About this trial
This observational study aims to collect standardized clinical data and biosamples from adults in university hospitals across Germany. The main goals are to create a cohort that combines clinical data, pathogen samples, and biosamples, with consent for future research. A pre-screening program tracks infection-related hospitalizations, helping detect pathogen changes early and respond quickly. Participants will be recruited if they have respiratory, bloodstream, gastrointestinal, emerging, or central nervous system infections. Data and biosamples will be collected at the start and end of the hospital stay, with additional visits if needed.
Eligibility criteria
Qualifiers
Fulfillment of all inclusion and no
Disqualifiers
Ability to perform all baseline visit data and biosample collections according to the study requirements no later than 48 hours (with an additional 48-hour period for weekends) after fulfilling all study and specific module inclusion and exclusion criteria
Signed informed consent form from all patients capable of giving consent and understanding all contents of the informed consent
Age ≥ 18 years.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Goethe University
Lead sponsor
German Federal Ministry of Education and Research
Collaborator