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Alternate Nicotine Delivery Systems and Airway Epithelial Biology

Alternate Nicotine Delivery Systems and Airway Epithelial Biology

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01974063
Enrollment
96
Registered
2013-11-01
Start date
2013-03-31
Completion date
2017-05-31
Last updated
2018-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking, Smoking Cessation

Keywords

Smoking, Smoking Cessation, Healthy Smoker, Shisha Smoker, Non-smoker

Brief summary

Cigarette smoking evokes major changes in the biology of the airway epithelium, the cell population that takes the brunt of the stress of cigarette smoke and the cell population central to the pathogenesis of chronic obstructive pulmonary disease (COPD) and lung cancer. The focus of this study is to identify the differences that two popular alternative nicotine delivery strategies, shisha and electronic cigarettes, have on the airway epithelium compared to cigarette smoking. We hypothesize that both alternative nicotine delivery strategies disorder airway epithelial biology, but in different ways than does cigarette smoking.

Detailed description

Hypothesis and Research Questions We hypothesize that shisha smoking and electronic cigarettes both disorder airway biology, but this disordered biology differs from that resulting from cigarette smoking, suggesting that these alternative nicotine delivery methods will cause lung disease, but perhaps with phenotypes different from that of cigarette smoking. Aim 1: To assess the hypothesis that shisha smoking disorders the biology of the airway epithelium, but that these changes are distinct from that of cigarette smokers. Aim 2: To evaluate the hypothesis that when the smoker switches from smoking cigarettes to smoking electronic cigarettes, there is a partial normalization of the disordered airway epithelial biology, but that this partial normalization is different from that associated from complete cessation of cigarette smoking. Standard and Experimental Procedures All of the study populations and assessments to be carried out in this protocol are already covered under the IRB approved protocol, Collection of Airway, Blood and/or Urine Specimens from Subjects for Research Studies (IRB #1204012331); the only purpose of this protocol is to formalize the timing of assessments so that the underlying hypothesis can be assessed. The above protocol is designed to assess gene expression in lung cells of nonsmokers, smokers and ex-smokers. The purpose of the present study is to asses if shisha smoking and electronic cigarettes both disorder airway biology, and see if this disordered biology differs from that resulting from cigarette smoking, suggesting that these alternative nicotine delivery methods will cause lung disease, but perhaps with phenotypes different from that of cigarette smoking. This new protocol will use our existing IRB approved protocol, Collection of Airway, Blood and/or Urine Specimens from Subjects for Research Studies (Airway) (IRB #1204012331), for all of the assessments and procedures of this study. This protocol is designed to formalize the time points at which we carry out the various test parameters (see Table II for a timeline of the study parameters). Recruitment for this protocol will be from the cohort of individuals who are recruited for the Airway study. Research subjects recruited into this protocol, will sign both the Airway informed consent form and also the consent form for this protocol. The standard clinical care of our pulmonary physicians is to encourage all smokers to stop smoking; hence, all research participants who smoke will be encouraged to stop smoking. If they decide to do so, they will receive standard of care smoking cessation aids including counseling and medications. Subjects enrolled in Group E of the study will receive an alternative nicotine delivery method such as electronic cigarettes.

Interventions

None listed

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Group A - Nonsmokers * All study subjects should be healthy according to the Weill Cornell IRB protocol #1204012331 and be willing and able to provide informed consent for the follow up study with repeated bronchoscopies. * Subjects will be male and female ≥18 yr of age. * Nonsmoker is defined as someone who has smoked \<100 cigarettes or \<10 shisha pipes per lifetime and whose urine nicotine \<2 ng/ml and/or urine cotinine \<5 ng/ml, at entry into the study. Group B - Current cigarette smokers * All study subjects should be healthy according to the Weill Cornell IRB protocol #1204012331 and willing and able to provide informed consent for the follow up study with repeated bronchoscopies. * Subjects will be male and female ≥18 years of age. * Active smoker is defined by self-report and urine nicotine \>30 ng/ml and/or urine cotinine \>50 ng/ml. Group C - Current shisha smokers * All study subjects should be healthy according to the Weill Cornell IRB protocol #1204012331 and willing and able to provide informed consent for the follow up study with repeated bronchoscopies. * Subjects will be male and female ≥18 yr of age. * Shisha smoker is defined by self-report of smoking \>4 pipes/wk and carboxyhemoglobin \>2.5. Group D - Current smokers who stop smoking * All study subjects should be healthy according to the Weill Cornell IRB protocol #1204012331 and willing and able to provide informed consent for the follow up study with repeated bronchoscopies. * Subjects will be male and female ≥18 years of age. * Current smoker is defined by self-report and urine nicotine \>30 ng/ml and/or urine cotinine \>50 ng/ml. * Subjects must be a current smoker willing to stop smoking with no contra indications to taking varenicline. Group E - Current smokers who switch to electronic cigarettes * All study subjects should be healthy according to the Weill Cornell IRB protocol #1204012331 and willing and able to provide informed consent for the follow up study with repeated bronchoscopies. * Subjects will be male and female ≥18 years of age. Current smoker is defined by self-report and urine nicotine \>30 ng/mL and/or urine cotinine \>50 ng/ml. * Subjects must be willing to switch from tobacco cigarettes to electronic cigarettes.

Exclusion criteria

All

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with gene expression changes in the small airway epithelium (SAE)Study individuals will be enrolled in the study for three months.We will measure the effect that shisha smoking has on the small airway epithelium (SAE) by measuring parameters such as the SAE gene expression, DNA methylation, telomere length and cilia length in pure shisha smokers (i.e., non-cigarette smokers.) We will compare these parameters to the same parameters measured in non-smokers and cigarette smokers.

Secondary

MeasureTime frameDescription
Number of participants with gene expression changes in the airway epitheliumStudy individuals will be enrolled in the study for three months.We will measure the small airway epithelium (SAE) of cigarette smokers who switch to smoking electronic cigarettes by measuring parameters such as the SAE gene expression, DNA methylation, telomere length and cilia length. We will compare these parameters to the same parameters measured in cigarette smokers who stop smoking completely.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026