Chicory fiber study seeks to unlock secrets of gut microbe changes
NCT ID NCT06528041
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how a prebiotic fiber from chicory root (inulin) changes gut bacteria in healthy adults aged 18-45. Over 13 weeks, participants take either inulin or a placebo (maltodextrin) and provide stool and blood samples. Researchers track changes in Bifidobacterium and other gut microbes, along with bowel habits, mood, and appetite. The goal is to understand why people's gut bacteria respond differently to the same fiber.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- chicory inulin (a prebiotic fiber supplement)
- What this could lead to
- If successful, this study could reveal how individuals respond differently to prebiotic fiber, helping personalize dietary recommendations for gut health.
- What could go wrong
- This is an early-stage, small study (52 healthy adults) focused on measuring changes, not treating a disease. Results may not apply to people with health conditions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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 52 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2024
- Expected to finish
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Jul 2026
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 45 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * adults aged 18-45 * BMI \>18.5 - \< 30 kg/m2 * Regular bowel movements (\> 4 days per week) Exclusion Criteria: * Self-reported sensitivity to FODMAPs and following a low FODMAP diet ((FODMAPS stands for fermentable oligosaccharides, disaccharides, monosaccharides and polyols). * Self-reported food allergies and sensitivities including gluten, dairy, nuts, soya and lactose etc. * Self-reported antibiotic treatment in the past 6 months. * Self-reported history of gastrointestinal disease and/or heart disease, cardiovascular, liver, and respiratory disorders, cancer and/or clinically relevant (pre) diabetes. * Self-reported to having undergone major surgery of the gastrointestinal tract, with the exception of cholecystectomy and appendectomy. * Self-reported smoking and/or self-reported drug or alcohol abuse. * Self-reported history of psychiatric and/or mood disorders including eating disorders. * Self-reported to be following a restrictive diet (i.e. ketogenic, intermittent fasting). * Pregnant and lactating women.
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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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Purdue University
RECRUITINGWest Lafayette, Indiana, 47907, United States
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