Effect of Postbiotic Product on Colonic Barriers in IBS
- Disease/Condition
- IBS - Irritable Bowel Syndrome
- Drug/Device/Intervention
- ReFerm(R)
- Study type
- Interventional
- Intervention type
- dietary supplement
- Primary sponsor
- Nordisk Rebalance A/S
- Location
- Linköping, Sweden
- Phase
- N/A
- Start date
- Dec 01, 2020
- End date
- Apr 30, 2022
- Enrollment
- 30 participants
Intestinal permeability
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT05475314
- Type
- Non-Device Trial
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.