Steroids In caRdiac Surgery Trial (SIRS Trial)
Cardiac Surgical Procedures, Cardiopulmonary Bypass, Systemic Inflammatory Response Syndrome
About this trial
This is an interventional treatment trial for Cardiac Surgical Procedures focused on measuring Cardiac Surgical Procedures, Cardiopulmonary Bypass, Systemic inflammatory Response Syndrome, Steroid, Myocardial Infarction, Randomized Clinical Trial
Eligibility Criteria
Inclusion Criteria:
- Age greater than 18 years
- Require CPB for any cardiac surgical procedure (such as CABG, Valve, Aorta, or combined procedures)
- Must have a EuroSCORE ≥ 6
- Provide written informed consent
NOTE: For participating sites in India, China and Hong Kong, the following eligibility criteria will be applied:
- Age greater than 18 years
- Require CPB for any cardiac surgical procedure (such as CABG, Valve, Aorta, or combined procedures)
Must have at least one of the following:
- EuroSCORE greater than or equal to 4 and undergoing valvular surgery
- EuroSCORE greater than or equal to 6 and undergoing any other cardiac surgery procedure (i.e. CABG, Aorta)
- Provide written informed consent
Exclusion Criteria:
- Use of systemic corticosteroids
- History of bacterial or fungal infection in last 30 days
- Allergy/intolerance to corticosteroids
- Will receive Aprotinin
- Previous participation in study
Sites / Locations
- Hamilton General Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Treatment
Placebo
500 mg of methylprednisolone divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation
500 mg of matching placebo (normal saline solution) divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation