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Crohn Disease clinical trials

View clinical trials related to Crohn Disease.

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NCT ID: NCT00138840 Completed - Crohn's Disease Clinical Trials

Study of STA-5326 Mesylate in Patients With Moderate to Severe Crohn's Disease

Start date: August 2005
Phase: Phase 2
Study type: Interventional

STA-5326 is an experimental drug that has been shown to block the release of interleukin-12 from peripheral blood mononuclear cells. Given this activity on the immune system, STA-5326 mesylate is a potential treatment for various autoimmune diseases, such as Crohn's disease, that are mediated by the inappropriate expression of Th1 cytokines. This study is evaluating the use of STA-5326 mesylate in patients with moderate to severe, active Crohn's disease. Study visits include a screening visit, 9 treatment period visits over 6 months and a follow-up visit that will occur 30 days following the end of treatment. Study drug treatment will continue for up to 6 months.

NCT ID: NCT00132899 Completed - Crohn's Disease Clinical Trials

COMMIT (Combination Of Maintenance Methotrexate-Infliximab Trial)

Start date: December 2005
Phase: Phase 3
Study type: Interventional

The primary objective is to compare the efficacy and safety of infliximab plus methotrexate to infliximab alone for the long-term control of signs and symptoms of Crohn's disease (CD) in patients with symptoms that are persistent enough to require corticosteroid therapy.

NCT ID: NCT00126373 Completed - Crohn Disease Clinical Trials

A Trial of Wellbutrin for Crohn's Disease

Start date: May 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators are testing the hypothesis that Wellbutrin (bupropion) can give a clinical remission in Crohn's disease.

NCT ID: NCT00114803 Completed - Ulcerative Colitis Clinical Trials

Nasal Calcitonin in the Treatment of Bone Mineral Loss in Children and Adolescents With Inflammatory Bowel Disease

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

The hypothesis underlying this study is that nasally administered calcitonin will stabilize or improve bone mineral density in young patients with ulcerative colitis or Crohn's disease. Patients who participate will receive either calcitonin or placebo and will have their bone mineral density measured at the start, at nine months, and at 18 months of study. Participants will also receive age appropriate doses of vitamin D and calcium supplements. Other serological measures of vitamin D status will be obtained every 3 months during the study.

NCT ID: NCT00114465 Completed - Crohn's Disease Clinical Trials

VSL#3 Versus Placebo in Maintenance of Remission in Crohn's Disease

Start date: June 2005
Phase: Phase 4
Study type: Interventional

The primary objective of the study is to compare the efficacy of the probiotic VSL#3 versus placebo, in addition to standard maintenance drugs, in maintaining remission in Crohn's disease (CD). The secondary objectives are: - To determine the time till flare of CD patients on VSL#3 compared to placebo. - To assess whether concurrent therapy with VSL#3 leads to an improvement in the quality of life (QOL). - To assess whether concurrent therapy with VSL#3 reduces the severity of a flare if it occurs.

NCT ID: NCT00109473 Completed - Crohn's Disease Clinical Trials

Trial of Growth Hormone Therapy in Pediatric Crohn's Disease

Start date: April 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether taking a growth hormone (GH) drug called somatropin causes the intestine of a person with Crohn's Disease (CD) to heal faster when compared to a person with Crohn's Disease that does not receive growth hormone drug.

NCT ID: NCT00106314 Completed - Crohn's Disease Clinical Trials

An Efficacy and Safety Evaluation of Inflabloc Cap in the Treatment of Patients With Crohn's Disease

Start date: January 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Inflabloc Cap (Dehydroepiandrosterone [DHEA]) in the treatment of patients with moderately active Crohn's disease.

NCT ID: NCT00105300 Completed - Crohn's Disease Clinical Trials

Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of Clinical Remission in Subjects With Crohn's Disease

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

The goal of this study is to test whether adalimumab can induce clinical remission in subjects with active Crohn's disease who have been initially treated with infliximab and either lost response or discontinued its use as a result of intolerance to the drug.

NCT ID: NCT00102921 Completed - Crohn Disease Clinical Trials

Safety and Activity Study of an Oral Medication to Treat Moderate to Severe Crohn's Disease

Start date: August 2004
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to investigate the effects of an investigational medication, called CCX282-B, on safety and on the some of the symptoms of Crohn's Disease in patients who are experiencing an active flare-up of moderate to severe Crohn's Disease.

NCT ID: NCT00101946 Completed - Crohn's Disease Clinical Trials

Nine-Weeks Treatment With 683699 In Subjects With Moderately-To-Severely Active Crohn's Disease

Start date: October 2004
Phase: Phase 2
Study type: Interventional

This study will evaluate the effectiveness and safety of the investigational drug 683699 in treating subjects with moderately to severely active CD (Crohn's Disease).