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SARS-CoV-2 diagnostic rapid testWiki

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Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (4)


Name (Synonyms) Correlation
drug1972 Quantitative analysis of SARS-CoV-2 antibodies Wiki 0.71
drug1973 Quantitative analysis of anti-SARS-CoV-2-antibodies Wiki 0.71
drug2942 pathogen reduced SARS-CoV-2 convalescent plasma Wiki 0.71
drug1822 Placebo Wiki 0.04

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D018352 Coronavirus Infections NIH 0.06

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There are 2 clinical trials

Clinical Trials


1 Herd Immunity Study SARS-CoV-2-CZ-Preval

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.

NCT04401085 COVID SARS-CoV 2 Diagnostic Test: SARS-CoV-2 diagnostic rapid test Diagnostic Test: Quantitative analysis of SARS-CoV-2 antibodies

Primary Outcomes

Description: Statistically, the primary objective is formulated as an estimate of the cumulative prevalence of SARS-CoV-2 positive individuals in geographically defined subpopulations of the Czech Republic with declared reliability of +/- 2%. For this primary objective, the required sample size in individual geographical cohorts is calculated. The positivity of SARS-CoV-2 individuals who have not been diagnosed with COVID-19 by a standard route of the detection will be assessed by the presence of specific IgM or IgG antibodies in the blood (antibody tests).

Measure: Estimation of the actual prevalence of SARS-CoV-2 positive persons in the Czech Republic.

Time: May 2020

Secondary Outcomes

Description: The proportion of SARS-CoV-2 positive persons who, according to the questionnaire, will not report any or minimal symptoms in the anamnesis.

Measure: Estimation of the proportion of people with a subclinical course of the disease

Time: May 2020

Measure: Estimation of the cumulative prevalence of the disease and the proportion of people with a subclinical course differences between subcohorts according to demographic, social and clinically relevant stratifications.

Time: May 2020

Description: The estimation will be calculated according to the prevalence of the disease in the population after excluding contraindications to blood donation (age, health status, etc.).

Measure: Estimation of the proportion of persons suitable for the donation of convalescent plasma

Time: May 2020

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

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.

NCT04453280 COVID SARS-CoV-2 Diagnostic Test: Quantitative analysis of anti-SARS-CoV-2-antibodies Diagnostic Test: SARS-CoV-2 diagnostic rapid test

Primary Outcomes

Description: The primary outcome is the determination of the concentration of anti-SARS-CoV-2 antibodies IgG, IgM, and IgA classes in relation to the categories of cured patients according to the time from the date of cure from the COVID-19 disease to the date of examination.

Measure: Determination of the concentration of anti-SARS-CoV-2 antibodies in relation to the categories of cured patients.

Time: May 2020

Secondary Outcomes

Description: The determination of the concentration of anti-SARS-CoV-2 antibodies IgG, IgM, and IgA classes in relation to the categories of cured patients according to their age: category 8-17, 18-39, 40-59, 60 and more years and according to the severity of the disease.

Measure: Determination of the concentration of anti-SARS-CoV-2 antibodies in relation to the age and to the severity of the disease.

Time: June 2020

Description: The quantification of the dependence of the change in the concentration of anti-SARS-CoV-2 antibodies IgG, IgM, and IgA classes on the time since cure (analysis by statistical model)

Measure: The quantification of the dependence of the change in the concentration of anti-SARS-CoV-2 antibodies.

Time: June 2020

Other Outcomes

Description: The identification of individuals in the study population, who can be contacted as voluntary donors of convalescent plasma, which is one of the therapeutic modalities in patients with severe COVID-19 disease.

Measure: The identification of potential donors of convalescent plasma.

Time: June2020


No related HPO nodes (Using clinical trials)