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Evaluation of Vitamin A and E Deficiency With Severity of SARS-COV-2 Disease: A Case-Control Study

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

COVID-19

Study type

Observational

Funder types

Other

Identifiers

NCT05946499
Vitamin A and E in COVID-19

Details and patient eligibility

About

Coronavirus disease 2019 (COVID-19) is a novel infectious disease that has been spreading worldwide Coronaviridae study group of the International Committee on taxonomy of viruses (2020). The clinical manifestation of COVID-19 can range from asymptomatic infection to critical illness with severe pneumonia, respiratory failure, and death.

Vitamin A is of special interest in the field of infectious diseases, especially for pulmonary infections. It is crucial for the development of normal lung tissue and tissue repair after injury due to infection. Therefore, it may play a role in recovery after severe COVID-19 pneumonia. Vitamin A has immune regulatory functions and positively affects both the innate and adaptive immune cell response.

The anti-oxidant Vitamin E, and trace element selenium, are major components of anti-oxidant defense. Epidemiological studies demonstrate that deficiencies in, either of these nutrients, alters immune responses and viral pathogenicity.

Data concerning vitamin A and E plasma levels in COVID-19 patients are lacking. Therefore, this study aims at characterizing vitamin A and E plasma levels in COVID-19 and analyzing the association of plasma levels with disease severity and outcome.

Full description

The aim of the current study is to evaluate the relation of plasma level of Vitamin A and E and their correlation with severity of SARS-COV2 disease.

Enrollment

90 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • COVID-19 positive patients by PCR (polymerase chain reaction) test
  • Patients aging 18 to 75 years

Exclusion criteria

  • Patients with known immunodeficiency - Patients with known lung diseases

Trial design

90 participants in 3 patient groups

Group A
Description:
30 ICU-admitted SARS-CoV-2- infected individuals with ARDS or in need of oxygen supplementation
Group B
Description:
30 ward-admitted SARS-CoV-2-infected individuals not suffering from ARDS and not in need of oxygen supplementation
Group C
Description:
30 sex and age-matched normal individuals

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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