Establishment of a Biobank for the Evaluation of Rapid Diagnostic Solutions
Condition(s) studied
Study summary
This multicenter prospective registry aims to establish a biobank of residual biological samples and associated clinical data from hospitalized patients. The registry will collect a wide range of specimens (serum, plasma, respiratory samples, urine, cerebrospinal fluid, biopsies) obtained during routine care, without any additional procedures. Data are pseudonymized and stored securely for up to 20 years. The biobank will be used to develop and evaluate rapid diagnostic tests (RDTs) for emerging infectious diseases and CBRN threats to improve epidemic preparedness and patient management.
Eligibility
Primary outcome measure(s)
- Number of residual clinical samples successfully collected, aliquoted, and stored with associated clinical and microbiological data — 36months (end of patient inclusion period)
Creation of a collection of residual biological samples (serum, plasma, urine, respiratory samples, CSF, biopsies, etc.) and associated clinical and microbiological data obtained during routine care
Trial sites (10)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | Recruiting |
| CHU Paul Brousse | Villejuif | France | Recruiting |
More Assistance Publique - Hôpitaux de Paris trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07411729 on ClinicalTrials.gov ↗ ← All trials in France