Clinical trial Recruiting at 1 site Observational Ages 18 and up

Rectal swab detection of ESBL, carbapenemases, and high-level cephalosporinase to predict C3G-resistant Enterobacteriaceae infections in ICU patients

Official title: Predictive Value of a Rectal Swab With Detection of Enterobacteria (ESBL-E), Carbapenemases, and High-level Cephalosporinase (HLC) on the Risk of Infections With C3G-resistant Enterobacteria in Intensive Care

Run by University Hospital, Strasbourg, France · NCT07345923 · Data updated 2026-11-12

This study tests whether a rectal swab that finds ESBL, carbapenemases, or high-level cephalosporinase can predict which adult ICU patients at Strasbourg are likely to get C3G-resistant Enterobacteriaceae infections.

More Enterobacteriaceae Infections trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment1000 (estimated)
SponsorUniversity Hospital, Strasbourg, France
Academic / other
Locations1 site (Strasbourg)
StatusRecruiting
StartedOctober 6, 2025
Main results expectedApril 2027
Study endsApril 2027
Registry record updatedJanuary 16, 2026
Trial IDNCT07345923 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult medical or surgical ICU patients at Strasbourg University Hospitals who underwent rectal screening for ESBL/HLC/carbapenemase carriage between January 1, 2024 and January 1, 2025.

Probably not a fit

Patients who were not screened with a rectal swab, were treated outside the specified ICUs or time window, were under 18, or who carry organisms not covered by these markers are unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational cohort of adult medical and surgical ICU patients at Strasbourg University Hospitals who had rectal screening for ESBL/HLC/carbapenemase carriage between January 1, 2024 and January 1, 2025. Investigators will link colonization results from rectal swabs to subsequent clinical and microbiology records to identify infections with C3G-resistant Enterobacteriaceae. No experimental interventions are given; the study analyzes existing diagnostic and outcome data to estimate predictive value. Findings aim to quantify how well carriage detected by rectal swab forecasts later resistant infections in this ICU population.

Why it matters

Potential benefit: If successful, the test could help identify ICU patients at high risk for resistant enterobacterial infections so clinicians can tailor empiric antibiotics and infection-control measures.

How similar studies have gone: Previous observational studies have shown that rectal carriage of ESBL- and carbapenemase-producing Enterobacteriaceae often predicts subsequent infection, though predictive accuracy varies by setting and the role of high-level cephalosporinase markers is less well established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patients (≥ 18 years old)
* Who have been in medical or surgical intensive care at Strasbourg University Hospitals (between January 1, 2024, and January 1, 2025)
* Who have undergone rectal screening for carriage of ESBL/HLC/carbapenemase-producing Enterobacteriaceae

Exclusion Criteria:

* Refusal to participate in the study

Where it's running

  • Service des Maladies Infectieuses et Tropicales - CHU de Strasbourg - France
    Strasbourg, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.