Influenca, RSV, Coronaviruses
Conditions
Interventions
Group 1: - Patients with acute infections from influenza, coronaviruses, or RSV will be asked to provide blood samples and nasopharyngeal swabs.
- Patients will be asked to complete a questionnaire
Sponsors
Universitätsklinikum Düsseldorf; Institut für Virologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Study participants are patients of the university hospital where the participant is recruited. - According to medical opinion, the information and the additional biomaterial sampling do not represent an additional burden for the study participants. - Ability to consent and agreement to participate in the study. - An infection with coronavirus, influenza or RSV was diagnosed by PCR or POCT testing. (index patients) /no infection (control patients).
Exclusion criteria
Exclusion criteria: - Missing capacity to consent - no consent to the study - < 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Investigation of the selection of virus variants and immunity (innate and adaptive) against influenza, RSV and coronaviruses | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation of results with questionnaire data: - Age and gender distribution - Symptom occurrence - Presence of pre-existing conditions | — |
Countries
Germany
Contacts
Public ContactAnna-Kathrin Schupp
Universitätsklinikum Düsseldorf, Institut für Virologie
Outcome results
None listed