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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of suvorexant, added to existing medications, for treatment-resistant insomnia in individuals with bipolar disorder. The investigators hypothesize that participants receiving suvorexant for one week will experience significantly greater improvement in sleep duration compared to participants receiving placebo.


Clinical Trial Description

Participants will be randomized to receive double-blind suvorexant or placebo for one week, after which all participants will receive open treatment with suvorexant for three months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02527564
Study type Interventional
Source Stanford University
Contact
Status Completed
Phase Phase 4
Start date September 2015
Completion date March 1, 2021

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