Share

L. CASEI DG® (LACTOBACILLUS PARACASEI CNCMI1572; ENTEROLACTIS®PLUS) IN THE TREATMENT OF PATIENTS WITH IRRITABLE BOWEL SYNDROME: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLELGROUP, PLACEBO CONTROLLED STUDY

L. CASEI DG® (LACTOBACILLUS PARACASEI CNCMI1572; ENTEROLACTIS® PLUS) in the treatment of patients with irritable bowel syndrome; a multicenter, randomized, double-blind, parallel-group, placebo-controlled study.

Project objectives

The overall aim of the study was to collect data to evaluate the effect of Lactobacillus casei DG (Enterolactis plus®) on abdominal symptoms in non-constipated patients with IBS.

Start and end date

2017 - ongoing

Project Manager

Prof. Michele Cicala

Coordinating institution of the project

Complex Operating Unit of Gastroenterology, Biomedical Campus University of Rome

Other Institutions involved

Pharmaceutical company SOFAR SpA (study sponsor)

QUICK LINKS
magnifiercrossmenuchevron-downchevron-leftchevron-right