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Taking people in CanadaNo phase

Tryptophan for Impaired AhR Signaling in Celiac Disease

Key facts

Where
Hamilton, CanadaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT05576038, who can take part

Where in Canada

  • McMaster UniversityHamilton, CanadaContact: David ArmstrongTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
McMaster University
Trial code
NCT05576038
Record updated
10 January 2025
Original description
This is a prospective, randomized, double-blind, placebo-controlled exploratory trial to evaluate the effect of L-tryptophan supplementation on celiac-related symptoms in individuals who have biopsy-confirmed celiac disease (CeD) and symptoms non-responsive to a gluten-free diet (GFD). Fifty participants, aged 18 to 75 years, who self-report persistent CeD-related symptoms despite taking a GFD for more than 1 year and who score > 40 on the Celiac Symptom Index (CSI) will be randomized to receive L-tryptophan or placebo for 3 weeks.Read full original descriptionShow less

Restoration of Impaired Microbiota-mediated Aryl Hydrocarbon Receptor Signaling in Celiac Disease by Oral Tryptophan Supplementation: an Exploratory, Pilot Trial

This is a prospective, randomized, double-blind, placebo-controlled exploratory trial to evaluate the effect of L-tryptophan supplementation on celiac-related symptoms in individuals who have biopsy-confirmed celiac disease (CeD) and symptoms non-responsive to a gluten-free diet (GFD). Fifty participants, aged 18 to 75 years, who self-report persistent CeD-related symptoms despite taking a GFD for more than 1 year and who score > 40 on the Celiac Symptom Index (CSI) will be randomized to receive L-tryptophan or placebo for 3 weeks.

Inclusion: 18 and 75 years of age; Celiac disease (CeD) diagnosis: Individuals with histological and serological evidence of CeD serology (positive biopsy and anti-tTG IgA); Persistent CeD related symptoms (>40 on the Celiac Symptom Index) despite >1 year of a gluten free diet (GFD).

Exclusion: Acid anti-secretory and antacid medications; Concurrent organic GI pathology other than benign polyps, haemorrhoids, lipomas, Helicobacter pylori infection, diverticulosis and melanosis coli; Chronic treatment with high dose opioids; Alcohol or drug abuse; Use of lithium and monoamine oxidase inhibitors (MAOIs); Current organic gastrointestinal or other autoimmune diseases, such as inflammatory bowel disease or diabetes mellitus (type 1); History of bariatric surgery, fundoplication or gastrectomy (partial or complete); Connective tissue disease; Allergy or sensitivity to any component of the study medication or placebo; Concurrent systemic disease and/or laboratory abnormalities considered by investigators to be a risk or that could interfere with data collection; Antibiotics, antibacterial agents or probiotics, currently, or within the last 8 weeks; Lactose and/or fructose intolerance; Participation in another dietary treatment study within the last 4 weeks.

ClinicalTrials.gov NCT05576038