Blood cardioplegia versus cold crystalloid cardioplegia: A prospective randomized study
Not Applicable
Recruiting
- Conditions
- Diseases which require aortic arch replacement
- Registration Number
- JPRN-jRCTs051220064
- Lead Sponsor
- Okada Kenji
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 52
Inclusion Criteria
1. Patients who receive aortic arch replacement
2. More than 20 years old
3. Patients who give written informed consent
Exclusion Criteria
1. Coronary artery stenosis (> 75%) which requires an intervention
2. Preoperative left ventricular systolic dysfunction (EF < 50%)
3. Emergent cases
4. Patients deemed inappropriate by the investigators
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method eft ventricular ejection fraction in thoracic cardioechography 7 days postoperatively
- Secondary Outcome Measures
Name Time Method In-hospital death<br>Overall survival<br>Incidence of low output syndrome<br>Incidence of postoperative myocardial infarction<br>Dosage of cardioplegia<br>CK / CK-MB release<br>Incidence of left ventricular diastolic dysfunction<br>Incidence of right ventricular systolic dysfunction<br>Incidence of ventricular arrhythmia after return to spontaneous rhythm<br>Incidence of new-onset atrial fibrillation 48 hours postoperatively<br>Requirement for implantation of permanent pacemaker<br>Incidence of cerebral stroke<br>Incidence of renal dysfunction<br>Duration of ventilatory support<br>Amount of intraoperative bleeding<br>Amount of intraoperative and postoperative transfusion<br>Re-exploration for bleeding<br>Occurence of diseases, etc.