Trial | NCT00205946  Report issue

Official Title

The Effects of Acute Administration of Bupropion on Neural Substrates Underlying Hedonic Capacity

  • Phase

    Phase 1

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Intervention/Treatment

    bupropion ...

  • Study Participants

    32
The purpose of the study is to evaluate the effects of a single-dose of Wellbutrin XL (bupropion hydrochloride) on reward processing.
A cardinal feature of Major Depressive Disorder is anhedonia, which is a lack of pleasure in normally enjoyable activities. In order to understand reward processing in depressed individuals it is also necessary to study reward processing in people who are not depressed. Bupropion, the active drug in the anti-depressant Wellbutrin XL, has been shown to increase brain reward functioning in animals. The goal of the present study is to investigate the effects of Wellbutrin XL administered to psychiatrically healthy individuals as they perform a computer task known to assess reward processing.
Study Started
Apr 30
2005
Study Completion
Jul 31
2007
Last Update
Dec 06
2007
Estimate

Drug Bupropion

150 mg of bupropion administered 5 hours before fMRI scanning

  • Other names: Wellbutrin XL

Drug Placebo

Administered 5 hours prior to fMRI scanning (randomly assigned, double blind)

Placebo Placebo Comparator

Bupropion Active Comparator

Criteria 

Inclusion Criteria:

Absence of medical, neurological, and psychiatric illness (including alcohol and substance abuse)
Non-Smoker
Right-handed (Chapman and Chapman 1987)
Ability to provide informed consent

Exclusion Criteria:

Predisposition to seizure (e.g. family history of a seizure disorder, history of head trauma) or current use of medications that lower the seizure threshold
History or current diagnosis of anorexia or bulimia
Alcohol or substance abuse within the past year
Current usage of Wellbutrin or Zyban or other drugs that contain bupropion
Recent discontinuation of alcohol or sedatives (including benzodiazepines)
Use of (in the last 2 weeks) medications that may have antidepressant properties (ex. some herbal supplements)
Known allergies to bupropion
Currently lactating, pregnant or believe you are likely to be pregnant (enrolled subjects who are not using reliable contraception and have engaged in sexual intercourse since their last menstrual period will be given a self-administered pregnancy test.)
Left-handed/ambidextrous
Evidence of neurological illness
Serious suicide or homicide risk

Concomitant medications other than those listed in the exclusion criteria will be considered on an individual basis. Oral contraceptives will be allowed.
No Results Posted