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Clinical Trials/NCT00737256
NCT00737256
Unknown
Phase 2

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

Paul Saenger1 site in 1 country44 target enrollmentAugust 2008

Overview

Phase
Phase 2
Intervention
Aripiprazole
Conditions
Schizophrenia
Sponsor
Paul Saenger
Enrollment
44
Locations
1
Primary Endpoint
The proportion of negative urine drug screen results will be significantly greater in the subjects treated with aripiprazole than in those treated with perphenazine.
Last Updated
13 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
May 2014
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Paul Saenger
Responsible Party
Sponsor Investigator
Principal Investigator

Paul Saenger

Executive Director

Denver Research Institute

Eligibility Criteria

Inclusion Criteria

  • Have a primary DSM-IV diagnosis of Schizophrenia or Schizoaffective disorder
  • Have a DSM-IV diagnosis of current cocaine dependence.
  • Are capable of reading, comprehending, and signing informed consent.
  • Agree to take Aripiprazole or Perphenazine as treatment for SCHZ and CD.
  • Agree to stop taking any other antipsychotic medication
  • 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

  • Under 18 years old or over 65 years old.
  • Refusal or inability to give informed consent,
  • 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),
  • A history of seizures or conditions that lower the seizure threshold
  • Have current suicidal ideation (history of suicide attempt in past 60 days)
  • Are actively psychotic which in the opinion of the investigator would preclude proper informed consenting or protocol adherence
  • Are receiving or plan to receive an agent metabolized by the Cytochrome P450-3A4 or -2D6 systems, including carbamazepine, ketoconazole, quinidine, fluoxetine, and paroxetine
  • WOCBP not on, or do not agree to use an acceptable form of contraception
  • Known sensitivity to aripiprazole or perphenazine
  • A diagnosis of current or past tardive dyskinesia

Arms & Interventions

1

Intervention: Aripiprazole

2

Intervention: Perphenazine

Outcomes

Primary Outcomes

The proportion of negative urine drug screen results will be significantly greater in the subjects treated with aripiprazole than in those treated with perphenazine.

Time Frame: Week 3 and Week 8 of study participation

Secondary Outcomes

  • 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)

Study Sites (1)

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