Skip to content

A Double-Blind, Controlled Study of Aripiprazole in Co-Morbid Schizophrenia and Cocaine Dependence

A Double-Blind, Controlled Study of Aripiprazole in Co-Morbid Schizophrenia and Cocaine Dependence

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00737256
Enrollment
44
Registered
2008-08-18
Start date
2008-08-31
Completion date
2014-05-31
Last updated
2012-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia, Cocaine Dependence

Brief summary

The purpose of this study is to gather systematic clinical data on whether aripiprazole, a partial dopamine agonist, beneficially affects schizophrenia plus cocaine dependence subjects. Since aripiprazole has established effects against schizophrenia, the study focuses on whether aripiprazole concurrently reduces co-morbid cocaine dependence in schizophrenia plus cocaine dependence sufferers compared to a standard typical antipsychotic treatment (perphenazine). The working hypothesis states that subjects in the aripiprazole treatment arm of the study will give fewer cocaine positive urine specimens as compared to the perphenazine control arm.

Interventions

DRUGAripiprazole

15-30 mg

8-16 mg

Sponsors

Paul Saenger
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Have a primary DSM-IV diagnosis of Schizophrenia or Schizoaffective disorder 2. Have a DSM-IV diagnosis of current cocaine dependence. 3. Are capable of reading, comprehending, and signing informed consent. 4. Agree to take Aripiprazole or Perphenazine as treatment for SCHZ and CD. 5. Agree to stop taking any other antipsychotic medication 6. If female and of child bearing potential (WOCBP) agree to use an acceptable form of birth control and have a negative pregnancy test within 2 days prior to starting study medication

Exclusion criteria

1. Under 18 years old or over 65 years old. 2. Refusal or inability to give informed consent, 3. Have a history of myocardial infarction or ischemic heart disease, heart failure or conduction abnormalities, cerebrovascular disease, or conditions that would predispose to hypotension (dehydration, hypovolemia), 4. A history of seizures or conditions that lower the seizure threshold 5. Have current suicidal ideation (history of suicide attempt in past 60 days) 6. Are actively psychotic which in the opinion of the investigator would preclude proper informed consenting or protocol adherence 7. Are receiving or plan to receive an agent metabolized by the Cytochrome P450-3A4 or -2D6 systems, including carbamazepine, ketoconazole, quinidine, fluoxetine, and paroxetine 8. WOCBP not on, or do not agree to use an acceptable form of contraception 9. Known sensitivity to aripiprazole or perphenazine 10. A diagnosis of current or past tardive dyskinesia 11. Pending legal charges or a court mandate for drug treatment 12. Currently taking concomitant medications that have been shown to reduce cocaine use, such as disulfiram 13. Clinically significant liver function abnormalities 14. Currently receiving depot neuroleptics

Design outcomes

Primary

MeasureTime frame
The proportion of negative urine drug screen results will be significantly greater in the subjects treated with aripiprazole than in those treated with perphenazine.Week 3 and Week 8 of study participation

Secondary

MeasureTime frame
The mean total self-report cocaine use days will be significantly fewer in subjects treated with aripiprazole than in those treated with perphenazine.End of study participation
The mean cocaine craving scores will be lower in subjects treated with aripiprazole than in those treated with perphenazine.End of study participation

Countries

United States

Contacts

Primary ContactJennifer Ratzlaff, MA
Jennifer.Ratzlaff@ucdenver.edu303-399-8020
Backup ContactBrandon Schmidt, MA
Brandon.Schmidt@ucedenver.edu303-399-8020

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026