Diagnostic accuracy and feasibility of a rapid SARS-CoV-2 (COVID-19) antigen test in general practice – a prospective multicenter validation and implementation study.
Phase 3
- Conditions
- COVID-19SARS-CoV-19 infectionU07.1COVID-19, virus identified
- Registration Number
- DRKS00023822
- Lead Sponsor
- niversitätsklinikum Würzburg Institut für Allgemeinmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 1518
Inclusion Criteria
respiratory symptoms (e.g. acute bronchitis or pneumonia, respiratory distress or fever)
- Acute hypo- or anosmia or hypo- or ageusia
Exclusion Criteria
symptomatic and asymptomatic patients in a nursing home, asymptomatic patients whose testing is done for follow-up reasons (travel history, contact person, etc.)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method -Validation of sensitivity, specificity, positive predictive value, negative predictive value of a rapid SARS-CoV-2 antigen tests in daily clinical routine
- Secondary Outcome Measures
Name Time Method