Clinical Pharmacology of Electronic Cigarettes

Not Applicable

Completed

Conditions: Nicotine Dependence

Interventions: Device: Tobacco Cigarette
Device: Electronic Cigarette

Registration Number: NCT02470754

Lead Sponsor: University of California, San Francisco

Brief Summary: The purpose of this study is to learn more about nicotine exposure and the safety of electronic cigarettes (EC). It will focus on the areas that are thought to most closely relate to the addictive potential of EC, namely: (1) EC as nicotine delivery devices, covering issues of nicotine intake and pharmacokinetics, temporal patterns of use and titration of nicotine; and (2) subjective effects of EC use, including relationship of use to reward, withdrawal and craving.

Detailed Description: Electronic cigarettes (EC) are nicotine delivery devices that generate a nicotine-containing aerosol which is inhaled by the user. EC are perceived by users to be useful in helping quitting smoking of conventional tobacco cigarettes (TC) as well as having a presumed lower risk of adverse health effects compared to TC, the potential for use in public places, reduced cost, and lack of the noxious clinging odors associated with TC use. Many believe that electronic cigarette (EC) function as nicotine delivery devices in the same way as tobacco cigarettes (TC), and that EC will prove to be just as addictive as TC, but this may not be the case because of fundamental differences in the design and method of use of these products. Investigators hypothesize that systemic nicotine exposure will be lower with EC compared to TC; that despite lower nicotine intake EC users will experience similar reward and no greater withdrawal symptoms or craving compared to TC; and that dual EC/ TC users will not titrate their daily intake of nicotine in the same way that TC smokers of high- vs low-yield nicotine TC do.

Investigators specifically focus on the areas that are thought to most closely relate to the addictive potential of EC, namely: (1) EC as nicotine delivery devices, covering issues of nicotine intake and pharmacokinetics, temporal patterns of use and titration of nicotine; and (2) subjective effects of EC use, including relationship of use to reward, withdrawal and craving. The investigators will also examine aspects of safety of EC use (by assessment of cardiovascular and hormonal effects of use and of biomarkers of exposure to potentially toxic constituents) and explore the identification and validation of biomarkers that may be useful in distinguishing EC from TC use. Study subjects will be dual users of TC and EC so that the investigators may compare both modalities of use in experienced users in a within-subject design.

The study will consist of two 1-week blocks (EC-only or TC-only conditions) with 4 days of outpatient ad libitum product use followed by 3 days in a clinical research ward to include a single-use pharmacokinetic study, monitoring of product use, subjective assessments, blood and urine collections to assess biomarkers, and a 24-hour period of cardiovascular monitoring. Two additional days at the end of the 2nd block will assess similar measurements during a period of nicotine-product abstention.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 38

Inclusion Criteria

Healthy on the basis of medical history and limited physical examination as described below:
- Heart rate < 105 BPM*
- Systolic Blood Pressure < 160 and > 90*
- Diastolic Blood Pressure < 100 and > 50*
- Body Mass Index ≤ 38.0 *Considered out of range if both machine and manual readings are above/below these thresholds.
Current regular "dual" user of both EC and conventional TC
EC device is one of the most popular 1st, 2nd or 3rd generation brands (with the exception of rebuildable atomizers) as determined at time of study commencement
Carbon monoxide ≥ 5 ppm or per discretion of Principal Investigator
Saliva cotinine ≥50 ng/ml or urine cotinine
Age: ≥ 21 years

Exclusion Criteria

Current regular use of selected psychiatric medications
Current regular use of cardiovascular medications for cardiovascular conditions including hypertension (Example: beta and alpha-blockers)
Current regular use of medications inducers of nicotine metabolizing enzymes CYP2A6 (Example: rifampicin, dexamethasone, phenobarbital, and other anticonvulsant drugs).
Use of other tobacco products
Pregnancy or breastfeeding (by history and pregnancy test)
Concurrent use of nicotine-containing medications
Drug/Alcohol Dependence
Positive toxicology test at the screening visit (THC okay)
Concurrent participation in another clinical trial
Inability to communicate in English
Planning to quit smoking within the next 60 days

