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Crohn's Disease clinical trials

View clinical trials related to Crohn's Disease.

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NCT ID: NCT01288053 Terminated - Crohn's Disease Clinical Trials

Non-myeloablative Allogeneic Hematopoietic Stem Cell Transplantation (NST) for Patients With Refractory Crohn's Disease

Start date: January 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Allogeneic transplantation has been a high-risk procedure, although non-myeloablative conditioning regimens (mini-transplantation) minimizes regimen related toxicity. The investigators, therefore, propose a phase I study of matched sibling allogeneic hematopoietic stem cell transplantation with non-myeloablative conditioning. In addition, graft versus host disease (GVHD) will be virtually eliminated by CAMPATH that removes donor T cells from the graft. The goal is to assess the toxicity/efficacy (phase I) of allogeneic non-myeloablative hematopoietic stem cell transplantation for high-risk Crohn's disease. In simplistic terms, this protocol is designed to ablate an aberrant immune system and then, similar to the use of marrow transplants for immunodeficient patients, reconstitute a new immune system with lymphocyte depleted marrow.

NCT ID: NCT01277289 Terminated - Crohn's Disease Clinical Trials

Intra-erythrocyte Dexamethasone Versus Placebo in Patients With Steroid-dependent Crohn's Disease

Crodex
Start date: June 3, 2009
Phase: Phase 3
Study type: Interventional

Primary objective: Assessment of the efficacy of EryDex vs PLACEBO in maintaining patients with steroid-dependent Crohn's disease in clinical remission throughout 12 months without oral steroids. Secondary objectives: 1. safety of EryDex 2. emergence of new adverse effects from steroids or disappearance of those possibly pre-existing in the various subgroups of patients; 3. duration of the period of remission; 4. evaluation of the hypophysis-adrenal function; 5. study of plasma concentrations of dexamethasone; 6. effect of therapy on the metabolism of calcium and on indexes of inflammation; 7. assessing the quality of life; 8. rate of surgical resection 9. evaluation of the indirect costs of care.

NCT ID: NCT01199302 Terminated - Crohn's Disease Clinical Trials

Long-term Safety Study of Brodalumab in Adults With Crohn's Disease

Start date: February 2, 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of long-term treatment with brodalumab in adults with Crohn's disease.

NCT ID: NCT01190839 Terminated - Crohn's Disease Clinical Trials

A Multicenter Trial Comparing REMICADE (Infliximab) and Placebo in the Prevention of Recurrence in Crohn's Disease (CD) Patients Undergoing Surgical Resection Who Are at an Increased Risk of Recurrence

Start date: November 2010
Phase: Phase 3
Study type: Interventional

REMICADE (infliximab) is a drug used to treat active Crohn's disease and is being tested in an experiment to see if it may be useful in preventing relapse of Crohn's disease after surgical resection. This study will compare the effects (both good and bad) of REMICADE (infliximab) to those of placebo. Placebo looks like the drug being studied but has no active ingredients.

NCT ID: NCT01182467 Terminated - Crohn's Disease Clinical Trials

Use of PET-CT in the Management of Crohn's Disease

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

Crohn's disease (CD) is an autoimmune disorder which affects over 700,000 people in the U.S. The disease can vary in severity and multiple drug classes are available to the disease depending on disease severity and complications. Our purpose will be to study how PET-CT scans can be used to better manage Crohn's Disease.

NCT ID: NCT01150890 Terminated - Crohn's Disease Clinical Trials

Brodalumab (AMG 827) in Adults With Moderate to Severe Crohn's Disease

Start date: November 9, 2010
Phase: Phase 2
Study type: Interventional

The study will examine the safety and effectiveness of brodalumab for the treatment of moderate to severe Crohn's disease. Participants will randomly assigned to receive either brodalumab or placebo (a lookalike liquid that doesn't have any drug in it) and neither the doctor nor the patient will know what treatment is being given.

NCT ID: NCT01094613 Terminated - Crohn's Disease Clinical Trials

Multicenter Clinical Efficacy and Safety Study of Delayed Release 6MP in Crohn's Disease

Start date: November 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The study is designed to evaluate the clinical efficacy and safety of daily treatment for 12 weeks of oral administration of a delayed release, locally delivered 6MP (mercaptopurine) drug (80 mg), as compared to standard Purinethol (at a dose of 1-1.5 mg/kg/body weight), in alleviating the clinical, immunological and mucosal signs and symptoms of moderately active Crohn's Disease

NCT ID: NCT01074580 Terminated - Crohn's Disease Clinical Trials

Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease

Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of this study is investigate if high frequency sonography and contrast enhanced sonography can be used to predict remission in patients with deterioration of Crohn's disease treated with steroids or tumor necrosis factor (TNF) alfa inhibitors.

NCT ID: NCT01046773 Terminated - Crohn's Disease Clinical Trials

Vitamin D Supplementation as Non-toxic Immunomodulation in Children With Crohn's Disease

Start date: January 2010
Phase: Phase 1
Study type: Interventional

IBD is caused by an abnormal immune response to the gut bacteria in people who are genetically predisposed. There has been a huge increase in the number of people diagnosed with IBD since World War II, likely due to changes in our environment. It is possible that the abundance of vitamin D in the body may be one of those environmental factors that the investigators can control to make patients with IBD better. Vitamin D acts on cells of the immune system and causes many effects, including the production of a "natural antibiotic" called cathelicidin. The investigators know that when people are supplemented with vitamin D, levels of cathelicidin produced by these immune cells increase. By supplementing children with Crohn's disease with vitamin D, the investigators may be able to alter their immune system "naturally," making their disease better. A consensus of vitamin D experts believes that vitamin D levels need to reach a level of 40-70 ng/mL in the blood in order to have effects on the immune system. Raising vitamin D levels to this range is one of the goals in the current study.

NCT ID: NCT01012726 Terminated - Crohn's Disease Clinical Trials

Study About the Effect of Doxycycline and Acetylcystein in the Treatment of CD-associated Fistulae

Start date: November 2009
Phase: N/A
Study type: Interventional

The investigators will study whether local instillation of Doxycycline and Acetylcystein results in fistula closure in CD patients.