Status:
UNKNOWN
Prilocaine or Bupivacaine for Spinal Anesthesiain Pregnant
Lead Sponsor:
University Hospital, Montpellier
Collaborating Sponsors:
Hopital Saint Roch
Conditions:
Cesarean
Eligibility:
FEMALE
18+ years
Phase:
PHASE2
Brief 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 operati...
Detailed Description
Prospective study, randomized into two parallel groups (Hyperbaric Prilocaïne versus hyperbaric Bupivacaine), double-blind, monocentric (Clinique Saint Roch in Montpellier). The number of subjects re...
Eligibility Criteria
Inclusion
- 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
Exclusion
Key Trial Info
Start Date :
May 7 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 30 2020
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT03433976
Start Date
May 7 2018
End Date
August 30 2020
Last Update
December 11 2018
Active Locations (1)
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1
Uhmontpellier
Montpellier, France, 34295