Renal function in pulsatile and non-pulsatile perfusion in patient undergoing coronary artery surgery.
Not Applicable
- Conditions
- Coronary artery disease.Chronic ischemic heart disease
- Registration Number
- IRCT20200825048509N1
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Age above 18 years
Coronary artery surgery
Exclusion Criteria
Suffering MI in the last two weeks
Off pump surgery
Urgent surgery
untreated diabetes
Abnormal liver function
Reduced level of consciousness before surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in renal function. Timepoint: Before surgery, during surgery, 24 hours after surgery, at the releasing time from hospital. Method of measurement: Getting blood and urine sample.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular pathways are affected by pulsatile vs. non-pulsatile perfusion on renal function in coronary surgery?
How does IRCT20200825048509N1 compare standard perfusion techniques in managing acute kidney injury post-coronary bypass?
Which biomarkers correlate with improved renal outcomes in pulsatile perfusion for patients with chronic ischemic heart disease?
What adverse events are associated with non-pulsatile perfusion in coronary artery disease patients and how are they managed?
Are there alternative perfusion systems or combination therapies that enhance renal protection in coronary surgery trials?