Study of Bupropion Versus Bupropion + Naltrexone for Smoking Cessation
Information source: National Institute on Drug Abuse (NIDA)
Information obtained from ClinicalTrials.gov on February 07, 2013 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Tobacco Use Disorder
Intervention: Bupropion (Drug); Bupropion + Naltrexone (Drug)
Phase: Phase 2/Phase 3
Status: Recruiting
Sponsored by: University of Minnesota - Clinical and Translational Science Institute Official(s) and/or principal investigator(s): Marc E Mooney, Ph.D., Principal Investigator, Affiliation: Univerisity of Minnesota
Overall contact: Marc E Mooney, Ph.D., Phone: 612-273-9732, Email: moon0078@umn.edu
Summary
The purpose of this study is to compare the effects of bupropion + placebo to bupropion +
naltrexone as treatments to help smokers quit.
Clinical Details
Official title: Phase II Randomized, Double-Blind Trial of Bupropion Versus Bupropion + Naltrexone for Smoking Cessation
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Primary outcome: Biochemically-verified point-prevalence abstinenceLikelihood of progression to a relapse (e.g., return to baseline smoking) following a slip at any time in study. Treatment completion. Daily cigarette smoking rate. Frequency and severity of bupropion and naltrexone side effects.
Secondary outcome: Attentional bias.Impulsivity. Nicotine withdrawal, craving and negative/positive affect.
Detailed description:
The purpose of this study is to compare the effects of bupropion + placebo to bupropion +
naltrexone as treatments to help smokers quit. Bupropion is an FDA-approved medication for
smoking cessation that is believed to provide relief from craving and withdrawal through
promotion of two neurotransmitter chemicals, dopamine and noradrenaline. Naltrexone is an
FDA-approved medication for the treatment of opiate and alcohol dependence, that appears to
function through blocking certain opiate receptors in the brain. It is expected that
bupropion + naltrexone will produce higher smoking quit rates than bupropion + placebo.
Bupropion alone is effective in alleviating some nicotine withdrawal complaints and craving
for nicotine. However, bupropion does not reduce the rewarding effects of slips to smoking.
Naltrexone alone is not generally effective as a smoking cessation medication, but it does
help to reduce the rewarding effects of slips to smoking. Thus, it may help to prevent full
relapse to smoking. In addition, naltrexone can help to reduce craving for cigarettes. It
is hypothesized that the differing complementary actions of the two drugs will help smokers
more than bupropion alone. In addition to examining smoking quit rates, the proposed study
will also look at psychological processes that change during smoking cessation including,
nicotine withdrawal, nicotine craving, mood, impulsivity, and attention
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- 18 years and older.
- Smoked at least 10 cigarettes/day for at least 1 year.
- English speaking.
- Females who are of childbearing potential must practice effective contraception and
meet the following criteria:
- Are instructed to avoid pregnancy through 30 days after the last dose of study
medication.
- Have a negative urine pregnancy test at baseline.
- Agree to use of the birth control methods listed: an oral contraceptive agent, an
intrauterine device (IUD), an implantable contraceptive (e. g., Norplant), or an
injectable contraceptive (e. g., Depo-Provera) for at least one month prior to
entering the study and will continue its use through at least 30 days after the last
dose of the study medication. A barrier method of contraception (e. g., condom or
diaphragm with spermicide) while participating in the study and 30 days after the
last dose of study medication.
- Willingness to reduce alcohol consumption during study to 2 or fewer standard
drinks/day (3 oz. of alcohol or two beers (12 oz.), or two 5 oz. glasses of wine).
- Willingness to not use illicit drugs during study period including marijuana.
Exclusion Criteria:
- Concurrent use of tobacco products (other than cigarettes) or nicotine products.
- Contraindications to use of bupropion (i. e., concurrent use of other forms of
bupropion, MAO inhibitors, anti-depressant medication, seizure disorder or any
clinical situation that might increase risk for seizures, past head injury, current
or prior diagnosis of bulimia or anorexia nervosa; bipolar disorder).
- Contraindications to use of naltrexone (i. e., past history of opioid abuse or
dependence or evidence of opioid use in the past 30 days; significant hepatocellular
injury as evidenced by liver enzyme levels over 3 times normal limits).
- Use of medications whose metabolism or effects may be adversely altered by bupropion
or naltrexone. Medications that contraindicate the use of bupropion include
theophylline, procarbazine, carbimazole, nialamide, pargyline, toloxatone,
iproniazid, and systemic steroids. Medications that contraindicate the use of
naltrexone include opioid analgesics and yohimbine.
- Current use of anti-seizure medications, disulfiram, or any medications that
significantly challenge liver functioning.
- Treatment for drug or alcohol dependence during the last year, or evidence of alcohol
abuse so severe that the patient is judged potentially unable to comply with the
protocol.
- Evidence of problem alcohol consumption based on AUDIT.
- Self-reported use of illicit drugs in the past 90 days (including opioids, but
excluding marijuana).
- Suicidal or homicidal ideation.
- Current major depression.
- History of bipolar disorder.
- Recent (within twelve months) myocardial infarction.
- Pregnant or lactating or planning pregnancy during treatment period.
- Having plans to leave the immediate geographical area within 9 months.
- Unwillingness or inability to given written informed consent.
Locations and Contacts
Marc E Mooney, Ph.D., Phone: 612-273-9732, Email: moon0078@umn.edu
Tobacco Use Research Center, University of Minnesota, Minneapolis, Minnesota 55414, United States; Recruiting Marc E Mooney, Ph.D., Phone: 612-273-9732, Email: moon0078@umn.edu Marc E Mooney, Ph.D., Principal Investigator
Additional Information
Tobacco Use Research Center Website, Study Page
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Starting date: November 2006
Last updated: December 2, 2009
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