Clinical Trials in France / NCT05872152
Recruiting
Not applicable
Impact of Fourier Transform Infrared Spectroscopy (FTIRS) in ICUs
NCT05872152 · tracked via the Priya Life Science France tracker
Condition(s) studied
Organ Failure, Multiple
Investigational drug(s) / intervention(s)
FTIR results
FTIR results: Weekly transmission of FTIRS typing of ESBL-E to centers
Study summary
This study will assess the impact of FTIRS typing on the spread of ESBL-E in intensive care units
Eligibility
Inclusion Criteria:
* Adult patients hospitalized in ICU
* ESBL-E carrier
Exclusion Criteria:
* none
Primary outcome measure(s)
- Baseline frequency of ESBL-E cross transmission as assessed by WGS — Month 9 to Month 12 (depending on centers, stepped wedge design)
Number of patients with hospital acquired ESBL-E / total number of ESBL-E carriers - Post intervention frequency of ESBL-E cross transmission as assessed by WGS — Month 24
Number of patients with hospital acquired ESBL-E / total number of ESBL-E carriers
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU CHEN | Caen | France | Recruiting |
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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 NCT05872152 on ClinicalTrials.gov ↗ ← All trials in France