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A RCT to Determine the Effect of ENDS Flavor Availability on Abstinence Within Smokers

NCT07172438 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 668

Last updated 2026-02-27

No results posted yet for this study

Summary

The overall purpose of this study will be to assess primary combustible cigarette users' abstinence from smoking their usual brand of combustible cigarettes at the end of the study, when provided with an electronic nicotine delivery system (ENDS) power unit (2) and varying levels of access to tobacco-flavored, menthol-flavored, or non-tobacco/non-menthol-flavored cartridge-based e-liquids (collectively referred to as the investigational product) within their assigned study arm over a three-month (ninety-day) period.

Conditions

  • Smoking
  • Tobacco

Interventions

OTHER

P2611222

Menthol flavor

OTHER

P2615022

Non-tobacco non-menthol flavor

OTHER

P2615122

Non-tobacco non-menthol flavor

OTHER

P2613422

Tobacco flavor

Sponsors & Collaborators

  • RAI Services Company

    lead INDUSTRY

Principal Investigators

  • Melissa Tapia, Ph.D. · RAIS Service Co

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2025-09-17
Primary Completion
2026-01-14
Completion
2026-01-14

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 NCT07172438 on ClinicalTrials.gov