COVID-19: Herd Immunity Study in the Czech Republic

NCT04401085 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 27000

Last updated 2020-06-01

No results posted yet for this study

Summary

The aim of the SARS-CoV-2-CZ-Preval study is to quantify the prevalence of individuals with a history of SARS-CoV-2 coronavirus infection in the Czech population, except for those diagnosed with COVID-19 by methods based on direct detection of SARS-CoV- 2, including individuals with a subclinical course of the disease.

Conditions

Interventions

DIAGNOSTIC_TEST

SARS-CoV-2 diagnostic rapid test

The rapid test detects the presence of antibodies against SARS-CoV-2 in the IgM and IgG class by the immunochromatographic reaction. It cannot detect early infection, the antibodies will probably appear two weeks after possible infection. The collection will be performed by finger puncture.

DIAGNOSTIC_TEST

Quantitative analysis of SARS-CoV-2 antibodies

The subsample from Olomouc region (Olomouc, Uničov, Litovel) is based on venous blood sampling and archiving for subsequent quantitative analysis of SARS-CoV-2 antibodies. These tests detect immunoglobulins M and G (IgM and IgG).

Sponsors & Collaborators

  • Ministry of Health, Czech Republic

    collaborator OTHER_GOV
  • Palacky University

    collaborator OTHER
  • Masaryk University

    collaborator OTHER
  • University of Ostrava

    collaborator OTHER
  • Faculty of Military Health Sciences, University of Defence in Brno

    collaborator UNKNOWN
  • Faculty of Health Studies, J. E. Purkyně University in Ústí nad Labem

    collaborator UNKNOWN
  • Charles University, Czech Republic

    collaborator OTHER
  • Institute for Clinical and Experimental Medicine

    collaborator OTHER_GOV
  • General University Hospital, Prague

    collaborator OTHER
  • University Hospital Olomouc

    collaborator OTHER
  • Brno University Hospital

    collaborator OTHER
  • Krajská zdravotní, a.s., Ústí nad Labem Region Hospitals

    collaborator UNKNOWN
  • Military University Hospital, Prague

    collaborator OTHER
  • Masaryk Memorial Cancer Institute

    collaborator OTHER
  • Czech Academy of Sciences

    collaborator OTHER
  • Czech Statistical Office

    collaborator UNKNOWN
  • Faculty of Medicine in Hradec Králové, Charles University

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

    lead OTHER_GOV

Principal Investigators

  • Roman Chlíbek, Prof. · University of Defence in Brno

  • Rastislav Maďar, Assoc. Prof. · University of Ostrava, Faculy of Medicine

  • Marián Hajdúch, Assoc. Prof. · Institute of Molecular and Translational Medicine

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

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

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

  • Věra Adámková, Prof. · Institute for Clinical and Experimental Medicine

  • Aleksi Šedo, Prof. · Charles University, First Faculty of Medicine

  • Vladimír Černý, Prof. · Charles University, Faculty of Medicine in Hradec Králové

  • Jaroslav Štěrba, Prof. · Brno University Hospital

  • David Feltl, Prof. · General University Hospital, Prague

  • Martin Repko, Prof. · Masaryk University, Faculty of Medicine

  • Dalibor Valík, Prof. · Masaryk Memorial Cancer Institute

  • Zdeněk Havel, Assoc. Prof. · J. E. Purkyně University in Ústí nad Labem, Faculty of Health Studies

Eligibility

Min Age
8 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-04-23
Primary Completion
2020-05-01
Completion
2020-05-01

Countries

  • Czechia

Study Locations

More Related Trials

Entities

Diseases

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 NCT04401085 on ClinicalTrials.gov