Closing Soon
Drug for Septic Shock, sponsored by The George Institute
Get in touch This trial recruits from July 2012 for 265 weeks
Janet Liang
Phone: +61 410 442 828
Email: Janet.Liang@waitematadhb.govt.nz
Inclusion Criteria
Age: From 18 Years To N/A
Gender: Both
Inclusion Criteria
Aged 18 years or older
Documented site of infection, or strong suspicion of infection, with 2 of the 4 clinical signs of inflammation:
Core temperature > 38°C or < 35°C
Heart rate > 90 beats per minute
White cell count > 12 x 109/L or < 4 x 109/L or > 10% immature neutrophils
Respiratory rate > 20 breaths per minute, or PaCO2 < 32 mmHg, or mechanical ventilation.
Being treated with mechanical ventilation at the time of randomisation
Being treated with vasopressors or inotropes to maintain a systolic blood pressure > 90mmHg, or mean arterial blood pressure > 60mmHg, or a MAP target set by the treating clinician for maintaining perfusion
Administration of vasopressors or inotropes for = 4 hours and present at time of randomisation.
Exclusion Criteria
Met all inclusion criteria more than 24 hours ago
Clinician expects to prescribe systemic corticosteroids for an indication other than septic shock (not including nebulised or inhaled corticosteroid)
Patients treated with etomidate
Patients receiving treatment with Amphotericin B for systemic fungal infections at time of randomisation
Patients with documented cerebral malaria at the time of randomisation
Patients with documented strongyloides infection at the time of randomisation
Death is deemed inevitable or imminent during this admission and either the attending physician, patient or surrogate legal decision maker is not committed to active treatment
Death from underlying disease is likely within 90 days
Patient has been previously enrolled in the ADRENAL study.
Exclusion Criteria
NCT01448109
A Randomised Blinded Placebo Controlled Trial of Hydrocortisone in Critically Ill Patients With Septic Shock
ADjunctive coRticosteroid trEatment iN criticAlly ilL Patients With Septic Shock