drugset / Trial / NCT07413744

The Gut - PRO Study

NCT07413744

RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and feasibility of an oral probiotic supplement (PS) intervention in individuals with dementia or mild-cognitive impairment (MCI) due to Alzheimer's disease or at risk of dementia due to Alzheimer's disease (AD). 40 participants will be enrolled and can expect to be on study for up to 1 year.

Timeline

Start
2026-08
Primary completion
2029-03
Completion
2029-03

Drugs

EvaluationDrugModalityDoseRoute
Subject VSL#3 Other / unclassified Oral

Indications