U07.1 U08.9
Conditions
Interventions
Group 1: COVID-19 patients in the Dessau Medical Center
Group 2: Anti-SARS-CoV2 vaccinated persons at the Dessau Medical Center (staff)
Group 3: Anti-SARS-CoV2 vaccinated hemato-oncolological patients
Sponsors
Städtisches Klinikum Dessau. Medizinische Hochschule Brandenburg Theodor Fontane
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Employees of the Dessau Medical Center, COVID-19 patients of the Dessau Medical Center, hemato-oncological patients of the Dessau Medical Center
Exclusion criteria
Exclusion criteria: Persons, who do not confirm their participation at the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| SARS-CoV2 antibody titre in serum - blood collection 2, 4, 8 12, 16, 32, 48 weeks after the second vaccination | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood count, CRP, BSG, C3, C4, circulating immune complexes, IL-6, IL-2 receptor, TNF-a, IL-4, IL-13 through blood control 2, 4, 8 12, 16, 32, 48 weeks after the second vaccination General symptoms, dermatological findings 2, 4, 8 12, 16, 32, 48 weeks after the second vaccination in the staff and the dermato-oncological patients of the Dessau Medical Center General symptoms, dermatological findings during COVID-19 infection and 2, 4, 8 12, 16, 32, 48 weeks after infection detection in COVID-19 patients of the Dessau Medical Center | — |
Countries
Germany
Contacts
Public ContactSabine Westphal
Institut für Klinische Chemie und Laboratoriumsdiagnostik, Städtisches Klinikum Dessau
Outcome results
None listed