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Clinical Trial Summary

This prospective, two-arm (parallel groups), double-blind, randomized, placebo-controlled, multi-center clinical trial will investigate the effects of an 8-week Bifidobacterium lactis HN019 supplementation on stool frequency and on other constipation parameters in adults suffering from functional constipation according to ROME III criteria. The hypothesis is that Bifidobacterium lactis HN019 is superior, in comparison with a placebo, for the increase of stool frequency of at least 1 stool per week.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04231162
Study type Interventional
Source Danisco
Contact
Status Completed
Phase N/A
Start date September 16, 2020
Completion date January 21, 2022

See also
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