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Study identifier: NCT06659380 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Probiotic Efficacy in Postmenopausal Women with Bacterial Vaginosis

Condition: Bacterial Vaginosis (BV) · Menopause  ·  Sponsor: Hasanuddin University

PhaseNA
Planned participants12
Who can joinFemale, N/A to no upper limit
Healthy volunteersYes

About this study

This study is a double-blind, randomized, controlled trial (RCT) aimed at evaluating the effects of Lactobacillus sp. probiotic administration on the vaginal microbiota changes in postmenopausal women with bacterial vaginosis and how its affect to immunology profile. Postmenopausal women diagnosed with bacterial vaginosis will be recruited as subjects as long as collected period in this study. All patients will receive Metronidazole antibiotic treatment then blind-randomly be divided into two groups: the treatment group, receiving Floragyn® probiotic tablets (Lapi, Indonesia), and the placebo group, receiving Cal 95® (Lapi, Indonesia). As a control, postmenopausal women without bacterial vaginosis will also be included and receive Floragyn® probiotic tablets only.

This description comes directly from the study's public registry record.

Talk to the study team

Yenti Purnamasari  ·  +628114058258  ·  yenti.purnamasari@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Alfa Farma Health Clinic, Obstetrics and Gynecology Doctor's Practice.Kendari, South East Sulawesi, IndonesiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06659380