Overview
Phenylephrine Versus Norepinephrine for Maintenance of Hemodynamic During Cesarean Section Under Spinal Anesthesia
Status:
Completed
Completed
Trial end date:
2020-12-02
2020-12-02
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Comparison between prophylactic continuous variable infusion of phenylephrine (starting dose 0,5mcg/kg/min) and norepinephrine tartrate (starting dose 0,1mcg/kg/min) to prevent hypotension and maintain cardiac output under spinal anesthesia during cesarean delivery.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Centre Hospitalier Régional d'OrléansTreatments:
Anesthetics
Bupivacaine
Morphine
Norepinephrine
Oxymetazoline
Phenylephrine
Sufentanil
Criteria
Inclusion Criteria:- Pregnancy higher than 36 weeks of amenorrhea
- Scheduled or semi-urgent (interval between decision and delivery by cesarean section
higher than 12hours) cesarean section under spinal anesthesia
Exclusion Criteria:
- Extreme height (less than 140cm; higher than 180cm)
- Weight less than 50kg
- Weight higher than 120kg
- Cardiovascular disease with use of cardiac medication (including antihypertensive
drug)
- Active neurological disease
- Anti-hypertension treatment.
- High blood pressure or severe pre-eclampsia
- American Society of Anesthesiologists physical status class higher than 3
- Placenta accrete/percreta
- Cesarean section scheduled under general anesthesia
- Contraindications to spinal anesthesia
- Minor (age less than 18 years old)
- Guardianship/ curatorship
- Anemia less than or equal to 8 g/dl
- Allergy to any study medication
- Simultaneous participation in another study