Study identifier:3591/9014
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Pharmacoeconomic analysis of first line meropenem versus standard antibiotic treatment in seriously infected secondary nosocomial sepsis syndrome patients. An open, randomized multi-center study.
Sepsis
Phase 4
No
Meropenem
All
160
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
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