The Gut - PRO Study
Part of paid clinical trials in Madison, Wisconsin.
- Sponsor
- University of Wisconsin, Madison
- Study ID
- NCT07413744
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 60 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Probiotic — DRUGA single dose of oral PS will be administered once daily for 6 months
- Placebo — OTHERA placebo will be given once daily for 6 months.
Study Details
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.
Key Dates
- First listed
- Feb 17, 2026
- Start date
- Sep 30, 2026
- Status verified
- Sep 2026
- Primary completion
- Sep 30, 2029
- Completion
- Sep 30, 2029
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cognitively Impaired due to AD: ProbioticDiagnosis of mild cognitive impairment (MCI) or dementia
- Placebo Comparator: Cognitively Impaired due to AD: PlaceboDiagnosis of mild cognitive impairment (MCI) or dementia
- Experimental: Cognitively Unimpaired Amyloid Positive: Probiotic
- Placebo Comparator: Cognitively Unimpaired Amyloid Positive: Placebo
Primary Outcome Measure
Safety: Proportion of participants with an adverse event (AE) occurring during any point of the study [ Time Frame: up to 36 weeks ]
Central Contacts
- Alfred Braceros, BA608-263-9485
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Wisconsin Hospitals and Clinics | Madison | Wisconsin | 53792 | Barbara Bendlin, PhD (PRINCIPAL_INVESTIGATOR) Federico Rey, PhD (PRINCIPAL_INVESTIGATOR) |
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