Nornicotine in Smokeless Tobacco as a Precursor for Carcinogen Exposure

NCT ID: NCT03998735

Last Updated: 2025-11-26

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 55 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-19
• Study Completion Date: 2026-08-31

Brief Summary

Our goal in this study is to investigate the extent of endogenous nitrosation of nornicotine in smokeless tobacco users as a function of nornicotine content in smokeless products. This study will lead to an understanding of the endogenous formation of NNN from nornicotine in humans, and will also investigate the effect of the reduction of nornicotine content in smokeless tobacco on the extent of endogenous NNN formation. The knowledge gained in this study will lead to the development of recommendations for the regulation, or potentially elimination, of nornicotine in smokeless tobacco products in order to minimize exposure to NNN in the users of these products.

Conditions

Smokeless Tobacco

Study Design

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

Study Groups

Group 1 (N=15)

160 µg/g herbal snuff, median level found in commercial moist snuff

Group Type: EXPERIMENTAL

Herbal Snuff (Smokeless Tobacco)

Intervention Type: DRUG

4 levels of \[D4\]nornicotine in herbal snuff

Group 2 (N=15)

70 µg/g herbal snuff, lowest level found in commercial moist snuff (rounded)

Group Type: EXPERIMENTAL

Herbal Snuff (Smokeless Tobacco)

Intervention Type: DRUG

4 levels of \[D4\]nornicotine in herbal snuff

Group 3 (N=15)

3.5 µg/g herbal snuff, 5% of the lowest level found in commercial moist snuff

Group Type: EXPERIMENTAL

Herbal Snuff (Smokeless Tobacco)

Intervention Type: DRUG

4 levels of \[D4\]nornicotine in herbal snuff

Group 4(N=10)

0 µg/g herbal snuff, control group will use unmodified herbal snuff

Group Type: ACTIVE_COMPARATOR

Herbal Snuff (Smokeless Tobacco)

Intervention Type: DRUG

4 levels of \[D4\]nornicotine in herbal snuff

Interventions

Herbal Snuff (Smokeless Tobacco)

4 levels of \[D4\]nornicotine in herbal snuff

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female adult smokeless tobacco users 18-65 years of age, using at least 3 tins of product per week for 6 months;
• Used the same brand for >80% of their smokeless tobacco use over the course of at least 6 months, and used this brand exclusively for at least two weeks prior to the eligibility screening;
• Not smoking or using any other nicotine or tobacco product in the past 2 weeks (expired CO < 6 ppm);
• Participants are in good physical health (no unstable medical condition) and good general oral health as determined by the licensed medical professional;
• Participants are in stable, good mental health (e.g. not currently, within the past 6 months, experiencing unstable or untreated psychiatric diagnosis, including substance abuse) as determined by the licensed medical professional;
• Participants who are not taking any medications that affect relevant metabolic enzymes;
• Women who are not pregnant or nursing or planning to become pregnant;
• Participants have provided written informed consent to participate in the study.

Exclusion Criteria

• Significant immune system disorders, respiratory diseases, kidney or liver diseases or any other medical disorders that may affect biomarker data as determined by the licensed medical professional;
• Vital signs out of range as determined by the licensed medical professional (participants failing for vital signs will be allowed to re-screen once):
• Evident poor oral health (significant gum recession, dental caries, tooth loss) as determined by the general oral health status check;
• Excessive drinking (e.g., 5 or more drinks daily) or problems with drinking or drugs (e.g., self-report of binge drinking alcohol or treatment for drug or alcohol abuse within last 3 months); to be assessed by PI or licensed medical professional;
• Regular smoking or tobacco use (e.g., greater than once a week) other than oral smokeless tobacco products;
• Currently (within the past 2 weeks) using nicotine replacement or other tobacco cessation products (to minimize confounding effects of another product);

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institutes of Health (NIH)

NIH

Sponsor Role: collaborator

Masonic Cancer Center, University of Minnesota

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Irina Stepanov, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota, Division of Environmental Health Sciences

Locations

Masonic Cancer Center

Minneapolis, Minnesota, United States

Countries

United States

Other Identifiers

SPH-2019-23251

Identifier Type: OTHER

Identifier Source: secondary_id

2019NTLS123

Identifier Type: -

Identifier Source: org_study_id

NCT02499198

Identifier Type: -

Identifier Source: nct_alias