Clinical Trials Directory

Trials / Completed

CompletedNCT06700785

A Pharmacokinetic Comparison of Three Butyrate Products

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
The Center for Applied Health Sciences, LLC · Industry
Sex
Male
Age
25 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study is a randomized, three-arm, interventional study of N=10 apparently healthy men. This study will quantify plasma butyrate responses to a single dose of three different butyrate products.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLysine butyrateLysine butyrate supplement. This study will compare plasma pharmacokinetic profiles of three commercially available butyrate supplements.
DIETARY_SUPPLEMENTSodium ButyrateOral sodium butyrate supplement.
DIETARY_SUPPLEMENTTributyrinOral tributyrin supplement.

Timeline

Start date
2024-05-03
Primary completion
2024-07-16
Completion
2024-09-12
First posted
2024-11-22
Last updated
2024-11-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06700785. Inclusion in this directory is not an endorsement.