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NCT05332626: LaBon

Lactobacillus Acidophilus and Postmenopausal Women

Completed NA Results posted Last updated 8 January 2026
What this trial tests

NA trial testing Probiotic group in Bone Loss in 90 participants. Completed in 1 July 2024.

Timeline
1 February 2022
Primary endpoint
1 July 2024
1 July 2024

Quick facts

Lead sponsorPoznan University of Life Sciences
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment90
Start date1 February 2022
Primary completion1 July 2024
Estimated completion1 July 2024
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Poznan University of Life Sciences

Who can join

Adults 45 to 70, female only, with Bone Loss or Post Menopausal Osteoporosis. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Calcium Primary · 2 years

measure the calcium concentration in serum and hair

GroupValue95% CI
Probiotic Group1.88± 0.44
Placebo Group2.04± 0.09
DXA Primary · 2 years

bone densitometry analysis

GroupValue95% CI
Probiotic Group1.12± 0.12
Placebo Group1.15± 0.11
Body Mass Secondary · 2 years

measure body mass in kilograms

GroupValue95% CI
Probiotics Group72.22± 15.21
Placebo Group73.88± 13.45
Calcium Intake Secondary · 2 years

assessing calcium intake with the questionnaire

GroupValue95% CI
Probiotics Group1,115.81± 529.76
Placebo Group894.72± 381.84
Biomarkers of Bone Turnover: CTX Secondary · 2 years

measure the concentration of C-terminal telopeptide of type I collagen (CTX) in serum

GroupValue95% CI
Probiotics Group5.67± 0.52
Placebo Group5.11± 0.52
Biomarkers of Bone Turnover: TRAP5b Secondary · 2 years

measure the concentration of tatrate-resistant acid phosphatase isoform-5b (TRAP5b) in serum

GroupValue95% CI
Probiotics Group26.09± 9.31
Placebo Group21.13± 6.33
Biomarkers of Bone Resorption: BSAP Secondary · 2 years

measure the concentration of bone-specific alkaline phosphatase (BSAP) in serum

GroupValue95% CI
Probiotics Group10.90± 1.56
Placebo Group11.38± 1.96
Biomarkers of Bone Resorption: PINP Secondary · 2 years

measure the concentration of N-terminal propeptide of type I procollagen (PINP) in serum

GroupValue95% CI
Probiotics Group2.64± 0.52
Placebo Group2.66± 0.52

Sponsor's own description

This study aims to evaluate the effect of Lactobacillus acidophilus supplementation on calcium status and bone densitometry in postmenopausal women in a randomized, double-blind placebo-controlled study.

Publications & conference data

4 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Targeting strategies for bone diseases: signaling pathways and clinical studies.
    Xu H, Wang W, Liu X, Huang W, et al · · 2023 · cited 97× · PMID 37198232 · DOI 10.1038/s41392-023-01467-8
  2. Effects of daily probiotic supplementation with <i>Lactobacillus acidophilus</i> on calcium status, bone metabolism biomarkers, and bone mineral density in postmenopausal women: a controlled and randomized clinical study.
    Harahap IA, Moszak M, Czlapka-Matyasik M, Skrypnik K, et al · · 2024 · cited 14× · PMID 39010860 · DOI 10.3389/fnut.2024.1401920
  3. The Link Between the Gut Microbiome and Bone Metastasis.
    Sevcikova A, Martiniakova M, Omelka R, Stevurkova V, et al · · 2024 · cited 5× · PMID 39596154 · DOI 10.3390/ijms252212086
  4. Nutraceuticals in osteoporosis prevention.
    Roseti L, Borciani G, Grassi F, Desando G, et al · · 2024 · cited 3× · PMID 39416651 · DOI 10.3389/fnut.2024.1445955

Verify or expand the search:

Other trials of Probiotic group

Trials testing the same drug.

Other recruiting trials for Bone Loss

Currently open trials in the same condition.

Other Poznan University of Life Sciences trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05332626.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing