The e-BILD Study: Effects of E-cigarettes on Lung Health in Teenagers.

Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Recruiting
CT.gov ID
NCT05105555
Collaborator
University of Bern (Other)
60
1
21.9
2.7

Study Details

Study Description

Brief Summary

Electronic nicotine delivery systems (ENDS/e-cigarettes/vaping) are increasingly popular among teenagers around the world. The safety and potential adverse effects of ENDS in this population are largely unknown. While the aerosol, that users inhale, appears safe under laboratory conditions, there are still open questions, which have not yet been assessed. These cover (a) differences in exposure to chemicals (such as metabolites of Volatile Organic Compounds (VOCs) and metabolites of Polycyclic Aromatic Hydrocarbons (PAHs)) between healthy teenagers using ENDS and healthy teenagers not vaping, (b) effects of exposure to such chemicals on the body (measured by lung health indicators: airway symptoms such as coughing; lung function and lung structure tests; immune response of airway cells exposed to vapor; markers of oxidative stress), and (c) the role of nicotine metabolism. It is unknown which lung health indicator/s is/are most relevant to assess the effect of ENDS on lung health in teenagers.

The primary hypothesis of this study is that there will be differences in exposure to chemicals, resulting in more or more severe airway symptoms in vaping teenagers compared to their non-vaping peers. While there might not yet exist any differences regarding lung function or structure, we expect already visible effects of vaping on the local immune response of primary cells isolated from airways in vaping teenagers as compared to non-vaping peers.

In this study, participants of the Bern Basel Infant Lung Development (BILD) cohort, a birth cohort of healthy term-born infants and their follow-up, will serve as healthy, non-vaping controls.1 Vaping teenagers will be recruited independently from the BILD study through advertisements and visits to Bernese schools. Both populations combined represent the study population of the e-BILD study. All e-BILD study participants will undergo the same investigations. While these are currently planned for once in a time (so-called cross-sectional design) to compare results from non-vaping BILD study participants to otherwise healthy but vaping teenagers, repeated measures might follow, depending on the findings of the first phase.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    60 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    The e-BILD Study: Effects of Electric Nicotine Delivery Systems (ENDS) on Pulmonary Health in Teenagers.
    Anticipated Study Start Date :
    Dec 1, 2021
    Anticipated Primary Completion Date :
    Sep 1, 2022
    Anticipated Study Completion Date :
    Sep 30, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Healthy controls

    In this study, participants of the Bern Basel Infant Lung Development (BILD) cohort, a birth cohort of healthy term-born infants and their follow-up, will serve as healthy, non-vaping controls.

    Vaping teenagers

    Vaping teenagers will be recruited independently from the BILD study through advertisements and visits to Bernese schools.

    Outcome Measures

    Primary Outcome Measures

    1. Correlation of the respiratory symptom coughing with vaping status (validated by exposure markers) [At baseline]

      Questions on frequency and intensity of coughing in past 12 months. Assessment of exposure markers (urinary concentrations of metabolites of VOCs (volatile organic compounds), urinary concentrations of metabolites of PAHs (Polycyclic aromatic hydrocarbons), urinary concentrations of urinary TSNA (Tobacco Specific Nitrosamines), urinary concentration of nicotine metabolites) to discriminate between vapers and non-vapers [Time Frame: at baseline] Urine sampling

    2. Correlation of the respiratory symptom wheezing with vaping status (validated by exposure markers) [At baseline]

      Questions on frequency and intensity of wheezing in past 12 months. Assessment of exposure markers (urinary concentrations of metabolites of VOCs (volatile organic compounds), urinary concentrations of metabolites of PAHs (Polycyclic aromatic hydrocarbons), urinary concentrations of urinary TSNA (Tobacco Specific Nitrosamines), urinary concentration of nicotine metabolites) to discriminate between vapers and non-vapers [Time Frame: at baseline] Urine sampling

    Secondary Outcome Measures

    1. Correlation of validated vaping status with lung function (spirometry) in healthy teenagers [At baseline]

      Assessment of lung function (spirometry)

    2. Correlation of validated vaping status with lung function (bodyplethysmography) in healthy teenagers [At baseline]

      Assessment of lung function (bodyplethysmography)

    3. Correlation of lung function (multiple breath washout) in healthy teenagers [At baseline]

      Assessment of lung function (multiple breath washout)

    4. Correlation of validated vaping status with airway inflammation (exhaled nitric oxide) in healthy teenagers. [At baseline]

      Assessment of levels of exhaled nitric oxide (eNO) measured by chemoluminescence analyzers in combination with ultrasound-based flow measurement.

    5. Correlation of validated vaping status with lung structure (magnetic resonance imaging, MRI) in healthy teenagers. [At baseline]

      Assessment of regional lung perfusion and ventilation.

    6. Correlation of validated vaping status with measures of oxidative stress in healthy teenagers. [At baseline]

      Measurement of oxidative stress metabolites in urine.

    7. Correlation of validated vaping status with ex vivo immune response of nasal epithelial cells in healthy teenagers. [At baseline]

      Assessment of nasal epithelial cell immune response collected by nasal brushing.

    8. Role of nicotine metabolism on lung health indicators. [At baseline]

      Measurement of nicotine metabolites in urine and saliva.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 19 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Informed consent as documented by signature

    • BILD study participants: see inclusion criteria of BILD study (NCT04286464), non-vaping

    • e-BILD: healthy, term-born, vaping at least weekly (might include healthy, vaping participants from BILD)

    Exclusion Criteria:

    • None, except for general exclusion criteria of BILD study (NCT04286464)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Insel, Bern University Hospital Bern Switzerland 3010

    Sponsors and Collaborators

    • University Hospital Inselspital, Berne
    • University of Bern

    Investigators

    • Principal Investigator: Julian Jakob, MD, Institute of Primary Health Care BIHAM, Bern University
    • Principal Investigator: Reto Auer, MD, MAS, Institute of Primary Health Care BIHAM, Bern University
    • Principal Investigator: Philipp Latzin, MD, PhD, Inselspital, Bern University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital Inselspital, Berne
    ClinicalTrials.gov Identifier:
    NCT05105555
    Other Study ID Numbers:
    • YTCR3419
    First Posted:
    Nov 3, 2021
    Last Update Posted:
    Dec 6, 2021
    Last Verified:
    Nov 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 6, 2021