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Kansas City, Kansas 66160


Little is known about the support needed to improve compliance with Chantix for smoking cessation. This is a two arm pilot study of African American smokers to provide varying levels of side effect management and compliance support during a 12 week treatment period. The primary aim of the study is to estimate the effect of induction support compared to standard care in increasing compliance with Chantix at month 3


Inclusion Criteria: - African American - 18-75 years of age - Smoke more than 10 cigarettes per day - Have a functioning telephone number - Be interested in quitting smoking - Be willing to take 3 months of Chantix - Be willing to complete all study visits Exclusion Criteria: - Renal impairment - Evidence or history of clinically significant allergic reactions to Chantix - Cardiovascular event in the past month - History of alcohol or drug abuse/dependency in the past year - Major depressive disorder in the last year requiring treatment - History of panic disorder - Psychosis, bipolar or eating disorder - Use of antidepressants, antipsychotics, mood stabilizers/anticonvulsants or naltrexone - Use of tobacco products other than cigarettes - Use of nicotine replacement therapy, buproprion, clonidine or nortriptyline in the month prior to enrollment - Prior use of Chantix - Women who are pregnant, contemplating getting pregnant or breastfeeding - Plans to move from Kansas City during the 3 month treatment phase - Another household member enrolled in the study



Primary Contact:

Principal Investigator
Nicole Nollen, PhD
University of Kansas

Backup Contact:


Location Contact:

Kansas City, Kansas 66160
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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