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Clinical Trial Summary

The purpose of this study is to evaluate the effects of oral administration of probiotic at 9 log colony forming unit (CFU)/day on vaginal microbiota profiles compared to placebo via the use of vaginal self-swab microbiota profiling.


Clinical Trial Description

1. To evaluate differences in general women's health of women on probiotic and placebo via the use of questionnaire. 2. To evaluate differences in immunity of women on probiotic and placebo via blood immunity profiling. 3. To evaluate differences in gut microbiota profiles of women on probiotic and placebo via blood fecal microbiota profiling. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05302687
Study type Interventional
Source Universiti Sains Malaysia
Contact
Status Completed
Phase Phase 2/Phase 3
Start date January 15, 2022
Completion date March 18, 2024

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