Antibody Detection in COVID-19 Cured Patients (SARS-CoV-2-CZ-Immunity)

NCT04453280 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 695

Last updated 2020-07-01

No results posted yet for this study

Summary

The aim of the SARS-CoV-2-CZ-Immunity study is to determine the time profile of the presence of antibodies against SARS-CoV-2 in blood plasma by quantification of antibodies or performing a rapid test in COVID-19 cured patients.

Conditions

Interventions

DIAGNOSTIC_TEST

Quantitative analysis of anti-SARS-CoV-2-antibodies

Plasma sampling will be collected and archived for subsequent quantitative analysis of anti-SARS-CoV-2 antibodies - IgG, IgM and IgA.

DIAGNOSTIC_TEST

SARS-CoV-2 diagnostic rapid test

The rapid test detects the presence of antibodies against SARS-CoV-2 by the immunochromatographic reaction.

Sponsors & Collaborators

  • Ministry of Health, Czech Republic

    collaborator OTHER_GOV
  • Masaryk University

    collaborator OTHER
  • Institute for Clinical and Experimental Medicine

    collaborator OTHER_GOV
  • Brno University Hospital

    collaborator OTHER
  • St. Anne's University Hospital Brno, Czech Republic

    collaborator OTHER
  • Masaryk Memorial Cancer Institute

    collaborator OTHER
  • Regional Public Health Office of the South Moravian Region based in Brno, Czech Republic

    collaborator UNKNOWN
  • Public Health Office of the Capital City of Prague, Czech Republic

    collaborator UNKNOWN
  • Regional Public Health Office of the Central Bohemian Region based in Prague, Czech Republic

    collaborator UNKNOWN
  • Institute of Health Information and Statistics of the Czech Republic

    lead OTHER_GOV

Principal Investigators

  • Roman Prymula, Prof. · Ministry of Health, Czech Republic

  • Jarmila Rážová, M.D., Ph.D. · Ministry of Health, Czech Republic

  • Ladislav Dušek, Prof. · Institute of Health Information and Statistics of the Czech Republic

  • Dalibor Valík, Prof. · Masaryk Memorial Cancer Institute

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-05-18
Primary Completion
2020-06-03
Completion
2020-06-03

Countries

  • Czechia

Study Locations

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Entities

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 NCT04453280 on ClinicalTrials.gov