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Healthy Lifetime Non-smokersNCT02585791

Evaluation of Acute and Subacute Effects of Nicotine Free Electronic Cigarette(NCFE) Vapors

A study testing Propylene Glycol, vegetable glycerin and PG+VG in people with Healthy Lifetime Non-smokers, run by University of Miami at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

This aim will examine the acute and subacute exposures to electronic cigarette (EC) vapor generated from e-liquids without nicotine (NFEC) on life-time non smokers subjects by measuring changes in nasal ion transport and TGF-β levels. Nasal ion transport will be assessed by nasal potential difference (NPD). Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Healthy Lifetime Non-smokers
What is being tested?
Propylene Glycol, vegetable glycerin and PG+VG
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
22 Feb 2017to 11 Dec 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Subjects will be over 18 years of age.
  • Healthy life-time non-smokers

Who cannot join

  • Presence of airflow obstruction (COPD, asthma, bronchiectasis)
  • Other concomitant inflammatory pulmonary disorders
  • Subjects with known pulmonary malignancies within 5 years
  • Subjects with prior thoracic surgery
  • Subjects with respiratory infection that required use of oral corticosteroids and/or antibiotics within the prior 3 months
  • Subjects with allergies to study medications
  • Subjects incapable of providing informed consent.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Miami School of Medicine

    Miami, Florida, 33136

Other trials in United States

About this study

Official title: EVALUATION OF ACUTE AND SUBACUTE EFFECTS OF NICOTINE FREE ELECTRONIC CIGARETTE (NFEC) VAPORS -Aim 2.1 of "Adverse Effects of Inhaled Nicotine From Tobacco and E-cigarettes".

This aim will examine the acute and subacute exposures to electronic cigarette (EC) vapor generated from e-liquids without nicotine (NFEC) on life-time non smokers subjects by measuring changes in nasal ion transport and TGF-β levels. Nasal ion transport will be assessed by nasal potential difference (NPD). Tumor growth factor (TGF)-β levels (mRNA and protein by ELISA) will be assessed on nasal cells and lavages.

Read the detailed description

The recent introduction of electronic cigarettes (ECs) to provide habitual smokers a source of nicotine without the need to inhale tobacco smoke is thought to reduce toxicity to airway epithelial cells. The use of ECs decreases use of traditional cigarettes diminishes nicotine withdrawal symptoms leads to opposite effects on exhaled NO levels compared to tobacco and may diminish stimulation of reward centers in the brain leading to less dependence due to the lack of other tobacco-derived chemicals. The manufacturers of ECs tout comparative safety as a reason to switch from traditional tobacco cigarettes to their products. However the dearth of data supporting this claim led the FDA to issue warning letters to these companies. For now, the World Health Organization recommends against EC use until ECs have been properly evaluated. On the other hand, the American Association of Public Health Physicians support the use of ECs as a means of "Harms Reduction" since ECs provide nicotine without the myriad of other toxic chemicals produced from burning tobacco. These recommendations are mostly due to theoretical considerations and expert opinion. Due to the novelty of the ECs, many concerns of their safety on health and long-term nicotine addiction remain unanswered due to a lack of studies that comprehensively evaluate their toxicity in the airways.

Moreover, ECs produce vapor mainly from propylene glycol (PG) or vegetable glycerin (VG) that are blended at different concentrations, making comprehensive testing more difficult.

The lack of consistent results demands a full evaluation of EC toxicity in the airway even when nicotine is not inhaled.

In our laboratory using cultures of primary normal human bronchial epithelial(NHBE) cells (either differentiating or fully differentiated) exposed to EC vapor or an equivalent volume of filtered air we have demonstrated that EC vapor can be delivered to fully differentiated NHBE cells and that high, but realistic puff numbers decrease ciliary beat frequency (CBF) as well as Large, Ca2+-activated K+ channels (BK channel) (the pore forming α subunit KCNMA1) and Forkhead box protein (FOXJ)-1 expression. We also have preliminary data of smoke exposure in vitro and in vivo, showing a negative effect of cigarette smoke and nicotine on parameters of mucociliary clearance (MCC) and nasal potential difference (NPD), a way to assess ion transport in vivo. These changes occurred in a TGF-β-dependent manner.

This study is designed to evaluate the airway toxicity of NFECs (Aim 2.1 of the project "Adverse effects of inhaled nicotine from tobacco and e-cigarettes").

PRIMARY ENDPOINT As the primary endpoint, we will assess the consequences of vaping EC liquid with no nicotine (NFEC) on cystic fibrosis transmembrane (CFTR)- and calcium-activated chloride channel (CaCC)-mediated chloride conductance in lifetime non-smokers using nasal potential difference (NPD) measurements.

We will use NPD as a primary endpoint because changes in most clinical parameters will only be seen after months or even years of exposure. For that particular reason, there is a recent surge to find alternative biomarkers that may be used as surrogate endpoints in shorter clinical trials. Since NPD directly measures the changes in ion transport expected to influence MCC and therefore overall outcome and since changes of NPD measurements are indirectly linked to lung function changes and MCC in trials with cystic fibrosis (CF) patients, we believe that NPD lends itself as a reasonable surrogate for MCC for this study.

