Pilot Study of Quetiapine Treatment for Cannabis Dependence
Information source: New York State Psychiatric Institute
Information obtained from ClinicalTrials.gov on October 19, 2009 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Cannabis Dependence
Intervention: quetiapine (Drug)
Phase: Phase 2
Status: Recruiting
Sponsored by: New York State Psychiatric Institute Official(s) and/or principal investigator(s): John J Mariani, MD, Principal Investigator, Affiliation: Columbia University
Overall contact: John J Mariani, MD, Phone: 212-543-5987, Email: jm2330@columbia.edu
Summary
Marijuana is the most commonly used illicit drug in the United States. However, the
treatment options for cannabis dependence are limited; notably, no effective pharmacotherapy
has been developed. Conceptually, the ideal medication treatment for cannabis dependence
would:
1. be safe when administered to patients actively using cannabis
2. reduce cannabis intake and promote abstinence
3. treat the symptoms of cannabis withdrawal
4. reduce craving and relapse risk
5. have a low abuse liability.
Conceptually, the pharmacodynamic and clinical actions of quetiapine suggest that it may be
useful for cannabis dependence. By antagonizing dopamine, quetiapine may interfere with the
reinforcing effects of cannabis, while serotonin type 2A, histamine type 1, and adrenergic
receptor antagonism may reduce cannabis withdrawal symptoms, primarily by sedating and
anxiolytic effects. The proposed research project is an open-label pilot study to evaluate
the tolerability and ideal target dosing range for quetiapine treatment of cannabis
dependence over an eight-week period. The purpose of this pilot study is to obtain
preliminary data regarding the potential efficacy, tolerability and safety of quetiapine
treatment of cannabis dependence before conducting a larger double-blind trial.
Clinical Details
Official title: Open-Label Pilot Study of Quetiapine Treatment for Cannabis Dependence
Study design: Treatment, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Primary outcome: Maximum tolerated dose of quetiapine
Secondary outcome: Cannabis Use
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Between the ages of 18-65
2. Meets DSM-IV criteria for current cannabis dependence
3. Seeking treatment for cannabis dependence
4. Reports using cannabis an average of five days per week over the past 28 days
5. Capable of giving informed consent and complying with study procedures
Exclusion Criteria:
1. Lifetime history of DSM-IV diagnosis of schizophrenia, schizoaffective disorder, or
bipolar disorder
2. Current DSM-IV criteria for any other psychiatric disorder that may, according to the
investigator's judgment, require either pharmacological or non-pharmacological
intervention over the course of the study
3. Receiving prescribed psychotropic medication
4. Known history of allergy, intolerance, or hypersensitivity to quetiapine
5. Pregnancy, lactation, or failure to use adequate contraceptive methods in female
patients who are currently engaging in sexual activity with men
6. Unstable medical conditions, such as poorly controlled diabetes or hypertension,
which might make participation hazardous
7. Current DSM-IV diagnosis of substance dependence other than cannabis or nicotine
dependence
8. Are legally mandated to participate in a substance use disorder treatment program
9. Increased risk for suicide
10. Diabetes (whether controlled or not), hyperglycemia (fasting glucose > 100 mg/dl),
obesity (BMI > 30) and elevated lipids (cholesterol > 200 mg/dl; triglycerides > 150
mg/dl).
Locations and Contacts
John J Mariani, MD, Phone: 212-543-5987, Email: jm2330@columbia.edu
Substance Treatment Research Service (STARS) of Columbia University, New York, New York 10032, United States; Recruiting
Additional Information
Substance Treatment Research Service (STARS) of Columbia University
Starting date: August 2009
Ending date: August 2010
Last updated: August 17, 2009
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