drugset / Trial / NCT03022526

CSE v. Epidural for Postpartum Depression

NCT03022526 ↗

Completed 61 enrolled Grace Lim, MD, MS
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this pilot prospective randomized control trial is to compare the initiation of labor epidural analgesia by combined spinal epidural vs. epidural for the influence on risk for postpartum depression symptoms. Investigators will randomize women to the receipt of CSE or E during labor, after measuring baseline psychological, psychosocial, and psychophysical factors related to pain and depression. The immediate research goals are to understand whether the association between labor pain and PPD is modifiable through the use of tailored anesthetic techniques.

Timeline

Start
2017-01
Primary completion
2019-12-31
Completion
2019-12-31

Outcome

Missed primary endpoint

registry analysis (superiority test); Combined Spinal Epidural (CSE) vs Epidural; p = 0.7463; t-test, 2 sided NCT03022526 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 0.083 % Intrathecal
Subject Fentanyl Other / unclassified 2 ug/ml Intrathecal

Indications