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Vilazodone Treatment for Marijuana Dependence

Primary Purpose

Marijuana Dependence

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Vilazodone
Placebo
Sponsored by
Medical University of South Carolina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Marijuana Dependence focused on measuring Marijuana, Vilazodone, Contingency management, Motivational enhancement therapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Must meet DSM-IV criteria for marijuana dependence
  • Must be between the ages of 18 and 65 years old
  • If female and of childbearing potential, must agree to use acceptable method of birth control for duration of the trial.
  • Cannabis-positive urine drug screen at screening
  • Must consent to random assignment
  • Must be able to read and provide informed consent

Exclusion Criteria:

  • Women who are pregnant, nursing, or plan to become pregnant during course of study
  • Must not have a history of or current psychotic disorder, bipolar disorder, or eating disorder
  • Must not pose a current suicidal or homicidal risk
  • Must not have evidence or history of serious medical disease
  • Must not require concomitant therapy with psychotropic medication or CYP3A4 inhibitors
  • Must not be currently dependent on other substances, with the exception of nicotine;
  • Patients who, in the investigator's opinion, would be unable to comply with study procedures or assessments

Sites / Locations

  • Medical University of South Carolina

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vilazodone

Placebo

Arm Description

Flexible dose up to 40 mg capsule daily

Flexible dose up to 40 mg capsule daily

Outcomes

Primary Outcome Measures

Percent Marijuana-negative Urine Drug Screens (UDS)
Participants submitted a urine sample weekly. Percentage of marijuana negative urine samples were calculated per group.

Secondary Outcome Measures

Weekly Cannabis Use Sessions
Self-report of weekly cannabis use sessions was measured using the Time Line Followback, a calendar-based instrument designed to assess substance consumption.
Marijuana Craving and Withdrawal
The Marijuana Craving Questionnaire (MCQ) is intended to measure marijuana craving in adults. It measures symptoms on four subscales: expectancy, purposefulness, emotionality, and compulsivity. The scale rates individual items from 1 (least craving) - 7 (most craving) with a composite scoring range of 12-84 and possible subscale scoring range of 3-21. It was administered weekly to all participants. Reported here is the mean MCQ purposefulness subscale score across 8 weeks.

Full Information

First Posted
April 5, 2012
Last Updated
July 8, 2016
Sponsor
Medical University of South Carolina
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01574183
Brief Title
Vilazodone Treatment for Marijuana Dependence
Official Title
Vilazodone Treatment for Marijuana Dependence
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
February 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of South Carolina
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Marijuana is the most commonly used illicit drug, yet few clinical trials have evaluated pharmacotherapy treatments for marijuana dependence. This study will evaluate the efficacy of vilazodone for reducing marijuana use in marijuana-dependent adults. A contingency management intervention (CM)and motivational enhancement therapy (MET)will be incorporated to encourage study engagement and retention, and genomic DNA will be extracted to characterize subjects according to polymorphisms of genes potentially relevant to the activity of vilazodone. It is hypothesized that vilazodone combined with MET and CM will reduce the percent of marijuana-positive urine drug screen results in marijuana-dependent individuals as compared to a placebo treatment combined with MET and CM.
Detailed Description
The purpose of this study is to determine if the medication vilazodone is effective in helping frequent marijuana smokers cut down or stop using marijuana. Vilazodone is FDA approved for the treatment of depression- in this study, vilazodone's effect on marijuana dependence is being investigated. Participation in the study takes 10 visits over a period of approximately two to three months. The first visit is a screening visit to determine if participants are eligible to participate. After the initial assessment visit, the weekly visits take about 30 minutes, with the exception of three therapy sessions which take approximately 60-90 minutes. The three therapy sessions will focus on participant's marijuana use and reasons they may have for stopping or cutting down on use. After completing an initial therapy session, participants will be randomly selected to receive the study medication, either vilazodone or placebo (a capsule that does not contain any active medication). Participants will have weekly study visits with a clinician. At each study visit, they will be asked to fill out forms and answer specific questions concerning their substance use, anxiety symptoms, and feelings in general. They will be providing urine samples to check for illegal drugs of abuse including marijuana and other drugs. They will also have blood samples drawn during to determine if you are taking the medication as directed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Marijuana Dependence
Keywords
Marijuana, Vilazodone, Contingency management, Motivational enhancement therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
76 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vilazodone
Arm Type
Experimental
Arm Description
Flexible dose up to 40 mg capsule daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Flexible dose up to 40 mg capsule daily
Intervention Type
Drug
Intervention Name(s)
Vilazodone
Other Intervention Name(s)
Viibryd
Intervention Description
up to 40 mg capsule daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
up to 40 mg capsule daily
Primary Outcome Measure Information:
Title
Percent Marijuana-negative Urine Drug Screens (UDS)
Description
Participants submitted a urine sample weekly. Percentage of marijuana negative urine samples were calculated per group.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Weekly Cannabis Use Sessions
Description
Self-report of weekly cannabis use sessions was measured using the Time Line Followback, a calendar-based instrument designed to assess substance consumption.
Time Frame
8 weeks
Title
Marijuana Craving and Withdrawal
Description
The Marijuana Craving Questionnaire (MCQ) is intended to measure marijuana craving in adults. It measures symptoms on four subscales: expectancy, purposefulness, emotionality, and compulsivity. The scale rates individual items from 1 (least craving) - 7 (most craving) with a composite scoring range of 12-84 and possible subscale scoring range of 3-21. It was administered weekly to all participants. Reported here is the mean MCQ purposefulness subscale score across 8 weeks.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Must meet DSM-IV criteria for marijuana dependence Must be between the ages of 18 and 65 years old If female and of childbearing potential, must agree to use acceptable method of birth control for duration of the trial. Cannabis-positive urine drug screen at screening Must consent to random assignment Must be able to read and provide informed consent Exclusion Criteria: Women who are pregnant, nursing, or plan to become pregnant during course of study Must not have a history of or current psychotic disorder, bipolar disorder, or eating disorder Must not pose a current suicidal or homicidal risk Must not have evidence or history of serious medical disease Must not require concomitant therapy with psychotropic medication or CYP3A4 inhibitors Must not be currently dependent on other substances, with the exception of nicotine; Patients who, in the investigator's opinion, would be unable to comply with study procedures or assessments
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aimee L McRae-Clark, PharmD, BCPP
Organizational Affiliation
Medical University of South Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Vilazodone Treatment for Marijuana Dependence

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