Actively Recruiting
The Effect of Two Different Doses of Noradrenaline on Hypotension Caused by Spinal Anesthesia for Cesarean Section
Led by Assiut University · Updated on 2025-08-29
100
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To compare two infusion rates of norepinephrine for prophylaxis against post-spinal hypotension during caesarean delivery.
CONDITIONS
Official Title
The Effect of Two Different Doses of Noradrenaline on Hypotension Caused by Spinal Anesthesia for Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women scheduled for cesarean section under spinal anesthesia
- Gestational age of at least 37 weeks
- Age between 19 and 40 years
- Height 150 cm or taller
- Weight 60 kg or more
- Body mass index less than 40 kg/m2
You will not qualify if you...
- Patient refusal to participate
- Contraindications to spinal anesthesia
- Allergy to norepinephrine or study drug
- Height less than 150 cm
- Weight less than 60 kg
- Body mass index 40 kg/m2 or higher
- Presence of cardiac diseases
- Hypertensive disorders during pregnancy
- Prepartum hemorrhage
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Assiut University Woman Health Hospital
Asyut, Egypt
Actively Recruiting
Research Team
Z
Zakaria A. Zakaria
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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