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Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Divalproex Sodium Extended-Release Tablets
Olanzapine
Risperidone
Sponsored by
Abbott
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

KEY INCLUSION CRITERIA: Acute exacerbation of schizophrenia as defined by: subject recently hospitalized or is in the process of being admitted to a hospital or an acute care inpatient psychiatric treatment facility; and has a PANNS Total score of 70 or greater at the time of screening and at randomization based on a 1-7 point scale; and has a score on any two of the four items from psychosis cluster of the BPRS (extracted from the PANSS) that correspond to the positive symptoms (hallucinatory behavior, unusual thought content, conceptual disorganization and suspiciousness) totaling 8 or greater; and has a total of 6 or greater on one of the following two pairs of items from the BPRS (extracted from the PANSS): hostility and uncooperativeness or excitement and tension. Current DSM-IV-TR diagnosis of schizophrenia as confirmed by the SCID Positive response to antipsychotics in the previous 2 years KEY EXCLUSION CRITERIA: Current diagnosis of schizoaffective disorder, drug-induced psychosis, manic episode or major depressive episode. At the time of screening, has been hospitalized for more than 14 days for the current episode Has ever taken clozapine Has had more than 3 psychiatric hospitalizations in the previous 6 months or has had more than 8 weeks of psychiatric hospitalization in the previous 12 months Has serious violent, homicidal, suicidal ideation Has received depot medications fluphenazine decanoate and/or haloperidol decanoate within 2 or 4 weeks prior to randomization respectively Urine toxicology screen is positive for phencyclidine (PCP), opiates, cocaine or amphetamines History of alcohol or substance dependence within the past month Has taken any valproate product for a psychiatric indication within the previous 30 days Has received an investigational drug within the last 30 days

Sites / Locations

Outcomes

Primary Outcome Measures

The psychiatric rating scale battery will include the PANSS, the CGI Scale, and the CDSS. The NOSIE, Overall Treatment Evaluation, Burden Questionnaire, and Quality of Life Scale.

Secondary Outcome Measures

The movement rating scale battery will include the Simpson-Angus Scale (SAS), the Barnes Akathisia Scale (BAS), and the Abnormal Involuntary Movement Scale (AIMS).

Full Information

First Posted
November 17, 2003
Last Updated
August 2, 2006
Sponsor
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT00073164
Brief Title
Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia
Official Title
A Study of the Safety and Efficacy of Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
August 2006
Overall Recruitment Status
Completed
Study Start Date
July 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Abbott

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to assess the 14-day and 12-week safety and efficacy of Depakote ER used in combination with either olanzapine or risperidone versus antipsychotic monotherapy with olanzapine or risperidone for the treatment of schizophrenia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
400 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Divalproex Sodium Extended-Release Tablets
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Intervention Type
Drug
Intervention Name(s)
Risperidone
Primary Outcome Measure Information:
Title
The psychiatric rating scale battery will include the PANSS, the CGI Scale, and the CDSS. The NOSIE, Overall Treatment Evaluation, Burden Questionnaire, and Quality of Life Scale.
Secondary Outcome Measure Information:
Title
The movement rating scale battery will include the Simpson-Angus Scale (SAS), the Barnes Akathisia Scale (BAS), and the Abnormal Involuntary Movement Scale (AIMS).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
KEY INCLUSION CRITERIA: Acute exacerbation of schizophrenia as defined by: subject recently hospitalized or is in the process of being admitted to a hospital or an acute care inpatient psychiatric treatment facility; and has a PANNS Total score of 70 or greater at the time of screening and at randomization based on a 1-7 point scale; and has a score on any two of the four items from psychosis cluster of the BPRS (extracted from the PANSS) that correspond to the positive symptoms (hallucinatory behavior, unusual thought content, conceptual disorganization and suspiciousness) totaling 8 or greater; and has a total of 6 or greater on one of the following two pairs of items from the BPRS (extracted from the PANSS): hostility and uncooperativeness or excitement and tension. Current DSM-IV-TR diagnosis of schizophrenia as confirmed by the SCID Positive response to antipsychotics in the previous 2 years KEY EXCLUSION CRITERIA: Current diagnosis of schizoaffective disorder, drug-induced psychosis, manic episode or major depressive episode. At the time of screening, has been hospitalized for more than 14 days for the current episode Has ever taken clozapine Has had more than 3 psychiatric hospitalizations in the previous 6 months or has had more than 8 weeks of psychiatric hospitalization in the previous 12 months Has serious violent, homicidal, suicidal ideation Has received depot medications fluphenazine decanoate and/or haloperidol decanoate within 2 or 4 weeks prior to randomization respectively Urine toxicology screen is positive for phencyclidine (PCP), opiates, cocaine or amphetamines History of alcohol or substance dependence within the past month Has taken any valproate product for a psychiatric indication within the previous 30 days Has received an investigational drug within the last 30 days
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Global Medical Information 800-633-9110
Organizational Affiliation
Abbott
Official's Role
Study Director
Facility Information:
City
Birmingham
State/Province
Alabama
Country
United States
City
Tuscaloosa
State/Province
Alabama
Country
United States
City
Anaheim
State/Province
California
Country
United States
City
Cerritos
State/Province
California
Country
United States
City
Chula Vista
State/Province
California
Country
United States
City
Garden Grove
State/Province
California
Country
United States
City
Glendale
State/Province
California
Country
United States
City
Los Angeles
State/Province
California
Country
United States
City
San Diego
State/Province
California
Country
United States
City
Denver
State/Province
Colorado
Country
United States
City
Gainsville
State/Province
Florida
Country
United States
City
Melbourne
State/Province
Florida
Country
United States
City
North Miami
State/Province
Florida
Country
United States
City
Winter Park
State/Province
Florida
Country
United States
City
Atlanta
State/Province
Georgia
Country
United States
City
Chicago
State/Province
Illinois
Country
United States
City
Hoffman Estates
State/Province
Illinois
Country
United States
City
Indianapolis
State/Province
Indiana
Country
United States
City
South Bend
State/Province
Indiana
Country
United States
City
Shreveport
State/Province
Louisiana
Country
United States
City
Rockville
State/Province
Maryland
Country
United States
City
Jackson
State/Province
Mississippi
Country
United States
City
Clementon
State/Province
New Jersey
Country
United States
City
Kenilworth
State/Province
New Jersey
Country
United States
City
Holliswood
State/Province
New York
Country
United States
City
New York
State/Province
New York
Country
United States
City
Butner
State/Province
North Carolina
Country
United States
City
Cincinnati
State/Province
Ohio
Country
United States
City
Cleveland
State/Province
Ohio
Country
United States
City
Oklahoma City
State/Province
Oklahoma
Country
United States
City
Philadelphia
State/Province
Pennsylvania
Country
United States
City
Austin
State/Province
Texas
Country
United States
City
Irving
State/Province
Texas
Country
United States
City
San Antonio
State/Province
Texas
Country
United States
City
Falls Church
State/Province
Virginia
Country
United States

12. IPD Sharing Statement

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Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia

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