Probiotic BC99 shows promise for gut health in overweight adults
NCT ID NCT06077383
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a probiotic called Weizmania Coagulans BC99 can improve gut bacteria and blood fat markers (like cholesterol) in overweight adults. 72 participants took either the probiotic or a placebo daily for 8 weeks. Researchers collected blood, urine, and stool samples to measure changes. The goal was to see if this probiotic could help manage weight-related health risks.
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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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72 people
The number who actually took part.
- Started
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Oct 2023
- Finished
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Jul 2024
- 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 65 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. All patients meet the diagnostic criteria for severe illness, and a body mass index (BMI) of ≥ 24kg/m2 is considered overweight; 2. Age 18-65 years old; 3. Without dieting or weight loss, and able to accept dietary intervention, maintain a low-carbon and healthy diet during the trial period; 4. Patients who understand clinical research and commit to complying with research requirements and procedures; 5. Patients who have signed informed consent forms. Able to complete research according to the requirements of the experimental protocol; Exclusion Criteria: 1. Taking items with similar functions to the test subjects in the short term can affect the judgment of the results; 2. Have taken antibiotics 2 weeks before recruitment; 3. Those who stop taking the test sample or add other drugs midway, and cannot determine the efficacy or have incomplete information; 4. Obesity caused by drug treatment (hormones, antidepressants, etc.), endocrine diseases, combined with severe liver and kidney dysfunction, water retention or muscle development; 5. Patients who are pregnant, lactating, stomatal, critically ill, or have potential health conditions that affect metabolism or weight; 6. Neuroendocrine system diseases (hypothyroidism, polycystic ovary syndrome, Cushing's syndrome, hypothalamic injury, etc.); 7. Have a clear history of gastrointestinal diseases (such as ulcers, gastrointestinal bleeding, irritable bowel syndrome, celiac disease, inflammatory bowel disease, Crohn's disease, or other diseases) and a history of surgery (such as weight loss surgery, bandaging surgery, gastrointestinal anastomosis surgery, and intestinal resection surgery); 8. Hereditary obesity Hereditary obesity (such as PWS, Down's syndrome), metabolic obesity (such as obesity reproductive impotence syndrome), endocrine obesity (such as Kirschner's syndrome, hypothyroidism), any disease affecting liver fibrosis or steatosis, metabolic disease (such as hypothyroidism/hyperthyroidism, type 1 or type 2 diabetes, etc.); 9. Patients who changed their diet type during the study period; 10. Patients with severe diseases such as cardiovascular, cerebrovascular, liver, kidney, and hematopoietic systems, as well as endocrine diseases, and mental illnesses; 11. According to the researcher's judgment, the condition of the subject does not qualify them to participate in the study.
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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
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Qilu hospital
Jinan, Shandong, 250012, China
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