CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 10 enrolled
Drug / intervention
L-carnitinedietary
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04908397
NCT04908397Phase 1Completed

Carnitine Consumption and Augmentation in Pulmonary Arterial Hypertension

Vanderbilt University Medical Center·interventional·Posted Jun 1, 2021·Updated Sep 30, 2025

In Brief

A Phase 1 clinical trial evaluating L-carnitine for Pulmonary Arterial Hypertension and 4 related conditions. Completed, enrolled 10 participants across 1 site.

Detailed Summary

In preparation for a future mechanistic study, investigators now propose to test the specific hypothesis that carnitine consumption is not reduced in PAH, that plasma carnitine levels are stable over time in PAH and that carnitine supplementation in PAH can increase plasma carnitine and thereby delivery of carnitine to the RV and possibly improve RV function. Investigators propose three aims in humans to test this mechanistic hypothesis, 1) Measure the oral consumption of carnitine in human PAH. This aim will use food diaries and carnitine supplement use questionnaires in PAH patients to test the hypothesis that carnitine supplementation is uncommon in PAH and food consumption is adequate. Aim 2) Measure the stability over time in plasma carnitine levels in PAH patients. This aim will test the hypothesis that plasma carnitine is not affected by disease severity and is stable over time in PAH patients. Investigators will measure plasma carnitine concentration and markers of fatty acid oxidation at Visit 1 and Visit 2. 3) Perform a mechanistic pilot study using carnitine supplementation to enhance circulating carnitine in PAH. This small pilot study will test the hypothesis that carnitine supplementation increases plasma carnitine (primary endpoint) and will test for physiologic effects using six minute walk testing, echocardiography and plasma markers of lipid metabolism.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedJun 1, 2021
Enrollment StartSep 29, 2021
Primary CompletionJun 1, 2023
Study CompletionJun 30, 2023
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 5.1 years ago

Interventions

L-carnitinedietary

supplement provided twice a day for 2 weeks