COVAG study - COVID 19 Antigen Study
Completed
- Conditions
- Covid-19U07.1COVID-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
Name Time Method Sensitivity and specificity of SARS-CoV-2 rapid detection tests. 31.03.2021.
- Secondary Outcome Measures
Name Time Method Sensitivity of rapid detection tests for different SARS-CoV-2 variants. 31.12.2021.