Escitalopram (Lexapro) for the Treatment of Postpartum Depression



Status:Completed
Conditions:Depression, Women's Studies
Therapuetic Areas:Psychiatry / Psychology, Reproductive
Healthy:No
Age Range:18 - 45
Updated:5/3/2014
Start Date:January 2009
End Date:November 2011
Contact:Stephanie D Connors, BS
Email:sdconnors@partners.org
Phone:617-724-6989

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Escitalopram for the Treatment of Postpartum Depression

The purpose of this study is to determine whether women with postpartum MDD will experience
a significant decrease in depressive symptoms from baseline over an eight-week treatment
intervention with escitalopram (Lexapro). Also, to determine whether women with postpartum
MDD will experience a significant decrease in anxiety symptoms.


Inclusion Criteria:

- Women ages 18 to 45 years old

- Subjects must meet criteria for a major depressive episode with symptoms developing
within three month of live childbirth

- Subjects must present within six months of childbirth

- MADRS score >15

- BAI score >10

- Subjects will be able to be treated on an outpatient basis

- Subjects will be able to provide written informed consent

Exclusion Criteria:

- Subjects who have taken any psychotropic medication, including antidepressants and
anti-anxiety medication, within the past two weeks (with the exception of
non-benzodiazepine medications used for sleep, including trazodone, zolpidem,
eszopiclone, etc)

- Suicidal ideation with active plan or intent, as determined by the investigator

- Presence of psychotic symptoms or homicidal ideation

- History of mania or hypomania

- Pregnant or breastfeeding

- Presence of chronic depression or dysthymia, or chronic or treatment resistant
anxiety disorders, as determined by investigator

- Active alcohol/substance abuse currently or within the past year

- Abnormal TSH, severe anemia, or uncontrolled hypertension
We found this trial at
1
site
185 Cambridge Street
Boston, Massachusetts 02114
617-724-5200
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from
Boston, MA
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