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Pharmacokinetics and Pharmacodynamics of Synthetic Nicotine and Nicotine Analogues

I

Insel Gruppe AG, University Hospital Bern

Status

Not yet enrolling

Conditions

Nicotine Analogues
Nicotine
Synthetic Nicotine
Vaping

Treatments

Other: Vaping of racemic nicotine (S-/R-nicotine)
Other: Vaping of synthetic S-nicotine
Other: Vaping of 6-methylnicotine

Study type

Interventional

Funder types

Other

Identifiers

NCT07348224
BASEC-ID 2025-01893

Details and patient eligibility

About

Electronic cigarettes are battery-operated devices that can produce an aerosol by heating a liquid which commonly contains nicotine. In recent years, products containing synthetically produced nicotine and nicotine analogues have entered the market. However, it remains unclear whether these types of nicotine have the same effects as conventional nicotine derived from the tobacco plant. The aim of this study is to investigate the effects of these nicotine types and to gain a better understanding of their respective mechanisms of action.

Full description

In the first part of the study, participants will use electronic cigarettes containing synthetic nicotine or nicotine analogs at three sessions in the hospital, following a specific schedule. In the second part, each product will be used for four days outside the hospital. The study is double-blind, meaning neither the participants nor the study team will know which product is being used.

The study comprises a total of seven appointments at the hospital. During these appointments, participants will be asked questions about their electronic cigarette and tobacco use, and samples of saliva, urine, and blood will be collected.

Enrollment

24 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men or women, age 18 or older at screening who have used EC with nicotine during at least 10 of the past 30 days
  • Saliva cotinine concentration of > 30 ng/mL at screening
  • Ability to communicate well with the investigator and to understand and comply with the requirements of the study
  • Women of child-bearing age engaging in sexual activities which can lead to pregnancy: willingness of using a reliable/hormonal contraception method during the study (hormonal, e.g. pill, intrauterine devices, or mechanical method, e.g. condom, diaphragm)
  • Signed informed consent form

Exclusion criteria

  • Known hypersensitivity/allergy to a content of the e-liquids
  • Smoking of more than 5 cigarettes per day in the past 30 days
  • Pregnant or lactating women
  • Intention to become pregnant during the course of the study
  • BMI < 18 or > 30 kg/m2 at screening
  • History or clinical evidence of alcoholism or drug abuse within the 3-year period prior to screening
  • Loss of ≥ 250 mL of blood within 3 months prior to screening, including blood donation
  • Treatment with an investigational drug within 30 days prior to screening
  • Treatment with prescribed or over-the-counter medications with known influence on CYP2A6 function within 1 week prior to screening (with the exception of contraception)
  • History or clinical evidence of any disease (e.g. gastrointestinal tract-disease) and/or existence of any surgical or medical condition, which in the opinion of the investigator might interfere with the absorption, distribution, metabolism or excretion of the study drugs, or which might increase the risk of toxicity.
  • Legal incapacity or limited legal capacity at screening
  • Any circumstances or conditions, which, in the opinion of the investigator, may affect full participation in the study or compliance with the protocol

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

24 participants in 3 patient groups

Synthetic S-Nicotine
Other group
Description:
Vaping of e-liquids contanining synthetic S-nicotine
Treatment:
Other: Vaping of synthetic S-nicotine
Racemic nicotine (S-/R-nicotine)
Other group
Description:
Vaping of e-liquids contanining synthetic racemic nicotine (containing both the S- and R-nicotine enantiomers)
Treatment:
Other: Vaping of racemic nicotine (S-/R-nicotine)
6-methylnicotine
Other group
Description:
Vaping of e-liquids contanining the nicotine analogue 6-methylnicotine (6MN)
Treatment:
Other: Vaping of 6-methylnicotine

Trial contacts and locations

1

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Central trial contact

Evangelia Liakoni, Prof.

Data sourced from clinicaltrials.gov

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