drugset / Trial / NCT04855799

GI Permeability Change in Response to Aquamin®

NCT04855799 ↗

Phase 2 Completed 35 enrolled James Varani
NaSingle-groupOpen-labelTreatment

Summary

This trial is being completed to learn about how Aquamin® affects gastrointestinal permeability, or the control of material passing from inside the gastrointestinal tract through the gut wall into the rest of the body, in people with ulcerative colitis (UC), Irritable Bowel Syndrome with diarrhea (IBS-D), and in healthy individuals.

Timeline

Start
2021-11-02
Primary completion
2024-03-11
Completion
2024-03-25

Outcome

Met primary endpoint

paper Overall, Aquamin ® supplementation reduced total post-intervention mannitol excretion by 29% (p = 0.024). PMID 41646788 ↗

paper the reduction at the 0-2 h interval reached statistical significance (p = 0.015). PMID 41646788 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Aquamin Other / unclassified 800 mg —