Examining the Effectiveness of the Nicotine Patch in Male and Female Smokers - 2

NCT ID: NCT00135746

Last Updated: 2017-01-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 128 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-05-31
• Study Completion Date: 2007-06-30

Brief Summary

Treatment studies have demonstrated that current smoking cessation techniques are less effective for women. The purpose of this study is to determine the role that gender plays on the effectiveness of nicotine replacement therapy. This may lead to improved cessation interventions for all smokers, particularly women.

Detailed Description

Currently, about 70 percent of smokers who try to quit by using smoking cessation treatments are unsuccessful. Treatment studies have demonstrated that current smoking cessation techniques are less effective for women. There is no clear explanation for this difference, but it may involve a differential response to nicotine replacement treatments (NRTs) and/or smoking-related stimuli. For women, NRT may be less effective at suppressing withdrawal or blunting the effects of smoking during a quit attempt. Women may also be more sensitive to smoking-related stimuli, such as the taste, sight, and smell of smoke. Tailoring treatment to the separate needs of subgroups, such as men and women, may produce better outcomes. The purpose of this study is to assess the influence of gender on the effectiveness of transdermal nicotine treatment in a group of male and female smokers.

Participants in this double-blind, dose-comparison study will complete separate sessions in a random order.

Each session will last approximately 6.5 hours and will correspond to a specific transdermal patch dose (0, 7, 14, or 21 mg). Objectively verified cigarette abstinence will be required before each session. Sessions will occur at least 48 hours apart to avoid carryover. Cognitive, behavioral, subjective, and physiological measures will occur during study visits. Specifically, the NRT dose response to tobacco suppression and cigarette blunting effects will be compared in women and men.

Conditions

Tobacco Use Disorder

Study Design

• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

nicotine transdermal system

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Daily cigarette use of 15 or more cigarettes for at least 2 years
• Screening CO level of or greater than 15 ppm
• Normal or corrected-to-normal vision
• Willing to abstain from tobacco products for 8 or more hours prior to testing

Exclusion Criteria

• History of chronic health problems or psychiatric conditions
• History of cardiovascular disease, low or high blood pressure, seizures, head injuries requiring hospital care, peptic ulcer, or diabetes
• Pregnancy (tested by urinalysis)
• Scores greater than 17 on the Beck Depression Inventory
• Lack of a high school degree or GED

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role: lead

Virginia Commonwealth University

OTHER

Sponsor Role: collaborator

Responsible Party

Virginia Commonwealth University

Principal Investigators

Thomas Eissenberg, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Virginia Commonwealth University

Locations

Behavioral Pharmacolgy Research Laboratory

Richmond, Virginia, United States

Countries

United States

Other Identifiers

R01-11082-2

Identifier Type: -

Identifier Source: secondary_id

DPMC

Identifier Type: -

Identifier Source: secondary_id

NIDA-11082-2

Identifier Type: -

Identifier Source: org_study_id