Could a poop transplant ease Parkinson's?
NCT ID NCT07597421
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether fecal microbiota transplantation (FMT) from healthy donors can improve motor and non-motor symptoms in people with Parkinson's disease. 58 participants will receive either FMT or a control, and their movement scores will be compared after 6 months. The goal is to see if changing gut bacteria can help manage the disease.
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 (FMT) from healthy donors
- What this could lead to
- If it works, this could point toward a new way to manage Parkinson's symptoms by targeting the gut-brain connection.
- What could go wrong
- This is a small, early pilot study, so results may not be conclusive. The procedure involves antibiotics and colonoscopy, which carry their own risks.
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 58 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2029
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 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1. Clinical diagnosis of idiopathic PD according to UK brain bank criteria. 2. PD disease duration ≧5 years to avoid the possible misdiagnosis of atypical parkinsonism. 3. Hoehn-Yahr stage 1-4 4. Using levodopa in a currently fixed dose. 5. Presence of motor complications (motor fluctuation or dyskinesia). 6. Written informed consent. 7. Age above 18. Exclusion Criteria: 1. Hoehn-Yahr stage 5. (wheelchair ridden or bedridden due to PD) 2. Dementia (MMSE\<24), history of encephalitis, or brain organic lesions, including congenital or acquired structural abnormalities (which were detected through brain computed tomography scan or Magnetic Resonance Imaging) may affect neurological function, leading to various neurological deficits and mpairing the cognitive function. 3. Current use of probiotics or in the past 3 months. 4. For women with childbearing potential. (Female participants are suggested to prevent pregnancy during this trial and undergo a pregnancy test before enrollment.) 5. Current need of antibiotics or use in the previous 3 months. 6. End stage renal disease caused uremic encephalopathy or liver cirrhosis caused hepatic encephalopathy 7. Immunocompromised state.
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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 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.
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