U07.1
Conditions
Interventions
Group 1: Patients with laboratory proven COVID-19
Primary and secondary pathophysiological changes and organ function as well as clinical intervention and potential biomarkers and surrogate markers
Sponsors
Charité Campus Virchow-Klinikum
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - Proven infection with SARS-CoV-2 (positive pathogen testing). - Willingness to participate in the study.
Exclusion criteria
Exclusion criteria: - Refusal to participate by patient, parent or appropriate legal representative. - Any conditions that prohibit supplemental blood-sampling.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| WHO scale for clinical improvement on day 15 | — |
Secondary
| Measure | Time frame |
|---|---|
| WHO scale for clinical improvement at discharge from hospital | — |
Countries
Germany
Contacts
Public ContactFlorian Kurth
Charité - Universitätsmedizin Berlin
Outcome results
None listed