Study Type
Interventional - Drug
SIRS was a multicentre, international, randomized, controlled, double-blind placebo-controlled trial of high-risk adult patients undergoing cardiopulmonary bypass.
Patients were randomly allocated to receive 500 mg of methylprednisolone divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation, or matching placebo.
Primary endpoint:
Adjudicated.
1) Total mortality within 30 days post-surgery and;
2) Composite of total mortality, MI, stroke, renal failure, or respiratory failure within 30 days post-surgery.
Interventional - Drug
Randomized, double-blind treatment, placebo control, parallel group
18
86
7507
2007-2014
PHRI
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