Clinical study on the monitoring of heparin concentration and patient prognosis in cardiac surgery under cardiopulmonary bypass
Not Applicable
- Conditions
- cardiac surgery under cardiopulmonary bypass
- Registration Number
- JPRN-UMIN000035112
- Lead Sponsor
- Department of Anesthesiology, Tokyo Medical University Hachioji Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1. Under 20 years old 2. Emergency operation 3. Major vascular surgery (circulatory arrest, selective cerebral perfusion) 4. Infective endocarditis 5. Patients with coagulation fibrinolysis abnormality by preoperative examination 6. Patient using auxiliary circulation before surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Amount of blood loss
- Secondary Outcome Measures
Name Time Method Amount of blood transfusion, heparin dosage, protamine dosage, time to extubation, length of ICU stay, blood coagulation and fibrinolysis function, anti-inflammatory effect, artificial lung inlet pressure and artificial lung outlet pressure