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Lactobacillus Acidophilus and Postmenopausal Women

NCT05332626 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2026-01-08

Study results available
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Summary

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.

Conditions

  • Bone Loss
  • Post Menopausal Osteoporosis
  • Mineralization

Interventions

DIETARY_SUPPLEMENT

Probiotic group

The probiotic gorup is focused on the treatment of postmenopause osteoporosis women with a capsule cointained 1x10\^9 CFU of Lactobacillus acidophilus UALa-01™/day (30 people)

DIETARY_SUPPLEMENT

Placebo group

The group is assigned on the treatment of postmenopause osteoporosis women without probiotic intervention (30 people)

Sponsors & Collaborators

  • Poznan University of Medical Sciences

    collaborator OTHER

  • Poznan University of Life Sciences

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
45 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-02-01
Primary Completion
2024-07-01
Completion
2024-07-01

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05332626 on ClinicalTrials.gov