Clinical Trial

The Effect of a Synbiotic on Intestinal Barrier Function and Microbiota Modulation in Middle-aged to Elderly Individuals With Excessive Body Weight

Study acronym: myBIOM
Recruiting
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Summary
The study is a single-center, randomized, double-blind, placebo-controlled study in middle-aged to elderly adults with excessive body weight. The study includes an 8-week intervention period followed by a 2-week follow-up period. The study will evaluate the effect of a synbiotic consisting of two probiotic strains and a prebiotic. The aim is to investigate the effect of the synbiotic on modulating the gut microbiota and improving markers of gastrointestinal permeability and integrity and gastrointestinal discomfort.
Protocol Amendment History 1 change
critical Recruitment opened 2026-04-16
Trial Details
NCT Number NCT07453823
Lead Sponsor Chr Hansen - part of Novonesis
Conditions Gastrointestinal Microbiome (Focus), Gastrointestinal Symptoms
Enrollment 90 participants
Start Date 2026-03-18
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-04-15