Actively Recruiting

Age: 18Years +
All Genders
NCT06838598

Structural and Microbiological Characterization of Arterial Catheter Biofilm in ICU's Patients Using Optical Coherence Tomography

Led by Centre Hospitalier William Morey - Chalon sur Saône · Updated on 2026-03-18

60

Participants Needed

2

Research Sites

182 weeks

Total Duration

On this page

Sponsors

C

Centre Hospitalier William Morey - Chalon sur Saône

Lead Sponsor

C

Centre Hospitalier Universitaire Dijon

Collaborating Sponsor

AI-Summary

What this Trial Is About

29.3% of bacteremias in intensive care units (ICU) are linked to vascular devices, including 7.7% to arterial catheters, with an influence on both morbility and mortality. It is now accepted that biofilm as a role on bacterial development on inner surface of vascular devices but there is yet a lack of clinical relevant data documenting a causal relation between biofilm formation and bacteremias. The investigators assume that a better structural and microbiological characterization of arterial catheter biofilm in ICU patients could help preventing bacteremias or have a more specific treatment when it appears.

CONDITIONS

Official Title

Structural and Microbiological Characterization of Arterial Catheter Biofilm in ICU's Patients Using Optical Coherence Tomography

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient or relative informed of the study and having declared their non-objection
  • Patient over 18 years old
  • Patient hospitalized in ICU with an arterial catheter
Not Eligible

You will not qualify if you...

  • Patient unable to express consent
  • Patient whose collection of the arterial catheter is impossible or for whom storage at 4�b0C is impossible
  • Patient with arterial catheter removed outside the usual procedure of the ICU
  • Patient admitted in ICU with an arterial catheter already in place

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

CHU Dijon Bourgogne

Dijon, Bourgogne-Franche-Comté, France, 21000

Actively Recruiting

2

CH Macon

Mâcon, Bourgogne-Franche-Comté, France, 71000

Actively Recruiting

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Research Team

F

Florian PERRAUD

CONTACT

T

Thomas MALDINEY

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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