Z20.8 U07.1
Conditions
Interventions
Group 1: Longitudinal observational study without intervention with the aim of building a database of symptoms of COVID-19 vaccination or COVID-19 disease or general complaints of subjects not vaccina
Sponsors
Charité - Universitätsmedizin Berlin
Eligibility
Sex/Gender
All
Age
18 Years to 105 Years
Inclusion criteria
Inclusion criteria: Included in the study are: - Subjects 18 years of age and older - Subjects who have received COVID-19 vaccination and have not had COVID-19. - Subjects who have received COVID-19 vaccination and have had COVID-19. - Subjects who had COVID-19 and were not vaccinated - Subjects who have not had COVID-19 disease. - Ability to give consent and signed informed consent form.
Exclusion criteria
Exclusion criteria: Subjects without an understanding of the German language will be excluded from the study. Participants will also be excluded if they are participating or have participated in another (clinical) study that has not been completed 3 months prior to study participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective parameter is to assess adverse vaccination reactions in COVID-19 vaccinated individuals compared to the adverse health effects in COVID-19 diseased and non-diseased individuals, respectively. The target parameter will be collected using a newly developed online questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| All other analyses involving predictors influencing vaccination responses or general or health impairments resulting from COVID-19 disease are exploratory. | — |
Countries
Germany
Contacts
Public ContactMaximilian Hinse
Institut für Sozialmedizin, Epidemiologie und Gesundheitsökonomie Charité – Universitätsmedizin Berlin
Outcome results
None listed