Oligofructose-enriched Inulin for the Treatment of Mild to Moderate Active Ulcerative Colitis
Launched by UNIVERSITY OF ALBERTA · Mar 19, 2014
Trial Information
Current as of June 19, 2025
Completed
Keywords
ClinConnect Summary
Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) of the colon which manifests as mucosal inflammation and ulceration. The disease affects various lengths of the colon. It cycles through periods of symptomatic relapse and asymptomatic remission. During relapse, patients suffer from frequent passage of watery diarrhea which may contain blood and mucous. Currently pharmacological treatments of mild to moderate UC consist of 5 amino salicylic acid (5 ASA), corticosteroids, and immunosuppressive agents such as azathioprine (Imuran), its metabolite 6-mercaptopurine (6-MP) and...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Males and females 18 - 65 years of age.
- • Diagnosis of ulcerative colitis established by previous endoscopies, with histology and clinical course consistent with diagnosis.
- • Colitis must extend for more than 15 cm above the anal verge, and involve at least the rectosigmoid.
- • Mild to moderately active ulcerative colitis defined by a minimum score of 3 and a maximum score of 8 on the 12 point Mayo scale. Mayo scores are assigned by (1) stool frequency, (2) rectal bleeding, (3) endoscopic findings and (4) physician's overall assessment of disease severity
- • At least one previous episode of ulcerative colitis, prior to the current episode
- • Duration of current symptomatic episode less than 4 weeks.
- • Ability to give valid informed consent.
- • For females of childbearing potential, a negative pregnancy test.
- Exclusion Criteria:
- • Crohn's disease or pouchitis.
- • Current infectious enteritis.
- • Use of oral steroids within the last 4 weeks of the screening visit.
- • Use of antibiotics within the last 2 weeks of the screening visit
- • Change in dose of oral 5-ASA products within the last 2 weeks of the screening visit.
- • Topical 5-ASA or steroids within 7 days prior to the baseline endoscopy
- • Use of immunosuppressive or biological agent within 3 months of screening.
- • Use of NSAIDS one week before screening.
- • Use of anti-diarrheal drugs within the last 1 week of the screening visit.
- • Use of probiotic preparations either prescribed or over-the-counter within two weeks of screening.
- • Use of natural health products within 2 weeks of screening (except multivitamins and minerals)
- • Significant hepatic, renal, endocrine, respiratory, neurological or cardiovascular disease as determined by the investigator
- • Imminent need for colectomy
- • Presence of severe UC (defined as a Mayo of 9 or greater)
- • Pregnancy or lactation
- • Inability to give a valid informed consent or to properly comply with study procedures for any reason.
About University Of Alberta
The University of Alberta, a leading research institution in Canada, is dedicated to advancing healthcare through innovative clinical trials. With a strong commitment to scientific excellence and community health, the university facilitates cutting-edge research across various medical disciplines. Its interdisciplinary approach fosters collaboration among researchers, clinicians, and students, ensuring that clinical trials are designed and conducted with the utmost rigor and ethical standards. By leveraging its extensive resources and expertise, the University of Alberta aims to translate research findings into meaningful advancements in patient care and public health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Edmonton, Alberta, Canada
Patients applied
Trial Officials
Levinus Dieleman, PhD
Principal Investigator
University of Alberta
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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