Efficacy and Safety of Modified Del Nido Cardioplegia in Adult Cardiac Surgeries
Phase 2
- Conditions
- Anaesthesia
- Registration Number
- PACTR202207730603285
- Lead Sponsor
- Cairo University Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 74
Inclusion Criteria
Age 18 years or older
Undergoing elective cardiothoracic surgical procedures requiring cardiopulmonary bypass with cross clamp time < 90 min
Exclusion Criteria
Patient refusal
Known allergy to any of the medications used in this study
Patients with coronary artery diseases
Patients with ejection fraction < 50%
Emergency surgeries
Patients on preoperative inotropic support and/or mechanical circulatory support
Redo surgeries
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The rhythm after removal of aortic cross clamp
- Secondary Outcome Measures
Name Time Method Reperfusion rhythm after removal of cross clamp;Potassium level immediately after aortic declamping;The number and the dose of DC shocks;CK, CKMB and Troponin T immediately after declamping.;Need for inotropes or vasopressor support and doses.;Need for anti-arrhythmia medication.;Ventricular ejection fraction change