Study & Design

Study Type: INTERVENTIONAL

Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
EC Block1/TC Block 2	Tobacco Cigarette	Participants will be randomized into one of two groups. In this group, participants will be assigned to Electronic Cigarettes only for Study Block #1, then crossover to Tobacco Cigarettes only for Study Block #2.
TC Block 1/EC Block 2	Electronic Cigarette	Participants will be randomized into one of two groups. In this group, participants will be assigned to Tobacco Cigarettes only for Study Block #1, then crossover to Electronic Cigarettes only for Study Block #2.
EC Block1/TC Block 2	Electronic Cigarette	Participants will be randomized into one of two groups. In this group, participants will be assigned to Electronic Cigarettes only for Study Block #1, then crossover to Tobacco Cigarettes only for Study Block #2.
TC Block 1/EC Block 2	Tobacco Cigarette	Participants will be randomized into one of two groups. In this group, participants will be assigned to Tobacco Cigarettes only for Study Block #1, then crossover to Electronic Cigarettes only for Study Block #2.

Primary Outcome Measures

Name	Time	Method
Standardized Session: Mean TMax	Inpatient Day 1, Up to 4 Hours post Session	Time (min) when Max Plasma Nicotine Concentration was achieved
Standardized Session: Mean CMax	Inpatient Day 1, Up to 4 Hours post Nicotine Administration	Maximum Plasma Nicotine Concentration (Cmax) (ng/mL)
Standardized Session: AUC 0-240	Inpatient Day 1, Up to 4 Hours post Session	Plasma Nicotine area-under-the curve from 0 to 4 Hours (min\*ng/ml)
PK-estimated Nicotine Dose	Inpatient Day 1, Up to 4 Hours post Session	Estimated in dose received (in milligrams) during the Standardized Session.

Secondary Outcome Measures

Name	Time	Method
Standardized Session: Positive and Negative Affect Score (Negative Affect)	Inpatient Day 1, Up to 4 Hours post Session	The PANAS Scale or Positive and Negative Affect Schedule (PANAS) is a self-report questionnaire. PANAS, (Sandín et al., 1999; Watson, Clark \& Tellegen, 1988).This instrument is composed of 20 items: 10 items measuring positive affective states and 10 items measuring negative affect states.This subscale measures a person's negative emotions. Scores range from 10- 50 with higher scores indicating stronger negative feelings.
Standardized Session: QSU Factor 1 (Smoking)	Inpatient Day 1, Up to 4 Hours post Session	Questionnaire for Smoking Urges Brief measures urge to smoke.Two factor scores and a total score were derived. Factor 1 represents the desire and intention to smoke with smoking perceived as rewarding, while Factor 2 represents an anticipation of relief from negative effect with an urgent desire to smoke. Scores range from 5 to 35 with higher scores indicating a higher level of craving.
Standardized Session: QSU Factor 2 (Smoking)	Inpatient Day 1, Up to 4 Hours post Session	Questionnaire for Smoking Urges Brief measures urge to smoke.Two factor scores and a total score were derived. Factor 1 represents the desire and intention to smoke with smoking perceived as rewarding, while Factor 2 represents an anticipation of relief from negative effect with an urgent desire to smoke. Scores range from 5 to 35 with higher scores indicating a higher level of craving.
Standardized Session: QSU Factor 1 (Vaping)	Inpatient Day 1, Up to 4 Hours post Session	Questionnaire for Smoking Urges Brief modified for e-cigarettes to measure urge to vape.Two factor scores and a total score were derived. Factor 1 represents the desire and intention to smoke with smoking perceived as rewarding, while Factor 2 represents an anticipation of relief from negative effect with an urgent desire to smoke.Scores range from 5 to 35 with higher scores indicating a higher level of craving.
Standardized Session: Minnesota Nicotine Withdrawal Scale	Inpatient Day 1, Up to 4 Hours post Session	Minnesota Nicotine Withdrawal Scale (MNWS) is a Self-Report Scale for measuring the severity of nicotine withdrawal symptoms.The possible range of scores for the 12-Item MNWS is between 0 and 48 with higher scores indicated greater withdrawal symptom severity.
Standardized Session: QSU Factor 2 (Vaping)	Inpatient Day 1, Up to 4 Hours post Session	Questionnaire for Smoking Urges Brief modified for e-cigarettes to measure urge to vape.Two factor scores and a total score were derived. Factor 1 represents the desire and intention to smoke with smoking perceived as rewarding, while Factor 2 represents an anticipation of relief from negative effect with an urgent desire to smoke. Scores range from 5 to 35 with higher scores indicating a higher level of craving.

Trial Locations

Locations (2): San Francisco General Hospital (SFGH)
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San Francisco, California, United States
University of California, San Francisco (UCSF)
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San Francisco, California, United States