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More info
You can access this
clinical trial
if you have
Depression, Postpartum or Labor Pain
and you are
between 18 and 50
years old
-
The phase for this study is not defined.
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The purpose

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.

Provided treatments

  • Procedure: CSE
  • Procedure: Epidural
  • Drug: Bupivacaine / fentaNYL

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT03022526. The sponsor of the trial is Grace Lim, MD, MS and it is looking for 46 volunteers for the current phase.
Official trial title:
Combined Spinal Epidural v. Epidural Labor Analgesia for Postpartum Depression Symptoms (COPE Trial): Pilot Randomized Control Trial