ClinicalTrials.Veeva

Menu

VITACOV: Vitamin D Polymorphisms and Severity of COVID-19 Infection

U

Universidade de Lisboa

Status

Completed

Conditions

COVID-19

Treatments

Other: Exposure

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04370808
VITACOV

Details and patient eligibility

About

Vitamin D deficiency has been linked to hypertension, autoimmune, infectious and cardiovascular diseases which are risk factors for COVID-19. Moreover, COVID-19 patients have a very high prevalence of hypovitaminosis D (Turin data). Taken together, we aim to investigate whether genetic variants in vitamin D-related genes contribute to a poor COVID-19 outcome, particularly in hypertension and CV patients, proposing thus a personalized therapeutics based on vitamin D supplementation in order to reduce the severity and deaths.

Full description

Collected data from Turin University indicate that hospitalized patients have a very high prevalence of hypovitaminosis D. Reports from China and Italy show that hypertension presents an increased risk of COVID-19-related death. Otherwise, observational studies suggest that 25(OH)D induces protection against respiratory pathogens while large-scale studies indicate that serum 25(OH)D-level is inversely correlated to hypertension prevalence. Recent published data (2020) shows that 66% of Portuguese adults present Vitamin D deficiency. HeartGenetics' genetic database with more than 8.500 Portuguese genotypes shows that the prevalence of vitamin D polymorphisms in this population is 4-fold higher than the EU average, increasing the risk of hypovitaminosis D.

Enrollment

517 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults of 18 years and above.
  • COVID-19 patients admitted with mild to severe disease (admission to isolation room) or critical patients (admission to ICU).
  • Available to comply with study protocol and sign informed consent.

Exclusion criteria

  • Patients diagnosed with COVID-19 not admitted to hospital.
  • Patients unable to provide informed consent.

Trial design

517 participants in 2 patient groups

Mild to severe disease
Description:
Mild to severe disease (admission to isolation room)
Treatment:
Other: Exposure
Critical patients
Description:
Critical patients (admission to ICU)
Treatment:
Other: Exposure

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems