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N/A N=52 Randomized Triple-blind Treatment

Impact of E-cigarette Nicotine Concentration on Compensation

Smoking Cessation

Enrolled (actual)
52
Serious AEs
0.0%
Results posted
Sep 2025
Primary outcome: Primary: Total Inhaled Volume — 416.5; 490.3 mL

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Electronic Cigarette with 5% Nicotine Concentration (Device); Electronic Cigarette with 1.8% Nicotine Concentration (Device)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
University of Kansas Medical Center
Primary completion
May 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Total Inhaled Volume
416.5; 490.3
SECONDARY
Participant Switch Trajectory
10; 6; 10; 13; 3; 0

Summary

The study will be the first to assess the impact of nicotine concentration on compensatory puffing (total inhaled volume), nicotine delivery, and switch patterns (percent exclusive EC, dual cig-EC, and cig only users) with an explicit focus on AA and White smokers.

Eligibility Criteria

Inclusion Criteria

  • identify as non-Hispanic white or non-Hispanic African American/Black
  • willing to switch from smoking to e-cigarettes for 6 weeks
  • speak and understand English
  • smoke greater than or equal to 25 of the last 30 days for the past 3 months
  • not previously used an e-cigarette for longer than 30 days
  • exhaled carbon monoxide of greater than or equal to 6ppm at screener visit
  • willing to abstain from marijuana for 12 hours prior to in-person lab visits
  • willing to abstain from smoking and vaping for 12 hours prior to 3 in-person lab visits

Exclusion Criteria

  • weekly use of an EC over the last six months
  • use of tobacco products other than cigarettes on greater than or equal to 10 days in the past 30 days
  • use of EC on more than 5 of the past 30 days
  • current use of cessation medications
  • pregnant, planning to become pregnant, or breastfeeding
  • past 30 day hospitalization/ER visit for psychiatric issue, seizure, stroke, or new heart problem
  • recent history of cardiovascular or pulmonary events in the past three months
  • treatment for alcohol or drug dependence in the past year
  • household member currently or previously enrolled in the study
  • current enrollment in a program aimed at changing smoking patterns
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05887947). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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