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COVID-19 Study on natural protection against SARS-CoV2 reinfections

Conditions
U07.1
COVID-19, virus identified
Registration Number
DRKS00023113
Lead Sponsor
Institut für VirologieUniversitätklinikum Bonn
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
1429
Inclusion Criteria

Consenting subjects who agree to participate in the study, regardless of age and acute or previous COVID-19 infection
Registered residents of the defined municipalities, either:
- Selection based on the COVID-19 Case Cluster Study (high prevalence Heinsberg district), or
- randomly selected index persons by the municipal administration of Rheinbach (low-prevalence region) from the population registration data regardless of age and regardless of an acute or previous COVID-19 infection, as well as their household members

Exclusion Criteria

Refusal of informed consent.
Contraindication for the described specimen collection methods (venipuncture or capillary blood collection via fingertip or throat swab)

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary endpoint is the prevalence of SARS/CoV-2 positive individuals in the study populations, defined as the number of participants with positive laboratory results (from at least one of the sample media taken in the study; the IgA value is excluded here because this test from the company Euroimmun has too low sensitivity and specificity) divided by the total number of study participants in the study period as well as the increase in new infections in the population of the already SARS-CoV-2 IgG/total antibody/PCR positive and the previously SARS-CoV-2 IgG/total antibody/PCR negative population.<br>
Secondary Outcome Measures
NameTimeMethod
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