Clinical trial Recruiting at 1 site Interventional Ages 18 to 45

Effects of chicory inulin on gut microbiota in healthy adults

Official title: Effect of Native Chicory Inulin Supplementation on Rates of Microbial Change Between Individuals

Run by Purdue University · NCT06528041 · Data updated 2026-11-12

This study tests whether taking chicory inulin can change the gut bacteria in healthy adults and see how it affects their bowel habits, mood, and appetite.

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Quick facts

Study typeInterventional
Ages18 Years to 45 Years
SexAll
Enrollment52 (estimated)
SponsorPurdue University
Academic / other
Locations1 site (West Lafayette, Indiana)
StatusRecruiting
StartedAugust 1, 2024
Main results expectedJuly 28, 2026
Study endsJuly 30, 2026
Registry record updatedDecember 11, 2025
Trial IDNCT06528041 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are healthy adults aged 18-45 with a BMI between 18.5 and 30 and regular bowel movements.

Probably not a fit

Patients with gastrointestinal diseases, food allergies, or those following a low FODMAP diet may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates how native chicory inulin affects the gut microbiota of healthy adult volunteers. Participants will undergo a one-week run-in phase to establish baseline data before being assigned to receive either chicory inulin or a maltodextrin placebo. The study aims to determine the rate and persistence of changes in gut microbiota, particularly focusing on the growth of Bifidobacterium, in response to the supplementation. Additionally, it will assess the impact of inulin on bowel habits, mood, and appetite.

Why it matters

Potential benefit: If successful, this study could enhance understanding of how prebiotics like chicory inulin can positively influence gut health and overall well-being.

How similar studies have gone: Previous studies have shown that inulin-type fructans can stimulate beneficial changes in gut microbiota, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Purdue University
    West Lafayette, Indiana, United States
    Recruiting

Study contacts

  • Principal investigator: Stephen Lindemann, PhD — Purdue University
  • Study coordinator: Stephen Lindemann, PhD
  • Email: lindems@purdue.edu
  • Phone: 765-494-9207

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.