Beta-Lactam Antibiotics InitiaL ExpoSure OptimisEd in CriticallY Ill Patients with SEpsis

Recruiting Phase 4 Interventional Study
Sepsis - to Reduce Mortality in the Intensive Care Unit Sepsis Septic Shock
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
980 (estimated)
Sponsor
Erasmus Medical Center · Other
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About This Trial

The aim of this study is to investigate if an initial short double dose of beta-lactam antibiotics will reduce mortality in critically ill patients with sepsis.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * ≥18 years of age * Receiving intravenous antibiotic therapy of the target drugs (including continuous infusion of beta-lactam antibiotics) * Primary infection * Admitted to the ICU * Meeting the Sepsis-3 criteria for septic shock: sepsis in addition to shock requiring the star…
Contacts

Birgit C.P. Koch, PharmD

0031107033202

b.koch@erasmusmc.nl

CONTACT