Pilot Study Evaluating the Use of Simultaneous HBV, HCV, and HIV Rapid Tests

NACompletedINTERVENTIONAL
Enrollment

327

Participants

Timeline

Start Date

February 28, 2013

Primary Completion Date

June 30, 2013

Study Completion Date

October 31, 2013

Conditions
HIVHepatitis BHepatitis CCarcinoma, HepatocellularAIDS
Interventions
OTHER

ELISA

Enzyme-linked immuno-assay (ELISA) will be used to determine hepatitis B surface antigen (HBsAg), anti-HBsAg antibody (anti-HBs Ab), anti-HCV antibody, and anti-HIV antibody status. Results will be given after test results are available (8-10 days).

OTHER

Rapid Test

A rapid test will be performed to determine the subjects' hepatitis B surface antigen (HBsAg, using VIKIA®), anti-HCV antibody (HCV, using OraQuick®), and anti-HIV antibody (HIV, using VIKIA®) status. Results will be given the same day.

Trial Locations (1)

75011

Consultation d'Accueil, de Soins et d'Orientation (CASO) de Médecins du Monde (MDM), Paris

Sponsors
All Listed Sponsors
collaborator

ANRS, Emerging Infectious Diseases

OTHER_GOV

collaborator

Gilead Sciences

INDUSTRY

collaborator

Roche Pharma AG

INDUSTRY

collaborator

Mairie de Paris

UNKNOWN

collaborator

BioMérieux

INDUSTRY

lead

Institut de Médecine et d'Epidémiologie Appliquée - Fondation Internationale Léon M'Ba

OTHER

NCT01790633 - Pilot Study Evaluating the Use of Simultaneous HBV, HCV, and HIV Rapid Tests | Biotech Hunter | Biotech Hunter