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View clinical trials related to Smoking.

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NCT ID: NCT02603627 Not yet recruiting - Lung Cancer Clinical Trials

Prevalence of COPD in Our Lung Cancer Population, Compared to Controls

Start date: December 2015
Phase: N/A
Study type: Observational

This study will investigate the prevalence of chronic obstructive pulmonary disease (COPD) in patients who are newly diagnosed with lung cancer and compare it to the prevalence of COPD in controls recruited from a smoking cessation clinic.

NCT ID: NCT01758276 Not yet recruiting - Smoking Clinical Trials

Obstetric Complications in Women Who Smoke During Pregnancy

Start date: January 2013
Phase: N/A
Study type: Observational

This will be a retrospective study. Details on all women who delivered in McGill University between 2001-2007 will be retrieved anonymously from the MOND database (McGill University Obstetrics and Neonatal database). Women will be divided to 2 groups according to their smoking status in pregnancy. Obstetric complications will be recorded in both groups.

NCT ID: NCT00819078 Not yet recruiting - Smoking Cessation Clinical Trials

Comparative Study of SR Bupropion for Adolescent Smoking Cessation

Start date: January 2009
Phase: N/A
Study type: Interventional

Bupropion has been used successfully and safely for smoking cessation in adults. It was also used in very few studies among adolescent population. Our hypothesis is that Bupropion would be effective and safe among the adoelscent psychiatric population. A double-blind randomized controlled-trial will be held to determine that.

NCT ID: NCT00647413 Not yet recruiting - Smoking Clinical Trials

Prevent Exposure to Tobacco Smoke at Home [Gesunde Atemluft zu Hause]

GESA
Start date: May 2008
Phase: N/A
Study type: Interventional

Background: Infants are at risk for tobacco-attributable diseases by being exposed to environmental tobacco smoke (ETS). International literature has shown that a home smoking ban can reduce ETS. The purpose of this study is to examine whether a brief feedback about urinary cotinine in infants and a counselling session about the consequences of ETS leads to a reduction of ETS. All families with children up to an age of three years in the study region will be contacted by mail and asked for participation in this study. They will be randomised into an intervention and one control group. The intervention group will receive a ETS counselling session and detailed analysis of urinary cotinine (a biomarker of ETS) at their home. They will further receive written feedback approx. 2 weeks later. The control group will be visited and will answer a questionnaire and will receive brochures about ETS. They will receive a standard analysis feedback of urinary cotinine. There will be oine further assessment/ visit 12 months later. The outcome of this study is an anlysis of urinary cotinine and smoking behaviour and changes in cotinine and smoking behaviour.

NCT ID: NCT00429208 Not yet recruiting - Smoking Clinical Trials

Effect Of Nicotine on Neurocognitive Performance of Cigarette Smokers

Start date: February 2007
Phase: N/A
Study type: Interventional

This research project addresses the hypothesis that a neurocognitive profile characterized by impairment of response inhibition and sustained attention may be a risk factor for smoking initiation and nicotine dependence among young women. Nicotine has short- term, facilitating effects on attention and response inhibition. Therefore, individuals who are impaired on cognitive functions such as these and initiate cigarette smoking may be more likely to maintain the habit and develop nicotine dependence. The research protocol specifically tests whether administration of nicotine to non-abstinent, regular cigarette smokers improves cognitive function in those domains where the participants had previously been shown to manifest performance deficits