The Gut - PRO Study
Probiotic Supplementation Safety and Feasibility Study in Preclinical Alzheimer's Disease
University of Wisconsin, Madison
40 participants
Sep 1, 2026
INTERVENTIONAL
Conditions
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.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
A single dose of oral PS will be administered once daily for 6 months
A placebo will be given once daily for 6 months.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07413744