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Treatment of Major Depressive Disorder With Psychotic Features.

Primary Purpose

Major Depression With Psychotic Features

Status
Terminated
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
risperidone
Sponsored by
Rush University Medical Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depression With Psychotic Features focused on measuring depression

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects will be men and women 18 to 70 years of age with major depression and psychosis that is either an initial episode or a recurrent episode (unipolar or bipolar). Subjects with an anxiety disorder or an additional mood disorder such as dysthymia are eligible. Baseline HDRS score of greater than 21. A baseline PANSS score of greater than 4 on at least one of the 5 psychosis items Exclusion Criteria: Pregnant women Women of child-bearing age who refuse a urine pregnancy test or who refuse to use a contraceptive technique when sexually active. Persons with other psychotic disorders; a mood disorder due to a general medical condition or substance-induced; a current substance dependence disorder; or a dementing disorder are excluded. Persons with serious, unstable medical illnesses.

Sites / Locations

  • Rush University Medical Center

Outcomes

Primary Outcome Measures

Hamilton Depression Rating Scale

Secondary Outcome Measures

Positive and Negative Symptom Scale

Full Information

First Posted
September 9, 2005
Last Updated
December 28, 2007
Sponsor
Rush University Medical Center
Collaborators
Janssen, LP
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1. Study Identification

Unique Protocol Identification Number
NCT00174590
Brief Title
Treatment of Major Depressive Disorder With Psychotic Features.
Official Title
Treatment of Major Depressive Disorder With Psychotic Features With Risperidone Monotherapy; Risperidone and Sertraline; or Haloperidol and Sertraline
Study Type
Interventional

2. Study Status

Record Verification Date
December 2007
Overall Recruitment Status
Terminated
Study Start Date
September 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Rush University Medical Center
Collaborators
Janssen, LP

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine the safety and efficacy of risperidone monotherapy in the treatment of psychotic depression. We hypothesize that risperidone is as equally as effective as haloperidol plus sertraline for depression with psychotic features
Detailed Description
Risperidone is a novel antipsychotic that is usually not associated with the adverse effects of neuroleptics. In addition, preliminary evidence suggests that it has additional mood stabilizing properties as compared with neuroleptics. We are examining the effect of risperidone alone for the treatment of psychotic depression. After providing written informed consent, subjects with major depression and psychosis will undergo a routine medical and neurological evaluation. If subjects qualify they will undergo a 3 to 7 day washout. Subjects will be randomly assigned under double-blind conditions to risperidone plus placebo; risperidone plus sertraline; or haloperidol (HPDL) plus sertraline in a prospective parallel design for a 6 week trial. Outcome measures include the Hamilton Rating Depression Scale, The Positive and Negative Symptom Scale and the Clinician Administered Ratings Scale for Mania and Simpson Angus Scale. Rating will be conducted on a weekly basis throughout the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depression With Psychotic Features
Keywords
depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
risperidone
Primary Outcome Measure Information:
Title
Hamilton Depression Rating Scale
Secondary Outcome Measure Information:
Title
Positive and Negative Symptom Scale

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects will be men and women 18 to 70 years of age with major depression and psychosis that is either an initial episode or a recurrent episode (unipolar or bipolar). Subjects with an anxiety disorder or an additional mood disorder such as dysthymia are eligible. Baseline HDRS score of greater than 21. A baseline PANSS score of greater than 4 on at least one of the 5 psychosis items Exclusion Criteria: Pregnant women Women of child-bearing age who refuse a urine pregnancy test or who refuse to use a contraceptive technique when sexually active. Persons with other psychotic disorders; a mood disorder due to a general medical condition or substance-induced; a current substance dependence disorder; or a dementing disorder are excluded. Persons with serious, unstable medical illnesses.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip g Janicak, MD
Organizational Affiliation
Rush University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Treatment of Major Depressive Disorder With Psychotic Features.

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