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Effect of Bifidobacterium Lactis HN019 on Colonic Transit Time and Digestive Symptoms

Gastrointestinal Symptoms Clinical Trial

Official title:
A Three‐Arm, Placebo Controlled, Double‐Blind, Single Center Study to Evaluate the Impact of Probiotic Strain Bifidobacterium Lactis HN019 on Intestinal Well‐Being, Colonic Transit Time and Digestive Discomfort

Clinical Trial Summary

The purpose of this study was to investigate the dose response effect of Bifidobacterium lactis HN019 supplementation on colonic transit time and gastrointestinal symptoms.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01171014
Study type Interventional
Source Fonterra Research Centre
Contact
Status Completed
Phase Phase 2/Phase 3
Start date June 2009
Completion date December 2009
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