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Clinical Trial Summary

A total of 120 subjects are expected to be recruited over a 3-year period starting after IRB approval, divided into two groups of 60 subjects, receiving PS23 or placebo, and completing a 6-week trial period.


Clinical Trial Description

There is still a lack of research to explore the interaction between high-pressure workers and probiotics to improve the intestinal microbiota and further affect its relationship with sleep, inflammation, and anti-oxidation, and further studies are still needed to confirm the clinical effect. A total of 120 subjects are expected to be recruited over a 3-year period starting after IRB approval, divided into two groups of 60 subjects, receiving PS23 or placebo, and completing a 6-week trial period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05826704
Study type Interventional
Source Mackay Memorial Hospital
Contact
Status Recruiting
Phase N/A
Start date December 30, 2022
Completion date December 30, 2025

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