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The Use of VSL#3 in Irritable Bowel Syndrome in Children — VSL#3  

Irritable Bowel Syndrome Clinical Trial

Official title:
The Use of VSL#3 in Irritable Bowel Syndrome in Children

Clinical Trial Summary

The goal of this study is to determine whether the oral administration of the probiotic VSL#3 under randomized, placebo-controlled conditions will improve symptoms of irritable bowel syndrome in children, safely.

Clinical Trial Description

Determine the safety and efficacy of different doses of VSL#3 in the treatment of children with irritable bowel syndrome: Children will be recruited from the pediatric gastroenterology clinic at The Children's Medical Center in Dayton, Ohio. Eighty four children will be enrolled in this controlled, double-blinded, randomized study. All children will have had a prior evaluation by a pediatric gastroenterologist who has diagnosed these patients with irritable bowel syndrome and excluded organic disease as a cause of the child's abdominal pain. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00932841
Study type Interventional
Source Dayton Children's Hospital
Contact
Status Terminated
Phase Phase 1
Start date January 2008
Completion date August 2011
View Details
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