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CSD1805: Study to Assess Nicotine Uptake and Product Use Behavior in Moist Snuff Consumers Using Two Moist Snuff Products

NCT03688776 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2020-09-25

No results posted yet for this study

Summary

The purpose of this study is to compare nicotine uptake and product use behavior during and following use of two moist snuff products in generally healthy, adult moist snuff users.

Conditions

  • Tobacco Use

Interventions

OTHER

1805AA

A moist snuff product

OTHER

1805AB

A moist snuff product

Sponsors & Collaborators

  • ICON Clinical Research Limited

    collaborator UNKNOWN

  • RAI Services Company

    lead INDUSTRY

Principal Investigators

  • Emanuel DeNoia, MD · ICON Clinical Research

  • Melanie Fein, MD · High Point Clinical Trial Center

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
21 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-10-19
Primary Completion
2018-12-02
Completion
2018-12-02

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03688776 on ClinicalTrials.gov