Overview

Phenylephrine Versus Norepinephrine for Maintenance of Hemodynamic During Cesarean Section Under Spinal Anesthesia

Status:
Completed
Trial end date:
2020-12-02
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Centre Hospitalier Régional d'Orléans
Treatments:
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