Abilify Therapy for Reducing Comorbid Substance Abuse

NCT ID: NCT00208169

Last Updated: 2007-08-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-03-31
• Study Completion Date: 2007-06-30

Brief Summary

It is hypothesized that the use of aripiprazole (Abilify) in patients with alcohol and/or drug dependence with comorbid psychiatric conditions will lead to:

• Reduction in the amount of alcohol and/or drugs used as measured by the Time Line Follow Back (TLFB) and the Addiction Severity Index (ASI)
• Reduction in cravings for alcohol and drugs as measured by the Penn Alcohol Craving Scale
• Reduction in symptoms of co-morbid psychiatric disorders compared to before starting aripiprazole.

Detailed Description

Substance abuse disorders are a major public health problem. With a current prevalence rate of 18%, substance abuse and dependence costs the nation over $300 billion per year in treatment costs and lost productivity. Approximately 20% of all patients attending primary care clinics and 35% of all patients attending psychiatric clinics meet Diagnostic and Statistical Manual IV (DSM IV) criteria for substance abuse or dependence.

The treatment of substance abuse and dependence disorders is complex and involves individual and group therapy, maintenance of sobriety, commitment to structured living, and participation in self-help groups. To date, pharmacotherapy for substance dependence disorders has had limited success. Several medications have been tested in the past, including tricyclic antidepressants, selective serotonin reuptake inhibitors, buspirone, bupropion, venlafaxine, nefazodone, bromocriptine, amantadine, naltrexone, and acamprosate. Of these, naltrexone has obtained an FDA indication for treatment of alcohol dependence, and acamprosate is in use in Europe. However, these medications are effective in only a relatively small proportion of patients. Benzodiazepines may be useful in treatment of withdrawal syndromes, but their potential for abuse and dependence limits their use in maintenance treatment.

This is an open label pilot study of aripiprazole therapy in the treatment of patients with substance use disorders and co-morbid disorders like Schizophrenia, Schizoaffective disorder, Bipolar disorder, Major depressive disorder, Anxiety (Panic disorder, Generalized Anxiety Disorder, Post-Traumatic Stress Disorder). While Aripiprazole has been approved for the treatment of Schizophrenia, its use in other psychiatric disorders is off label use. Increasing evidence suggests that Aripiprazole might offer some benefit for other psychiatric disorders besides Schizophrenia.

Conditions

Schizophrenia; Schizoaffective Disorder; Bipolar Disorder; Major Depressive Disorder; Anxiety Disorders; Substance Abuse

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

Aripiprazole start dose at 5 mg/day by day 4-6 increase to 10 mg/da and day 7 and subsequent visits flexible dosing from 10 up to 30 mg/day.

Group Type: EXPERIMENTAL

Aripiprazole

Intervention Type: DRUG

Interventions

Aripiprazole

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Ages 19 - 65

2. Diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, major depressive disorder, or anxiety (panic disorder, generalized anxiety disorder, or post-traumatic stress disorder) as confirmed by Mini International Neuropsychiatric Interview (MINI) structured assessment

3. Diagnosis of comorbid substance abuse/dependence as confirmed by the MINI structured assessment

4. Ability to provide signed informed consent

5. Stable general medical health

6. Ability to attend outpatient research clinic.

Exclusion Criteria

1. Dangerous to self or others

2. Pregnancy, or inability or unwillingness to use approved methods of birth control

3. Inability or unwillingness to provide signed informed consent

4. Inability to attend outpatient research clinic

5. Medical conditions, which would preclude use of aripiprazole

6. Absolute need for ongoing treatment with antipsychotic other than aripiprazole

7. Medical instability defined as likelihood of needing to change prescription medication during the course of the study

8. Patients with prior unsuccessful treatment with aripiprazole

9. Patients with a psychiatric diagnosis of only antisocial personality disorder or only an eating disorder and comorbid substance abuse/dependence.

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Bristol-Myers Squibb

INDUSTRY

Sponsor Role: collaborator

Creighton University

OTHER

Sponsor Role: lead

Principal Investigators

Pirzada S. Sattar, M.D.

Role: PRINCIPAL_INVESTIGATOR

Creighton University

Locations

Creighton University Psychiatry and Research Center

Omaha, Nebraska, United States

Countries

United States

Other Identifiers

05-13685

Identifier Type: -

Identifier Source: org_study_id