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L. Casei DG® in Patients With Irritable Bowel Syndrome. — PROBE2  

IBS - Irritable Bowel Syndrome Clinical Trial

Official title:
L. Casei DG® (Lactobacillus Paracasei CNCMI1572) in the Treatment of Patients With Irritable Bowel Syndrome: a Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo Controlled Study.

Clinical Trial Summary

To assess the effect of L. casei DG® (Lactobacillus paracasei CNCMI1572; Enterolactis® plus) on abdominal symptoms and gut microbiota metabolism/composition in non constipated patients with IBS (Irritable Bowel Syndrome). Patients will be randomized to receive L. casei DG® capsules, b.i.d. for 12 weeks the a 4 weeks Follow Up period will follow.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03449628
Study type Interventional
Source SOFAR S.p.A.
Contact
Status Completed
Phase N/A
Start date November 6, 2017
Completion date December 30, 2021
View Details
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