Add-On Ramelteon in Bipolar I Disorder With Clinically Significant Sleep Disturbance

Bipolar Disorder Clinical Trial

Official title: A Randomized, Double-Blind, Placebo-Controlled Study of Add-On Ramelteon in Ambulatory Bipolar I Disorder With Clinically Significant Sleep Disturbance

Status Terminated

Clinical Trial Summary

The purpose of this research study is to evaluate the safety and efficacy of ramelteon (Rozerem™) as an add-on treatment for sleep problems in patients with bipolar disorder. This study will determine whether or not the addition of ramelteon to ongoing medication(s) for bipolar disorder is useful in improving sleep.

Clinical Trial Description

This is a randomized, double-blind, placebo-controlled, parallel-group, single site, 8-week trial of add-on ramelteon in outpatient adults (18-65 years old, inclusive) with lifetime bipolar I disorder, with mild to moderate manic symptoms, and currently experiencing a clinically significant sleep disturbance. Approximately 60 subjects will be screened to obtain 30 subjects who enroll in the 8-week trial. Subjects will be randomized to ramelteon or placebo in a double-blind manner as add-on to current treatment. Any other psychotropic medications that the subject is taking at the initiation of participation in this protocol should be continued unchanged throughout the course of this study, except in instances in which these medications require dose reduction for management of side effects. Efficacy and safety assessments will be performed weekly, and the presence of treatment-emergent adverse events will be monitored and recorded. ;

Related Conditions & MeSH terms

• Bipolar Disorder
• Disease
• Dyssomnias
• Insomnia
• Parasomnias
• Sleep Initiation and Maintenance Disorders
• Sleep Wake Disorders

• NCT number: NCT00585208
• Study type: Interventional
• Source: Lindner Center of HOPE
• Status: Terminated
• Phase: Phase 3
• Start date: December 2007
• Completion date: December 2010