Evaluating a new method for identifying pathogens and antibiotic resistance in sepsis patients

Is this trial a fit for you?

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

What this trial studies

This observational study focuses on the IDBIORIV method for identifying pathogens and testing antibiotic susceptibility in patients diagnosed with sepsis. Sepsis is a critical condition resulting from bloodstream infections, and timely identification of the causative microorganisms is crucial for effective treatment. The study aims to assess the performance of this method compared to standard techniques used in clinical microbiology laboratories. By improving the speed and accuracy of pathogen identification, the study seeks to enhance patient outcomes and reduce mortality associated with sepsis.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult or child patient
* Hospitalized in one of the departments registered with Hospices Civils de Lyon
* Showing signs of infection
* Confirmed by a 1st positive blood culture
* Patient or close relative (trustworthy person or family member) or holder of parental authority who has given his or her non-objection after receiving the information note

Exclusion Criteria:

* Patients under court protection
* Patients under guardianship or curatorship

Where it's running

• Femme Mère enfant Hospital
  Bron, France Recruiting
• Femme Mère Enfant Hospital
  Bron, France Recruiting
• Louis Pradel Hospital
  Bron, France Recruiting
• Louis Pradel Hospital
  Bron, France Recruiting
• Louis Pradel Hospital
  Bron, France Recruiting
• Pierre Wertheimer Hospital
  Bron, France Recruiting

Study contacts

• Study coordinator: François VANDENESCH, Pr
• Email: francois.vandenesch@univ-lyon1.fr
• Phone: 4 72 07 11 11

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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.