Prilocaine or Bupivacaine for Spinal Anesthesiain Pregnant

• Status: Unknown status
• Trial end date: 2020-08-30
• Target enrollment: 0
• Participant gender: Female

Summary

The planned cesarean section is an intervention with a standard operating time of less than 40 minutes in trained teams. Hyperbaric Bupivacaine is the local anesthetic (LA) reference for these operations. But the duration of its motor block is generally greater than 3 hours. The purpose of this study is to show a reduction in motor block time with hyperbaric Prilocaine by at least 30 minutes, which would allow mothers and their children to return to the maternity ward earlier and thus improve the circulation of patients within the maternity's PACU.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University Hospital, Montpellier
• Collaborator: Hopital Saint Roch
• Treatments: Anesthetics; Bupivacaine; Prilocaine

Criteria

Inclusion Criteria:

• Normal pregnancy

• Scheduled caesarean section

• Non-multiple pregnancy

• Age of patient: 18 years and over

• Height of patient: between 155 and 175 cm

• Affiliated patients or beneficiaries of a Social Security System

• Signature of the patient's consent

Exclusion criteria:

• Patient <18 years

• Pathological pregnancy

• Multiple pregnancy

• Emergency caesarean

• Patients who cannot give informed consent (not French speaking)

• Refusal of the patient

• Contraindications to spinal anesthesia

• Contraindications to Prilocaine

• Contraindications to Bupivacaine