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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03920319
Other study ID # Brody011
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date January 1, 2004
Est. completion date December 31, 2005

Study information

Verified date April 2019
Source University of California, Los Angeles
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Randomized, double-blind, before-after controlled trial to assess changes in regional brain activation in response to cigarette-related cues from before to after treatment with bupropion (vs placebo).


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date December 31, 2005
Est. primary completion date December 31, 2005
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Treatment-seeking cigarette smoker

- Meet DSM-IV criteria for nicotine dependence

- Negative result on urine test for drug use during screening

Exclusion Criteria:

- History of any Axis I psychiatric diagnosis other than nicotine dependence

- 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bupropion
Bupropion 150 mg sustained release
Other:
Placebo


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of California, Los Angeles

Outcome

Type Measure Description Time frame Safety issue
Primary Craving ratings Participants were instructed to respond from 1 (definitely not) to 5 (definitely) on the question, "I crave a cigarette right now", after viewing video cues. 8 weeks
Secondary Exhaled carbon monoxide (CO) Participants were asked to hold their breath for as long as possible, ideally 15 seconds, then to breathe out slowly into the mouthpiece of a CO monitor, aiming to empty the lungs completely. 8 weeks
Secondary Cigarettes per day Self-reported number of cigarettes smoked daily during the past 7 days [??] 8 weeks
Secondary Fagerström Test for Nicotine Dependence (FTND) The FTND contains six items that evaluate the quantity of cigarette consumption, the compulsion to use, and dependence. The yes/no items are scored from 0 to 1 and multiple-choice items are scored from 0 to 3. The items are summed to yield a total score of 0-10. The higher the total Fagerström score, the more intense is the patient's physical dependence on nicotine. 8 weeks
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