The Effect of Two Different Doses of Noradrenaline on Hypotension Caused by Spinal Anesthesia for Cesarean Section
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age19-40
SponsorAssiut University
About this trial
To compare two infusion rates of norepinephrine for prophylaxis against post-spinal hypotension during caesarean delivery.
Eligibility criteria
Qualifiers
Pregnant women scheduled for cesarean section under spinal anesthesia
Gestational age of at least 37 weeks
Disqualifiers
Patient refusal
Contraindications of spinal anesthesia
Allergy to the study drug
Height<150 cm, weight < 60 kg, body mass index (BMI) ≥40 kg/m2.
Trial design
Treatments tested in this trial
- Norepinephrine (0.1)
- Norepinephrine (0.075)
Treatment groups
100 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov