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Prilocaine or Bupivacaine for Spinal Anesthesiain Pregnant

NCT03433976 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2018-12-11

No results posted yet for this study

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.

Conditions

  • Cesarean

Interventions

DRUG

spinal anesthesia

spinal anesthesia for planned cesarean sections

Sponsors & Collaborators

  • Hopital Saint Roch

    collaborator OTHER

  • University Hospital, Montpellier

    lead OTHER

Principal Investigators

  • christophe DADURE · University Hospital, Montpellier

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-07
Primary Completion
2020-05-07
Completion
2020-08-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03433976 on ClinicalTrials.gov