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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03433976
Study type Interventional
Source University Hospital, Montpellier
Contact christophe DADURE, MD, PhD
Phone 467338256
Email c-dadure@chu-montpellier.fr
Status Recruiting
Phase Phase 2
Start date May 7, 2018
Completion date August 30, 2020

See also
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Completed NCT03147781 - Auricular Therapy for Postpartum Lactation N/A