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RECRUITING
NCT07787026
NA

Assessing the Short-Term Effects of Multi-Fiber Supplementation on Gut Health

Sponsor: Brown University

View on ClinicalTrials.gov

Summary

This is a randomized, parallel-group interventional study evaluating the short-term gastrointestinal effects of a standardized multi-fiber supplement in healthy adults. Approximately 100 participants (50 per arm) aged 18 and older will be randomized to receive either the multi-fiber supplement or a control (flavoring agent only) daily for 10 days. Objectives include assessing effects on stool characteristics, specifically frequency and consistency, as well as changes in metagenomically inferred short-chain fatty acid production potential from the microbiota. Eligible participants must be free of chronic disease, acute illness, and recent antibiotic, probiotic, or prebiotic use. Total participation duration is 10 days.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-08

Completion Date

2029-08

Last Updated

2026-08-26

Healthy Volunteers

Yes

Interventions

DIETARY_SUPPLEMENT

Prebiotic

Formulated prebiotic supplement designed to be accessible to gut microbiota members and assist with bowel movement regularity

DIETARY_SUPPLEMENT

Placebo

Placebo supplementation intervention, with only flavoring agents and no prebiotic fiber

Locations (1)

Biomedical Center

Providence, Rhode Island, United States