Vitamin D and Zinc Supplementation for Improving Treatment Outcomes Among COVID-19 Patients in India

Last updated: September 15, 2022
Sponsor: Harvard School of Public Health (HSPH)
Overall Status: Completed

Phase

3

Condition

Covid-19

Treatment

N/A

Clinical Study ID

NCT04641195
VR3- 172649
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to assess the effect of vitamin D and/or zinc supplementation on improving COVID-19 treatment outcomes. The effects of vitamin D, zinc, and both vitamin D and zinc together will be investigated among COVID-19 patients in India.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Aged >=18 years old
  • Polymerase chain reaction (PCR) or Rapid Antigen Test (RAT)-confirmed infection withSARS-COV2
  • Provide informed consent

Exclusion

Exclusion Criteria:

  • Pregnancy
  • Enrollment in other clinical trials

Study Design

Total Participants: 181
Study Start date:
April 22, 2021
Estimated Completion Date:
August 01, 2022

Study Description

This study is a 2x2 factorial randomized double-blind, placebo-controlled trial to examine the effectiveness of vitamin D and zinc supplements as immune-based therapy among COVID-19 patients in India. The study is also examining the immunological response to COVID-19 and the effect of the intervention on specific biomarkers of immune and endothelial activation that are independent and quantitative predictors of severity and mortality in other severe infections. The primary aims are to determine the effect of vitamin D supplementation versus placebo on time to recovery among patients hospitalized with COVID-19; and to determine the effect of zinc supplementation versus placebo on time to recovery among patients hospitalized with COVID-19. As secondary aims, this study is also investigating the effect of vitamin D or zinc supplementation on all-cause mortality. necessity for assisted ventilation, individual symptoms duration, duration of hospital stay and biomarkers including vitamin D, Zinc, Interleukin 6 (IL-6), Angiopoietin-2, sTREM-1, immunoglobulin G (IgG) and immunoglobulin M (IgM).

Eligible individuals are randomly assigned to one of four groups: (1) Vitamin D (180,000 IU bolus at enrollment, followed by 2000 IU daily); (2) Zinc (placebo at enrollment followed by one daily dose of 40 mg); (3) Vitamin D and Zinc; or (4) Placebo. Daily supplements start at the hospital and continue after discharge for a total of 8 weeks. Active data collection occurs daily while patients are hospitalized and at least twice per week via telephone after discharge. A clinical exam occurs at 8 weeks and longer-term symptoms are assessed at 3 months.

Connect with a study center

  • Saifee Hospital

    Mumbai, Maharashtra
    India

    Site Not Available

  • King Edward Memorial (KEM) Hospital

    Pune, Maharashtra
    India

    Site Not Available

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