NCT05475314

Effect of Postbiotic Product on Colonic Barriers in IBS

A Postbiotic Fermented Oat Gruel May Have a Beneficial Effect on the Colonic Mucosal Barrier in Patients With Irritable Bowel Syndrome
Nordisk Rebalance A/S·ClinicalTrials.gov·dietary supplementCompleted
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
ReFerm(R)
Study type
Interventional
Intervention type
dietary supplement
Sponsor & location
Primary sponsor
Nordisk Rebalance A/S
Location
Linköping, Sweden
Timeline & enrollment
Phase
N/A
Start date
Dec 01, 2020
End date
Apr 30, 2022
Enrollment
30 participants
Primary outcome

Intestinal permeability

Summary

Impaired intestinal permeability and microbial dysbiosis are important pathophysiological
 mechanisms underlying irritable bowel syndrome (IBS). ReFerm®, also called Profermin®, is a
 postbiotic product of oat gruel fermented with Lactobacillus plantarum 299v. In this
 experimental study, we investigated whether ReFerm® has a beneficial effect on the intestinal
 epithelial barrier function in patients with IBS.

ICD-10 classifications
Irritable bowel syndrome with predominant constipation [IBS-C]Irritable bowel syndromeIrritable bowel syndrome with predominant diarrhoea [IBS-D]Irritable bowel syndrome with mixed bowel habits [IBS-M]Other and unspecified irritable bowel syndrome
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05475314
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05475314 through Pure Global AI's free database. This phase not specified trial is sponsored by Nordisk Rebalance A/S and is currently Completed. The study focuses on IBS - Irritable Bowel Syndrome. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.