Treatment of Schizophrenia and Comorbid Cannabis Use Disorder: Comparing Clozapine to Treatment-as-Usual
NCT ID: NCT00498550
Last Updated: 2019-03-13
Study Results
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View full resultsBasic Information
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COMPLETED
PHASE4
31 participants
INTERVENTIONAL
2000-10-31
2009-03-31
Brief Summary
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Detailed Description
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This study will enroll individuals with schizophrenia who are currently taking any oral antipsychotic other than clozapine, including those taking up to two oral antipsychotic, and who are also addicted to marijuana. The study will begin with a 1-week assessment phase, during which all participants will continue taking olanzapine or risperidone. Participants will undergo a physical examination and have blood drawn for laboratory tests. Information pertaining to their medical, psychiatric, and substance use history will also be collected. Urine tests and breathalyzers will be used to screen for the presence of alcohol and drugs. Following the assessment phase, participants will be randomly assigned to switch to clozapine or remain on their prestudy antipsychotic for 12 weeks. Participants remaining on their prestudy antipsychotic treatment will continue to receive the same dose for the entire study. Participants taking clozapine will initially receive a daily dose of 12.5 mg, which will be increased to a maximum of 400 mg per day, as tolerated. Study visits will take place once a week. At each visit, medication side effects, physical and psychological symptoms, substance use, treatment services received, and living situation will be assessed. Blood will be drawn for laboratory tests. Drug and alcohol levels will be monitored three times a week through urine and breathalyzer tests. Quality of life questionnaires will be administered once a month.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Clozapine
Clozapine, Clozaril
Clozapine
Clozapine up to 550mg per day
Treatment as usual
Treatment as usual with any antipsychotic other than Clozapine.
Treatment as usual
Remain on pre-study antipsychotic treatment
Interventions
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Clozapine
Clozapine up to 550mg per day
Treatment as usual
Remain on pre-study antipsychotic treatment
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Meets diagnostic criteria for marijuana use disorder, as determined by a rating of 3 or higher on the Drug Use Scale (Abuse or Dependence)
* Used marijuana on 5 or more days during the 3 weeks prior to study entry
* Taking any oral antipsychotic other than clozapine in the month prior to study entry. (Patients may take a second oral antipsychotic medication, if approved by the Medication Adjustment Group)
* If female, willing to use effective contraception throughout the study
Exclusion Criteria
* Currently taking clozapine
* Currently taking other psychotropic medications for the treatment of substance use (e.g., disulfiram, naltrexone, acamprosate, inderol, tegretol, topiramate, and pramipexole)
* Participated in a clinical trial of an investigational drug within 30 days of study entry
* Currently participating in a psychosocial intervention clinical trial
* Has medical or legal problems that may entail a jail or hospital stay during the study
* Has a developmental disability that would make study participation difficult
* Currently enrolled in a live-in treatment program for substance use disorders
* Pregnant or plans to become pregnant during the study
18 Years
65 Years
ALL
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
University of Missouri, Kansas City
OTHER
VA Medical Center-West Los Angeles
FED
University of South Carolina
OTHER
Dartmouth-Hitchcock Medical Center
OTHER
Responsible Party
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Alan Green
Principal Investigator
Principal Investigators
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Alan Green, MD
Role: PRINCIPAL_INVESTIGATOR
Dartmouth-Hitchcock Medical Center
Locations
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West LA VAHCS
Los Angeles, California, United States
University Missouri
Kansas City, Missouri, United States
Mental Health Center of Greater Manchester
Manchester, New Hampshire, United States
University South Carolina
Columbia, South Carolina, United States
Countries
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Other Identifiers
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DPMCDA
Identifier Type: -
Identifier Source: secondary_id
NCT00149955
Identifier Type: -
Identifier Source: org_study_id
NCT00149955
Identifier Type: -
Identifier Source: nct_alias
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