Depakote ER in Bipolar Depression
Depression, Bipolar
About this trial
This is an interventional treatment trial for Depression, Bipolar
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
Sites / Locations
- Stanford University Bipolar Disorders Clinic
Arms of the Study
Arm 1
Experimental
Depakote ER
Depakote ER up to 1500 mg/day