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Clinical Trial Summary

The purpose of this study is to analyse the effect of probiotic supplement on symptoms of irritable bowel syndrome.


Clinical Trial Description

The aim of the intervention is to analyse the effect of a probiotic supplement in a dose-responsive set up on symptoms of irritable bowel syndrome (IBS). Fulfillment of Rome III criteria will be used as inclusion criterion. Subjective assessment of bowel symptoms, IBS-related quality of life and adequate relief will be assessed as outcome measures. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT01475929
Study type Interventional
Source Danisco
Contact
Status Terminated
Phase Phase 2
Start date June 2011
Completion date May 2012

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