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Clinical Trial Summary

An acceptance and feasibility study for immediate ART initiation and storage of laboratory specimens for individuals with suspected acute HIV infection who are diagnosed in one of the 7 participating emergency rooms


Clinical Trial Description

Individuals with suspected acute HIV infection willing to start immediate ART treatment will be given the ART regimen (bictegravir 50mg + tenofovir alafenamide 25 mg + emtricitabine 200 mg fixed dose combination) on the day of diagnosis. Those patients beginning immediate ART in the ED who are willing to have additional laboratory specimens drawn in the ED and become part of a cohort to receive ART and have ongoing biological specimens obtained and will be followed for 48 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03711253
Study type Interventional
Source University of Southern California
Contact Esther Lim, MPH
Phone (323) 865-1645
Email Esther.Lim@med.usc.edu
Status Not yet recruiting
Phase Phase 4
Start date November 2018
Completion date November 2021

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