Gut bacteria pill tested for weight loss
NCT ID NCT06030362
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a probiotic (a mix of good bacteria) can help adults with obesity lose weight when combined with healthy lifestyle changes. About 100 people aged 18-50 with a BMI between 25 and 40 will take either the probiotic or a placebo for several weeks. Researchers will check changes in gut bacteria, blood markers, and stress levels to see if the probiotic is safe and helpful.
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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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2023
- Expected to finish
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Jul 2027
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 50 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: * Ages 18-50 * BMI 25-40 * Male and Female * Not Pregnant or Nursing Exclusion Criteria: * Co-morbidities including but not limited to: * Type 1 (insulin dependent) diabetes * vascular disease * drastic weight loss (more than 10lbs over the preceding 2months) * frequent strenuous exercise (i.e. marathon runners/heavy weight lifting) * abdominal surgeries including weight loss surgery or partial/complete resection of stomach or bowel * untreated thyroid disease * neurological disease * Major medical condition the PI/MD feels would put the subject at risk or interfere with data collection. * Chronic pain * Diagnosed DSM IV active psychiatric illness including eating disorders. Must not be active or present for at least 2 years. Participants with a positive endorsement on the MINI+ will be excluded. * Using medications known to affect hunger/satiety/appetite * Pregnant, lactating, postpartum less than 6months. * Women of childbearing potential who are not practicing birth control or are planning to get pregnant during the study. * Use of oral/IV antibiotics within the last 3 months * Use of probiotics in the last 3 months. * Heavy use of alcohol and drugs will be determined by a positive endorsement on the MINI+. If the MINI+ is positive for alcohol or drug dependence or abuse, the participant will be excluded. In regards to tobacco use, participants will be excluded if they smoke more than 1/2 pack per day. * Cannabis use will not be exclusionary. If the MINI+ is positive for drug dependence or abuse, the participant will be excluded. * Significant change in usual diet and/or weight loss of more than 10lbs in the last 2 months. * Anyone taking medicines on the medication exclusion list. * Non-English Speakers (due to the use of validated questionnaires and limited availability of translated copies, participants must be fluent in English so that they will be able to read and follow directions easily. * Maintenance pharmacotherapies will not be exclusionary so long as they have been on a stable dose for 6months. * Body weight at enrollment greater than 400lbs. * Exclude from Optional MRI if: participant is unable to safely participate in the MRI (claustrophobia, presence of devices affected by MRI such as pacemakers, neurostimulators, metallic foreign bodies, etc.).
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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 of California
RECRUITINGLos Angeles, California, 90095, United States
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