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Depakote ER in Bipolar Depression

Primary Purpose

Depression, Bipolar

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Depakote ER
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression, Bipolar

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Bipolar I, II or NOS currently suffering from depression Both: both female and male participants are being studied Adults 18 years and older of any race Exclusion Criteria: Schizophrenia or schizoaffective disorder and other disorders excluded at the discretion of the investigator's discretion Substance dependence within the past 3 months and abuse within the past 2 weeks prior to study. Positive screen for psychoactive drugs, stimulants or drugs of abuse (excluding marijuana, as long as dependence and abuse are ruled out according to DSM-IV) Significant risk harm to self or others based on history and mental status exam Clinically significant or unstable medical condition Unstable thyroid pathology and treatment initiated or altered within the past 3 months Clinically significant abnormal laboratory test results, vital signs, as judged by the investigators Women pregnant or nursing, or WOCBP who do not use adequate contraception or who are judged to be unreliable in their use of contraception Subjects who failed (because of inefficacy or adverse effects) an adequate trial of Depakote; eligible patient's may not have received Depakote within 30 days of screen

Sites / Locations

  • Stanford University Bipolar Disorders Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Depakote ER

Arm Description

Depakote ER up to 1500 mg/day

Outcomes

Primary Outcome Measures

Montgomery Asberg Depression Rating Scale (MADRS)
The Montgomery-Åsberg Depression Rating Scale (MADRS) is a ten-item diagnostic questionnaire which psychiatrists use to measure the severity of depressive episodes in patients with mood disorders. Higher MADRS score indicates more severe depression the overall score ranges from 0 to 60. Usual cutoff points are: 0 to 6 - normal/symptom absent 7 to 19 - mild depression 20 to 34 - moderate depression >34 - severe depression.

Secondary Outcome Measures

Response to the Divalproex-ER in Acute Bipolar 2 Depression.
A reduction greater than or equal to 50% in MADRS total score from baseline to the endpoint.

Full Information

First Posted
September 13, 2005
Last Updated
March 1, 2017
Sponsor
Stanford University
Collaborators
Abbott, National Alliance for Research on Schizophrenia and Depression
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1. Study Identification

Unique Protocol Identification Number
NCT00186186
Brief Title
Depakote ER in Bipolar Depression
Official Title
Depakote ER in Bipolar Depression
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
January 2009 (Actual)
Study Completion Date
January 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
Abbott, National Alliance for Research on Schizophrenia and Depression

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine the safety and efficacy of Depakote ER in bipolar depression and to evaluate metabolic and GABA changes with Depakote ER administration using PET and MRI/MRS brain imaging techniques.
Detailed Description
Mood disorders are important public health problems. Bipolar disorder is a major psychiatric disorder characterized by mood cycles alternating between mania and depression and affects approximately 1% of the population. Most patients are treated beginning in the early twenties and then embark on a course marked by multiple recurrences, hospitalizations, and encounters with legal authorities. These disorders inflict substantial morbidity which yields important deficits in occupational and interpersonal function. The risk of suicide in mood disorders may be as high as 10%. Although the outlook for recovery from acute manic or depressive episodes is generally excellent, the long-term prognosis of the disorder varies tremendously across the patient population. The introduction of lithium, anticonvulsants and atypical antipsychotics significantly changes the outlook for bipolar disorder, with some individuals on chronic treatment attaining complete remission and indefinite prophylaxis against mood episodes. However, such optimum outcomes may be limited to as few as one-third to one-half of all treated patients. The remaining experiences various combinations of breakthrough mood episodes, including chronic mood instability, persistent depression, and rapid cycling. Very little research has been conducted with bipolar disorder, and no medications have an FDA indication to treat bipolar depression. Previous studies suggest that Depakote is promising in the treatment of mixed and depressed episodes of bipolar disorder. This study utilizes the extended release formulation of divalproex sodium, with demonstrated increased tolerability. We propose investigating safety, tolerability and efficacy of Depakote ER monotherapy in Bipolar I, II or NOS depression, and monitoring associated changes in brain GABA levels. In addition, we intend to evaluate and assess the differences between brain metabolic rate and GABA levels in bipolar disorder patients and healthy volunteers.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Depakote ER
Arm Type
Experimental
Arm Description
Depakote ER up to 1500 mg/day
Intervention Type
Drug
Intervention Name(s)
Depakote ER
Intervention Description
Depakote ER
Primary Outcome Measure Information:
Title
Montgomery Asberg Depression Rating Scale (MADRS)
Description
The Montgomery-Åsberg Depression Rating Scale (MADRS) is a ten-item diagnostic questionnaire which psychiatrists use to measure the severity of depressive episodes in patients with mood disorders. Higher MADRS score indicates more severe depression the overall score ranges from 0 to 60. Usual cutoff points are: 0 to 6 - normal/symptom absent 7 to 19 - mild depression 20 to 34 - moderate depression >34 - severe depression.
Time Frame
Baseline, 7 weeks
Secondary Outcome Measure Information:
Title
Response to the Divalproex-ER in Acute Bipolar 2 Depression.
Description
A reduction greater than or equal to 50% in MADRS total score from baseline to the endpoint.
Time Frame
7 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Bipolar I, II or NOS currently suffering from depression Both: both female and male participants are being studied Adults 18 years and older of any race Exclusion Criteria: Schizophrenia or schizoaffective disorder and other disorders excluded at the discretion of the investigator's discretion Substance dependence within the past 3 months and abuse within the past 2 weeks prior to study. Positive screen for psychoactive drugs, stimulants or drugs of abuse (excluding marijuana, as long as dependence and abuse are ruled out according to DSM-IV) Significant risk harm to self or others based on history and mental status exam Clinically significant or unstable medical condition Unstable thyroid pathology and treatment initiated or altered within the past 3 months Clinically significant abnormal laboratory test results, vital signs, as judged by the investigators Women pregnant or nursing, or WOCBP who do not use adequate contraception or who are judged to be unreliable in their use of contraception Subjects who failed (because of inefficacy or adverse effects) an adequate trial of Depakote; eligible patient's may not have received Depakote within 30 days of screen
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Terence A. Ketter, MD
Organizational Affiliation
Stanford University, Department of Psychiatry and Behavioral Sciences
Official's Role
Study Director
Facility Information:
Facility Name
Stanford University Bipolar Disorders Clinic
City
Stanford
State/Province
California
ZIP/Postal Code
94305-5723
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19923006
Citation
Wang PW, Nowakowska C, Chandler RA, Hill SJ, Nam JY, Culver JL, Keller KL, Ketter TA. Divalproex extended-release in acute bipolar II depression. J Affect Disord. 2010 Jul;124(1-2):170-3. doi: 10.1016/j.jad.2009.10.021.
Results Reference
result

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Depakote ER in Bipolar Depression

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