Actively Recruiting
Hemodynamic Effects of a High Dose Versus Low Dose Propofol During Induction of Anesthesia.
Led by Ain Shams University · Updated on 2024-11-26
70
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The investigators will test the hemodynamic effects of a high dose versus low dose Propofol during induction of anesthesia.
CONDITIONS
Official Title
Hemodynamic Effects of a High Dose Versus Low Dose Propofol During Induction of Anesthesia.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age from 21 to 40 years old
- Patients with ASA classification I and II
- Undergoing scheduled elective surgery
You will not qualify if you...
- Declining to give written informed consent
- ASA classification III to V
- Morbid obesity with BMI greater than 40 kg/m2
- Severe intraoperative hypotension requiring large fluid treatment
- Severe or uncontrolled hypertension (NIBP >150/100), congestive heart failure, moderate to severe valvular heart disease, uncontrolled arrhythmia, heart rate over 100 bpm
- Significant hepatic or renal disorder
- Uncontrolled diabetes mellitus type 1 or type 2 with complications
- Pregnancy or menstruation
- Anemia with hemoglobin less than 9.0 g/dL
- Hypersensitivity to soybean oil, egg lecithin, or glycerol
- Medical substance abuse
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ain Shams university
Cairo, Abbaseya, Egypt, 11517
Actively Recruiting
Research Team
H
Hadeer S Saied, MBBCH
CONTACT
H
Hadeer S Saied, M.B.B.CH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here