Expired Study
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West Allis, Wisconsin 53214


The purpose of this study is to determine whether the Smoke-Break nicotine delivery device can help smokers quit smoking, while avoiding many of the side effects associated with other smoking cessation products.

Study summary:

The study has been completed and published. The published study manuscript can be found here: http://www.biomedcentral.com/1471-2458/10/155


Inclusion Criteria: - Volunteer is at least 18 years of age. - Volunteer currently smokes cigarettes, cigars or other forms of tobacco products for at least one year. - Volunteer wants to quit smoking. - Volunteer will be fully informed as to the nature of the study. - Volunteer will have no known allergy to any product ingredients as listed in the informed consent. - Volunteer agrees to a confidential pretest questionnaire and periodic monitoring as to the effectiveness of the smoking cessation regimen. - Volunteers are not currently using another nicotine replacement therapy. - Volunteer will agree to use birth control measures while on the study. Exclusion Criteria: - Volunteer has a known allergy or hypersensitivity to nicotine or other related ingredients as outlined in the informed consent. - Volunteer does not desire to quit smoking. - Volunteer is using another nicotine replacement therapy. - Volunteer is pregnant or breast-feeding. - Volunteer has a history of heart disease or advanced diabetes. - Volunteer indicates on the application that they smoke ten (10) or fewer cigarettes per day. - Volunteer is using a daily prescription medicine for depression or asthma. - Volunteer is using a non-nicotine smoke cessation drug, such as Zyban or Chantix. - Volunteer is an employee of Smoke-Break Inc., or is personally known to an employee of Smoke-Break Inc.



Primary Contact:

Principal Investigator
Nicholas Geimer, MD
Smoke-Break, Inc.

Backup Contact:


Location Contact:

West Allis, Wisconsin 53214
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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