Actively Recruiting
Processed Electroencephalography-guided General Anesthesia and Outcomes in Major Abdominal Surgery
Led by Assiut University · Updated on 2025-02-04
162
Participants Needed
1
Research Sites
99 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate whether the reduction in the amount of intraoperative norepinephrine required to prevent hypotension, facilitated by processed electroencephalography (pEEG) -guided general anesthesia, will lead to a decrease in postoperative complications, particularly acute kidney injury (AKI).
CONDITIONS
Official Title
Processed Electroencephalography-guided General Anesthesia and Outcomes in Major Abdominal Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for major abdominal surgery lasting more than 2 hours under general anesthesia
- American Society of Anesthesiologists Physical Status (ASA) score I-III
- Age between 18 and 70 years
- Both male and female patients
You will not qualify if you...
- Emergency surgeries
- Uncontrolled hypertension (systolic blood pressure >150 mm Hg) despite medication
- Recent acute cardiovascular events such as heart failure or acute coronary syndrome
- Chronic kidney disease with glomerular filtration rate below 30 ml/min/1.73 m² or requiring renal replacement therapy
- Severe liver failure indicated by elevated liver enzymes, bilirubin, or low prothrombin time
- Preoperative sepsis or septic shock
- Pregnancy
- Patient refusal to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Assiut University Hospitals
Asyut, Egypt
Actively Recruiting
Research Team
W
Walaa H Mohamed, Assistant Lecturer
CONTACT
M
Mostafa S Abbas, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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