A Safety and Efficacy Study of Eszopiclone 3 Mg Compared to Placebo in Subjects With Insomnia Related to Major Depressive Disorder.
Information source: Sepracor, Inc.
Information obtained from ClinicalTrials.gov on October 19, 2007 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Insomnia; Depressive Disorder, Major
Intervention: Eszopiclone (Drug)
Phase: Phase 3
Status: Completed
Sponsored by: Sepracor, Inc.
Summary
To evaluate subjective sleep efficacy in subjects with insomnia related to major depressive disorder.
Clinical Details
Study design: Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Eligibility
Minimum age: 21 Years.
Maximum age: 64 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Male or female patients with primary insomnia related to major depressive disorder.
Exclusion Criteria:
-
Locations and Contacts
Additional Information
Last updated: August 23, 2006
|