Rapid Recognition of Corticosteroid Resistant or Sensitive Sepsis
Recruiting
N/A
Interventional Study
Sepsis
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