Randomized controlled trial of a comparison between ritonavir-boosted atazanavir with tenofovir plus emtricitabine versus rilpivirine with tenofovir plus emtricitabine in occupational post-exposure prophylaxis for HIV infectio
Phase 4
Recruiting
- Conditions
- Occupational post-exposure prophylaxis for HIV infectionComparisonRilpivirineRitonavir-boosted atazanavirexposure prophylaxisRandomized controlled trial
- Registration Number
- TCTR20190311001
- Lead Sponsor
- King Chulalongkorn Memorial Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 82
Inclusion Criteria
>18-year-old of age
occupational exposure to HIV less than 72 hours
Exclusion Criteria
non-occupational exposure to HIV
allergic to study drugs
HIV-negative source
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Completion rate 28 days after initiation of intervention Chi-square test
- Secondary Outcome Measures
Name Time Method Adherence 28 days after initiation of intervention Chi square test,Side effects 28 days after initiation of intervention Chi square test,Change of total bilirubin level 28 days after initiation of intervention student t-test,Seroconversion 28 days & 90 days after initiation of intervention Chi square test