Clinical Trial

Efficacy of PosBion® Postbiotic Supplementation in Adults With Irritable Bowel Syndrome

Completed
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Summary
Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder characterized by recurrent abdominal pain and altered bowel habits, often associated with impaired intestinal barrier function, low-grade inflammation, and dysregulation of the gut-brain axis. Postbiotics have emerged as a promising therapeutic approach due to their immunomodulatory, anti-inflammatory, and gut barrier-protective properties. This completed single-arm, open-label clinical study evaluated the efficacy of PosBion® postbiotic supplementation in adults with IBS over a 12-week intervention period. The study assessed changes in IBS symptom severity, quality of life, gastrointestinal health, inflammatory biomarkers, intestinal barrier integrity, mucosal immunity, oxidative stress, and gut-brain axis biomarkers using validated questionnaires and salivary biomarker analyses.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-07.
Trial Details
NCT Number NCT07699926
Lead Sponsor My Myracle Sdn.Bhd
Collaborators: UCSI University
Conditions IBS (Irritable Bowel Syndrome), IBD (Inflammatory Bowel Disease), Gut Health
Enrollment 55 participants
Start Date 2026-01-01
Primary Completion 2026-05-31 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-14