Gut bacteria byproducts may tame inflammation and shield the brain
NCT ID NCT07713641
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 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: * 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
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Endotoxemia are added.
By submitting, you agree to our Terms of use
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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)
RECRUITINGLeuven, 3000, Belgium
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A handful of peanuts a day: could it sharpen teen brains?
- Herbal extract may turn gym sessions into stress relief and brain boost
- Mindfulness body scan may calm stress and inflammation after floods
- Strawberries as medicine? trial tests whether the fruit can calm inflammation and boost insulin response
- Mindfulness may tame the Body's stress fire after repeated floods
- Soy compound could tame HIV-Related inflammation and protect the heart