Surveillance of rEspiratory viruses iN healThcare and anImal workers in the NethErLands

• Conditions: airway infection; respiratory infection; 10047438

• Registration Number: NL-OMON56919
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

18 years old and above

Exclusion Criteria

none

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study endpoint is the early detection of respiratory virus infections<br /><br>that occur in HCW or AW, and the identification of the causative agent during<br /><br>the observation period. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary study endpoints include the assessment of local and systemic<br /><br>virus-specific immune responses, risk factors, data on infection kinetics, and<br /><br>genetic variation between causative viruses after a respiratory tract infection<br /><br>or vaccination against respiratory viruses. </p><br>