RecruitingNot ApplicableNCT06104631

A Prospective Trial in Patients With Crohn's Disease in Remission and Having Irritable Bowel Syndrome-like Symptoms

A 10-week Randomized Double-blinded Crossover Trial of BiOkuris® Chitin-glucan Based Formulation Versus Placebo in Patients With Crohn's Disease in Remission and Having Irritable Bowel Syndrome-like Symptoms


Sponsor

Biokuris s.a.

Enrollment

50 participants

Start Date

Mar 12, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Crohn's disease is a chronic and complex inflammatory bowel disease affecting the gastrointestinal tract, causing symptoms like abdominal pain, diarrhea, and fatigue. While its exact cause is unclear, it involves genetic, environmental, and immunological factors. Crohn's disease can lead to nutrient deficiencies and has unpredictable flare-ups and remission periods. During the remission phases, irritable bowel syndrome (IBS)-like symptoms can persist in 50% of patients, for which no satisfactory treatment is available yet. Chitin-glucan is prebiotic, obtained by extraction, isolation and purification from a fungal resource: the mycelium of Aspergillus niger (a microscopic fungus of the Ascomycetes family) of which it composes the cell walls. The biopolymer consists essentially of two types of polysaccharide chains: chitin (poly-N-acetyl-D-glucosamine) and beta-(1,3)-D-glucan (D-glucose units linked essentially via beta-1,3 bonds). Because of its beta bond, human intestinal enzymes cannot digest it, as a result, the majority of chitin-glucan can reach the colon where it can be fermented by the microbiota. By modulating the composition and/or activity of the intestinal microbiota, fermentation of chitin-glucan could have beneficial effects on health. The aim of the RELIEVE study is to assess if BK003 could improve the relief of global symptoms, individual symptoms, stool consistency and frequency of evacuations, quality of life, anxiety, and depression in patients with Crohn's disease in remission without treatment or with stable maintenance therapy and having IBS-like symptoms and to confirm the product's safety.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying a new treatment approach for people with Crohn's disease that is in remission but who still experience irritable bowel syndrome (IBS)-like symptoms such as abdominal pain, bloating, or altered bowel habits — even though their inflammation is under control. **You may be eligible if...** - You are 18–75 years old - You have Crohn's disease that has been in steroid-free remission for more than 3 months - You still experience IBS-like symptoms (meeting Rome IV criteria) - You have significant abdominal pain (Likert score ≥ 3) - You own a smartphone or tablet and can read and write in French - You are willing to maintain your current medications and lifestyle habits during the study **You may NOT be eligible if...** - You have other gastrointestinal conditions (bowel narrowing, cancer history, active Crohn's complications) - You have active flaring Crohn's disease with measurable inflammation - You are pregnant or not using reliable birth control - You have certain dietary restrictions that make the study diet impossible Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERBK003

The product is a combination of chitin-glucan and other dietary complement components. The dosage of chitin-glucan is 3 g/day. The product is a powder for oral administration 1x/day.

OTHERPlacebo

The placebo product has the same composition in excipient, same form and same posology as BK003.


Locations(2)

CHU Liege - Gastroenterology

Liège, Belgium

CHU Lille - Gastroenterology

Lille, France

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NCT06104631