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Irritable Bowel Syndrome and Food Sensitivity

Irritable Bowel Syndrome Clinical Trial

Official title:
Irritable Bowel Syndrome and Food Sensitivity: Assessing Clinical Outcomes and Inflammatory Cellular Pathways

Clinical Trial Summary

The primary objective of the clinical trial portion of this study is to assess whether an individualized dietary plan based on a commercial food sensitivity assay provides specific benefit in a randomized controlled trial in adults with irritable bowel syndrome (IBS).

Clinical Trial Description

This is a parallel group, randomized control trial, powered to assess changes in validated outcomes in adult patients with symptomatic irritable bowel syndrome. Subjects will receive dietary counseling and be asked to adhere to dietary instructions for 4 weeks. Assessments will occur at baseline, 4-weeks, and 8-weeks post-baseline. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02186743
Study type Interventional
Source Yale University
Contact
Status Completed
Phase N/A
Start date July 2014
Completion date January 2016
View Details
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