Clinical Trials Directory

Trials / Completed

CompletedNCT01837485

Probiotics in the Treatment of Irritable Bowel Syndrome

Evaluation of the Effects of Lactol Probiotic in Comparison With Placebo on Symptoms of Irritable Bowel Syndrome

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
82 (actual)
Sponsor
Islamic Azad University, Najafabad Branch · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Some evidences have shown that probiotics are effective in the treatment of irritable bowel syndrome. Because few evidences are available in our population, we investigated if probiotics are effective in our patients as well. We hypothesize that the probiotic Lactol which contains Lactobacillus Sporogenes reduces the symptoms of irritable bowel syndrome.

Conditions

Interventions

TypeNameDescription
DRUGLactolThe Symbiotic Lactol® (Bioplus Life Sciences Pvt.) was applied 3 times a day for 3 months. Lactol is composed of the followings; Lactobacillus Sporogenes (15 × 107 Spores), Fructo-Oligosaccharides, Microcrystalline Cellulose, Sodium starch Glycolate, Povidone, Hypermellose Stearate, Sillicon Dioxide, and Propylene Glycol.
DRUGPlaceboPlacebo pill was applied 3 times a day for 3 months

Timeline

Start date
2011-08-01
Primary completion
2013-01-01
Completion
2013-03-01
First posted
2013-04-23
Last updated
2013-04-23

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT01837485. Inclusion in this directory is not an endorsement.