Efficacy and Safety of Acetyl L-Carnitine in COVID-19 Patients With Mild-to-Moderate Disease

Sponsor
Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04623619
Collaborator
(none)
100
2
7.5

Study Details

Study Description

Brief Summary

Different studies showed that acetyl L-Carnitine (LC) positively affects the development and maturation of T lymphocytes, involved in the immune response to viral agents. It also contributes to the inhibition of ROS production and to the remodulation of the cytokine network typical of the systemic inflammatory syndrome.

Given the potential protective effects of LC, it is suggested as a supportive and therapeutic option in patients with coronavirus infection. Given this background, in the light of the current COVID-19 emergency, it is the intention of the investigators to conduct a prospective, randomized, open-label, controlled study in the cohort of hospitalized patients with covid-19 pneumonia, administering 2 gr of LC orally in addition to the standard of care therapy (SOC).

The investigators hypothesize that the use of LC will be associated with an earlier improvement of clinical and biohumoral parameters after 14 days of LC treatment when compared to the group of patients provided with standard care.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Acetyl L-Carnitine
N/A

Detailed Description

Different studies showed that acetyl L-Carnitine (LC) positively affects the development and maturation of T lymphocytes, involved in the immune response to viral agents. It also contributes to the inhibition of ROS production and to the remodulation of the cytokine network typical of the systemic inflammatory syndrome.

SARS-CoV-2 virus activates the human cell ACE2 receptor, triggering a series of deleterious events. In COVID19, renin-angiotensin is upregulated and the pathway is overexpressed and a progressive cytokine storm is always observed. In all these pathogenic processes, LC could play a modifier function to enhance condition. LC can be beneficial to the antioxidant effects of Angiotensin II by inhibiting NF-kB and down-regulating NOX1and NOX2. For LC, an anti-apoptotic and genome-stabilizer role was estimated by inhibiting pro-apoptotic caspases and activating PARP-1. LC is an immunomodulator that downregulates pro-inflammatory cytokines including TNF-α, IL-6, and IL-1 that could extinguish the cytokine storm. LC can also serve as a protective agent against COVID19 cardiotoxicity due to disruption in the ACE2-mediated signaling pathway, cytokine storm, pulmonary dysfunction, and side effects of medications.

In patients with coronavirus infection, provided LC's possible protective effects, it is suggested as a supportive and therapeutic alternative.

Given this background, in the light of the current COVID-19 emergency, it is the intention of the investigators to conduct a prospective, randomized, open-label, controlled study in the cohort of hospitalized patients with covid-19 pneumonia, administering 2 gr of LC orally in addition to the standard of care therapy (SOC).

The investigators hypothesize that the use of LC will be associated with an earlier improvement of clinical and humoral parameters after 14 days of LC treatment when compared to the group of patients provided with standard care.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Prospective, randomized, open-label, controlled studyProspective, randomized, open-label, controlled study
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Use of Acetyl L-Carnitine in Patients With Covid-19 Pneumonia
Anticipated Study Start Date :
Dec 15, 2020
Anticipated Primary Completion Date :
Apr 29, 2021
Anticipated Study Completion Date :
Jul 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Acetyl L-Carnitine

Acetyl L-Carnitine

Dietary Supplement: Acetyl L-Carnitine
Administering 2 gr of Acetyl L-Carnitine orally in addition to the standard of care therapy for 14 days

No Intervention: Standard of care

Standard of care

Outcome Measures

Primary Outcome Measures

  1. In-hospital mortality [72 hours]

    Change of hospital mortality

Secondary Outcome Measures

  1. C reactive protein (CRP) levels [72 hours]

    Reduction of CRP levels > 50% in comparison with CRP levels at the admission, within 72 hours after the administration

  2. IL-6 levels [72 hours]

    Reduction of IL-6 levels > 50% in comparison with IL-6 at the admission, within 72 hours after the administration

  3. D-dimer levels [72 hours]

    Reduction of D-dimer levels > 50% in comparison with D-dimer at the admission, within 72 hours after the administration

  4. Hospital stay [up to 24 weeks]

    Length of hospital stay

  5. Duration of positive PCR swab [5 days]

    Time length of negativization of PCR molecular swab

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Positive swab test of SARS-CoV-2

  • Pneumonia related to SARS-CoV-2

  • Signature of informed consent

Exclusion Criteria:
  • Unsigned informed consent

  • Negative swab test of SARS-CoV-2

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo

Investigators

  • Principal Investigator: Antonio Cascio, MD, PhD, University of Palermo, Italy

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Antonio Cascio, Direttore UOC Malattie Infettive e Tropicali, Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo
ClinicalTrials.gov Identifier:
NCT04623619
Other Study ID Numbers:
  • 20201109
First Posted:
Nov 10, 2020
Last Update Posted:
Nov 17, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Antonio Cascio, Direttore UOC Malattie Infettive e Tropicali, Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 17, 2020