The Clinical Impact of Cobas® Eplex Blood Culture Panels for the Diagnosis of Bacteremia and Fungemia

Recruiting N/A Interventional Study
Bloodstream Infection
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
200 (estimated)
Sponsor
University Hospital, Antwerp · Other
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About This Trial
A quality improvement study on the diagnostics and clinical management of bloodstream infection episodes. Patients of all ages and genders with positive blood cultures collected for standard patient care are included in the study. In the intervention group of patients, positive blood cultures will be analysed with the cobas® eplex (Roche) blood culture panels in addition to conventional, standard-…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with onset of BSI at the emergency department or general wards * Patients hospitalized from blood draw (at least 24h) * For pediatric patient only BSI episodes caused by gram-negative organisms Exclusion Criteria: * Patients deceased at the time of the positive bloo…
Contacts

Sien De Koster, PhD

+32 3 821 36 72

Sien.DeKoster@uza.be

CONTACT

Thomas Demuyser, PhD

+32 3 436 82 86

thomas.demuyser@uza.be

CONTACT