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Colitis, Ulcerative clinical trials

View clinical trials related to Colitis, Ulcerative.

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NCT ID: NCT01848561 Active, not recruiting - Clinical trials for Ulcerative Colitis (UC)

A Long-Term Registry of Humira® (Adalimumab) in Patients With Moderately to Severely Active Ulcerative Colitis (UC)

Start date: April 29, 2013
Phase:
Study type: Observational

This is a registry study to evaluate the long-term safety and effectiveness of adalimumab in patients with moderately to severely active UC who are treated as recommended in the product label.

NCT ID: NCT01757964 Active, not recruiting - Ulcerative Colitis Clinical Trials

Bacteriotherapy in Pediatric Inflammatory Bowel Disease

Start date: December 2012
Phase: Phase 1
Study type: Interventional

In this study, the investigators want to see if Bacteriotherapy (also referred to as stool transplantation) improves the symptoms and decreases inflammation in children with Inflammatory Bowel Disease (IBD). Examples of IBD are Crohn's Disease and Ulcerative Colitis. Additionally, researchers want to learn whether this experimental therapy delays the need for starting additional medications to treat pediatric IBD.

NCT ID: NCT01586533 Active, not recruiting - Ulcerative Colitis Clinical Trials

Study of the Safety and Efficacy of Zoenasa® Versus Mesalamine Enema in Subjects With Left-Sided Ulcerative Colitis

Start date: June 2012
Phase: Phase 2
Study type: Interventional

This double-blind, randomized, comparator-controlled Phase II study is designed to establish the safety and efficacy of Zoenasa Rectal Gel compared to mesalamine enema in subjects with left-sided ulcerative colitis, as measured by the modified ulcerative colitis disease activity index (UCDAI), over 6 weeks of treatment. In this study, two cohorts of subjects will receive either Zoenasa-1:4 (1.0g NAC; 4.0g 5-ASA) investigational drug enema therapy or comparator mesalamine enema (4.0g 5-ASA). The study will enroll subjects randomized equally into the 2 cohorts. Each cohort will enroll approximately 60 subjects. The two arms of the trial will be enrolled concurrently in a randomized fashion.

NCT ID: NCT01505842 Active, not recruiting - Ulcerative Colitis Clinical Trials

Chromoendoscopy for Dysplasia Detection in Chronic Inflammatory Bowel Disease

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

Patients with longstanding ulcerative colitis or crohn's disease in the large bowel have an increased risk of developing cancer. The purpose of this study is to determine if visualizing of the mucosa in details using a dye spray (indigo-carmine) will result in detection of more abnormalities than conventional colonoscopy without dye spray.

NCT ID: NCT01221428 Active, not recruiting - Ulcerative Colitis Clinical Trials

Umbilical Cord Mesenchymal Stem Cells Infusion for Ulcerative Colitis

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

The purpose of this study is to determine whether umbilical cord Mesenchymal Stem Cells of treatment for ulcerative colitis is safe and effective.

NCT ID: NCT01169207 Active, not recruiting - Clinical trials for Inflammatory Bowel Disease

Johns Hopkins Crohn's Disease and Ulcerative Colitis Study

Start date: July 1996
Phase:
Study type: Observational

Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), is a idiopathic, chronic and frequently disabling inflammatory disorder of the intestines characterized by a dysregulated mucosal immune response that affect more than a million Americans. This current protocol was established in 1996 with the goal of identifying the genetic and environmental components that contribute to the development of IBD, especially in families.

NCT ID: NCT01011322 Active, not recruiting - Ulcerative Colitis Clinical Trials

A Study to Investigate the Efficacy of LT-02 in Patients With Mesalazine Refractory Ulcerative Colitis

Start date: December 2009
Phase: Phase 2
Study type: Interventional

The participation in this clinical study will last approximately 21 weeks with a 1 week screening period and a 12 weeks treatment duration. If the study doctor finds, that the patients disease has significantly improved he/she will enter a treatment free follow-up period of 8 weeks. In total the study consists of 5 to 6 clinical visits (V1 - V6) and 1 telephone follow-up call.

NCT ID: NCT00606346 Active, not recruiting - Ulcerative Colitis Clinical Trials

A Multicenter, Prospective, Long-term, Observational Registry of Pediatric Patients With Inflammatory Bowel Disease

DEVELOP
Start date: May 31, 2007
Phase:
Study type: Observational

The purpose of this study is to evaluate the long-term safety and clinical status of pediatric patients with Inflammatory Bowel Disease (IBD). Particular attention will be directed to recording safety outcomes reported in association with infliximab and other prescribed IBD therapies. In addition, information on disease status and quality of life will be collected.

NCT ID: NCT00510978 Active, not recruiting - Ulcerative Colitis Clinical Trials

Probiotics in GastroIntestinal Disorders

PROGID
Start date: January 2002
Phase: Phase 2/Phase 3
Study type: Interventional

All of us have millions of bacteria living in our gut. These bacteria are very important to our health providing us with protection against infections of the gut, allowing us to gain extra nutritional value from food we eat and helping our immune system. Changes in the balance of these many bacteria can make us vulnerable to infections both from within and from outside the gut. Certain bacteria may also be directly associated with some diseases of the gut. Research by doctors and scientists into relationships between the bacteria normally found in our gut and certain diseases of the gut is helping to develop food supplements and other therapies to treat these diseases. This study involves research into the usefulness and safety of two probiotic products in maintaining remission in Crohn's disease and ulcerative colitis. Approximately 360 patients with Crohn's disease and ulcerative colitis from Ireland, Finland and Spain will be involved in the study. The yoghurts used in this study contain either Lactobacillus salivarius subsp. salivarius or Bifidobacterium infantis.