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Starting soon Observational

Biofilm-induced Antimicrobial Resistance RIsk ERadication in Critical Care Central Venous Catheters

NCT07546994 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-04
Last updated
2026-04-23

Condition(s) studied

Catheter-Related InfectionsBiofilmsInfection Prevention

Investigational drug(s) / intervention(s)

Microbial analysis of catheter biofilm

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Central venous catheters (conventional central venous lines, dialysis catheters, PICC lines) showing positive microbiological culture taken from adult patients in the critical care units (intensive care units, post-operative intensive care units and post-resuscitation intensive care units) * Patient consent is free, informed, and non-opposition, provided after delivery of an information letter and oral explanation. Exclusion Criteria: * None

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)

FacilityCityRegionStatus
CH d'Alès Alès France
CHU de Nîmes Nîmes France
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 NCT07546994 on ClinicalTrials.gov ↗ ← All trials in France