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Clinical Trial Summary

Eligible participants will be randomized and receive either the probioic or placebo supplement to consume daily for 28-days. Three check-in visits will occur every 7 days of study participation. Participants will be expected to complete a daily study diary documenting their investigational product use/adverse events and a daily bowel habits diary documenting each bowel movement. Blood samples, stool samples, and questionnaires will be completed for study outcome analysis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04223388
Study type Interventional
Source Church & Dwight Company, Inc.
Contact Mal Evans, PhD
Phone 5194389374
Email mevans@kgkscience.com
Status Recruiting
Phase N/A
Start date December 18, 2019
Completion date April 2020

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