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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | L-Carnitine | 500 mg tablets of L-Carnitine taken 3 times daily before meals. |
| DIETARY_SUPPLEMENT | Placebo | 500 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.