Epidemiology of Bacteremia at Two Tertiary ICUs in Switzerland
NCT ID: NCT05236283
Last Updated: 2023-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
395 participants
OBSERVATIONAL
2022-02-01
2022-03-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Bern ICU
Blood Culture
Blood Culture
Lausanne ICU
Blood Culture
Blood Culture
Interventions
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Blood Culture
Blood Culture
Eligibility Criteria
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Inclusion Criteria
1. was treated at the ICU/IMC at the time of blood culture collection;
2. or has been admitted to ICU/IMC in the 48 hours after blood culture collection
Exclusion Criteria
* coagulase negative staphylococci;
* Bacillus spp.;
* Corynebacterium spp.;
* Propionibacterium spp.;
* Aerococcus spp.;
* Micrococcus spp.
2. Explicit documentation that the patient does not want to participate in any study
18 Years
ALL
No
Sponsors
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Insel Gruppe AG, University Hospital Bern
OTHER
Responsible Party
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Principal Investigators
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Josef Prazak, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Insel Gruppe AG, University Hospital Bern
Locations
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Departement of Intensive Care Medicine
Bern, , Switzerland
Countries
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References
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Zuercher P, Moser A, Frey MC, Pagani JL, Buetti N, Eggimann P, Daneman N, Fowler R, Que YA, Prazak J. The effect of duration of antimicrobial treatment for bacteremia in critically ill patients on in-hospital mortality - Retrospective double center analysis. J Crit Care. 2023 Apr;74:154257. doi: 10.1016/j.jcrc.2023.154257. Epub 2023 Jan 23.
Other Identifiers
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2021-02302
Identifier Type: -
Identifier Source: org_study_id
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