Early Phase 1
N=35
Bronchoscopy in Determining the Effect of E-Cigarette Smoking on Biomarkers in the Lungs
Cigarette Smoker · Current Every Day Smoker
Bottom Line
View on ClinicalTrials.gov: NCT03691350 ↗Enrolled (actual)
35
Serious AEs
0.0%
Results posted
Apr 2026
Primary outcome: Primary: Changes in Cytokines — 0.2473; -0.04988; -0.1137; -0.05875 pg/ml
Study Design & Population
- Study type
- Interventional
- Phase
- Early Phase 1
- Interventions
- Bronchoscopy with Bronchoalveolar Lavage (Procedure); Cigarette (Drug); Electronic Cigarette (Other); Laboratory Biomarker Analysis (Other); Nicotine Replacement (Drug); Questionnaire Administration (Other)
- Age
- Adult · 21+ yrs
- Sex
- All
- Sponsor
- Ohio State University Comprehensive Cancer Center
- Primary completion
- Oct 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Changes in Cytokines |
0.2473; -0.04988; -0.1137; -0.05875; 0.04439; -0.01088 | — |
| PRIMARY Changes in Cell Counts |
367938; -42479; -147825; -340625; 4.25; -4.667 | — |
| SECONDARY Changes in Fractional Exhaled Nitric Oxide (FeNO) Levels |
0; 3.5; 1.2; -0.5 | — |
| SECONDARY Changes in Messenger (m) Ribonucleic Acid (RNA) and microRNA (miRNA) Gene Expression Analyzed Using Sequencing |
— | — |
| SECONDARY Changes in Deoxyribonucleic Acid (DNA) Gene Methylation |
0; 0; 0; 0 | — |
| SECONDARY Changes in the Microbiome in BAL Cells and Saliva |
0; 0; 0; 0 | — |
| SECONDARY Changes in Untargeted Metabolomics Using Mass Spectrometry |
0; 0; 0; 0 | — |
Summary
This trial studies biomarkers obtained by bronchoscopy (bronchoalveolar lavage and lung brushings) to determine the effect of smoking e-cigarettes on the lungs. Studying samples of lung cells from participants who smoke e-cigarettes may help doctors learn more about changes that occur in deoxyribonucleic acid and identify biomarkers related to cancer.
Eligibility Criteria
Inclusion Criteria
- Smokers who smoke >= 5 filtered cigarettes/day for >= 1 year
- No unstable or significant medical conditions as determined by medical history to ensure safety of the subject, to minimize the effects of poor health on biomarker measures and to maximize compliance to study procedures
- Able to read adequately to complete the survey and related study documents or give consent
- Subject has provided written informed consent to participate in the study
Exclusion Criteria
- Regular consumption of roll your own cigarettes
- Immune system disorders requiring medication
- Prior diagnosis of chronic pulmonary disease (e.g., asthma with regular use of medications, chronic obstructive pulmonary disease [COPD], chronic bronchitis, and restrictive lung disease)
- Acute bronchitis or pneumonia within 1 year
- Reported history of diagnosed kidney or liver disease
- Any medical disorder that will increase the risk from bronchoscopy, affect biomarker data, or increase risk of an adverse effect from e-cig use
- General anesthesia within 1 year
- Regular use of inhalant medications in the last 2 months
- Use of antibiotics in prior 30 days
- Use of steroids, including corticosteroids, in prior 30 days
- Allergies to study medications, such as, lidocaine, Versed, fentanyl or Cetacaine
- Allergies to propylene glycol/glycerin or flavors
- History of hypersensitivity to varenicline
- Bronchoscopy or any other lung procedure for any reason within the previous 6 months
- Current or recent (within three months) alcohol or drug abuse problems
- Regularly smoked marijuana within the prior 3 months
- Use of an e-cigarette or other combustible tobacco products in the prior 3 months
- Currently using nicotine replacement or other tobacco cessation products (to minimize confounding effects of another product) or intention to quit in next three months
- Adverse reaction to previous e-cig use
- Body mass index (BMI) > 40 (risk of unstable airway)
- Pregnant or breastfeeding - if the subject is female, a urine pregnancy test at no cost to the subject will be done on the day of bronchoscopy
- Unable to read for comprehension or completion of study documents
Data sourced from ClinicalTrials.gov (NCT03691350). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.