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OpenTrials
Completed

NCT Number: NCT05535751

Cefepime vs. Carbapenems for Treating AmpC β-lactamase-producing Enterobacteriaceae Bloodstream Infections

Recent international recommendations suggest the use of carbapenem rather than cefepime in this situation, but with a low level of evidence, given the few existing studies. As cefepime is a less broad-spectrum antibiotic than carbapenems, its use would limit the selection of multidrug-resistant bacteria.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Service des maladies infectieuses et tropicales - CHU de Strasbourg - France

Strasbourg, 67091, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patient (≥18 years of age)
  • managed within a study center for high-grade cephalosporinase-producing bacteremia
  • Not objecting to the reuse of their health data for scientific research purposes.

Exclusion criteria

  • Patient who has expressed opposition to the reuse of their data for scientific research purposes.
  • Resistance to Cefepime or carbapenems
  • Multiple bacteremia
  • Treatment with a molecule other than Cefepime or carbapenem.

Treatment and study plan

Primary outcomes

  1. Hospital mortality

    Time frame: 30 days after infection

Sponsors and collaborators

Lead sponsor

University Hospital, Strasbourg, France

Other

Registry information

Acronym: CARBAPENEM

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Sep 10, 2022
Registry last updated
Dec 13, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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