Bipolar Disorder Clinical Trial
Official title:
Valproate Efficacy in Cocaine-Bipolar Comorbidity
This proposal will test the efficacy of a promising pharmacological approach for the treatment of comorbid cocaine dependence and bipolar disorder. We propose a randomized, double blind, placebo controlled 12-week trial to test the efficacy of Divalproex sodium (Valproate) plus treatment as usual compared to placebo plus treatment as usual in decreasing cocaine use and stabilizing mood symptoms among patients with comorbid cocaine dependence and bipolar disorder. Treatment as usual includes the use of lithium carbonate for mood stabilization plus supportive psychosocial treatment.
Bipolar disorder has the highest rate of association with cocaine and other substance use
disorders than any other major severe psychiatric syndrome. This comorbidity represents a
major treatment challenge and is associated with severe disability, morbidity, and
heightened risk for suicide.
The aims of this study are:
1. Examine the efficacy of valproate plus treatment as usual compared to placebo plus
treatment as usual in decreasing cocaine use in patients with cocaine dependence and
comorbid bipolar disorder.
2. Determine whether primary vs. secondary cocaine dependence, bipolar subtype (depressed
vs. manic/mixed) and the presence of additional substance use disorders moderate the
association between treatment and cocaine use outcome.
3. Assess the effects of medication compliance and mood symptoms as mediators of cocaine
use outcome.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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