Clinical Trials Directory

Trials / Completed

CompletedNCT01099696

Study to Evaluate a Probiotic in Healthy Subjects With a History of Abdominal Discomfort and Bloating

A Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Evaluate the Benefit of a Probiotic (Bifidobacterium Infantis 35624) in Healthy Subjects With a History of Abdominal Discomfort and Bloating

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
302 (actual)
Sponsor
Procter and Gamble · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This is a multicenter, double-blind, randomized, placebo-controlled, 6-week study of a probiotic for abdominal discomfort and bloating in healthy subjects.

Detailed description

This is a multicenter, double-blind, randomized, placebo-controlled, parallel-group, 6-week study of a probiotic for abdominal discomfort and bloating in healthy subjects.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTB. infantis 35624B. infantis 35624 in white capsules
DIETARY_SUPPLEMENTplacebowhite placebo capsules

Timeline

Start date
2010-04-01
Primary completion
2010-10-01
Completion
2010-10-01
First posted
2010-04-07
Last updated
2012-12-20

Locations

10 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01099696. Inclusion in this directory is not an endorsement.

Study to Evaluate a Probiotic in Healthy Subjects With a History of Abdominal Discomfort and Bloating (NCT01099696) · Clinical Trials Directory