Clozapine for Cannabis Use in Schizophrenia (CLOCS)
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|ClinicalTrials.gov Identifier: NCT01639872|
Recruitment Status : Completed
First Posted : July 13, 2012
Last Update Posted : March 23, 2018
Many individuals with schizophrenia also suffer from marijuana addiction that worsens their problems related to schizophrenia. Most of the medications prescribed for schizophrenia have no effect on reducing marijuana use. Preliminary data suggests that clozapine, an atypical antipsychotic, may limit marijuana use in people diagnosed with schizophrenia, but it is not commonly used due to its side effects and is reserved for people who do not respond to other antipsychotic medications.
In the proposed study, 132 individuals who are diagnosed with both schizophrenia and a cannabis use disorder will be randomized to a 12-week treatment course with either clozapine or risperidone (another commonly prescribed antipsychotic medication) to test the hypothesis that patient treated with clozapine will have decreased cannabis use as compared to patients treated with risperidone.
Should this study indicate that clozapine will lessen marijuana use in persons diagnosed with schizophrenia more than risperidone, it will provide evidence needed to begin to shift clinical practice toward its use in this population.
|Condition or disease||Intervention/treatment||Phase|
|Schizophrenia Cannabis Abuse Cannabis Dependence Dual Diagnosis||Drug: Clozapine Drug: Risperidone||Phase 4|
Cannabis use disorder (CUD), which is up to ten times more common in patients with schizophrenia (SCZ) than in the general population, worsens the course of this severe psychiatric disorder. Since SCZ occurs in 1% of the population, the co-occurrence of CUD in 13% to 42% of people with this disorder presents society with an important public health problem. Unfortunately, most antipsychotics available for treatment of patients with SCZ do not appear to limit their cannabis use. Moreover, the one antipsychotic that preliminary data suggest may well limit cannabis use in these patients, clozapine (CLOZ), is not used for this purpose; it is reserved for patients whose psychosis is treatment resistant.
The overarching idea behind this proposal, however, is that CLOZ's use is being unreasonably restricted and should be made more widely available for patients with SCZ who have a co-occurring CUD but whose psychosis is not necessarily treatment resistant. This notion is supported by our preliminary clinical and animal data on the effects of CLOZ, as well as our neurobiological model of the basis of cannabis use in patients with SCZ that provides a pharmacologic rationale for this effect of CLOZ.
Even given all the arguments favoring the potential benefits of CLOZ in patients with SCZ and CUD, however, its side effect profile will likely limit its use until a fully powered study demonstrates its ability to decrease cannabis use in patients with SCZ. This proposal aims to launch such a study. If, as we hypothesize, this study confirms and extends our previous preliminary data of the effects of CLOZ in patients with SCZ and CUD, it will provide a strong impetus to expand the use of CLOZ in this population.
In the proposed study, 132 patients who are comorbid for both SCZ and CUD will be randomized to a 12-week treatment course with either CLOZ or risperidone (RISP) to test the hypothesis that patients treated with CLOZ will have decreased cannabis use as compared to patients treated with RISP. In addition, the study will determine whether patients treated with CLOZ will have improvements in psychiatric symptoms, quality of life neuropsychological functions as compared to those taking RISP. We will also explore whether patients taking CLOZ show improved reward responsiveness as compared to those taking RISP. Finally, this study will explore whether those patients with the val/val genotype at the COMT Val158Met locus are more likely to decrease cannabis use during CLOZ treatment than are those without the val/val COMT genotype.
Should this study indicate that CLOZ will lessen cannabis use in patients with SCZ more than RISP, it will provide evidence needed to begin to shift clinical practice toward its use in these patients.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||50 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Clozapine for Cannabis Use Disorder in Schizophrenia|
|Actual Study Start Date :||May 1, 2013|
|Actual Primary Completion Date :||March 29, 2017|
|Actual Study Completion Date :||March 29, 2017|
Clozapine: target dose of 400mg per day with a maximum dose of 550mg per day
Other Name: Clozaril
|Active Comparator: Risperidone||
Clozapine: target dose of 4mg per day with a maximum dose of 6mg per day
Other Name: Risperdal
- Intensity of cannabis use [ Time Frame: up to 12 weeks ]Intensity of cannabis use will be assessed by the amount of cannabis consumed each week
- Frequency of cannabis use [ Time Frame: up to 12 weeks ]Frequency of cannabis use will be assessed by the days of use per week.
- Symptoms of Schizophrenia [ Time Frame: up to 12 weeks ]Symptoms of schizophrenia will be measured using the scores on standardized assessments, including the Brief Psychiatric Rating Scale, the Schedule for the Assessment of Negative Symptoms, and the Clinical Global Inventory
- Quality of Life [ Time Frame: Monthly for three months ]Quality of life will be assessed based on scores on the Quality of Life scale and the "subjective section" from the Quality of Life Interview
- Neuropsychological functioning [ Time Frame: Every 6 weeks for three months ]Neuropsychological functioning will be assessed using the MATRICS Consensus Cognitive Battery;
- Reward responsiveness [ Time Frame: Every 6 weeks for three months ]We will assess reward responsiveness using the computerized Probabilistic Reward Task. This task measures the extent to which a participant biases their responding toward a more rewarded versus less rewarded stimulus consistent with the view that frequency of responding is increased toward reinforcers.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01639872
|United States, California|
|CNS Network Inc|
|Garden Grove, California, United States, 92845|
|Pacific Research Partners|
|Oakland, California, United States, 94607|
|United States, Florida|
|University of Miami|
|Miami, Florida, United States, 33136|
|United States, Massachusetts|
|Unversity of Massachusetts Medical School|
|Worcester, Massachusetts, United States, 01605|
|United States, Michigan|
|Michigan State University / Cherry Street Health Services|
|Grand Rapids, Michigan, United States, 49503|
|United States, New Hampshire|
|Dartmouth Hitchcock Medical Center|
|Lebanon, New Hampshire, United States, 03756|
|United States, North Carolina|
|University of North Carolina/UNC Center for Excellence in Community Mental Health|
|Raleigh, North Carolina, United States, 27610|
|United States, South Carolina|
|University of South Carolina|
|Columbia, South Carolina, United States, 29203|
|United States, Vermont|
|Rutland Regional Medical Center|
|Rutland, Vermont, United States, 05701|
|Study Chair:||Alan I Green, MD||Dartmouth College|