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Epidural Dexamethasone for Labor Analgesia: the Effects on Ropivacaine Consumption and Labour Outcome — DEXAPER  

Obstetric Pain Clinical Trial

Official title:
Epidural Dexamethasone for Labor Analgesia: the Effects on Ropivacaine Consumption and Labour Outcome. A Randomized Double Blind Placebo Study

Clinical Trial Summary

To assess the efficacy of epidural dexamethasone administration, compared to placebo, in reducing local anesthetics consumption during labor epidural analgesia in parturient women

Clinical Trial Description

It is hypothesized that reducing the consumption of local anesthetics during labor epidural analgesia could lower their side effects (rate of motor block, nausea and emesis during labor, maternal hypotension, maternal fever) and improve the duration of the second part of the labor, and the new-born adaptation to child-birth and during the first 24 hours. The use of instruments for assisted vaginal delivery and the needs to perform emergency cesarean could also be impacted.

The efficacy of the dexamethasone will be assessed by the hourly Ropivacaine consumption (milligrams/hour) measured from randomization time to the end of epidural analgesia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02857465
Study type Interventional
Source Centre Hospitalier Universitaire de la Réunion
Contact
Status Withdrawn
Phase Phase 3
Start date January 2017
Completion date June 2017
View Details
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