Scientists probe gut bugs and sugar link in IBS pain
NCT ID NCT07337707
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at why some people with irritable bowel syndrome (IBS) feel more belly pain after eating fructose (a sugar found in fruit). Researchers will check the gut bacteria and other body signals in 60 IBS patients. No new treatment is tested — the goal is to better understand the connection between fructose, gut microbes, and pain.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: For all groups: * Patients with IBS defined by current Rome criteria (currently IV) * Adult, aged 18 to 75 * Regulatory criteria : * Membership of a social security scheme * Adult having read and understood the information letter and signed the consent form * Woman of childbearing age with effective contraception for the duration of the study such as oestroprogestins, intrauterine device, tubal ligation, vasectomised partner or sexual abstinence (no heterosexual intercourse for 1 month and a negative urine pregnancy test at inclusion). * Postmenopausal women: confirmatory diagnosis (non-medically induced amenorrhoea for at least 12 months prior to the inclusion visit or biologically documented) * Women of childbearing age who have been rendered surgically infertile (e.g. hysterectomy, bilateral salpingectomy, bilateral oophorectomy). For the IBS group with fructose malabsorption and visceral hypersensitivity (named group of interest, MalF-HyperSens) (1): * 25g fructose breath test in favour of fructose malabsorption * Rectal barostat finding visceral hypersensitivity For the IBS group with fructose malabsorption and without visceral hypersensitivity (known as the MalF-NormoSens group) (2): * Fructose breath test at 25g dose in favour of fructose malabsorption * Rectal barostat finding no visceral hypersensitivity For the IBS group without fructose malabsorption and visceral hypersensitivity (named NormoF-HyperSens group) (3): * Fructose breath test at 25g dose in favour of no fructose malabsorption * Rectal barostat finding visceral hypersensitivity For the IBS group without fructose malabsorption or visceral hypersensitivity (called the NormoF-NormoSens group) (4): * Fructose breath test at a dose of 25g in favour of the absence of fructose malabsorption * Rectal barostat finding no visceral hypersensitivity Exclusion Criteria: * Patient who has not undergone a fructose breath test or a barostat in our department in the last 10 years. * Patient with organic digestive pathology (chronic inflammatory bowel disease, microscopic colitis, digestive cancer, celiac disease) * Systemic antibiotic use (oral, IV or IM) in the month prior to inclusion * Regulatory criteria : * Pregnant or parturient or breast-feeding woman or proven absence of contraception, * Person deprived of liberty by an administrative or judicial decision or person placed under court protection / sub- guardianship or curatorship, * Person undergoing research participating in another trial / having participated in another trial within a period of 2 weeks, * History of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol or preventing him/her from giving informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHU de Rouen
Rouen, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Herbal capsules take on gut bacteria: a new hope for IBS?
- Could a Dual-Action supplement tame irritable bowel syndrome?
- Could an Anti-Inflammatory diet designed for Crohn's disease also tame IBS?
- Scientists hunt for the exact FODMAPs that trigger IBS pain
- Gut-Brain connection in IBS: scientists hunt for clues to anxiety and depression
- Could a nerve pain drug soothe IBS symptoms?