U07.1
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Signed informed consent. 2. At least one positive SARS-CoV-2 swab/PCR-test (groups b-e). 3. Availability of data (e.g. discharge letters) to assign the patient in one of the groups (asymptomatic/mild/severe) and to document the course of the COVID-19-disease. 4. Subject/patient is at least 18 years old and able to give informed consent.
Exclusion criteria
Exclusion criteria: 1. Every disease or status that does not allow the blood drawing according to the assessment of the consenting physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This trial does not fall under the German drug or device law as no drug is applied; only one blood drawing takes place. The aim of this trial is to compare SARS-CoV-2-specific serum parameters (e.g. IgG-, IgA-, IgM-level, lipids etc.) of different populations (SARS-CoV-2-seronegative subjects, patients with acute COVID-19 disease as well as of recovered SARS-CoV-2-patients with asymptomatic/mild/severe disease). This trial is designed to establish assays that can be used in the future to clinical trials with patients suffering from COVID-19. The results of this trial might also be used in drug development projects. | — |
Countries
Germany