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Qualifying participants will be provided with a diagnostic test for SIBO, and will follow a 8 week course of probiotics (or placebo), with sampling for microbiome changes at several time points. 

Probiotic Efficacy in Bloating

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STUDY DESIGN

A double-blind, randomized, placebo-controlled clinical study in patients with diagnosed or suspected Small Intestinal Bacterial Overgrowth (SIBO).

A Study in Partnership with Lallemand Health Solutions




Qualifying participants will be provided with a diagnostic breath test for small bacterial overgrowth, complete daily and weekly questionnaires, will follow an 8 week course of probiotics (or placebo), with sampling for microbiome changes at several time points. 

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Ethics approval ID: HREBA.CTC-23-0061

TO BE ELIGIBLE FOR THE STUDY, YOU MUST MEET AT LEAST THE FOLLOWING CRITERIA

18 - 55 years of AGE

Suffer from bloating, diarrhea or abdominal pain

Follow an 8 week 
course of Probiotics

Male or female

Upon enrollment you will receive a diagnostic Breath Test to confirm your eligibility. 

Formulation designed for SIBO
note: some participants will receive a placebo

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