Open-Label Depakote ER in Patients With Bipolar I or II Depression and Alcohol Abuse or Dependence

• Status: Withdrawn
• Trial end date: 2005-05-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to determine if Divalproex Sodium can be used to Treat and Prevent Depression in Patients with Bipolar Disorder who have Comorbid Alcohol Dependence/Abuse.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: The University of Texas Medical Branch, Galveston
• Treatments: Ethanol; Valproic Acid

Criteria

Inclusion Criteria:

• MADRS >= 20 at screen and 18 at baseline

• YMRS =< 11 at screen and baseline

• DMS-IV criteria for past manic or hypomanic episode based on the SCID

• DSM-VI criteria for alcohol dependence or abuse based on the SCID.

• Alcohol dependence/abuse confirmed by corroboration from family member

• Negative urine pregnancy test

Exclusion Criteria:

• Inability to give informed consent

• Inability to give reliable assessment of alcohol consumption

• Evidence of alcohol consumption one week prior to baseline

• Liver function tests greater than 3X upper limit of normal at screen

• History of active hepatitis or hepatic encephalopathy

• History of pancreatitis

• History of adverse reaction to divalproex sodium

• History of seizure other than directly associated w/prior alcohol withdrawl

• History of major head trauma with LOC > 10 min. or skull fracture

• Hisotry of hypertension or neurologic illness

• If female, not practicing an effective form of birth control