Gut check: can poop pills from young donors turn back the biological clock?
NCT ID NCT07826793
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers at Stanford University are testing whether fecal microbiome transplants from young, healthy donors and a fermented, plant-rich high-fiber diet can reduce markers of inflammation and biological aging. The trial enrolls 80 adults aged 40 and older who are in generally good health. Participants are randomly assigned to one of four groups for eight weeks: diet alone, transplant alone, diet plus transplant, or a placebo transplant. The main measure is the change in DunedinPACE, a blood test that estimates how fast a person is aging biologically.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- fecal microbiota transplant capsules from young healthy donors, plus a fermented plant-rich high-fiber diet
- What this could lead to
- If the approach works, it could point toward diet and microbiome-based ways to slow biological aging and lower inflammation in healthy older adults.
- What could go wrong
- This is an early Phase 2 trial with 80 participants, so any effect on aging markers may be small or fade. Fecal transplants can cause temporary digestive upset, and the diet may be hard for some people to follow.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
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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40 years and older
- 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: * Able and willing to provide written informed consent prior to completion of any study procedures. * Age ≥40 years at the time of consent. * In generally good health, as determined by medical history, medication review, and investigator assessment. * Willing and able to comply with all study procedures, assessments, and study-related restrictions for the duration of participation. * Willing to adhere to the study's lifestyle considerations for the duration of the study (maintain usual diet unless assigned to the diet arm; maintain usual physical activity; avoid non-essential systemic antibiotics; avoid probiotic/prebiotic/synbiotic supplements). * Willing and able to attend all required in-person study visits at Stanford University and complete remote assessments, if applicable. Exclusion Criteria: * Moderate or severe irritable bowel syndrome (IBS). * Current or prior diagnosis of inflammatory bowel disease (IBD), including ulcerative colitis, Crohn's disease, or indeterminate colitis. * Active gastrointestinal disease, including infectious gastroenteritis, colitis, gastritis, recurrent Clostridioides difficile infection, untreated Helicobacter pylori infection, or clinically significant malabsorption disorders (e.g., celiac disease). * Major gastrointestinal surgery within the past 5 years (excluding cholecystectomy and appendectomy), or history of major bowel resection at any time. * Body mass index (BMI) ≥40 kg/m². * Diabetes mellitus. * Hyperthyroidism or uncontrolled hypothyroidism. * Clinically significant renal disease. * Clinically significant hepatic disease or significant liver enzyme abnormalities. * Clinically significant cardiovascular disease. * Autoimmune or systemic inflammatory disease. * Current malignancy or history of malignancy within the past 5 years, excluding adequately treated non-melanoma skin cancer. * Current use of immunosuppressive medications, including systemic corticosteroids, thiopurines, methotrexate, calcineurin inhibitors, biologic agents, or other immunosuppressive therapies. * Receipt of fecal microbiota transplantation (FMT) within the previous 12 months. * Use of systemic antibiotic therapy within 30 days prior to enrollment or anticipated antibiotic use during the study period. * Use of probiotic supplements, prebiotic supplements, synbiotics, or live microbial therapeutics within 30 days prior to enrollment. * Current use or use within the previous 6 months of medications prescribed primarily for weight loss. * Current use of medications known to significantly affect body weight unless the medication and dose have remained stable for at least 6 months prior to enrollment. * Neurodevelopmental, psychiatric, neurological, or neuromuscular disorders that, in the opinion of the investigator, may impair the participant's ability to provide informed consent, comply with study procedures, or complete study assessments. * Current diagnosis of schizophrenia, bipolar disorder, or other severe psychiatric illness that may interfere with study participation. * Current substance use disorder. * Current smoking or nicotine use, including cigarettes, cigars, electronic cigarettes, vaping products, or nicotine replacement therapy. * History of anaphylaxis or severe allergic reaction to study-related dietary components. * Planned major dietary change, initiation of a structured weight-loss program, or initiation of a specialized therapeutic diet during the study period. * Concurrent participation in another interventional clinical trial. * Any other medical, psychiatric, or social condition that, in the opinion of the investigator, could compromise participant safety, study compliance, or interpretation of study outcomes. * Pregnancy or breastfeeding * Known immunodeficiency state, including HIV infection, primary immunodeficiency, active hematologic or solid-organ malignancy under treatment, or other clinically significant immunocompromise, independent of medication use. * Dysphagia or any condition impairing the ability to swallow oral capsules.
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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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Stanford University
Stanford, California, 94305, United States
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