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Efficacy and Safety of a Probiotic Formulation in Adults With Irritable Bowel Syndrome With Diarrhea (IBS-D)

IBS - Irritable Bowel Syndrome Clinical Trial

Official title:
Efficacy and Safety of a Probiotic Formulation in Adults With Irritable Bowel Syndrome With Diarrhea (IBS-D): A Multicenter, Randomized, Prospective, Placebo-Controlled, Double-Blind, Phase IV Clinical Study

Clinical Trial Summary

The purpose of the study is to monitor safety and to evaluate the efficacy of a probiotic formulation on abdominal pain, abnormal defecation, comorbid mood disorders (anxiety and depression) as well as general quality of life in adults with IBS-D.

Clinical Trial Description

To monitor safety and to evaluate the efficacy of a probiotic formulation on severity of gastrointestinal symptoms (abdominal pain, abnormal defecation), anxiety, depression and quality of life in adult participants with IBS-D. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05509725
Study type Interventional
Source Lallemand Health Solutions
Contact Burcu Sume
Phone +90 312 479 88 75
Email burcus@croturk.com
Status Recruiting
Phase Phase 4
Start date August 11, 2022
Completion date November 2024
View Details
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