Could poop transplants treat diabetes and heart disease?
NCT ID NCT07421947
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tests whether fecal microbiota transplantation (FMT) can change the gut microbiome in 30 people with type 2 diabetes and stable coronary artery disease. Participants receive processed stool from healthy donors via colonoscopy. The goal is to see if this alters gut bacteria and possibly improves metabolic and heart health markers.
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 transplantation (processed stool from healthy donors given via colonoscopy)
- What this could lead to
- If successful, this could point toward a new way to treat type 2 diabetes and heart disease by adjusting gut bacteria.
- What could go wrong
- This is a very small pilot study (30 people) with no control group, so results may not be reliable or generalizable. The procedure carries risks like infection or bowel perforation.
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
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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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 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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18 to 75 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 (Recipients): Age ≥18 years and ≤75 years Diagnosis of type 2 diabetes mellitus Stable coronary artery disease Platelet count ≥50 × 10⁹/L within 2 days prior to FMT Hemoglobin ≥8.5 g/dL within 2 days prior to FMT International normalized ratio (INR) ≤1.5 within 2 days prior to FMT Willingness to undergo fecal microbiota transplantation (FMT) via colonoscopy Signed informed consent Exclusion Criteria (Recipients): Pregnancy or breastfeeding Women of childbearing potential not using adequate contraception Acute coronary syndrome within 12 months Requirement for dual antiplatelet therapy Relevant moderate or severe valvular heart disease Severe kidney dysfunction (estimated GFR \<30 mL/min) Significant liver dysfunction Contraindications to colonoscopy or FMT Systemic steroid or immunosuppressive therapy Antibiotic therapy within 3 months Ongoing infectious disease Active malignancy Participation in another interventional study Life expectancy \<12 months Inability to provide informed consent Inclusion Criteria (Donors): Healthy participants ≥18 years and \<60 years Eligibility for stool donation according to institutional donor screening procedures Negative donor screening results Signed informed consent Exclusion Criteria (Donors): History of gastrointestinal disease History of metabolic, autoimmune, or chronic inflammatory disease History of infectious disease Recent antibiotic therapy High-risk behavior for transmissible diseases Contraindications to colonoscopy Pregnancy or breastfeeding
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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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University Hospital Zurich
Zurich, Canton of Zurich, 8091, Switzerland
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