Clinical Trials Directory

Trials / Completed

CompletedNCT00616889

Effect of Quetiapine on Sleep Architecture in Bipolar Depression and Major Depressive Disorder

Effects of Seroquel on Sleep Architecture in Patients With Bipolar Depression or Major Depressive Disorder - An Open Label Study

Status
Completed
Phase
Study type
Observational
Enrollment
15 (actual)
Sponsor
Queen's University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Clinical practice indicates that Quetiapine has sedating properties, and its sedative effects may play an important role in restoring quality of sleep in patients with various psychiatric conditions who frequently experience sleep disturbances as part of their illness. It is well known that depressive disorders are very frequently associated with significant sleep disturbance. Sleep disruption is a feature of Bipolar Disorder during both Depressed and Manic/Hypomanic episodes. Considering that Seroquel has good antidepressant properties (Calabrese, 2004), the investigators suggest that Seroquel's effect on sleep architecture contributes to its antidepressant properties.

Detailed description

Primary Objective: To assess the objective (polysomnographic) change in sleep quality before and after introduction of Seroquel (Quetiapine) in treatment of patients with Bipolar Depression or Major Depressive Disorder. Secondary Objectives: To assess the objective (polysomnographic) and subjective changes in sleep quality parameters before and at different stages after introduction of Seroquel (Quetiapine) treatment, longitudinally, and to correlate these changes with measures of illness severity. Study Design: Prospective polysomnographic (PSG) study of patients before and after treatment with Seroquel (Quetiapine). PSG recordings will be done three (optional four) times during the study: before starting the Seroquel (Quetiapine) (baseline), at day 2 to 4 (early) and day 21 to 28 (longer term). (Optional fourth PSG can be done at day 42-56). PSG will be completed at patients home with a portable PSG.

Conditions

Interventions

TypeNameDescription
DRUGSeroquelThe dosage is flexible from 50-600 mg based on the investigator's clinical judgement and patient tolerance. It may be raised or lowered at will.

Timeline

Start date
2006-05-01
Primary completion
2009-01-01
Completion
2009-01-01
First posted
2008-02-15
Last updated
2015-12-16

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00616889. Inclusion in this directory is not an endorsement.