Personalized B-fructan Diet in Inflammatory Bowel Disease Patients
Inflammatory Bowel Diseases | Ulcerative ColitisThis study aims to examine patient tolerability of personalized dietary fibre consumption recommendations (high-pectin diet versus high-B-fructan diet based on personalized responses), provided by an IBD dietician, based on our novel translational research findings.
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Conditions de participation
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Sexe:
ALL -
Âges admissibles:
6 to 39
Critères de participation
Inclusion Criteria:
* Children (age 6-17) or young adults (age 18-39).
* Known or suspected UC or IBDU \[there will be 2 control group: non-IBD (undergoing colonoscopy but found not to have IBD; and healthy (no GI symptoms, so not required to have colonoscopy; could be family members)\]
* For UC: Remission-mild-moderate disease: Mayo score \<10
* Clinical indication for sedated colonoscopy
* Disease location: E2-E4
* Stable treatment (not on steroids; biologics or immunomodulator not changed in last month)
* High likelihood that patients will be able to collect all samples and provide all data
Exclusion Criteria:
* Use of antibiotics for a week or more over the last 3 months
* Use of probiotics or prebiotics at pharmacological doses (adding fibre sources to food or probiotics in yogurt, for example, are allowed)
* History of abdominal surgery, including appendectomy
* Documented enteric infection during the 3 months prior to endoscopy
* Presence of non-IBD bowel conditions (e.g., celiac), anatomical or mucosal abnormalities, motility disorder
* Presence of a systemic disease requiring treatment (cancer, ischemic heart disease, kidney failure, etc)
* Proctitis (E1)
* Systemic steroids (above 10 mg/day of Prednisone)
* Topical therapy within 1 week of endoscopy
* Recent change in IBD treatment (started biologics or IM over the last month)
* Pregnancy or planning to become pregnant during the study
* Inability to understand or sign the consent
Lieu de l'étude
Health Sciences Centre Hospital
Health Sciences Centre HospitalWinnipeg, Manitoba
Canada
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University of Alberta Hospital
University of Alberta HospitalEdmonton, Alberta
Canada
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- Étude parrainée par
- University of Manitoba
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05615779