Actively Recruiting

Phase 3
Age: 18Years - 75Years
All Genders
NCT05120752

Efficacy of a Low FODMAP Diet in the Absence of Lactose Malabsorption in Moderate to Severe ROME IV IBS.

Led by Universitair Ziekenhuis Brussel · Updated on 2025-12-18

60

Participants Needed

1

Research Sites

321 weeks

Total Duration

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AI-Summary

What this Trial Is About

Irritable bowel syndrome (IBS) is a frequently encountered disorder. According to the Rome IV criteria, it is characterized by abdominal pain associated with a change in stool frequency or con-sistency, or with symptomatic improvement by defecation (Mearin 2016). Associated symptoms, such as bloating and flatulence, are frequently reported. The underlying pathophysiology remains obscure, although several pathways have been proposed. Low-grade immune activation, visceral hypersensitivity, alteration in gut microbiome have all been reported (Mearin 2016). As diet exerts an impact on all these pathophysiological mechanisms, the role of dietary intervention receives spe-cial attention, with special interest in the role played by so-called fermentable oligo-, di-, monosac-charides and polyols (FODMAPs). Multiple studies indicated the beneficial effects of the low FODMAP diet in at least part of the patients (Halmos 2014, Eswaran 2016, Staudacher 2017). As a disaccharide, lactose is part of the FODMAPs. Lactose intolerance (LI) results from lactose malabsorption (LM) secondary to insufficient hydrolysis of the disaccharide lactose into galactose and glucose (Misselwitz 2019). The undigested lactose will eventually reach the colon, resulting in fermentation from colonic bacteria with production of different compounds such as short chain fat-ty acids, carbon dioxide, H2 and methane (Catanzaro 2021). These compounds have an osmotic effect and can stimulate colonic contractions. In patients suffering from LI, these pathophysiologi-cal mechanisms generate symptoms such as abdominal pain and cramps, flatulence, diarrhea, in-creased bowel sounds, among others, similar to the mechanisms by which FODMAPs induce symp-toms of IBS. As dairy products are highly present in our Western diet, LI will often be considered in patients presenting with such symptoms and they will be referred for further testing. When LM is diagnosed, a lactose-free diet (LFD) will be advocated to alleviate symptoms. While the earlier-mentioned studies investigated symptomatic improvement by the low FODMAP diet, it remains uncertain whether this restrictive diet remains beneficial in patients without evidence of LM. In a recent study the low FODMAP diet and LFD provided comparable improvement in symptom severity (Krieger-Grübel 2020). This study aims to: * Assess the improvement in IBS symptoms and quality of life (QOL) by a low FODMAP di-et when lactose malabsorption has been previously excluded; * Compare the improvement in IBS symptoms and QOL obtained by a low FODMAP diet to a lactose free diet (data from the PreVaIL study).

CONDITIONS

Official Title

Efficacy of a Low FODMAP Diet in the Absence of Lactose Malabsorption in Moderate to Severe ROME IV IBS.

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 - 75 years
  • Fulfilling the ROME IV criteria for IBS
  • Moderate symptom severity as defined by a IBS-SSS > 175
  • Consumption of lactose containing products
Not Eligible

You will not qualify if you...

  • Clinical suspicion of an organic disorder different from lactose intolerance or IBS (excluded before inclusion)
  • Known lactose intolerance
  • Known inflammatory bowel disorder
  • Known major intestinal motility disorder
  • Alcohol abuse (more than 14 units per week) or other substance abuse
  • Active psychiatric disorder
  • Known systemic or autoimmune disorder affecting the gastrointestinal system
  • Prior abdominal surgery except appendectomy
  • Any prior cancer diagnosis except basocellular carcinoma
  • Current chemotherapy
  • History of gastroenteritis in the past 8 weeks
  • Intake of antibiotics, prebiotics, or probiotics during the past 8 weeks
  • Use of dietary supplements unless stable dose for more than 8 weeks
  • Treatment with neuromodulators unless stable dose for more than 12 weeks
  • Treatment with spasmolytic agents, opioids, loperamide, gelatin tannate, or mucoprotectants during the past 8 weeks
  • Previous use of lactose-free or low FODMAP diet

AI-Screening

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Trial Site Locations

Total: 1 location

1

UZ Brussel

Jette, Brussels Capital, Belgium, 1090

Actively Recruiting

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Research Team

S

Sébastien Kindt, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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