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Clinical Trial Summary

The primary objective of this study is to assess the safety and efficacy of Salix Probiotic Blend, administered orally for 30 days, in participants with functional gastrointestinal (GI) disturbances.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04155801
Study type Interventional
Source Bausch Health Americas, Inc.
Contact
Status Completed
Phase N/A
Start date October 11, 2019
Completion date February 14, 2020

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