Biofilm-induced Antimicrobial Resistance RIsk ERadication in Critical Care Central Venous Catheters
Condition(s) studied
Investigational drug(s) / intervention(s)
Microbial analysis of catheter biofilm: Identification and sampling of the catheter, standard microbiological analysis, inclusion and transfer (INSERM platform), biofilm analysis, and collection of associated data (clinical, biological and related to the catheter).
Study summary
Central venous catheter (CVC) infections are a frequent and serious nosocomial complication in critical care, leading to increased morbidity, mortality, and costs. The pathophysiology of these infections relies on the formation of a biofilm, an organized microbial structure that confers exceptional tolerance to anti-infectives and the immune system. However, data concerning the characteristics of the in vivo biofilm (kinetics, composition, endo- vs. extraluminal organization) on central venous catheters in intensive care patients are very limited, hindering the development of effective and targeted prevention strategies.
The main aim of this study is to quantify the density and describe the spatial distribution (extra- and intraluminal compartments) of the biofilm on infected or colonized central venous catheters, prospectively collected from patients in the critical care units.
Eligibility
Primary outcome measure(s)
- Concentration (density) of viable bacterial biofilm — Baseline
Measured in Colony Forming Units per millilitre (CFU/mL) for each compartment of the central venous catheter (internal and external lumen of the catheter)
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| CH d'Alès | Alès | France | |
| CHU de Nîmes | Nîmes | France |
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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 NCT07546994 on ClinicalTrials.gov ↗ ← All trials in France