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N/A N=22 Randomized Other

Comparative Abuse Liability Among African American and White Smokers

Tobacco Use Disorder

Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Jul 2023
Primary outcome: Primary: Nicotine Delivery — 14.13; 6.79; 9.15 ng/mL — p=0.002

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
E-cigarette and Heat not burn (Combination_product)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
University of Kansas Medical Center
Primary completion
Aug 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Nicotine Delivery
14.13; 6.79; 9.15 0.002 sig

Summary

The study is a randomized crossover trial. Current smokers will complete a session with each product: usual brand cigarette, e-cigarette, and heat-not-burn. The objective of this survey is to assess for ongoing use of study products and is part of safety monitoring.

Eligibility Criteria

Inclusion Criteria

  • Non-Hispanic African American or white/Caucasian,
  • ≥21 years old, smoke 5-30 cigarettes per day,
  • daily cigarette smoker
  • smoked at current rate for at least 6 months
  • interested in trying e-cigarettes and heat not burn products
  • not interested in or unable/unwilling to quit cigarette smoking
  • willing to complete three in-person study visits
  • willing to have IV catheter placed

Exclusion Criteria

  • Interested in quitting cigarettes in the next 30 days
  • use of smoking cessation pharmacotherapy in the past 30 days
  • use of non-cigarette tobacco products in the past 30 days
  • use of e-cigarettes >5x in lifetime
  • use of e-cigarettes ≥4 of the past 30 days
  • use of heat not burn products >5x in lifetime
  • use of heat not burn products ≥4 of the past 30 days
  • weight 10 miles from study site (Fairway CRU)
  • current enrollment is a research study or program that aims to alter tobacco use
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04646668). 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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