Innovate, Involve, Inspire

ConditionHCV
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorFrontline AIDS

About this trial

The study will test a Community-based Simplified HCV Testing and Treatment Algorithm (CBSA), implemented at community harm reduction fixed or mobile sites.

All potential participants with positive anti-HCV test will undergo diagnostic procedures including HCV-RNA testing. Those eligible for CBSA will be prescribed a fixed dose combination tablet: sofosbuvir/daclatasvir.

Sustained virologic response (SVR) will be assessed 12 weeks after treatment completion. All those who achieve SVR will be tested for HCV\_RNA at six and 12 months after SVR12.

Eligibility criteria

Qualifiers

Drug use in the past 90 days

Age 18 and above

Positive for HCV RNA

Disqualifiers

No meeting inclusion criteria

Pregnancy

Trial design

Treatments tested in this trial

  • Community-based Simplified HCV Testing and Treatment Algorithm

Treatment groups

1,454 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators

Frontline AIDS

Lead sponsor

Alliance for the Public's Health

Collaborator