Safety and Efficacy of Early Administration of Dexamethasone in High-risk Sepsis
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Trial Parameters
ConditionSepsis
SponsorCHA University
Study TypeINTERVENTIONAL
PhasePhase 1, Phase 2
Enrollment102
SexALL
Min Age19 Years
Max AgeN/A
Start Date2021-01-15
Completion2025-12-30
Interventions
Dexamethasone
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Brief Summary
The purpose of this study is to investigate the safety and efficacy of early administration of two different doses of dexamethasone in high risk septic patients.
Eligibility Criteria
Inclusion Criteria: * Sepsis defined by Sepsis-3 definition * Initial systolic blood pressure \< 90mmHg or blood lactate level \>2mmol/L Exclusion Criteria: * advanced directive for "Do not resuscitation" * recent systemic administration of glucocorticoid (4 weeks) * recent systemic administration of chemotherapy (4 weeks) * recent systemic administration of immunosuppressant (4 weeks) * expected life less than 90 days * Transferred from other hospital * Sepsis diagnosed 24 hours after ED admission * Use of etomidate in ED * pregnant or on lactation * no informed consent
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