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Clinical Trial Summary

A randomized, double-blind, placebo-controlled pilot study in patients with IBS-D according to Rome IV criteria evaluating the clinical efficacy and safety of oral administration of 2g G-PUR® tid compared to placebo in a cohort of 30 patients over an active treatment period of 12 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04138186
Study type Interventional
Source Glock Health, Science and Research GmbH
Contact Michael Wolzt, Prof. Dr.
Phone +43 (0)1 40400
Email michael.wolzt@meduniwien.ac.at
Status Recruiting
Phase N/A
Start date October 2, 2019
Completion date February 2021

See also
  Status Clinical Trial Phase
Completed NCT00394173 - Efficacy, Safety and Tolerability of DNK333 (25 mg Bid) in Women With Diarrhea-predominant Irritable Bowel Syndrome (IBS-D) Phase 2
Completed NCT03931785 - A Study of MD-7246 to Treat Abdominal Pain in Patients With Diarrhea-predominant Irritable Bowel Syndrome Phase 2