Clinical Pharmacology of Electronic Cigarettes

Nicotine Dependence Clinical Trial

Official title:

Clinical Pharmacology of Electronic Cigarettes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02470754
• Other study ID #: 15635
• Secondary ID: R01DA039264NCI-2
• Status: Completed
• Phase: N/A
• Start date: July 23, 2015
• Est. completion date: February 2, 2018

Study information

• Verified date: June 2023
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: February 2, 2018
• Est. primary completion date: February 2, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Nicotine Dependence
• Tobacco Use Disorder

Intervention

Device:
• Tobacco Cigarette
Usual brand tobacco cigarette smoked by study participant.
• Electronic Cigarette
Usual brand electronic cigarettes smoked by study participant.

Locations

Country	Name	City	State
United States	San Francisco General Hospital (SFGH)	San Francisco	California
United States	University of California, San Francisco (UCSF)	San Francisco	California

Sponsors (4)

Lead Sponsor	Collaborator
University of California, San Francisco	National Institute on Drug Abuse (NIDA), National Institutes of Health (NIH), Roswell Park Cancer Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Standardized Session: Half-life	Estimated Time (min) to reduce the plasma nicotine concentration by half based on observed pharmacokinetics.	Inpatient Day 1, Up to 4 Hours post Session
Primary	Standardized Session: Mean CMax	Maximum Plasma Nicotine Concentration (Cmax) (ng/mL)	Inpatient Day 1, Up to 4 Hours post Nicotine Administration
Primary	Standardized Session: Mean TMax	Time (min) when Max Plasma Nicotine Concentration was achieved	Inpatient Day 1, Up to 4 Hours post Session
Primary	Standardized Session: AUC 0-240	Plasma Nicotine area-under-the curve from 0 to 4 Hours (min*ng/ml)	Inpatient Day 1, Up to 4 Hours post Session
Primary	PK-estimated Nicotine Dose	Estimated in dose received (in milligrams) during the Standardized Session.	Inpatient Day 1, Up to 4 Hours post Session
Secondary	Standardized Session: QSU Factor 1 (Vaping)	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.	Inpatient Day 1, Up to 4 Hours post Session
Secondary	Standardized Session: Positive and Negative Affect Score (Negative Affect)	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.	Inpatient Day 1, Up to 4 Hours post Session
Secondary	Standardized Session: Minnesota Nicotine Withdrawal Scale	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.	Inpatient Day 1, Up to 4 Hours post Session
Secondary	Standardized Session: QSU Factor 2 (Vaping)	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.	Inpatient Day 1, Up to 4 Hours post Session
Secondary	Standardized Session: QSU Factor 1 (Smoking)	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.	Inpatient Day 1, Up to 4 Hours post Session
Secondary	Standardized Session: QSU Factor 2 (Smoking)	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.	Inpatient Day 1, Up to 4 Hours post Session