COVID-19: Herd Immunity Study in the Czech Republic
NCT04401085 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 27000
Last updated 2020-06-01
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
- COVID
- SARS-CoV 2
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
-
Xpert MTB/RIF Ultra Trial
NCT07135622 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the QuantiFERON-TB Test.
NCT02253537 ·Status: COMPLETED
-
Biomarkers for Therapy Response in Drug-resistant Tuberculosis
NCT02597621 ·Status: COMPLETED
-
Lung Innate Immunity and Microbiome After Tuberculosis Exposure
NCT06526689 ·Status: RECRUITING
-
Whole Genome Sequencing of Tuberculosis for Disease Control in Madagascar
NCT05406453 ·Status: COMPLETED ·Phase: NA
-
The Clinical Utility of QuantiFERON in the Diagnosis of Active Tuberculosis
NCT00982969 ·Status: COMPLETED
-
Evaluation of the QuantiFERON-TB Test.
NCT02256839 ·Status: COMPLETED
-
ImmuneSense™ COVID-19 Cross-Reactivity Study
NCT05112874 ·Status: WITHDRAWN
-
Effect of Xpert MTB/RIF on Patient Outcomes
NCT02729532 ·Status: COMPLETED
-
ImmuneSense COVID-19 Variant Study
NCT05054088 ·Status: COMPLETED
-
Prospective Evaluation of Novel Diagnostics for Tuberculosis in KwaZulu-Natal, South Africa
NCT04583904 ·Status: COMPLETED
-
Evaluation of Centralised TB Assay Solutions
NCT04147676 ·Status: COMPLETED
-
Azithromycin as Host-directed Therapy for Pulmonary Tuberculosis
NCT03160638 ·Status: COMPLETED ·Phase: PHASE2
-
Epidemiologic Study to Assess the IGRA Positivity in Populations With a High TB Burden
NCT05190146 ·Status: COMPLETED
-
Post-Trial Tuberculosis Case Finding: A Substudy of CoVPN 3008
NCT06585683 ·Status: COMPLETED
-
Functional Exhaustion of T Cells in COVID19 Patients
NCT04470323 ·Status: UNKNOWN
-
QuantiFERON Change During Anti-tuberculosis Medication
NCT01038830 ·Status: COMPLETED
-
Active Close Contact Investigation of Tuberculosis Through Computer-aided Detection and Stool Xpert MTB/RIF Among People Living in Ethiopia
NCT05818059 ·Status: UNKNOWN ·Phase: NA
-
Feasibility of Centralized Therapeutic Drug Monitoring of Fluoroquinolones in Multi-Drug Resistant Tuberculosis Patients
NCT03409315 ·Status: UNKNOWN
-
Tuberculosis as a Risk Factor for a Worse Outcome Post-Sars-CoV-2 Infection
NCT05643781 ·Status: COMPLETED
-
Study on Antibody Persistence and Immune Memory of Inactivated COVID-19 Vaccine
NCT05072496 ·Status: COMPLETED
-
Prevalence of Latent Tuberculosis Infection in Health-care Workers and Students
NCT05756582 ·Status: RECRUITING
-
Evaluation of the 4th Generation QuantiFERON-TB Test (QFT-Plus) for the Detection of Tuberculosis Infection
NCT02687529 ·Status: COMPLETED
-
A Study on Changes in IFN-gamma Levels Following Anti-TNF Treatment in Patients Undergoing Serial QuantiFERON-TB Gold In-Tube
NCT01475409 ·Status: COMPLETED ·Phase: NA
-
The Time of Positive Conversion of Interferon-γ Releasing Assay After Tuberculosis Exposure
NCT00981071 ·Status: COMPLETED