JRA) is the most common chronic inflammatory disease in children, and may be related to genetics. Having two siblings who both have JRA in one family is rare. The purpose of this registry is to collect patient information and blood samples from qualifying JRA siblings and their families. The goal of the registry is to further understanding of JRA as related to genetics.

NCT ID: NCT00078806 Terminated - Clinical trials for Juvenile Rheumatoid Arthritis

Safety and Efficacy Study of Etanercept (Enbrel®) In Children With Systemic Onset Juvenile Rheumatoid Arthritis

Start date: June 4, 2001
Phase: Phase 3
Study type: Interventional

The primary objective of this study was to determine the efficacy of etanercept in pediatric patients with systemically active system onset juvenile rheumatoid arthritis (SOJRA).

NCT ID: NCT00078793 Completed - Clinical trials for Juvenile Rheumatoid Arthritis

Registry of Etanercept (Enbrel®) In Children With Juvenile Rheumatoid Arthritis

Start date: June 2000
Phase: N/A
Study type: Observational

This study will evaluate long-term safety of etanercept with or without other DMARDs in children with polyarticular course or systemic juvenile rheumatoid arthritis (JRA) compared to a cohort of subjects with polyarticular or systemic JRA receiving methotrexate with or without other DMARDs.

NCT ID: NCT00029042 Terminated - Clinical trials for Juvenile Rheumatoid Arthritis

Infliximab to Treat Children With Juvenile Rheumatoid Arthritis

Start date: January 2002
Phase: Phase 2
Study type: Interventional

This study will determine whether a stepwise increase of the drug infliximab (Remicade® (Registered Trademark)) controls juvenile rheumatoid arthritis more effectively than a fixed dose. It will look at the safety and effectiveness of increasing the dose to a maximum of 15mg/kg body weight per dose, examining the drug's effect on bone and cartilage, and whether it can improve abnormal growth, metabolism and hormones. Infliximab is approved for treating adults with rheumatoid arthritis and Crohn's disease. Children between 4 and 17 years of age with active juvenile rheumatoid arthritis who do not respond adequately to standard therapy may be eligible for this study. Participants will receive nine infusions of infliximab during this 62-week study. The drug is given intravenously (IV, into a vein) over 2 hours. The first three infusions will be at a dose of 5 mg/kg of body weight. Children who improve on this regimen will receive another 6 infusions at the same dose. Children who do not significantly improve on 5 mg/kg at the end of 6 weeks (the third infusion) may continue with phase 2 of the study, in which they will be randomly assigned to receive either: 1) 6 additional doses of the drug at 5 mg/kg per dose, or 2) a gradually increased dose to a maximum of 15 mg/kg. In addition, all children will continue to take methotrexate at the same dose as when they entered the study. Participants will visit the NIH Clinical Center 12 times (about every 8 weeks) during the study for the following tests and procedures: - History and physical examination, including a complete joint exam - Puberty assessment - breast development in girls, testicle size in boys, and pubic hair - Height and weight measurements Children will have imaging studies (x-rays, MRI and Dexa scan) at the beginning and end of the study and will collect a 24-hour urine sample before each infliximab infusion. Patients may elect to have an endocrine evaluation. This involves Clinical Center hospitalizations for 1-1/2 days on visits 1, 4 and 12. Small amounts of blood will be drawn every 20 minutes (through an indwelling catheter to avoid multiple needle sticks) for 8 hours while the child sleeps. The blood will be examined for the normal rhythm of growth hormone and other substances in the body and how they are affected by arthritis. Participants will complete a questionnaire once a year for 2 years to provide information on their health status and any problems that might be related to the study drug.

NCT ID: NCT00010335 Completed - Clinical trials for Systemic Lupus Erythematosus

Pilot Study of Total Body Irradiation in Combination With Cyclophosphamide, Anti-thymocyte Globulin, and Autologous CD34-Selected Peripheral Blood Stem Cell Transplantation in Children With Refractory Autoimmune Disorders

Start date: November 2000
Phase: Phase 1
Study type: Interventional

OBJECTIVES: I. Determine the safety and long term complications of total body irradiation in combination with cyclophosphamide, anti-thymocyte globulin, and autologous CD34-selected peripheral blood stem cell (PBSC) transplantation in children with refractory autoimmune disorders. II. Determine the efficacy of this treatment regimen in these patients. III. Determine the reconstitution of immunity after autologous CD34-selected PBSC transplantation in these patients. IV. Determine engraftment of autologous CD34-selected PBSC in these patients.