Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Exposure
  • Influenza
  • Prevention
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Patients randomly allocated into 3 or 7-days postexposure chemoprophylaxis groupMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Younger than 18 years
Gender
Both males and females

Description

Only applies to patients hospitalized due to other than influenza reasons. If a proven contact with influenza has taken place (influenza diagnosed by signs/symptoms and positive rapid influenza diagnostic test and/or PCR), a patient may be enrolled.

Only applies to patients hospitalized due to other than influenza reasons. If a proven contact with influenza has taken place (influenza diagnosed by signs/symptoms and positive rapid influenza diagnostic test and/or PCR), a patient may be enrolled.

Tracking Information

NCT #
NCT04297462
Collaborators
Not Provided
Investigators
Principal Investigator: August E. Wrotek, MD PhD The Centre of Postgraduate Medical Education