Eszopiclone for the Treatment of Posttraumatic Stress Disorder

Status Completed

Clinical Trial Summary

The purpose of this study is to determine if eszopiclone relative to placebo (sugar pill) is effective and tolerable for people with posttraumatic stress disorder (PTSD)-related sleep disturbance. The investigators will also examine the impact of treatment on sleep patterns, memory recall bias, and level of inflammatory markers (cytokines). The investigators predict eszopiclone will lead to greater improvement than placebo in measures of PTSD symptoms, memory recall bias, and level of inflammatory markers.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01605253
Study type	Interventional
Source	Rush University Medical Center
Contact
Status	Completed
Phase	Phase 4
Start date	March 2012
Completion date	December 2015

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