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Selective Serotonin Reuptake Inhibitors (SSRIs) in Borderline Personality Disorder

Borderline Personality Disorder Clinical Trial

Official title:
SSRIs and Self-harm in Borderline Personality Disorder

Clinical Trial Summary

The goal of this study is to examine the effectiveness the selective serotonin reuptake inhibitor (SSRI) escitalopram (also known by the trade name "Lexapro") in reducing desire to self-harm and actual self-harming among young adults with borderline personality disorder who are also currently depressed. Subjects will receive either escitalopram or placebo for eight weeks. During this time subjects will be make weekly visits to see the psychiatrist and record their thoughts and feelings several times each day using an electronic diary.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01103180
Study type Interventional
Source University of Chicago
Contact
Status Terminated
Phase Phase 2
Start date September 2010
Completion date November 2014
View Details
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