- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03153761
CSD170201: A Study to Evaluate the Exposure to Tobacco Constituents From Two Moist Snuff Products
April 9, 2018 updated by: RAI Services Company
CSD170201: A Crossover Study to Evaluate the Exposure to Tobacco Constituents From Two Moist Snuff Products
This study will evaluate exposure to tobacco constituents from two moist snuff products, and provide a basis for comparing mouth-level exposure (MLE) in moist snuff users after use of each of the two moist snuff products.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This will be an unblinded, single-center, randomized, two-way crossover study, conducted in generally healthy, adult moist snuff users who will be randomly assigned to the order in which they will use two moist snuff study products (comparator product, test product).
Enrolled subjects will use one of each of the study products exclusively for approximately one week (seven days +1/-2 day) prior to a test visit, with a different product used each week over a two-week period.
During each test visit, subjects will use study product ad libitum during a 6-hour period.
Expectoration will be collected from the subjects during each product use.
The used study product will be collected after use.
Blood samples will be collected at each test visit, prior to study product use, for determination of plasma cotinine levels.
Study Type
Interventional
Enrollment (Actual)
53
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Georgia
-
Stockbridge, Georgia, United States, 30281
- Clinical Research Atlanta
-
-
Texas
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San Antonio, Texas, United States, 78229
- Clinical Trials of Texas
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Able to read, understand, and willing to sign an Informed Consent Form (ICF) written in English;
- Generally healthy males and females, 21 years of age or older, at Screening-Enrollment Visit;
- Self-reports currently using at least two cans of moist snuff per week;
- Self-reports that moist snuff is the only tobacco- or nicotine-containing product used within 30 days of the Screening-Enrollment Visit;
- Usual brand (UB) of moist snuff is one of the products specified in the protocol;
- Used their UB product for ≥ 3 months;
- Subject is not delaying a decision to quit using moist snuff to participate in the study;
- Agrees to exclusively use the study products and not use any other tobacco- or nicotine-containing products during the course of the study;
- Able to safely perform the required study procedures, as determined by the Investigator.
Exclusion Criteria:
- Self-reported history of heart disease, kidney disease, diabetes, liver disease, uncontrolled hypertension, or uncontrolled hypercholesterolemia;
- At risk for heart disease, i.e., obesity (body mass index [BMI] > 43 kg/m2), as determined by the Investigator;
- Females ≥ 35 years of age currently using systemic, estrogen-containing contraception, or hormone replacement therapy;
- Use of any medication or substance that aids in smoking cessation, including but not limited to any nicotine replacement therapy (NRT) (e.g., nicotine gum, lozenge, patch), varenicline (Chantix®), bupropion (Wellbutrin®, Zyban®), or lobelia extract within 30 days prior to the Screening-Enrollment Visit;
- Females who are pregnant or breastfeeding, or plan to become pregnant during the course of the study;
- Participation in another clinical study within 30 days prior to the Screening-Enrollment Visit. (The 30-day window for each subject will be derived from the date of the last study event in the previous study to the Screening-Enrollment Visit of the current study);
- Determined by the Investigator to be ineligible for the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: CSD170201AA, CSD170201AB Use Group
Use of product CSD170201AA exclusively for approximately one week (seven days +1/-2 day) prior to a test visit, followed by use of product CSD170201AB exclusively for approximately one week (seven days +1/-2 day) prior to a test visit.
|
A moist snuff product
A moist snuff product
|
Experimental: CSD170201AB, CSD170201AA Use Group
Use of product CSD170201AB exclusively for approximately one week (seven days +1/-2 day) prior to a test visit, followed by use of product CSD170201AA exclusively for approximately one week (seven days +1/-2 day) prior to a test visit.
|
A moist snuff product
A moist snuff product
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Mouth-Level Exposure (MLE) of nicotine per gram (or product)
Time Frame: 6 hours
|
6 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Nathan Segall, MD, Clinical Research Atlanta
- Principal Investigator: Jason Miller, DO, Clinical Trials of Texas
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 8, 2017
Primary Completion (Actual)
November 17, 2017
Study Completion (Actual)
November 17, 2017
Study Registration Dates
First Submitted
May 12, 2017
First Submitted That Met QC Criteria
May 12, 2017
First Posted (Actual)
May 15, 2017
Study Record Updates
Last Update Posted (Actual)
April 10, 2018
Last Update Submitted That Met QC Criteria
April 9, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- CSD170201
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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