Prophylactic Treatment With Oseltamivir
Not Applicable
Completed
- Conditions
- Influenza, Human
- Interventions
- 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
Group Intervention Description 10 days Oseltamivir Oral Capsule for 10 days post-exposure oral oseltamivir 75 mg once daily for 10 days post-exposure 5 days Oseltamivir Oral Capsule for 5 days post-exposure oral oseltamivir 75 mg once daily for 5 days post-exposure
- Primary Outcome Measures
Name Time Method Occurrence of influenza like illness 10 days after oseltamivir prophylactic therapy 10 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
Name Time Method
Trial Locations
- Locations (1)
University Medical center Ljubljana
🇸🇮Ljubljana, Slovenia