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Clinical Trial Summary

Participants experiencing recurrent gastrointestinal symptoms in this double-blind, randomized, controlled trial will receive either a commercially-available probiotic dietary supplement or placebo. The investigators hypothesize that participants in the probiotic dietary supplement group will experience greater improvement in their gastrointestinal symptoms than participants in the placebo group.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02277431
Study type Interventional
Source University of Maryland, Baltimore
Contact
Status Completed
Phase Phase 2/Phase 3
Start date December 2014
Completion date October 2015

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