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临床试验/NCT02185898
NCT02185898已完成不适用

A Single-Center Evaluation of Environmental Emissions From Electronic Cigarettes and Tobacco-Burning Cigarettes

R.J. Reynolds Vapor Company2 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2014年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
71
试验地点
2
主要终点
To assess differences in levels of selected SHS constituents in an environmental test chamber after human smoking of e-cigarette #1, #2, and #3 compared to after human smoking of tobacco-burning cigarettes.

研究概览

简要总结

This study will assess environmental emissions of selected compounds in a test chamber after cigarette smoking or e-cigarette vaping.

详细描述

Secondhand smoke is the aged and diluted combination of smoke exhaled by a smoker and sidestream smoke (smoke from the lit end of a cigarette). Electronic cigarettes are different from tobacco-burning cigarettes in that they produce vapor, not smoke. For consistency with common usage, secondhand smoke (SHS) refers to true secondhand smoke from cigarettes and secondhand vapor from e-cigarettes.

The goals of this study are to 1) increase understanding of the composition of SHS from e-cigarettes, 2) quantitatively compare the amount of SHS generated by e-cigarettes and a market sample of commercial e-cigarettes to leading brand styles of commercial tobacco-burning cigarettes, and 3) quantitate the emission factors of e-cigarettes including the market-sample e-cigarettes.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
21 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able to read, understand, and willing to sign an Informed Consent Form (ICF) and complete questionnaires written in English.
  • Generally healthy males or females, 21 years of age or older at Screening.
  • Able to meet cohort-specific requirements as follows:
  • Cohort 1 - Leading U.S. tobacco-burning non-menthol cigarette, and
  • Cohort 2 - Leading U.S. tobacco-burning menthol cigarette:
  • self-reports at the Screening Visit smoking at least 5 cigarettes per day and inhaling the smoke, for at least 3 months prior to Screening
  • self-reports smoking Leading U.S. tobacco-burning non-menthol cigarette or Leading U.S. tobacco-burning menthol cigarette as usual brand (UB) cigarettes [UB cigarette is defined as the cigarette brand style currently smoked most frequently by the participant];
  • Cohort 3 - Electronic cigarette #1 smokers, and
  • Cohort 4 - Electronic cigarette #2 smokers:
  • self-reports at the Screening Visit smoking a non-menthol e-cigarette at least once per day, for at least 3 months prior to Screening;
  • willing to switch from using their current e-cigarette brand style to using a different e-cigarette brand style during the study;
  • Cohort 5 - Electronic cigarette #3 smokers:
  • self-reports at the Screening Visit smoking a menthol e-cigarette at least once per day, for at least 3 months prior to Screening;
  • willing to switch from using their current e-cigarette brand style to using a different e-cigarette brand style during the study;
  • Cohort 6 - U.S Market-sample electronic cigarette smokers:
  • self-reports at the Screening Visit smoking the selected U.S. market-sample e-cigarettes (menthol or non-menthol) at least once per day, for at least three months prior to Screening;
  • willing to continue exclusive use of their preferred style (flavor) of e-cigarette during the study.
  • Females of childbearing potential must be willing to use a form of contraception acceptable to the Investigator from the time of signing informed consent until study discharge or be surgically sterile for at least 90 days prior to enrollment;
  • Able to safely perform the required study procedures, as determined by the Investigator.

排除标准

  • Clinically significant or unstable/uncontrolled acute or chronic medical conditions at Screening, as determined by the Investigator, that would preclude a participant from participating safely in the study (e.g., hypertension, asthma, or other lung disease; cardiac disease; neurological disease; or psychiatric disorders) based on screening assessments such as safety labs and medical history or physical examination at Enrollment;
  • Self-reports or safety labs indicate diabetes;
  • At risk for heart disease, as determined by the Investigator;
  • Use of medicine for treatment of depression or asthma;
  • Systolic blood pressure of ≥150 mmHg or a diastolic blood pressure of ≥95 mmHg, measured after being seated for 5 minutes;
  • Postponing a decision to quit smoking (defined as planning a quit attempt within 30 days of the Screening Visit) to participate in this study;
  • Employed by a tobacco company, the study site, or environmental test chamber vendor;
  • Females who have a positive pregnancy test, are pregnant, breastfeeding, or intend to become pregnant during the course of the study;
  • History of claustrophobia;
  • Regularly exposed to solvent fumes or gasoline (e.g., painter, gas-station mini mart employee);
  • Determined by the Investigator to be inappropriate for this study, including a participant who is unable to communicate or unwilling to cooperate with the clinical staff.

研究组 & 干预措施

Electronic cigarette #2

Experimental

VUSE® (original flavor, 29 mg nicotine)

干预措施: Electronic cigarette #2 (Other)

Leading U.S. tobacco-burning non-menthol cigarette

Active Comparator

Leading U.S. non-menthol cigarette

干预措施: Leading U.S. non-menthol cigarette (Other)

Leading U.S. tobacco-burning menthol cigarette

Active Comparator

Leading U.S. menthol cigarette

干预措施: Leading U.S. menthol cigarette (Other)

Electronic cigarette #1

Experimental

VUSE® (menthol flavor, 29 mg nicotine)

干预措施: Electronic cigarette #1 (Other)

Electronic cigarette #3

Experimental

VUSE® (original flavor, 14 mg nicotine)

干预措施: Electronic cigarette #3 (Other)

U.S. Market-sample electronic cigarettes (two brands)

Experimental

blu™ (any variety) and NJOY® (any variety)

干预措施: U.S. Market-sample electronic cigarettes (Other)

结局指标

主要结局

To assess differences in levels of selected SHS constituents in an environmental test chamber after human smoking of e-cigarette #1, #2, and #3 compared to after human smoking of tobacco-burning cigarettes.

时间窗: 2 weeks for participants in Cohorts 1 and 2; and approximately 4 weeks for participants in Cohorts 3, 4, and 5

次要结局

  • To determine selected SHS constituent emission factors for each tobacco-burning cigarette, each e-cigarette, and the market-sample e-cigarettes (collectively).(2 weeks for participants in Cohorts 1, 2, and 6; and approximately 4 weeks for participants in Cohorts 3, 4, and 5)
  • To assess the differences in levels of selected SHS constituents in an environmental test chamber after human smoking of e-cigarettes and tobacco-burning cigarettes compared to after a non-smoking blank condition.(2 weeks for participants in Cohorts 1, 2, and 6; and approximately 4 weeks for participants in Cohorts 3, 4, and 5)
  • To assess differences in levels of additional selected SHS constituents in an environmental test chamber after human smoking of e-cigarettes compared to after human smoking of tobacco-burning cigarettes.(2 weeks for participants in Cohorts 1, 2, and 6; and approximately 4 weeks for participants in Cohorts 3, 4, and 5)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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