SECONDARY ENDPOINTS Nasal nitric oxide and TGF-ß levels in nasal lavage and cells will be also collected to correlate with the changes on NPD results after exposure to NFEC.

STUDY DESIGN This aim will examine whether acute and subacute exposures to NFEC vapors have adverse effects on lifetime non-smokers by measuring changes in nasal ion transport and TGF-β levels. Nasal ion transport will be assessed by nasal potential difference (NPD), which measures the voltage potential resulting from epithelial ion fluxes (both Na+ absorption and Cl- and K+ secretion at the mucosal surface in vivo. In normal airway epithelia, Na+ absorption is the primary ion transport activity so that the resulting airway surface potential difference is negative with reference to the interstitium. Ion transport across nasal epithelia is representative for findings in distal airways. We also believe that NPD is a reasonably sensitive biomarker for this study as discussed below. Therefore, we will evaluate the acute effects of NFEC vapor generated from the nicotine-carrier system ("e-liquid" without nicotine) and the subacute effect after a 7-days exposure to the NFEC.

Since the major difference between the ECs is the amount of vapor produced per puff, we will focus on a commonly used mini and mid-sized EC: Halo (The Halo company, USA) and eGo-T® (Joyetech Co., Ltd., ShenZhen China), and examine different vapor fluids or "e-liquids" (100% PG, 50% PG/50% VG and 100% VG) without nicotine.

Being tested
Propylene Glycol, vegetable glycerin, PG+VG
Keywords
electronic cigarette, airway inflammation, nasal potential difference
Medical subject headings
Vaping

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Propylene GlycolOther

    inhaled Propylene Glycol (PG) by vaporing

  • vegetable glycerinOther

    inhaled vegetable glycerin (VG) by vaporing

  • PG+VGOther

    inhaled PG+VG by vaporing

Study groups in NCT02585791
Study groupRoleWhat they receive
vape NFEC containing 100% PGExperimentalSubjects will then be instructed how to use the NFEC (eGo-T® with light emitting diode (LED) display) for 1 week of regularly vaping NFEC containing 100% Propylene Glycol . Subjects will be given the eGo-T®, which contains a 1.2 ml refillable cartridge and a 1100 mAh battery with an LED display to record the number of puffs. Subjects will be asked to puff 100x per day (equivalent to ~10-11 cigarettes) for 7 days. We will accept a vaping range of 80-120 times a day.
Receives: Other: Propylene Glycol
vape 100% vegetable glycerin -VGExperimentalSubjects will then be instructed how to use the NFEC (eGo-T® with LED display) for 1 week of regularly vaping NFEC containing 100% VG. Subjects will be given the eGo-T®, which contains a 1.2 ml refillable cartridge and a 1100 mAh battery with an LED display to record the number of puffs. Subjects will be asked to puff 100x per day (equivalent to ~10-11 cigarettes) for 7 days. We will accept a vaping range of 80-120 times a day.
Receives: Other: vegetable glycerin
vape PG+VGExperimentalSubjects will then be instructed how to use the NFEC (eGo-T® with LED display) for 1 week of regularly vaping NFEC containing 50% PG and 50% VG. Subjects will be given the eGo-T®, which contains a 1.2 ml refillable cartridge and a 1100 milliamp hours (mAh) battery with an LED display to record the number of puffs. Subjects will be asked to puff 100x per day (equivalent to ~10-11 cigarettes) for 7 days. We will accept a vaping range of 80-120 times a day.
Receives: Other: PG+VG

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. changes on nasal potential difference (NPD) measurements

    NPD will be measured at baseline and 7 days after the vapor

    Measured: before and after 7 days of vapor

Secondary outcomes (2)
  1. changes on nasal nitric oxide

    Nitric oxide will be measured at baseline and 7 days after the vapor

    Measured: before and after 7 days of vapor

  2. changes on TGF-ß levels in nasal lavage

    TGF-ß will be measured at baseline and 7 days after the vapor

    Measured: before and after 7 days of vapor

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Oct 2015 (estimated)
  2. Study start22 Feb 2017
  3. Primary completion11 Nov 2019
  4. Study completion11 Dec 2019

Why it stopped: due to recent release reports from CDC about lung injury due to vaping, the PI and IRB decided to terminate the study

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Single group
Masking
Single blind
Who is masked
Participant
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02585791
Sponsor's protocol ID
20150373
Status last verified
Jan 2020
First submitted
22 Oct 2015
Last updated
14 Jan 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Propylene Glycol, vegetable glycerin and PG+VG in people with Healthy Lifetime Non-smokers, run by University of Miami at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 14 Jan 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: due to recent release reports from CDC about lung injury due to vaping, the PI and IRB decided to terminate the study). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

changes on nasal potential difference (NPD) measurements (time frame: before and after 7 days of vapor). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jan 2020.

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