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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.
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Inclusion criteria
Provide informed consent for participation in this study.
Patient sample must meet at least one of the criteria below:
1. Positive samples (serum or plasma) from individuals who meet at least one of the following conditions:
HIV-1 Ab positive
HIV-2 Ab positive
HCV-Ab positive
HBsAg positive
Positive for at least TPHA, with those positive for both TPHA and VDRL ideally included 2. Negative samples (serum or plasma) from individuals who meet at least one of the following conditions:
Blood donors
Hospitalized patients or individuals coming to the clinic
Vulnerable populations (such as: drug users, prison population, ...) 3. Negative samples (serum or plasma) containing potential interfering substances from individuals who meet at least one of the following conditions:
Being a pregnant woman
Infected with at least one of the following viruses or bacteria: hepatitis A virus (HAV), hepatitis E virus (HEV), tuberculosis (TB), gonorrhoea, chlamydia, influenza virus, Covid-19
Presenting any of the following criteria:
Exclusion criteria
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Data sourced from clinicaltrials.gov
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