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Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depakote Plus Olanzapine in Stable Subjects During the Maintenance Phase of Bipolar Illness

Primary Purpose

Bipolar Disorder

Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Divalproex Sodium (Delayed-Release Tablets)
Divalproex Sodium (Extended-Release Tablets)
Olanzapine
Sponsored by
Abbott
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring Bipolar Disorder - Mania

Eligibility Criteria

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

Inclusion Criteria: DSM-IV-TR primary diagnosis of Bipolar I Disorder as confirmed by the SCID Outpatient receiving treatment with a combination of Depakote plus olanzapine for their bipolar illness and considered clinically stable (e.g., no more than minimal symptoms, no psychiatric hospitalizations, no increase in intensity of clinical interventions) for the preceding 4 months Identified at Screening a most bothersome side effect listed in the UKU which makes switching to monotherapy desirable MRS total score < 12 on two consecutive ratings, separated by at least 5 days (Screening and Day 1) DSS score < 13 on two consecutive ratings, separated by at least five days (Screening and Day 1) CGI-S score < 3 on two consecutive ratings, separated by at least five days (Screening and Day 1) Serum valproate level > 45 mcg/mL, and a maximum allowable dose of Depakote of 3000 mg/day at Screening Olanzapine dose between 5 and 20 mg/day at Screening Exclusion Criteria: History of schizophrenia or schizoaffective disorder Axis I (e.g., anxiety disorder) or Axis II (e.g., personality disorder) that would interfere with compliance or confound interpretation of study results Has taken antipsychotics, mood stabilizers, or anticonvulsants (unless specifically for seizure control) other than Depakote or olanzapine in the four months prior to randomization. Other psychotropics (e.g., antidepressants, anxiolytics) with the exception of stimulants, that have been used routinely to maintain stability in the preceding four months may be continued, but not increased or decreased Has first manic episode after age 60 Has ever taken clozapine Has received depot neuroleptic medication within six months of randomization Urine toxicology screen is positive for phencyclidine (PCP), opiates, cocaine or amphetamines History of active alcohol or substance abuse/dependence within 90 days prior to Screening Known history of non-response to either Depakote or olanzapine monotherapy for the treatment of bipolar disorder

Sites / Locations

  • Behavioral and Medical Research, LLC
  • Synergy Clinical Research
  • Clinical Trial Management
  • Segal Institute for Clinical Research
  • Rush Presbyterian - St. Luke's
  • University of Louisville Outpatient Psychiatry
  • University of Mississippi Medical Center
  • Creighton University Department of Psychiatry
  • Lake Mead Hospital
  • NYU School of Medicine
  • University Hospital of Cleveland
  • R. Ranjan, MD & Associates, Inc.
  • IPS Research
  • UTMB Dept. of Psychiatry
  • Zablocki VAMC

Outcomes

Primary Outcome Measures

CGI-s
CGI-i
MRS
DSS
SADS-C

Secondary Outcome Measures

Full Information

First Posted
October 16, 2003
Last Updated
August 2, 2006
Sponsor
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT00071253
Brief Title
Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depakote Plus Olanzapine in Stable Subjects During the Maintenance Phase of Bipolar Illness
Official Title
A Randomized, Double-Blind Study of Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depakote Plus Olanzapine in Stable Subjects During the Maintenance Phase of Bipolar Illness
Study Type
Interventional

2. Study Status

Record Verification Date
August 2006
Overall Recruitment Status
Terminated
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 efficacy and safety of continued combination therapy using Depakote plus olanzapine, vs. Depakote monotherapy and olanzapine monotherapy in stable subjects during the maintenance phase of bipolar illness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
Bipolar Disorder - Mania

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
180 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Divalproex Sodium (Delayed-Release Tablets)
Intervention Type
Drug
Intervention Name(s)
Divalproex Sodium (Extended-Release Tablets)
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Primary Outcome Measure Information:
Title
CGI-s
Title
CGI-i
Title
MRS
Title
DSS
Title
SADS-C

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: DSM-IV-TR primary diagnosis of Bipolar I Disorder as confirmed by the SCID Outpatient receiving treatment with a combination of Depakote plus olanzapine for their bipolar illness and considered clinically stable (e.g., no more than minimal symptoms, no psychiatric hospitalizations, no increase in intensity of clinical interventions) for the preceding 4 months Identified at Screening a most bothersome side effect listed in the UKU which makes switching to monotherapy desirable MRS total score < 12 on two consecutive ratings, separated by at least 5 days (Screening and Day 1) DSS score < 13 on two consecutive ratings, separated by at least five days (Screening and Day 1) CGI-S score < 3 on two consecutive ratings, separated by at least five days (Screening and Day 1) Serum valproate level > 45 mcg/mL, and a maximum allowable dose of Depakote of 3000 mg/day at Screening Olanzapine dose between 5 and 20 mg/day at Screening Exclusion Criteria: History of schizophrenia or schizoaffective disorder Axis I (e.g., anxiety disorder) or Axis II (e.g., personality disorder) that would interfere with compliance or confound interpretation of study results Has taken antipsychotics, mood stabilizers, or anticonvulsants (unless specifically for seizure control) other than Depakote or olanzapine in the four months prior to randomization. Other psychotropics (e.g., antidepressants, anxiolytics) with the exception of stimulants, that have been used routinely to maintain stability in the preceding four months may be continued, but not increased or decreased Has first manic episode after age 60 Has ever taken clozapine Has received depot neuroleptic medication within six months of randomization Urine toxicology screen is positive for phencyclidine (PCP), opiates, cocaine or amphetamines History of active alcohol or substance abuse/dependence within 90 days prior to Screening Known history of non-response to either Depakote or olanzapine monotherapy for the treatment of bipolar disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Global Medical Information
Organizational Affiliation
Abbott
Official's Role
Study Director
Facility Information:
Facility Name
Behavioral and Medical Research, LLC
City
Anaheim
State/Province
California
ZIP/Postal Code
92805
Country
United States
Facility Name
Synergy Clinical Research
City
Chula Vista
State/Province
California
ZIP/Postal Code
91910
Country
United States
Facility Name
Clinical Trial Management
City
Fort Meyers
State/Province
Florida
ZIP/Postal Code
33907
Country
United States
Facility Name
Segal Institute for Clinical Research
City
North Miami
State/Province
Florida
ZIP/Postal Code
33161
Country
United States
Facility Name
Rush Presbyterian - St. Luke's
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
University of Louisville Outpatient Psychiatry
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
Facility Name
University of Mississippi Medical Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
Facility Name
Creighton University Department of Psychiatry
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68131
Country
United States
Facility Name
Lake Mead Hospital
City
North Las Vegas
State/Province
Nevada
ZIP/Postal Code
89030
Country
United States
Facility Name
NYU School of Medicine
City
New York City
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
University Hospital of Cleveland
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
R. Ranjan, MD & Associates, Inc.
City
Lyndhurst
State/Province
Ohio
ZIP/Postal Code
44124
Country
United States
Facility Name
IPS Research
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73103
Country
United States
Facility Name
UTMB Dept. of Psychiatry
City
Galveston
State/Province
Texas
ZIP/Postal Code
77555-0197
Country
United States
Facility Name
Zablocki VAMC
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53295
Country
United States

12. IPD Sharing Statement

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Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depakote Plus Olanzapine in Stable Subjects During the Maintenance Phase of Bipolar Illness

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