Actively Recruiting
Hantavirus Registry - HantaReg
Led by University of Cologne · Updated on 2025-12-17
200
Participants Needed
1
Research Sites
560 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Hantavirus disease are zoonotic infections and remain a clinical challenge with globally increasing incidence and multiple serious outbreak situations in Europe within the last years. Hantavirus disease encompasses two clinical syndromes, hemorrhagic fever with renal syndrome (HFRS) and hantavirus cardiopulmonary syndrome (HCPS) caused by Old World and New World hantaviruses, respectively. Depending on the causative Old World hantavirus species, clinical course of HFRS can vary from mild to moderate to severe. At present, there is no specific therapy available for hantavirus disease. As the clinical course of hantavirus disease is dependent on the causing viral pathogen and as there worrisome hints that clinical course HFRS and HCPS overlap, further studies with regard to the disease course are mandatory. Furthermore, the examination of attributable mortality and costs of hantavirus disease will need to be studied on a multinational basis and therefore HantaReg will particularly use a matched case control design.
CONDITIONS
Official Title
Hantavirus Registry - HantaReg
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Laboratory-confirmed hantavirus infection by serology or molecular tests
- Clinical evidence of nephropathia epidemica or hemorrhagic fever with renal syndrome (HFRS)
- Clinical evidence of hantavirus cardiopulmonary syndrome (HCPS)
You will not qualify if you...
- Laboratory-confirmed hantavirus infection without clinical signs of nephropathia epidemica, HFRS, or HCPS
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital of Cologne
Cologne, North-Rhine Westfalia, Germany, 50937
Actively Recruiting
Research Team
F
Felix Köhler, MD
CONTACT
F
Felix Köhler, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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