Gut bacteria supplement shows promise for weight loss
NCT ID NCT06964919
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed trial tested whether a heat-killed probiotic called Akkermansia muciniphila Akk11 could help overweight or obese adults lose weight and improve their metabolism. 61 participants took either the probiotic or a placebo capsule daily for 12 weeks, while following a low-carb diet. Researchers measured changes in body weight, BMI, waist size, and blood fats like cholesterol.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Heat-killed Akkermansia muciniphila Akk11 probiotic capsules
- What this could lead to
- If it works, this could offer a natural probiotic supplement to help with weight loss and improve cholesterol levels in overweight people.
- What could go wrong
- This is a small, early-stage trial with only 61 participants. The effects may be modest, and results might not apply to everyone. As a dietary supplement, it is not a substitute for lifestyle changes.
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
-
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
-
61 people
The number who actually took part.
- Started
-
Mar 2025
- Finished
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Jan 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
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: 1. A body mass index (BMI) of ≥24 kg/m²; 2. Willingness to provide written informed consent to participate in the study; 3. Agreement to adhere to the study protocol and restrictions, including a low-carbohydrate, energy-restricted diet; 4. No plans for conception from 14 days before screening until 6 months after the trial, with a commitment to using effective contraception. Exclusion Criteria: 1. Use of products similar to the test product in the near term that may affect the results; 2. Presence of mental or neurological disorders, celiac disease, lactose intolerance, or allergies; 3. Pregnant, breastfeeding, or planning pregnancy; 4. Irritable Bowel Syndrome (IBS), Ulcerative Colitis, Hepatic Cirrhosis, or Diabetes Mellitus; 5. Antibiotic use within the past three months; 6. Failure to consume the test product as required or attend follow-ups on time, making efficacy assessment impossible; 7. Smoking more than 10 cigarettes a day; 8. Allergy to probiotic products; 9. Other participants deemed unsuitable for the study by the investigator.
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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.
Contacts and locations
Locations
-
The School of Food and Bioengineering, Henan University of Science and Technolog
Luoyang, Henan, 471000, China
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