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Evaluation of Inflammatory Cytokines During COVID-19

Conditions
Covid19
Interventions
Diagnostic Test: Blood sample
Registration Number
NCT04824495
Lead Sponsor
University of Vienna
Brief Summary

The aim of this study is to evaluate pro-inflammatory cytokines as well as microvesicles during the course of SARS-CoV2 infection in the context of clinical parameters.

Detailed Description

In this prospective trial, 100 patients with an acute SARS-CoV2 infection are enrolled. After confirmation of COVID-19, blood samples are taken for evaluation of various inflammatory cyokines and microvesicles at day 1, 5, 9 and 13 during hospitalisation and are interpreted in the context of clinical parameters.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Age > 18 years
  • Confirmation of acute SARS-CoV2 infection
  • Ability to provide informed consent
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Patients with acute COVID-19Blood sample-
Primary Outcome Measures
NameTimeMethod
Cytokine level in context with clinical parameters2 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Medical University of Vienna

🇦🇹

Vienna, Austria

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