Effect of Propofol in coronary bypass surgery
Phase 3
Recruiting
- Conditions
- Comparison of Outcomes Between Propofol and Dexmedetomidine in Post-Coronary Artery Bypass Graft Patients.
- Registration Number
- IRCT20240207060924N1
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 92
Inclusion Criteria
Having informed consent
Patients must meet inclusion criteria, i.e. be elective and referred for open heart surgery only
Age should be between 35 and 80 years old
Performed by the same surgeon
The maximum duration of the surgery must be 6 hours
All were operated with a cardiopulmonary pump
Valve surgery should not be performed at the same time as CABG
Exclusion Criteria
Patient is not a candidate for elective CABG surgery
Duration of surgery is more than 6 hours
Patients have not had surgery outside of the cardiopulmonary pump
Patients outside the 35-80 age range
The patient has the right to withdraw at any stage of the research
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method