Comparison of Body warming devices and clinical outcomes after Heart Surgery: randomized Clinical Trial
- Conditions
- HypothermiaRewarmingCardiac SurgeryCardiopulmonary BypassHemorrhageH02.403.810.803E04.292.413C23.888.119.565E02.760.731C23.550.414
- Registration Number
- RBR-5t582g
- Lead Sponsor
- niversidade Federal de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Age 18 years or older; submitted to elective coronary artery bypass grafting with Cardiopulmonary bypass; Intensive Care unit admission temperature below 36 ° C and greater than 32 ° C.
Other surgical corrections associated with coronary artery bypass grafting with Cardiopulmonary bypass; use of circulatory support devices, intra-aortic Balloon Counterpulsation; extracorporeal membrane oxygenation ; ventricular percutaneous circulatory assistance previus cardiac surgery; patients with chronic renal disease; intraoperative cardiac arrest, immunosuppressed patients; acquired or hereditary coagulation disorders; liver disease
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method