Prilocaine or Bupivacaine for Spinal Anesthesiain Pregnant
Last updated on July 2021Recruitment
- Recruitment Status
- Unknown status
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Cesarean
- Type
- Interventional
- Phase
- Phase 2
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Participant)Primary Purpose: Treatment
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Only males
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 required is 50 patients, 25 per group.
Prospective study, randomized into two parallel groups (Hyperbaric Prilocaïne versus hyperbaric Bupivacaine), double-blind, monocentric (Clinique Saint Roch in Montpellier). The number of subjects required is 50 patients, 25 per group.
Tracking Information
- NCT #
- NCT03433976
- Collaborators
- Hopital Saint Roch
- Investigators
- Principal Investigator: christophe DADURE University Hospital, Montpellier