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Prophylactic Treatment With Oseltamivir

Registration Number
NCT03899571
Lead Sponsor
University Medical Centre Ljubljana
Brief Summary

The purpose of this study is to compare the efficacy of 5-day versus 10-day oseltamivir prophylactic treatment in patients who had been exposed to influenza.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
222
Inclusion Criteria
  • 18 years or older
  • exposure to influenza during hospitalization
  • risk factors for influenza complications
  • consent for participation obtained
Exclusion Criteria
  • younger than 18 years
  • hematological malignancy
  • hospitalized in intensive care unit
  • refusal to participate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
10 daysOseltamivir Oral Capsule for 10 days post-exposureoral oseltamivir 75 mg once daily for 10 days post-exposure
5 daysOseltamivir Oral Capsule for 5 days post-exposureoral oseltamivir 75 mg once daily for 5 days post-exposure
Primary Outcome Measures
NameTimeMethod
Occurrence of influenza like illness 10 days after oseltamivir prophylactic therapy10 days after oseltamivir prophylactic therapy

Experiencing influenza like illness as self assessed by a patient and/or as assessed by a medical doctor while on prophylaxis with oseltamivir and during the following 10 days.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Medical center Ljubljana

🇸🇮

Ljubljana, Slovenia

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