Viewing Study NCT00174603



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Study NCT ID: NCT00174603
Status: TERMINATED
Last Update Posted: 2008-01-10
First Post: 2005-09-09

Brief Title: Treatment of Depression With Quetiapine
Sponsor: Rush University Medical Center
Organization: Rush University Medical Center

Study Overview

Official Title: Treatment of Major Depressive Disorder With Psychotic Features With Quetiapine Monotherapy Quetiapine and Citalopram or Haloperidol and Citalopram
Status: TERMINATED
Status Verified Date: 2007-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Unable to recruit subjects
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to examine the mood stabilizing and antipsychotic properties of quetiapine in the treatment of depression by comparing subjects who were randomly assigned to either quetiapine monotherapy quetiapine and citalopram or haloperidol and citalopram We hypothesize that quetiapine monotherapy would have similar effects to the combination of a first generation antipsychotic plus an antidepressant for the treatment of a major depressive episode with psychosis
Detailed Description: Thus current practice for treating psychotic depression is to combine an antidepressant with an antipsychotic However there are limitations to this approach The rate of response is still lower than in other forms of major depression Janicak et al 2001 The rate of noncompliance is higher in this group and the incidence of adverse effects related to the antipsychotic is increased Janicak et al 2001 As a result studies have examined alternative treatments The present study proposes to examine quetiapines antipsychotic and mood stabilizing properties for the treatment of a major depressive disorder with psychotic features Subjects will be randomized to either quetipine monotherapy quetiapine and citalopram or haloperidol and citalopram

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None