Measuring Smoking Behaviors While Using Varenicline

Nicotine Dependence Clinical Trial

Official title:

Assessment of Smoking Topography and Behaviors During Response to Varenicline

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00948155
• Other study ID #: 808930
• Status: Completed
• Phase: Phase 4
• First received: July 28, 2009
• Last updated: December 15, 2014
• Start date: January 2009
• Est. completion date: November 2010

Study information

• Verified date: December 2014
• Source: University of Pennsylvania
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This study will demonstrate the behavioral responses to varenicline, helping to better understand its mechanisms. Hypotheses for the study are to observe decreases in smoking topography and nicotine cigarette choice on varenicline, relative to placebo; and decreases on day 21 relative to day 7 during varenicline treatment. We also propose to examine if extended duration of treatment has clinical significance in decreasing smoking behaviors, thus increasing the efficacy of varenicline.

Description:

This study is designed to examine the behavioral responses a cigarette smoker may have to using varenicline. Behavioral responses may help to better understand its mechanisms which in turn could improve treatment outcomes. The primary hypothesis for the study is to observe decreases in smoking topography, an objective measure of smoking behavior or puffing, on varenicline, relative to placebo; and decreases on day 21 relative to day 7 during varenicline treatment. We will also examine puffing and nicotine cigarette choices during lab visits at baseline, and Days 7 and 21. We also propose to examine if extended duration of treatment has clinical significance in decreasing smoking behaviors, thus potentially increasing the efficacy of varenicline.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: November 2010
• Est. primary completion date: November 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 21 Years to 65 Years

Eligibility

Inclusion Criteria:

• self report minimum 10 daily cigarettes

• self report smoking every day past 5 years

• between the ages 21-65

• self report intention to try to quit smoking in the next 6 months

Exclusion Criteria:

• self reported use of any nicotine-containing products other than non-menthol cigarettes

• self reported history or current treatment of substance abuse (other than nicotine dependence)

• self reported alcohol use greater than 25 standard drinks per week;

• currently pregnant, planned pregnancy or lactating (females: negative urine pregnancy screen)

• self reported history or current diagnosis of any Axis 1 disorders except past depression

• self reported serious or unstable disease within past year

• self reported history of epilepsy or seizure disorder;

• self reported history or current diagnosis of COPD (chronic obstructive pulmonary disease), cardiovascular disease, heart attack, or uncontrolled hypertension

• self reported kidney function impairment

• any current or recent (30 day) use of: smoking cessation medications, anti-psychotics, anti-depressants, anti-anxiety, panic medications, stimulants or opiate-containing medications

• less than 5 years of daily smoking

• any medical condition or concomitant medication that could compromise participant safety or treatment

• provide a baseline carbon monoxide (CO) reading < 10 ppm

• self reported use of non filtered cigarettes

• inability to provide informed consent or complete any of the study tasks as determined by the Principal Investigator and/or Study Physician

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Nicotine Dependence

Intervention

Drug:
• Varenicline
Intervention Drug (Varenicline (Chantix) will be administered in standard dosing in pill format: 0.5 mg days 1-3; 0.5 mg bid daily days 4-7; 1.0 mg bid daily days 8-21.

Locations

Country	Name	City	State
United States	Tobacco Use Research Center	Philadelphia	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
University of Pennsylvania	Pfizer

Country where clinical trial is conducted

United States, 

References & Publications (1)

Ashare RL, Tang KZ, Mesaros AC, Blair IA, Leone F, Strasser AA. Effects of 21 days of varenicline versus placebo on smoking behaviors and urges among non-treatment seeking smokers. J Psychopharmacol. 2012 Oct;26(10):1383-90. doi: 10.1177/0269881112449397. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Smoking Topography: Total Puff Volume	Total puff volume was created by summing all of the puffs from the cigarette smoked in the lab at each time point (each lab visit). This value represents the total volume of smoke extracted from a single cigarette and it a standard measure of smoking behavior. A total puff volume represents the total smoking volume from a cigarette. Values are reported in milliliters. Value of interest is the average puff volume across all sessions for all participants in a group and is reported as a key measure of smoking behavior. Analyses were repeated measures analysis of variance where individual, time and drug were within factors.	Days 1-21 of each of 2 study periods	No
Primary	The Number of Choices of a Nicotine Containing Cigarette Compared to a Non-nicotine Cigarette.	Participants were given 4 puff choices (between a nicotine containing and de-nicotinized cigarette) on 6 study visits, for a total of 24 choices. Number of puffs reported is average across both study periods.	Days 1, 7, 21 of each of two 21 day study periods	No
Primary	Daily Cigarette Consumption	Average of the number of cigarettes smoked per day	Two 21 day study periods	No
Secondary	Total Nicotine Metabolites From Urine Samples	Total urinary metabolites from urine samples collected at Day 1 and Day 21	Samples from Day 1 and Day 21 of two 21 day Periods	No
Secondary	Nicotine Levels From Urine Samples	Nicotine levels from urine samples collected at Day 1 and Day 21.	Samples from Day 1 and Day 21 of two 21 day Periods	No
Secondary	Cotinine Levels From Urine Samples	Cotinine levels from urine samples collected at Day 1 and Day 21.	Samples from Day 1 and Day 21 of two 21 day Periods	No
Secondary	Carbon Monoxide Levels	Exhaled breath carbon monoxide levels collected at Day 1 and Day 21 sessions. Alveolar carbon monoxide is a validated assessment of smoke exposure.	Samples from Day 1 and Day 21 of two 21 day Periods	No
Secondary	Subjective Measures to Assess Smoking Urges	Craving for cigarettes was assessed with the 32-item Questionnaire of Smoking Urges (QSU) during each study visit. In order to calculate the QSU measure, each item is rated on a Likert-type scale from 1 (strongly disagree) to 7 (strongly agree). The values are then summed to create a single total score. Well validated 2 factor subscale scores were also created by summing the item scores for the 2 factors: Factor 1 reflects the desire to smoke for pleasure and Factor 2 reflects urges to smoke to relieve withdrawal-related negative affect. Internal consistency for each scale across all time points was high (Cronbach's a > 0.95, 0.85, and 0.95 for Factor 1, Factor 2, and QSU total, respectively). Scale range is 1-7 where 1 is low urge to smoke and 7 represents high urge to smoke. Data was collected at each time point but outcome measure of interest is end of period.	Days 21 of each of the two 21-day study periods, range 1(low)-7(high)	No