Study Results
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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COMPLETED
PHASE1
34 participants
INTERVENTIONAL
2004-01-01
2005-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
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Bupropion
Participants assigned to 150mg of bupropion daily for the first 3 days, followed by titration up to 2 pills daily, separated by 8 hours, for the remaining 8 weeks of treatment.
Bupropion
Bupropion 150 mg sustained release
Placebo
Participants assigned to pill placebo daily for the first 3 days, followed by titration up to 2 pills daily, separated by 8 hours, for the remaining 8 weeks of treatment.
Placebo
Interventions
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Bupropion
Bupropion 150 mg sustained release
Placebo
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Meet DSM-IV criteria for nicotine dependence
* Negative result on urine test for drug use during screening
Exclusion Criteria
* Medical conditions that might affect brain function
* Current use of medications that could alter brain function
* Pregnancy
* Current illicit drug use other than occasional use of marijuana
18 Years
65 Years
ALL
No
Sponsors
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University of California, Los Angeles
OTHER
Responsible Party
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Other Identifiers
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Brody011
Identifier Type: -
Identifier Source: org_study_id
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