Nabilone & Marijuana Addiction

NCT ID: NCT01025700

Last Updated: 2011-02-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-06-30

Study Completion Date

2010-10-31

Brief Summary

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Safety of Nabilone in reducing marijuana craving

Detailed Description

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

Conditions

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Marijuana Smoking

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Cesemat

Group Type EXPERIMENTAL

Cesemat

Intervention Type DRUG

1 mg capsule per day for 21 days

Placebo

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Cesemat

1 mg capsule per day for 21 days

Intervention Type DRUG

Other Intervention Names

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Nabilone

Eligibility Criteria

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Inclusion Criteria

* 19 years or older
* History of marijuana use
Minimum Eligible Age

19 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of British Columbia

OTHER

Sponsor Role lead

Responsible Party

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University of British Columbia

Principal Investigators

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Shaohua Lu, MD

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Locations

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Vancouver General Hospital - Psychiatry Outpatient

Vancouver, British Columbia, Canada

Site Status

Countries

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Canada

Other Identifiers

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H08-01999

Identifier Type: -

Identifier Source: org_study_id

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