Condition: Combined Point of Care Diagnostic of HIV, HBV and HCV · Sponsor: MagIA Diagnostics
Prospective, cross-sectional, adaptative study to evaluate the clinical performance of the In-Vitro Diagnostics Medical Device MagIA IBC (a Multiplex Point-of-Care Test for the detection of HIV, HBV and HCV) in detecting anti-HIV antibodies (HIV-Ab), anti-HCV antibodies (HCV-Ab), and HBs antigens (HBs-Ag) in serum, plasma, venous blood and capillary blood. If not prescribed for the patient care, blood drawings, and finger pricks will be performed on the patient for the purpose of the clinical study. The Study includes a Technical Adjustment Phase (to identify optimized acquisition parameters and to define the decision threshold for the diagnostic) followed by a Validation Phase (to validate the concordance between the matrices and to evaluate the Specificity and the Sensibility of the diagnostics). Validation Phase is between Sept. 2024 and still ongoing.
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| Hopital Européen de Marseille | Marseille, France, France | Completed |
| Centre Hospitalier de Perpignan - Equipe Mobile Hépatites | Perpignan, France | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06082336