Occupational post-
Conditions
Interventions
Tenofovir/Emtricitabine (300/200) + Rilpivirine (25),Tenofovir/Emtricitabine (300/200) + Ritonavir-
boosted atazanavir (300/100)
Active Comparator Drug,Experimental Drug
TDF/FTC+RPV,TDF/FTC+ATV/r
Sponsors
King Chulalongkorn Memorial Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: >18-year-old of age occupational exposure to HIV less than 72 hours
Exclusion criteria
Exclusion criteria: non-occupational exposure to HIV allergic to study drugs HIV-negative source
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Completion rate 28 days after initiation of intervention Chi-square test | — |
Secondary
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
Thailand
Contacts
Public ContactPreut Assawaworrarit
Unaffiliated
Outcome results
None listed