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Nabilone & Marijuana Addiction

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ClinicalTrials.gov Identifier: NCT01025700
Recruitment Status : Completed
First Posted : December 3, 2009
Last Update Posted : February 17, 2011
Information provided by:
University of British Columbia

Brief Summary:
Safety of Nabilone in reducing marijuana craving

Condition or disease Intervention/treatment Phase
Marijuana Smoking Drug: Cesemat Phase 2 Phase 3

Detailed Description:
Randomized double blind trial into the safety and efficacy of Cesemat for the treatment of marijuana use

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 35 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Double-Blind Placebo Control Study on the Use of Nabilone for Outpatient Management of Acute Marijuana Withdrawal
Study Start Date : June 2009
Primary Completion Date : June 2010
Study Completion Date : October 2010

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Marijuana
Drug Information available for: Nabilone
U.S. FDA Resources

Arm Intervention/treatment
Experimental: Cesemat Drug: Cesemat
1 mg capsule per day for 21 days
Other Name: Nabilone
No Intervention: Placebo

Primary Outcome Measures :
  1. Safety and tolerability to Nabilone

Secondary Outcome Measures :
  1. Marijuana craving questionnaire

Information from the National Library of Medicine

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Ages Eligible for Study:   19 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • 19 years or older
  • History of marijuana use

Information from the National Library of Medicine

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): NCT01025700

Canada, British Columbia
Vancouver General Hospital - Psychiatry Outpatient
Vancouver, British Columbia, Canada
Sponsors and Collaborators
University of British Columbia
Principal Investigator: Shaohua Lu, MD University of British Columbia

Responsible Party: Shaohua Lu, MD, University of British Columbia
ClinicalTrials.gov Identifier: NCT01025700     History of Changes
Other Study ID Numbers: H08-01999
First Posted: December 3, 2009    Key Record Dates
Last Update Posted: February 17, 2011
Last Verified: February 2011

Keywords provided by University of British Columbia:

Additional relevant MeSH terms:
Marijuana Abuse
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders
Autonomic Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Gastrointestinal Agents
Anti-Anxiety Agents
Tranquilizing Agents
Central Nervous System Depressants
Psychotropic Drugs