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Colitis clinical trials

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NCT ID: NCT00620126 Completed - Ulcerative Colitis Clinical Trials

The Home Telemanagement (UC HAT) Trial for Patients With Ulcerative Colitis

UCHAT
Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if home automated telemanagement improves bowel symptoms, quality of life, compliance with medications, and health care utilization compared to best available care in patients with ulcerative colitis.

NCT ID: NCT00619489 Completed - Ulcerative Colitis Clinical Trials

Long Term Safety of Vedolizumab (MLN0002) in Patients With Ulcerative Colitis and Crohn's Disease

Start date: December 2007
Phase: Phase 2
Study type: Interventional

This was an open-label study to provide an opportunity for participants with Ulcerative Colitis (UC) who previously completed Study C13002 (NCT01177228), and for treatment-naïve participants with UC or Crohn's Disease (CD) to receive treatment with vedolizumab, and to determine the long term safety of vedolizumab in patients afflicted with these diseases.

NCT ID: NCT00616434 Completed - Clinical trials for Active Ulcerative Colitis

A Phase 2 Study of Interferon Beta-1a (Avonex®) in Ulcerative Colitis

Start date: May 2008
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to evaluate the clinical activity of interferon beta-1a in participants with moderate to severe ulcerative colitis (UC). Secondary objectives of this study are to determine (i) the safety and tolerability of interferon beta-1a in participants with moderate to severe UC, and (ii) the percentage of participants, with a decrease in the Simple Clinical Colitis Activity Index (SCCAI) score of ≥3 points at Week 8.

NCT ID: NCT00604422 Completed - Ulcerative Colitis Clinical Trials

Evaluation of the PillCamâ„¢ Colon Capsule Endoscopy (PCCE) in Detection & Classification of Ulcerative Colitis

Start date: April 2007
Phase:
Study type: Observational

To evaluate the ability of the PillCam® Colon Capsule Endoscope to detect and classify Ulcerative colitis

NCT ID: NCT00603733 Completed - Clinical trials for Active Ulcerative Colitis

Canadian Active & Maintenance Modified Pentasa Study

CAMMP
Start date: October 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate that the new modified oral extended-release Pentasa® 500mg tablet is at least as efficacious as the currently marketed Pentasa® 500mg tablet in active mild to moderate Ulcerative Colitis and also in maintenance of quiescent disease.

NCT ID: NCT00587236 Completed - Colitis, Ulcerative Clinical Trials

Compare Conventional Colonosocpy to Endoscopic AFI, NBI for Dysplasia Detection for Ulcerative Colitis & Cholangitis

Start date: March 2006
Phase: N/A
Study type: Observational

This study is being done to: To attempt to increase the detection of precancerous colon tissue in patients with chronic ulcerative colitis and primary sclerosing cholangitis; To determine if an investigational scope that can look at the lining of the colon in different ways will help the doctor identify abnormal tissue in patients with chronic ulcerative colitis and concurrent primary sclerosing cholangitis; and To determine if this investigational scope can accurately detect precancerous or cancerous tissue in patients with chronic ulcerative colitis that are known to have had cancerous or precancerous tissue in the past.

NCT ID: NCT00586599 Completed - Ulcerative Colitis Clinical Trials

Levels of the Stat4 Alpha and Stat4 Beta Isoforms in PBMCs From Patients With Crohn's Disease and Ulcerative Colitis

Start date: August 2007
Phase: N/A
Study type: Interventional

The goal in these studies will be to assess the relative levels of the Stat4 alpha and Stat4 beta isoforms in PBMCs from patients with Crohn's Disease, ulcerative colitis, celiac disease or from control patients. We hypothesize that the beta to alpha ratio will be higher in patients with active disease and that there will be a correlation between the ratio and the severity of disease.

NCT ID: NCT00586352 Completed - Ulcerative Colitis Clinical Trials

Protein Metabolism in Newly Diagnosed Pediatric Inflammatory Bowel Disease

Start date: January 2006
Phase: N/A
Study type: Interventional

Inflammatory bowel disease, which includes both Crohn's disease and ulcerative colitis, is a disease of the gastrointestinal tract leading to symptoms of abdominal pain, diarrhea, and growth disturbance. Crohn's disease is a chronic inflammatory process that may affect any part of the gastrointestinal tract, whereas ulcerative colitis is typically present only in the colon. Children with inflammatory bowel disease frequently suffer from disturbances in growth, which may continue into adulthood and result in altered growth outcomes. The metabolic response to inflammatory bowel disease, including increased protein breakdown and decreased protein synthesis may play a significant role in the resulting malnutrition and growth failure from which children with inflammatory bowel disease suffer. The purpose of this study is to compare the rates of protein synthesis within the mucosal lining of the gastrointestinal tract in children Crohn's disease or ulcerative colitis to children who have normal endoscopic examinations. By comparing children with inflammatory bowel disease to normal children, we can begin to determine how alterations in protein metabolism within the lining of the gastrointestinal tract affect whole body protein metabolism, and its consequent effects on growth. In those patients diagnosed with Crohn's disease or ulcerative colitis, a follow-up study will be conducted two weeks following the initiation of steroid therapy to determine its effects on protein metabolism. We hypothesize that children with active inflammatory bowel disease will have increased rates of protein synthesis in the lining of the gastrointestinal tract than patients who have normal endoscopy, and that increases in protein breakdown and protein synthesis will be improved following steroid therapy in children with newly diagnosed inflammatory bowel disease.

NCT ID: NCT00577473 Completed - Ulcerative Colitis Clinical Trials

Safety and Efficacy of Asacol 4.8 g/Day Versus Asacol 2.4 g/Day (ASCEND I)

ASCEND I
Start date: February 2001
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of Asacol 4.8 g/day (800 mg tablet) versus Asacol 2.4 g/day (400 mg tablet

NCT ID: NCT00573794 Completed - Ulcerative Colitis Clinical Trials

Long-term Open-label Safety and Efficacy Study of Adalimumab in Subjects With Ulcerative Colitis

Start date: November 28, 2007
Phase: Phase 3
Study type: Interventional

To assess the long-term safety and maintenance of response of adalimumab in subjects with ulcerative colitis who participated in and successfully completed M06-826 (NCT00385736) or M06-827 (NCT00408629).