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Prospective collection of data and biomaterial of COVID-19 at the location Würzburg

Conditions
U07.1
COVID-19, virus identified
Registration Number
DRKS00022402
Lead Sponsor
niversitätsklinikum Würzburg
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
94
Inclusion Criteria

Symptomatic COVID-19 infection,
Hospital admission

Exclusion Criteria

None

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mortality: Registration via clinical information system or (when consent has been given) by information of relatives or family doctor. Data is collected at baseline (during hospital stay), 3, 12 and 24 months after admission.<br><br>Non-fatal complication: pulmonary co-infection, bloodstream infection, thromboembolic event. Data is collected at baseline (during hospital stay) via clinical information system.<br><br>Quality of life: Registration via structured interview and standardized questionnaire (EQ-5D). Data is collected at 3, 12 and 24 months after admission.<br>
Secondary Outcome Measures
NameTimeMethod
identification of immune response or comorbidities due to COVID-19 infection
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