Clinical Trials Directory

Trials / Completed

CompletedNCT03193125

Carnitine and Liver Mitochondria Fatty Acid Processing

Effects of Carnitine Supplementation on Liver Mitochondria Fatty Acid Processing

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Pennington Biomedical Research Center · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers
Accepted

Summary

This double-blind, placebo-controlled randomized trial will assess whether 14 days of oral carnitine supplementation modifies mitochondrial fatty acid processing in healthy young adults.

Detailed description

This project will use stable isotope techniques and magnetic resonance spectroscopy (MRS) to take a first step toward clarifying how the benefit of oral carnitine supplementation depends on basal mitochondrial fatty acid processing (MFAP) and MFAP modification, with a specific focus on the liver. Approximately 24 healthy young individuals will be enrolled, with 20 expected to complete. Before and after 14 days of oral carnitine supplementation or placebo, MFAP will be measured using measures of acetyl-carnitine concentration (from long-TE proton MRS) and de novo lipogenesis (DNL, from analysis of blood metabolites following 13C-labeled acetate infusion and high-fructose drink challenge). The MFAP measures will be collected before and after loading participants with a high-fructose drink. Fructose is solely metabolized by the liver.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTL-Carnitine500 mg tablets of L-Carnitine taken 3 times daily before meals.
DIETARY_SUPPLEMENTPlacebo500 mg tablets of L-Carnitine taken 3 times daily before meals.

Timeline

Start date
2017-05-15
Primary completion
2018-05-11
Completion
2018-05-11
First posted
2017-06-20
Last updated
2022-09-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03193125. Inclusion in this directory is not an endorsement.