Continuous Infusion of Norepinephrine vs Phenylephrine During Spinal Anesthesia for Cesarean Section (INPEACE)
Recruiting
Phase 4
Interventional Study
Cesarean Section Complications
Hypotension
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 140 (estimated)
- Sponsor
- Hassan II University · Other
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About This Trial
The goal of this clinical trial is to compare norepinephrine and ephedrine in maintaining blood pressure during spinal anaesthesia for elective cesarean delivery. The main questions it aims to answer are:
* Do phenylephrine and norepinephrine administered as manually controlled continuous infusion during elective cesarean delivery have different effects on neonatal outcome ?
* Do phenylephrine an…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Full-term, singleton, pregnant women, nonlaboring.
* Scheduled for elective cesarean delivery under spinal anesthesia,
* American Society of Anesthesiologists physical status : 1 or 2
* Baseline systolic BP between 90 and 140 mm Hg.
Exclusion Criteria:
* Known fetal abnormal…
Contacts