Efficacy of Suvorexant to Treat Insomnia Related to Bipolar Disorder

Status Completed

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

Bipolar Disorder
Insomnia
Sleep Initiation and Maintenance Disorders

Clinical Trial Details

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

View Details

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