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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of the oral administration of Lactobacillus reuteri in treating infantile colic as defined by the Rome III criteria. Forty breastfed infants aged from 29 days to 3 months will be enrolled and blinded randomized to receive orally L.reuteri or placebo. The rate of responders (reduction of daily crying time >50% compared to the baseline) will be assessed at day 7, day 14 and day 21 in both groups. The average daily crying time as well as the associated digestive symptoms will also be analyzed.


Clinical Trial Description

NOTE: The study never started. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01887444
Study type Interventional
Source BioGaia AB
Contact
Status Withdrawn
Phase N/A
Start date October 2013
Completion date September 2014

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