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NCT ID: NCT00689611 Completed - Clinical trials for Myocardial Infarction

Zyban as an Effective Smoking Cessation Aid for Patients Following an Acute Coronary Syndrome: The ZESCA Trial

ZESCA
Start date: December 2005
Phase: Phase 3
Study type: Interventional

Patients who continue to smoke after a heart attack have a 35% increased risk of a recurrent event or death compared with those who quit. Many patients attempt to stop smoking after a heart attack, but relapse rates approach 66%. A variety of smoking cessation aids have been shown to be effective for the general population. However, bupropion is the only non-nicotine replacement therapy shown to improve abstinence rates in healthy young smokers. Furthermore, nicotine replacement therapies (NRTs) are contraindicated in the immediate period following a heart attack because of the undesirable effects of nicotine. Although bupropion has been successfully used to reduce smoking rates in healthy young populations, its efficacy and safety in the setting of patients recovering from an ACS is unknown. These patients, if they continue to smoke, are at exceptionally high risk for recurrent cardiac events. If bupropion is effective in this population, it will have a major impact on secondary prevention of recurrent clinical events in patients who suffer a heart attack.

NCT ID: NCT00683839 Completed - Smoking Clinical Trials

Tobacco Cessation Via Public Health Dental Clinics

PHD2
Start date: January 2006
Phase: Phase 2
Study type: Interventional

The study will examine the effectiveness of public health dental practitioners using a brief office based intervention designed to help patients quit smoking or smokeless tobacco use, as compared to usual care.

NCT ID: NCT00672256 Completed - Smoking Clinical Trials

Neuroimaging Decision Making and Response Inhibition During Smoking Abstinence

SmokeAtt02
Start date: January 2007
Phase: N/A
Study type: Interventional

The broad objective of this proposal is to identify functional neuroanatomical correlates of impairments in response inhibition during smoking abstinence. We will measure changes in performance and regional blood oxygenation levels using functional magnetic resonance imaging (fMRI)while smokers complete tasks designed to assess decision making and response inhibition. Our primary hypothesis is that smoking abstinence will result in impaired response inhibition accompanied by decreases in blood-oxygenation-level-dependent (BOLD) fMRI signal in brain regions associated with these cognitive processes including frontal cortex and the ventral striatum. Abstinence may also result in performance-related increases in activation in brain regions associated with effortful processing including the anterior cingulate cortex in effort to compensate for deficits in other regions.

NCT ID: NCT00670904 Completed - Smoking Clinical Trials

Randomized Trial Assessing the Effectiveness of a Pharmacist-Delivered Program for Smoking Cessation

Start date: October 2005
Phase: N/A
Study type: Interventional

This randomized trial compared the effectiveness of a three session pharmacist-delivered group program for smoking versus one 5 to 10 minute standard care session delivered over the telephone on 7-day point prevalence quit rates. Participants in both groups were offered their choice of bupropion IR or nicotine patch at no cost. At 6 months after the established quit date, self-reported cessation was biochemically verified using tests for urinary cotinine.

NCT ID: NCT00670514 Completed - Smoking Clinical Trials

Smoking Cessation in a Dentistry Setting

Start date: April 2003
Phase: N/A
Study type: Interventional

Aim: to assess relative effectiveness of a high and a low intensity intervention for smoking cessation support in a dental clinic setting. Method: 300 smokers were randomly assigned to support with either low (LTI) or high treatment intensity (HTI). Main outcome measures were self-reported point-prevalence and continuous abstinence (≥183 days).

NCT ID: NCT00665704 Completed - Smoking Clinical Trials

Tobacco Tactics Website for Veteran Smokers

Start date: March 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to develop an evidence-based Tobacco Tactics website tailored to veterans based on an intervention tested in the VA.

NCT ID: NCT00664404 Completed - Smoking Clinical Trials

Genetic Differences in Limbic Activation Associated With Nicotine Withdrawal

Start date: April 2008
Phase: Phase 3
Study type: Interventional

Objectives: - To evaluate neural correlates associated with emotional processing during nicotine withdrawal preferentially involving the amygdala and associated areas within the corticolimbic and mesolimbic circuitry. We hypothesize that relative to a pre-quit baseline, post-quit nicotine withdrawal will result in increased activity to negative emotional cues, in contrast to other cues, in one or more areas of interest, and particularly in the right cerebral hemisphere. - To determine if bupropion and varenicline moderate patterns of brain activation during post-quit nicotine withdrawal. We hypothesize that relative to placebo, bupropion and varenicline will attenuate the effects of post-quit nicotine withdrawal on emotional processing, reducing activation to negative emotional cues, relative to other cues, in one or more areas of interest, and particularly in the right cerebral hemisphere. - To determine if genotype (DRD2 TaqA2 allele and the ins variant of the -141C ins/del DRD2) moderates patterns of brain activation during post-quit nicotine withdrawal.

NCT ID: NCT00662766 Completed - Smoking Clinical Trials

Intervention With Black Currant Seed Press Residues in Healthy Subjects

Start date: September 2005
Phase: N/A
Study type: Interventional

The study was performed to investigate the effects of the consumption of black currant seed press residues, which were baked into bread.

NCT ID: NCT00657020 Completed - Smoking Clinical Trials

Functional Magnetic Resonance Imaging (fMRI) Investigation of Nicotine Withdrawal Symptoms

Start date: September 2007
Phase: Phase 4
Study type: Interventional

A single center, double blind, randomized, placebo controlled, two-treatments, two-period crossover study conducted in adult smokers.

NCT ID: NCT00650585 Completed - Smoking Clinical Trials

An Effectiveness Trial of Project ALERT

Start date: May 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to replicate a longitudinal evaluation of Project ALERT, a substance abuse prevention program that targets middle school students.