Gut bacteria byproducts may tame inflammation and shield the brain

NCT ID NCT07713641

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time

Summary

This study tests whether short-chain fatty acids (SCFAs) — substances naturally produced by gut bacteria — can reduce inflammation and protect thinking skills. Healthy adults receive either SCFA capsules or a placebo, then a low dose of a bacterial substance that briefly activates the immune system, causing mild flu-like symptoms. Researchers measure inflammation in the blood and test memory, inhibition, and mental flexibility to see if SCFAs help.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
short-chain fatty acid colon-delivery capsules (sodium acetate, sodium butyrate, sodium propionate)
What this could lead to
If it works, this could point toward a dietary supplement that reduces inflammation and protects mental performance during immune challenges.
What could go wrong
This is a small, early-phase trial in healthy people using a temporary lab-induced inflammation, so results may not apply to real infections or chronic 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

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

About 56 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2025

Expected to finish

Mar 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 45 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Voluntary written informed consent obtained prior to any study procedure * Healthy, with no gastrointestinal or psychological complaints * Age 18-45 years * BMI 18.5-27 kg/m2 * Proficiency in English and/or Dutch Exclusion Criteria: * History of previous or current neurological disorder (e.g., epilepsy, multiple sclerosis, migraine with aura) * History of previous or current psychiatric disorder (e.g., depression, anxiety disorders, bipolar disorder, schizophrenia) * History of previous or current gastrointestinal disorder (e.g., Crohn's disease, ulcerative colitis, irritable bowel syndrome) * History of previous or current endocrine disorder (e.g., diabetes, thyroid disorders, polycystic ovary syndrome) * History of immune system disorder, including inflammatory, autoimmune, or severe allergic conditions (e.g., rheumatoid arthritis, lupus, celiac disease, or severe allergies such as anaphylaxis) * History of neuropsychiatric disorder (e.g., ADHD, autism spectrum disorder, learning disorder, Tourette's syndrome) * History of major head trauma (e.g., concussion with loss of consciousness or long-term symptoms) * History of severe infection (e.g., sepsis, pneumonia requiring hospitalization, meningitis, endocarditis, or other systemic infection requiring hospitalization, intravenous antibiotics, or intensive care) * One or more diagnoses based on the Mini International Neuropsychiatric Interview (MINI) * One or more diagnoses based on ROME-IV criteria for gastrointestinal disorders * Any disorder that, in the investigator's opinion, might jeopardise the participant's safety or compliance with the protocol * Any prior or concomitant treatment that might jeopardise the participant's safety or compromise the integrity of the study * Participation in an interventional trial with an investigational medicinal product (IMP) or device * Current or recent (past month) prescribed medication use, with particular attention to cardiovascular drugs, steroids, NSAIDs, and centrally-acting drugs (excluding isolated over-the-counter use such as ibuprofen or paracetamol, and hormonal contraceptives in women) * Use of psychotropic medication within the past year (e.g., antidepressants, anxiolytics, antipsychotics) * Use of antibiotics within three months preceding the study * Use of pre- or probiotics within one month preceding the study * Current or recent (past month) infection (e.g., common cold, influenza, COVID-19) * Recent (past month) vaccination * Pregnant or lactating women * Previous or current substance or alcohol dependence or abuse (\>2 units/day or \>14 units/week) * Smoking * Night-shift work * Adherence to special diets (e.g., vegan, vegetarian, weight-loss, lactose-free, gluten-free) * Previous experience with or knowledge of any of the cognitive tasks used in the study (questionnaires excluded) * C-reactive protein higher than 0.5mg/dL on the day of the injection. * Colour vision deficiency or colour-blindness

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Conditions

The condition(s) this trial relates to.

Endotoxemia Inflammation inflammatory disease Inhibition, Psychological van der Woude syndrome

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • University Hospital Leuven (UZ Leuven)

    RECRUITING

    Leuven, 3000, Belgium

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