CTI-01 (Ethyl Pyruvate) Safety and Complication Prevention in Cardiac Surgery Patients on Cardiopulmonary Bypass (CPB)
Coronary Disease, Heart Valve Diseases
About this trial
This is an interventional prevention trial for Coronary Disease focused on measuring Coronary artery bypass grafting, Heart valve prosthesis implantation, Cardiopulmonary bypass, Oxidative stress, Inflammation, Endotoxemia
Eligibility Criteria
Inclusion Criteria: Parsonnet additive risk score greater than or equal to 15 Scheduled CABG (coronary artery bypass grafting) and/or cardiac valve repair or replacement surgery using cardiopulmonary bypass Exclusion Criteria: Emergency cardiac surgery Significant concomitant surgery Minimally invasive or thoracic surgical approach Preoperative mechanical assist device Body weight <50 kg or >140 kg Active systemic infection Creatinine >3.0 mg/dL History of hematologic or coagulation disorders History of malignancy (past year)or organ transplantation Use of immunosuppressive drugs or current immunosuppressed condition
Sites / Locations
- Saddleback Memorial Medical Center
- University of Southern California
- Kaiser Permanente
- Washington Hospital Center
- University of Florida
- Research Support Personnel
- Peninsula Regional Medical Center
- Baystate Medical Center
- Nebraska Methodist Hospital
- NYU Medical Center
- Duke University Medical Center
- East Carolina University - Brody School of Medicine
- Hospital of the University of Pennsylvania
- Chester County Hospital - The Cardiovasular Center
- St. Luke's Episcopal Hospital/Texas Heart Institute
- MultiCare Health System
- Medical College of Wisconsin - VA Medical Center