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Divalproex Sodium (Depakote) for Explosive Tempers in Adolescents and Adults

Information source: New York State Psychiatric Institute
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Attention Deficit and Disruptive Behavior Disorders; Marijuana Abuse

Intervention: Divalproex Sodium (Depakote) (Drug); divalproex sodium (Drug)

Phase: Phase 3

Status: Active, not recruiting

Sponsored by: New York State Psychiatric Institute

Official(s) and/or principal investigator(s):
Stephen Donovan, MD, Principal Investigator, Affiliation: New York State Psychiatric Institute

Summary

The purpose of this study is to compare the effectiveness of divalproex sodium (Depakote) versus placebo in treating disruptive behavior disorder and explosive tempers in adolescents and adults.

Clinical Details

Official title: Parallel Groups Study of Divalproex Sodium (Depakote) for Irritable, Explosive Adults & Adolescents

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Primary outcome: Symptoms of disruptive behavior disorder (measured throughout the study and at Week 6)

Detailed description: Disruptive behavior disorders among children and adolescents are readily diagnosed; however, few individuals with such disorders receive drug treatment. Depakote is a mood stabilizing medication that may be beneficial in treating individuals with disruptive behavior disorders. The purpose of this study is to examine the effectiveness of Depakote in reducing temper outbursts and improving mood in individuals with disruptive behavior disorders. In addition, this study will determine the safety and effectiveness of Depakote in treating individuals with substance disorders who also have disruptive behavior disorders. This study will last 6 weeks. Participants will be randomly assigned to receive treatment with Depakote or placebo. Medication will be given in a single evening dose if tolerated; otherwise, medication will be given twice per day. Participants will be assigned to a fixed-flexible dosing schedule and dosages will increase based on weight. All participants will attend weekly psychotherapy and family counseling sessions throughout the study. Participants who are substance abusers will also receive substance abuse counseling. Weekly study visits will include a physical exam, blood collection, and drug tests. Teachers and guidance counselors will be contacted to assess the participant's behavior from week to week. Some participants will complete a follow-up study, in which they will take part in phone interviews.

Eligibility

Minimum age: 12 Years. Maximum age: 55 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Meets DSM-IV criteria for a disruptive behavior disorder (e. g., oppositional/defiant

disorder, conduct disorder)

- Explosive temper, defined as four or more outbursts of rage, property destruction, or

fighting per month

- Mood liability, defined as having multiple, daily, distinct shifts from normal to

irritable mood with withdrawn or boisterous behavior

- Chronic symptoms, defined of at least 1 year duration when not receiving treatment

- Impairment from the above symptoms in two or more areas, including school, the law,

family, substance use, peers, or work (as manifested by a GAF score of 55 or less)

- Symptoms not limited to a particular place or to particular intimate relationships

- General good health

- Custodial parent or guardian gives informed consent

Exclusion Criteria:

- History of non drug-induced psychosis

- Seizure or other neurologic disturbance

- Pregnant

- Moderate to severe mental retardation

- Sexually active females who refuse to use an adequate method of contraception for the

duration of the study

- Significant medical problems

- Current suicidal or homicidal ideation

- Uses barbiturates

- Refusal to permit weekly contact with school officials

- Bipolar I or II disorder

- Major depressive disorder

- First degree relative with bipolar I or II disorder

- Attention deficit/hyperactivity disorder

- Post traumatic stress disorder

- Clinical evidence of hyperandrogenism in a female

- Liver disease

- Thrombocytopenia

- Pancreatic disease

Locations and Contacts

New York State Psychiatric Institute, New York, New York 10032, United States
Additional Information

Starting date: February 2000
Last updated: March 6, 2014

Page last updated: August 20, 2015

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