Rapid Recognition of Corticosteroid Resistant or Sensitive Sepsis

Recruiting N/A Interventional Study
Sepsis
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
1,800 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Other
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About This Trial
Main objective and primary endpoint: To compare the effect hydrocortisone plus fludrocortisone vs. placebo on a composite of death or persistent organ dysfunction - defined as continued dependency on mechanical ventilation, new renal replacement therapy, or vasopressors - assessed at 90 days on intensive care unit (ICU) adults and having different biological profiles for immune responses and corti…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patient ≥18 years old; 2. Admitted to ICU with proven or suspected infection as the main diagnosis; 3. Community acquired pneumonia related sepsis or vasopressors dependency (norepinephrine, epinephrine, vasopressin, dopamine, phenylephrine) or septic shock (vasopressor to ma…
Contacts

Djillali ANNANE, MD, PhD

+33 1 47 10 77 87

djillali.annane@aphp.fr

CONTACT