The Effect of Two Different Doses of Noradrenaline on Hypotension Caused by Spinal Anesthesia for Cesarean Section
Recruiting
N/A
Interventional Study
Cesarean Section
Hypotension
Norepinephrine
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 19 – 40
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- Assiut University · Other
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About This Trial
To compare two infusion rates of norepinephrine for prophylaxis against post-spinal hypotension during caesarean delivery.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant women scheduled for cesarean section under spinal anesthesia
* Gestational age of at least 37 weeks
Exclusion Criteria:
* Patient refusal
* Contraindications of spinal anesthesia
* Allergy to the study drug
* Height\<150 cm, weight \< 60 kg, body mass index (BMI) ≥4…
Contacts