Efficacy of a Dietary Supplementation in Reducing Hospital Admissions for COVID-19. Randomized Clinical Trial

NCT04751669 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 252

Last updated 2024-03-25

No results posted yet for this study

Summary

A double-blind, placebo-controlled, randomized clinical trial to assess efficacy of micronutrient dietary supplementation in reducing hospital admissions for COVID-19 and incidence of Long Covid.

We want to assess the need for hospital admission for severe acute respiratory syndrome Corona Virus-2 (SARS-CoV-2) infection in outpatients diagnosed of COVID-19 disease, taking a micronutrient supplementation for 14 days. The outcome Will be measured within 1 month after beginning the study treatment. The patients will be followed-up for a period of 180 days for the incidence of Long Covid

Conditions

  • Covid19

Interventions

DIETARY_SUPPLEMENT

Vitamin and trace elements

Dietary supplement oral route, once a day, during 14 days

DIETARY_SUPPLEMENT

Placebo

Dietary supplement (placebo) oral route, once a day, during 14 days

Sponsors & Collaborators

  • Germans Trias i Pujol Hospital

    collaborator OTHER
  • Fundació Institut Germans Trias i Pujol

    lead OTHER

Principal Investigators

  • Teresa M Tomasa-Irriguible, MD-PhD · Hospital Germans Trias i Pujol- Intensive Care Unit

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-09
Primary Completion
2023-10-26
Completion
2023-10-26

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04751669 on ClinicalTrials.gov