Gut Permeability

2

Review clinical trials related to Gut Permeability. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Modulation of Gut Microbiota Composition and Gut Permeability Profiles by Multispecies Synbiotic Supplementation in Hemodialysis Patients

Chronic kidney disease (CKD) patients undergoing maintenance hemodialysis experience profound alterations in their gut microbiota, leading to dysbiosis and increased gut permeability. This disruption facilitates the translocation of endotoxins and gut-derived uremic toxins such as indoxyl sulfate and p-cresyl sulfate into the systemic circulation, contributing to heightened systemic inflammation, cardiovascular disease risk, and accelerated CKD progression. Synbiotic supplementation, particularly multispecies formulations, has emerged as a promising therapeutic strategy to restore gut microbial balance, enhance intestinal barrier integrity, and reduce the systemic burden of deleterious microbial metabolites. These probiotics potentially improve clinical outcomes by modulating inflammatory pathways and decreasing circulating levels of uremic toxins. Despite these insights, few clinical trials have comprehensively assessed the effects of multispecies synbiotic on fecal microbiome composition, gut permeability and uremic toxin profiles in hemodialysis patients. This pilot study aims to fill this gap by evaluating the modulatory effects of a 12-week multispecies synbiotic intervention.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tungs' Taichung Metroharbour HospitalUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older receiving maintenance hemodialysis patients for at...

Use of probiotic supplements within the last month; [+4]

Status: Recruiting

Effects of Effera Human Lactoferrin at One Dose Compared to Placebo on Gut Permeability

The purpose of this study is to evaluate the impact of 28-day supplementation with effera human lactoferrin, compared to a placebo control product on indicators of gut barrier health in males and females

Participants needed: 46
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Helaina Inc.Updated: Jun 25, 2025Locations: 1
Eligibility criteria

Male or premenopausal female, 18 - 40 years of age, inclusive [+3]

Clinically important GI condition that would potentially interfere with the eval... [+28]