RecruitingPhase 1NCT07413744

The Gut - PRO Study

Probiotic Supplementation Safety and Feasibility Study in Preclinical Alzheimer's Disease


Sponsor

University of Wisconsin, Madison

Enrollment

40 participants

Start Date

Sep 1, 2026

Study Type

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

Min Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Placebo and a drug called Probiotic for people with alzheimer disease. The study is currently recruiting participants at 1 location. People eligible for this study include aged 60 Years and older.

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

DRUGProbiotic

A single dose of oral PS will be administered once daily for 6 months

OTHERPlacebo

A placebo will be given once daily for 6 months.


Locations(1)

University of Wisconsin Hospitals and Clinics

Madison, Wisconsin, United States

View Full Details on ClinicalTrials.gov

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NCT07413744


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