Clinical Trials Directory

Trials / Completed

CompletedNCT03359499

Impact of Bacillus Clausii Administration on Irritable Bowel Syndrome Patients

Impact of Bacillus Clausii Administration on Irritable Bowel Syndrome Patients - a Pilot Study

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Hospital Britanico · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Probiotics have been proposed as useful therapeutic alternatives for the treatment of irritable bowel syndrome patients. Bacillus clausii is a probiotic that has been used for the treatment of acute diarrhea among adults and pediatric patients, as well as an adjunctive therapy for the treatment for Helicobacter pylori infection. It has been proposed that Bacillus clausii is effective for the treatment of irritable bowel syndrome-related symptoms (especially diarrhea and bloating) in non-controlled trials. The aim of the proposed investigation is to determine whether the administration of Bacillus clausii during two weeks plus dietary advice compared to antispasmodics plus dietary advice would be an effective and safe alternative.

Conditions

Interventions

TypeNameDescription
DRUGBacillus clausiiOral suspension administered BID
DRUGTrimebutineOne tablet of 200 mg of trimebutine administered BID

Timeline

Start date
2017-08-12
Primary completion
2017-10-25
Completion
2017-11-23
First posted
2017-12-02
Last updated
2018-03-13

Locations

1 site across 1 country: Argentina

Source: ClinicalTrials.gov record NCT03359499. Inclusion in this directory is not an endorsement.