NCT05236283

Brief Summary

The objectives of the retrospective cohort study is to describe the actual current practice of antibiotic treatment duration for bloodstream infections in critically ill patients at two tertiary hospitals (ICU Inselspital Bern and ICU CHUV Lausanne), to examine patient, pathogen and infectious syndrome factors associated with selection of shortened treatment duration, and to describe the expected time course of clinical resolution among bacteremic patients.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
395

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 1, 2022

Completed
Same day until next milestone

Study Start

First participant enrolled

February 1, 2022

Completed
10 days until next milestone

First Posted

Study publicly available on registry

February 11, 2022

Completed
18 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2022

Completed
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2022

Completed
Last Updated

January 26, 2023

Status Verified

January 1, 2023

Enrollment Period

28 days

First QC Date

February 1, 2022

Last Update Submit

January 25, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Antibiotic Treatment Duration

    Days of adequate antibiotic treatment in Patients with Bacteremia

    Hospital discharge, expected to be on average ca. 15-20 days

Secondary Outcomes (2)

  • Days of ICU stay

    ICU discharge, expected to be on average ca. 5-15 days

  • Days of hospital stay

    Hospital discharge, expected to be on average ca. 15-25 days

Study Arms (2)

Bern ICU

Diagnostic Test: Blood Culture

Lausanne ICU

Diagnostic Test: Blood Culture

Interventions

Blood CultureDIAGNOSTIC_TEST

Blood Culture

Bern ICULausanne ICU

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patient is critically ill at the time the blood culture was collected and was treated at the ICU/IMC at the time of blood culture collection or has been admitted to ICU/IMC in the 48 hours after blood culture collection.

You may qualify if:

  • Patient has a positive blood culture with a pathogenic organism Patient is critically ill at the time the blood culture was collected as defined by the following:
  • was treated at the ICU/IMC at the time of blood culture collection;
  • or has been admitted to ICU/IMC in the 48 hours after blood culture collection

You may not qualify if:

  • Patient has a single positive blood culture with a common contaminant organism:
  • coagulase negative staphylococci;
  • Bacillus spp.;
  • Corynebacterium spp.;
  • Propionibacterium spp.;
  • Aerococcus spp.;
  • Micrococcus spp.
  • Explicit documentation that the patient does not want to participate in any study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Departement of Intensive Care Medicine

Bern, Switzerland

Location

Related Publications (1)

  • 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.

MeSH Terms

Conditions

Bacteremia

Interventions

Blood Culture

Condition Hierarchy (Ancestors)

Bacterial InfectionsBacterial Infections and MycosesInfectionsSepsisSystemic Inflammatory Response SyndromeInflammationPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Microbiological TechniquesClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisInvestigative Techniques

Study Officials

  • Josef Prazak, MD, PhD

    Insel Gruppe AG, University Hospital Bern

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 1, 2022

First Posted

February 11, 2022

Study Start

February 1, 2022

Primary Completion

March 1, 2022

Study Completion

March 30, 2022

Last Updated

January 26, 2023

Record last verified: 2023-01

Locations