Tiny gut biopsies reveal Probiotic's inner workings
NCT ID NCT07366749
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study looks at how a single dose of a probiotic supplement changes gene activity and sugar patterns in the small intestine of 8 healthy adults. Participants will take the probiotic alone, with fiber, or a placebo, then have a small tissue sample taken the next morning. The goal is to understand how the probiotic works and whether simpler stool samples can replace gut biopsies in future studies.
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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 8 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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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 60 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.
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: * Signed informed consent. * Age 18-60 years. * BMI 18.5 - 29.9 kg/m². * Willing to avoid probiotics, fermented foods, and maintain stable diet/lifestyle for the study duration. Exclusion Criteria: * Chronic GI, inflammatory, metabolic (including renal), or significant psychiatric disease. * Acute infection/allergy within 2 weeks. * Regular use of NSAIDs, antibiotics, steroids, immunomodulators. * Alcohol \>9 units/week. * Use of recreational drugs, tobacco, or nicotine. * Known allergy to local anesthetics or sedatives for gastroscopy. * Bleeding disorder or use of anticoagulants. * Use of probiotics or antibiotics within 4 weeks prior. * Pregnancy, breastfeeding, or planning pregnancy. * Any condition deemed by investigator to compromise safety or data integrity
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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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Örebro University, Campus USO, School of medical sciences
Örebro, Örebro Lan, 703 62, Sweden
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