Duloxetine for the Treatment of Postpartum Depression

Withdrawn before enrolling · Not applicable

Conditions studied: Postpartum Depression, Major Depressive Disorder

In brief

The purpose of this study is to assess whether the antidepressant, duloxetine, is equally effective as a treatment for subjects who have a Postpartum Onset Depression compared to subjects who have an onset of Major Depressive Disorder prior to delivery. The hypothesis is that duloxetine will be as effective in subjects with Postpartum Major Depressive Disorder as in subjects with a Major Depressive Disorder.

Key facts

Study ID
NCT00617045
Run by
Yale University
People needed
0
Starts
2007-07-01
Expected to finish
2013-05-01
Last updated by the study team
2016-06-17

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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