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Programmed Intermittent Epidural Bolus Versus Continuous Infusion in Labour Analgesia

Labor Pain Clinical Trial

Official title:
Programmed Intermittent Epidural Bolus Versus Continuous Infusion When Added to Patient-controlled Epidural Analgesia on Bupivacaine Consumption in Labour Analgesia: a Randomized Controlled Trial

Clinical Trial Summary

This study aims to establish if programmed intermittent epidural bolus combined to patient controlled analgesia in labour analgesia will lower the hourly bupivacaine consumption when compared to continuous infusion combined with patient controlled analgesia. The investigators' hypothesis is that the use of programmed intermittent epidural bolus will lower the hourly bupivacaine consumption.

Clinical Trial Description

Patients are randomised to receive either a programmed bolus of 6ml each 45 minutes or a continuous infusion of 8ml/h. In each group, they have the possibility to add a PCEA bolus of 6ml every 20min as needed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03730753
Study type Interventional
Source Université de Sherbrooke
Contact Isabelle Caron, Dr.
Phone +1 819 346-1110
Email isabelle.caron4@usherbrooke.ca
Status Recruiting
Phase N/A
Start date June 1, 2019
Completion date June 30, 2025
View Details
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