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COVAG study - COVID 19 Antigen Study

Completed
Conditions
Covid-19
U07.1
COVID-19, virus identified
Registration Number
DRKS00026956
Lead Sponsor
Synlab Academy, Synlab Holding Deutschland GmbH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
3733
Inclusion Criteria

Subjects eligible for inclusion in this study must meet the following criteria:
1. Signed informed consent must be obtained prior to study participation. The patient must be capable of understanding the nature, significance and implication of the trial.
2. Age 18 years or more

Exclusion Criteria

1. Lack of informed consent
2. Inability to understand the nature, significance and implication of the trial.
3. Severe clinical conditions requiring emergency hospitalization
4. Children and adolescents under the age of 18 years

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sensitivity and specificity of SARS-CoV-2 rapid detection tests. 31.03.2021.
Secondary Outcome Measures
NameTimeMethod
Sensitivity of rapid detection tests for different SARS-CoV-2 variants. 31.12.2021.
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