Clinical trial Recruiting at 5 sites Observational

Creating a database for tracking drug-resistant bacterial infections in Switzerland

Official title: Development of a Swiss Surveillance Database for Molecular Epidemiology of Hypervirulent and Multi-drug Resistant Pathogens

Run by University Hospital, Basel, Switzerland · NCT04172025 · Data updated 2026-11-12

This study is creating a database to help track drug-resistant bacterial infections in Switzerland, connecting information from hospitals and veterinary labs to improve public health responses.

Quick facts

Study typeObservational
SexAll
Enrollment10000 (estimated)
SponsorUniversity Hospital, Basel, Switzerland
Academic / other
Locations5 sites (Basel and 4 other locations)
StatusRecruiting
StartedSeptember 30, 2019
Main results expectedDecember 31, 2029
Study endsDecember 31, 2029
Registry record updatedMay 14, 2025
Trial IDNCT04172025 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients with infections or colonizations by multidrug-resistant or virulent bacterial pathogens who have available genomic and epidemiological data.

Probably not a fit

Patients without infections or colonizations by the specified pathogens or those who decline to provide consent may not benefit from this study.

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

What this trial studies

This project aims to develop a shared surveillance database that connects human and veterinary microbiology laboratories in Switzerland. The database will facilitate near real-time molecular epidemiology, allowing for effective tracking of hypervirulent and multidrug-resistant bacterial pathogens. By analyzing previously collected genomic and epidemiological data, the study seeks to enhance outbreak recognition and transmission monitoring across different environments, including humans, animals, and the environment. The focus is on improving public health responses to significant bacterial infections.

Why it matters

Potential benefit: If successful, this initiative could significantly improve the rapid identification and management of outbreaks caused by drug-resistant pathogens, ultimately reducing morbidity and mortality.

How similar studies have gone: While the approach of creating a shared surveillance database is innovative, similar studies have shown promise in improving outbreak management and pathogen tracking.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* All patients with either colonisations or infections with either a bacterial or a viral pathogen, where whole genome sequencing data and available minimal epidemiological, demographic and clinical data
* Pathogens included into analysis are: Multidrug-resistant bacteria include: methicillin resistant Staphylococcus aureus (MRSA), Carbapenemase- and/or extended spectrum betalactamase (ESBL)-producing Enterobacteriaceae and non-fermenting bacteria including Pseudomonas aeruginosa and Acinetobacter baumannii, Vancomycin resistant Enterococcus faecium, and others; virulent bacteria include: Neisseria meningitidis, Neisseria gonorrhoeae, Mycobacterium tuberculosis, Campylobacter spp., Salmonella spp., Legionella pneumophila, Listeria monocytogenes, and Streptococcus pneumoniae, and others; Viruses include: Influenza viruses, Measles virus, Enterovirus E68, Respiratory Syncytial Virus and others.

Exclusion Criteria:

* Decline to sign a general consent or any other declining statement against using data for research purposes.

Where it's running

  • University Hospital Basel
    Basel, Switzerland
    Recruiting
  • University of Bern
    Bern, Switzerland
    Recruiting
  • University Hospital Geneva
    Geneva, Switzerland
    Recruiting
  • University Hospital Lausanne CHUV
    Lausanne, Switzerland
    Recruiting
  • University of Zurich
    Zurich, Switzerland
    Recruiting

Study contacts

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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.
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.