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Dose Ranging Study With the Probiotic Combination (VSL#3) in Diarrhea IBS

IBS Clinical Trial

Official title:
A Randomized, Multi-center, Double-blind, Placebo Controlled, Dose Ranging Study With VSL#3 in Diarrhea Predominant IBS Patients

Clinical Trial Summary

To evaluate the effects of VSL#3 on symptoms associated with diarrhea predominant IBS

Clinical Trial Description

The study will evaluate 2 doses of VSL#3 and placebo over a 4 week period in patients presenting with diarrhea predominant IBS symptoms. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00179582
Study type Interventional
Source Beth Israel Deaconess Medical Center
Contact
Status Terminated
Phase N/A
Start date January 2005
Completion date January 2006
View Details
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