About this trial

Performance study to evaluate the clinical performance of the In-Vitro Diagnostics Medical Device MagIA H3S (a Multiplex Point-of-Care test for the combined detection of Human Immunodeficiency Virus (HIV), Hepatitis B and C and Syphilis) from serum, plasma samples collected prospectively or retrospectively in Ivory Coast and Kenya.

Eligibility criteria

Qualifiers

Provide informed consent for participation in this study.

HIV-1 Ab positive

HIV-2 Ab positive

HCV-Ab positive

Disqualifiers

Samples from patients below 18 years of age

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

2
Côte d’Ivoire
Centre de Diagnostic et de Recherche sur le SIDA et les autres Maladies Infectieuses - CHU Treichville Abidjan Côte d’Ivoire
Kenya
Kenya Medical Research Institute (KEMRI) Nairobi Kenya

Sponsors and collaborators

MagIA Diagnostics

Lead sponsor

Institut Pasteur

Collaborator

Kenya Medical Research Institute

Collaborator

Programme PAC-CI, Site ANRS-MIE de Côte d'Ivoire

Collaborator