Highdose Nicotine Patch Therapy for Smokeless Tobacco Use

NCT ID: NCT00939029

Last Updated: 2014-05-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 52 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-07-31
• Study Completion Date: 2013-06-30

Brief Summary

Smokeless tobacco use ("chewing") is associated with negative health effects. To date, no medications have been shown to help chewers quit long-term. High dose nicotine patch therapy may improve the chances that chewers can quit for good. If found to be effective, chewers may use this treatment to help them quit and reduce their risk for negative health effects.

Detailed Description

Approximately 8.2 million (3.3%) of Americans ≥ 12 years of age are current smokeless tobacco (ST) users, and the prevalence of ST use has increased over the past three years. ST is increasingly being promoted as a harm reduction strategy for cigarette smoking, and two of the world's largest cigarette manufacturers have entered the ST market. ST use is estimated to be the greatest exogenous source of human exposure to cancer-causing nitrosamines. ST has been associated with oral and extra-oral cancer as well as cardiovascular and cerebrovascular mortality.

A need for efficacious interventions exists as 64% of ST users report the desire to quit. However, no pharmacotherapy has proven efficacy for increasing long-term (> 6 months) tobacco abstinence rates among ST users compared to placebo. New pharmacotherapies, drug combinations, and improved dosing of existing pharmacotherapies are needed. Previous research with nicotine patches for ST users using standard doses (up to 21 mg/day) have not increased long-term abstinence rates. However, studies of higher dose nicotine patch therapy (up to 63 mg/day) in ST users have demonstrated a dose-dependent reduction in tobacco withdrawal symptoms as well as preliminary evidence of increased long-term (> 6 months) abstinence rates compared to lower doses. The purpose of this study is to evaluate the efficacy of high dose nicotine patch therapy (42 mg/day) for increasing the 7-day point prevalence and prolonged all tobacco and ST abstinence rates at end-of-treatment (week 8), 12 and 24 weeks compared to placebo in ST users who use ≥ 3 cans/pouches per week when all subjects receive behavioral treatment for tobacco dependence. To accomplish our aims, we will randomize 60 ST users in a clinical pilot study. The work will be conducted at the Mayo Clinic in Rochester, MN.

Conditions

Smokeless Tobacco Use

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Active

2 nicotine patches each at 21 mg/day for a total of 42 mg/day for 8 weeks

Group Type: ACTIVE_COMPARATOR

nicotine replacement therapy (nicotine patches)

Intervention Type: DRUG

2- 21 mg patches per day for 8 weeks

placebo

2 patches (containing non active ingredients) per day for 8 weeks

Group Type: PLACEBO_COMPARATOR

placebo NRT

Intervention Type: DRUG

2 placebo patches (containing no active ingredient)per day for 8 weeks

Interventions

nicotine replacement therapy (nicotine patches)

2- 21 mg patches per day for 8 weeks

Intervention Type: DRUG

placebo NRT

2 placebo patches (containing no active ingredient)per day for 8 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. are at least 18 years of age and at most 55 years of age;

2. report daily ST use for the past 12 months;

3. identify ST as their primary tobacco product;

4. use an average of ≥ 3 cans/pouches per week;

5. are in general good health (determined by medical history and screening physical examination);

6. have been provided with, understand, and have signed the informed consent.

Exclusion Criteria

1. are currently using (past 30 days) any other behavioral or pharmacologic tobacco treatment program;

2. are currently pregnant or lactating;

3. have had unstable angina, myocardial infarction, or coronary angioplasty within the past 3 months;

4. have a history of arrhythmia or an abnormal tracing on the baseline EKG;

5. have a blood pressure of greater than 140/90 or a pulse of more than 110 beats per minute;

6. have a history of severe skin allergies or dermatoses;

7. have a history of intolerance to nicotine patches;

8. have another member of their household already participating in this study;

9. are taking a medication known to interact with nicotine (i.e., clozapine);

10. are taking any prescription medication for depression or asthma

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Mayo Clinic

OTHER

Sponsor Role: lead

Responsible Party

Jon Ebbert

Priniciple Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jon O Ebbert, MD

Role: STUDY_CHAIR

Mayo Clinic

Locations

Mayo Clinic

Rochester, Minnesota, United States

Countries

United States

References

Ebbert JO, Croghan IT, Schroeder DR, Hurt RD. A randomized phase II clinical trial of high-dose nicotine patch therapy for smokeless tobacco users. Nicotine Tob Res. 2013 Dec;15(12):2037-44. doi: 10.1093/ntr/ntt097. Epub 2013 Jul 19.

Reference Type: RESULT

PMID: 23873976 (View on PubMed)

Other Identifiers

CA140125

Identifier Type: -

Identifier Source: secondary_id

09-001763

Identifier Type: -

Identifier Source: secondary_id

09-002581

Identifier Type: -

Identifier Source: org_study_id