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Recruiting Observational

Establishment of a Biobank for the Evaluation of Rapid Diagnostic Solutions

NCT07411729 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-06-03
Last updated
2026-02-17

Condition(s) studied

Emerging Infectious DiseasesCommunicable DiseasesBiological Warfare AgentsZoonosesDisease Outbreaks

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (≥ 18 years old) hospitalized in one of the participating centers at Bicêtre or Paul Brousse hospitals, for whom residual biological samples are available as part of routine care in one or more participating hospital departments. * Covered by, or entitled to, the French social security system (excluding State Medical Aid - AME). * Patient or legal representative/trusted person informed about the registry and having provided written consent to participate. Exclusion Criteria: * Patients under judicial protection (guardianship or curatorship). * Patients deprived of liberty by judicial or administrative decision. * Patients not speaking French and not accompanied by a translator.

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)

FacilityCityRegionStatus
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
Official registry record

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