Gut check: can poop pills from young donors turn back the biological clock?

NCT ID NCT07826793

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
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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 Results may not be published yet.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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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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

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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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 80 people

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

Expected to start

Dec 2026

An estimate. Start dates often move.

Expected to finish

Jun 2028

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

40 years and older

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: * 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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Contacts and locations

Locations

  • Stanford University

    Stanford, California, 94305, United States

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