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Effectiveness of Nefazodone and Bupropion in Treating Marijuana Dependent Individuals
This study has been completed.
Study NCT00249509   Information provided by National Institute on Drug Abuse (NIDA)
First Received: November 3, 2005   Last Updated: October 15, 2009   History of Changes

November 3, 2005
October 15, 2009
September 2000
September 2004   (final data collection date for primary outcome measure)
Marijuana use
Marijuna use
Complete list of historical versions of study NCT00249509 on ClinicalTrials.gov Archive Site
Marijuana withdrawal
Same as current
 
Effectiveness of Nefazodone and Bupropion in Treating Marijuana Dependent Individuals
Marijuana Pharmacotherapies: Controlled Clinical Trials With Nefazodone and Bupropion

Recent research has identified the following withdrawal symptoms to be associated with abruptly stopping marijuana use: anxiety, irritability, bodily aches and pains, and difficulty sleeping. These symptoms resemble those of both depression and nicotine withdrawal, suggesting that a similar treatment drug may be useful. This study will evaluate the effectiveness of two antidepressant drugs, bupropion and nefazodone, in reducing withdrawal symptoms in marijuana dependent individuals.

There have been few controlled studies that focus on treatments for marijuana dependence. The symptoms associated with marijuana withdrawal, including anxiety, irritability, bodily aches and pains, and difficulty sleeping, resemble those caused by depression and nicotine withdrawal. Therefore, antidepressant or nicotine withdrawal medications may be effective in treating marijuana dependence. Nefazodone and bupropion are two medications currently used to treat depression. The purpose of this study is to determine the effectiveness of nefazodone and bupropion in alleviating marijuana withdrawal symptoms. In addition, this study will evaluate whether these medications successfully treat marijuana dependent individuals in terms of treatment adherence and drug abstinence.

Participants in this double-blind trial will be randomly assigned to receive nefazodone, bupropion, or placebo. Daily doses of medication will be provided to participants in dated pill boxes; pill boxes will then be returned to the study nurse at each study visit. Medication will be taken in three daily doses; one of the doses will be a nonmedicated pill. Nefazodone will initially be given at a dose of 150 mg per day, which participants will take at bedtime. Every 5 days, the daily dose will increase by 150 mg, to a maximal dose of 600 mg of nefazodone per day. Bupropion will be given at an initial dose of 150 mg, which participants will take in the morning. After 3 days, the daily dose will increase to a total dose of 300 mg of bupropion per day.

Study visits will occur daily, at which time participants will complete drug use and withdrawal symptom reports. In addition, participants will partake in weekly therapy visits, which will consist of four sessions of motivational enhancement therapy followed by sessions of relapse prevention therapy. Bi-weekly psychiatry visits will include evaluations on substance use behavior and overall clinical symptoms, and will last 15-30 minutes.

Phase II
Interventional
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Marijuana Abuse
  • Drug: Nefazodone
  • Drug: Bupropion
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
132
September 2004
September 2004   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Meets DSM-IV criteria for current marijuana dependence
  • Uses at least 5 marijuana joints per week
  • Currently seeking treatment for marijuana dependence
  • Used marijuana in a maladaptive pattern in the 6 months prior to study entry

Exclusion Criteria:

  • History of seizures or unexplained loss of consciousness
  • Significant and unstable psychiatric condition (e.g., schizophrenia, bipolar disorder)
  • Chronic organic mental disorder
  • Dependent on any substances of abuse other than marijuana
  • Currently at significant suicidal risk
  • Unstable physical disorder that may represent a severe untreated condition, such as hypertension (blood pressure greater than 150/90), elevated transaminase levels, or unstable diabetes
  • Current or suspected coronary vascular disease
  • Has taken a monoamine oxidase inhibitor in the 2 weeks prior to study entry
  • Currently taking terfenedine, cisapride, astemizole, or pimozide
  • History of an allergic reaction to bupropion or nefazodone
  • If female, pregnant, breastfeeding, or unwilling to use an adequate method of contraception for the duration of the study
Both
18 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00249509
Frances R. Levin, M.D, NYSPI
NIDA-13191-1, R01-DA013191-1, DPMC
National Institute on Drug Abuse (NIDA)
 
Principal Investigator: David Mcdowell, MD New York State Psychiatric Institute
National Institute on Drug Abuse (NIDA)
October 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP