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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&#45
exposure prophylaxis for HIV infection
Comparison
Rilpivirine
Ritonavir&#45
boosted atazanavir
exposure prophylaxis
Randomized 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
NameTimeMethod
Completion rate 28 days after initiation of intervention Chi-square test
Secondary Outcome Measures
NameTimeMethod
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
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