An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatment of Mania/Bipolar Disorder

Study Identifier
M02-540
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Bipolar Disorder
  • Study Drug
  • Divalproex Sodium (Depakote ER)
  • Phase
    CSR.ORG
    Sex
    Female & Male
    Age
    18 - 65 Years

    Protocol Summary

    The purpose of this study is to determine the safety and effectiveness of Depakote ER

    compared to placebo in the treatment of bipolar disorder, manic or mixed type in adults.

    Study Locations

    Location
    Status
    Location
    Comprehensive Neuroscience of SCA
    Cerritos, California, United States, 90703
    Status
    Not applicable
    Location
    AVI Clinical Research
    Torrance, California, United States, 90505
    Status
    Not applicable
    Location
    Washington Hospital Center
    Washington, District of Columbia, United States, 20010
    Status
    Not applicable
    Location
    Mark Lerman, MD
    Hoffman Estates, Illinois, United States, 60194
    Status
    Not applicable
    Location
    University of Louisville Bipolar Research Program
    Louisville, Kentucky, United States, 40202
    Status
    Not applicable
    Location
    Brentwood Research Inst.
    Shreveport, Louisiana, United States, 71101
    Status
    Not applicable
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