Evidence map›Paper›PMID 37545576›Full record

ArticleFrontiers in nutrition2023

A randomized clinical trial to evaluate the efficacy of L-carnitine L-tartrate to modulate the effects of SARS-CoV-2 infection.

Roberto Badaro, Josiane Dantas Viana Barbosa, Cesar Augusto de Araujo Neto, Bruna Aparecida Souza Machado, Milena Botelho Pereira Soares, Valter de Senna, Marcelo Taddeo, Lila Teixeira de Araújo, Shane Durkee, Raymond Donninger and 2 more

Abstract read
In one paragraph

Article in Frontiers in nutrition, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Roberto BadaroInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Josiane Dantas Viana BarbosaInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Cesar Augusto de Araujo NetoInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Bruna Aparecida Souza MachadoInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Milena Botelho Pereira SoaresInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Valter de SennaInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Marcelo TaddeoInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Lila Teixeira de AraújoInstitute of Health Technologies (ITS), University Center SENAI/CIMATEC, Salvador, Bahia, Brazil.
Shane DurkeeResearch and Development, Lonza Greenwood, LLC, Greenwood, SC, United States.
Raymond DonningerResearch and Development, Lonza Biologics, Slough, United Kingdom.
Kevin JudgeResearch and Development, Lonza Greenwood, LLC, Greenwood, SC, United States.
Zainulabedin SaiyedResearch and Development, Lonza Greenwood, LLC, Greenwood, SC, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: L-carnitine (LC) has been associated with inflammatory mediator reduction and with downregulating the angiotensin-converting enzyme-2 (ACE2) receptor, which is the target of SARS-CoV-2 attachment. Methods: This pilot phase 2 randomized, double-blind placebo-controlled trial contained two cohorts. Cohort 1 comprised 101 individuals with negative RT-PCR SARS-CoV-2 test results who cohabitated with an individual diagnosed with SARS-CoV-2 infection. Cohort 2 comprised 122 individuals with positive SARS-CoV-2 RT-PCR test results who were asymptomatic or had mild COVID-19 pneumonia symptoms. Participants in each cohort were randomized 1:1 to receive either 2 g elemental oral LC supplementation or placebo daily for 21 days. Primary endpoints included adverse events, SARS-CoV-2 infection incidence in Cohort 1, and disease progressions in Cohort 2. Secondary endpoints included between-group laboratory profile comparisons and Cohort 2 ACE1/ACE2 plasma levels. Disease progression was compared between the Cohort 2 groups using chest computed tomography. Results: In Cohort 1, two SARS-CoV-2 infections occurred in each group. The common adverse events included headache, dyspnea, and tiredness. In Cohort 2, platelet counts were elevated, and fibrinogen levels reduced in the LC group compared with those of the placebo group. Conclusion: Our study showed that LC was well-tolerated and suggests it modulates coagulation pathways. Furthermore, chest computed tomography images of the Cohort 2 LC group showed significant lung lesion improvement, suggesting that LC may slow COVID-19 progression.

Indexed as

COVID-19infectionL-carnitinepneumoniaSARS-CoV-2

Identifiers

PMID37545576
PMCPMC10400325

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.