Probiotic shows promise in preventing menopause bone loss
NCT ID NCT05332626
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether taking a probiotic called Lactobacillus acidophilus can help prevent bone loss and osteoporosis in women after menopause. 90 women aged 45-70 with a BMI between 27 and 35 took either the probiotic or a placebo. Researchers measured calcium levels and bone density to see if the supplement made a difference.
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
-
90 people
The number who actually took part.
- Started
-
Feb 2022
- Finished
-
Jul 2024
- Lead sponsor
-
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
-
45 to 70 years
- Sex
-
Female participants only
- Healthy volunteers
-
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. Women aged 45 to 70 years old with more than one year since last menstruation; 2. Body mass index (BMI): 27.0 kg/m2 to 34.9 kg/m2; 3. All female participants who accepted bone densitometry measurement Exclusion Criteria: 1. The secondary form of obesity, the pharmacological treatment for obesity (in the three months before the study), history of bariatric surgery; 2. Other gastrointestinal disorders, especially: inflammatory bowel diseases, celiac disease, gastritis and duodenitis, pancreatic disorders, gastrointestinal symptoms suggestive of irritable bowel syndrome; 3. Pharmacotherapy of lipid disorders or hypertension in the three months before enrollment 4. Clinically significant acute inflammatory process (elevated hsCRP) 5. Abnormal kidney function (GFR \<60mL/min/1,73m2); 6. Participation in a body mass management study; 7. The use of drugs known to modify body mass or food intake; 8. Hormone replacement therapy; 9. History of following alternative diets (diets with the altered amount of macronutrients, vegan or vegetarian diets, high-fiber diet, a diet with high quantities of fermented food (\>400 g/day), diet fortified with prebiotics- and probiotics-functional food, elimination diets, low-calorie diets) within three months before the study; 10. History of use of any dietary supplements, including calcium, in the three months before the study; 11. History of intake of antibiotics, probiotics, prebiotics (and synbiotics) within three months before the study; 12. Type 2 diabetes - - requiring the introduction and/or change of pharmacological treatment in the 2 years before the trial or during intervention; 13. Dyslipidemia - requiring the introduction and/or change of pharmacological treatment in the 6 months before the trial or during intervention; 14. Hypertension - requiring the introduction and/or change of pharmacological treatment in the 6 months before the trial or during intervention; 15. Another chronic pharmacotherapy: nonsteroidal anti-inflammatory drugs, proton pump inhibitors, anticoagulants, drugs causing metabolic alteration, e.g., SFAs (second-generation antipsychotics); 16. Diseases requiring nutritional requirement and chronic supplementation; 17. Alcohol (\>20g/d), nicotine or drug abuse; 18. Mental disorders, including eating disorders; 19. Cancer, autoimmune diseases; 20. Any other condition that, in the opinion of the investigators, would make participation not in the best interest of the subject, or could prevent, limit, or confound the efficacy of the study any diseases, disorders, and therapies, which may influence on final results of the study or pose a risk for subjects health.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Bone loss are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
Poznan University of Life Sciences
Poznan, Greater Poland Voivodeship, 60-624, Poland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Two ways to rebuild a Child's bone: which holds up?
- A common supplement may shield bones in kidney disease — a trial puts it to the test
- Could a single abutment placement save your jawbone?
- Drilling speed showdown: which dental implant technique preserves bone better?
- Denture cap showdown: which material saves more bone?
- Bone-Saving drug may shield patients after bariatric surgery