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NOT YET RECRUITING
NCT07611370
PHASE1

Evaluating the Effects of Propionate and Butyrate Supplementation on the Intestinal Health of Healthy Volunteers

Sponsor: City of Hope Medical Center

View on ClinicalTrials.gov

Summary

This clinical trial evaluates how propionate and butyrate supplementation alters intestinal health in healthy volunteers and whether it would be feasible to administer these supplements to patients undergoing allogeneic hematopoietic stem cell transplant in the future. Propionate and butyrate are short chain fatty acids naturally produced in the intestines during the fermentation of dietary fibers. Greater levels of propionate and butyrate may improve intestinal barrier function, and propionate specifically has been shown to modulate immunity, energy metabolism, and gut-brain communication. The protective effects of propionate and butyrate supplementation on intestinal health may be especially beneficial for patients undergoing donor stem cell transplant, as these patients can experience significant gastrointestinal injury during treatment. The results of this study may help researchers determine whether propionate and butyrate supplementation positively alters the gut microbiome and whether or not supplementation could be used in the future for patients undergoing a donor stem cell transplant.

Official title: A Pilot Feasibility Study of Oral Administration of Microencapsulated Propionate and Butyrate in Healthy Volunteers

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2026-09-30

Completion Date

2027-06-30

Last Updated

2026-05-28

Healthy Volunteers

Yes

Interventions

PROCEDURE

Biospecimen Collection

Undergo collection of blood samples

DRUG

Microencapsulated Sodium Butyrate

Given PO

DRUG

Microencapsulated Sodium Propionate

Given PO

Locations (1)

City of Hope Medical Center

Duarte, California, United States