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N/A N=68 Randomized Other

A Trial of E-cigarettes in Current Cigarette Smokers

Smoking · Nicotine Dependence · Nicotine Dependence, Other Tobacco Product

Enrolled (actual)
68
Serious AEs
0.0%
Results posted
Apr 2018
Primary outcome: Primary: Uptake of Electronic Nicotine Delivery Systems (ENDS) — 57.14; 32; 13.64 percentage of participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
electronic cigarette (Other); cigarette group (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Medical University of South Carolina
Primary completion
May 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Uptake of Electronic Nicotine Delivery Systems (ENDS)
57.14; 32; 13.64
PRIMARY
Independent Purchase of an ENDs Product
57; 28; 14
PRIMARY
% Quit Attempts
47.6; 40; 27.3
PRIMARY
Point Prevalence Abstinence
9.5; 4.0; 4.6

Summary

The purpose of this study is to examine cigarette smokers' use of electronic cigarettes (e-cigarettes), and how use of e-cigarettes affects short term smoking behavior.

Eligibility Criteria

Inclusion Criteria

  • age 18+
  • current smoker of at least 5 cigarettes per day for at least 1 year
  • at least some concern for health effects of smoking
  • having an easily accessible email address

Exclusion Criteria

  • past six month use of any e-cigarette
  • lifetime ever purchase of any e-cigarette
  • recent history of cardiovascular distress (heart attack in past year; arrhythmia; uncontrolled hypertension)
  • recent history (past 3 months) of Chronic Obstructive Pulmonary Disease (COPD), cancer (any non-dermatologic), or uncontrolled diabetes mellitus
  • pregnant or breastfeeding
  • any major current psychiatric impairment, including current alcohol/drug abuse/dependence
  • use of non-cigarette tobacco products (e.g., cigarillos) in the last 30 days
  • current use of any smoking cessation medications
  • current enrollment in a smoking cessation treatment study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02357173). 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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