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Toxins and Delivery in e-Cigarette Users (TADEUS)

Q

Queen Mary University of London

Status

Completed

Conditions

Smoking Cessation

Treatments

Other: e-Cigarette

Study type

Observational

Funder types

Other

Identifiers

NCT01714778
QMUL201208a

Details and patient eligibility

About

Electronic cigarettes or "e-cigarettes" (EC) may have a potential public health benefit as a safer alternative to smoking and possibly also as an aid in tobacco dependence treatment. However, there are concerns about their safety and whether they can deliver nicotine consistently and in doses necessary for such effects.

To be able to consider the safety of ECs and their potential in harm reduction, data are needed comparing the exposure to the potential toxicant, acrolein, in smokers of conventional cigarettes, users of EC, and people who use both products at the same time.

To accurately assess EC nicotine delivery, data are needed from people who use them regularly, as there is some evidence of higher and faster nicotine absorption in experienced users compared with naïve users who try them once in an artificial laboratory setting.

This study will provide information on both of these issues. Forty smokers will be given EC to use, in addition to behavioural support, as part of a stop smoking attempt. Levels of acrolein and nicotine will be measured before and after 4 weeks of EC use.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Smokers who want help in quitting
  • Aged 18 or over

Exclusion criteria

  • Women who are pregnant or breastfeeding
  • People with any current serious illness

Trial design

40 participants in 1 patient group

e-Cigarette
Description:
Smokers attempting to quit with behavioural support and e-Cigarettes.
Treatment:
Other: e-Cigarette

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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