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Effectiveness of Nefazodone and Bupropion in Treating Marijuana Dependent Individuals

Marijuana Pharmacotherapies: Controlled Clinical Trials With Nefazodone and Bupropion

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00249509
Enrollment
132
Registered
2005-11-07
Start date
2000-09-30
Completion date
2004-09-30
Last updated
2017-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Marijuana Abuse

Keywords

marijuana dependence

Brief summary

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.

Detailed description

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.

Interventions

DRUGBupropion

Sponsors

National Institute on Drug Abuse (NIDA)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Marijuana use

Secondary

MeasureTime frame
Marijuana withdrawal

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026