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E-Cig UseNCT06860698

The Impact of Chronic E-Cigarette Usage on Microvascular Health

An observational study of E-Cig Use, run by Virginia Commonwealth University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study is focused on investigating the mechanisms involved in microvascular health in subjects that use e-cigarettes frequently. To explore microvascular health, different techniques and compounds. Read more about this study

Who is it for?
Ages 18 to 29 yearsHealthy volunteers can take part
Conditions the study is for
E-Cig Use
What is being tested?
E-cig use
How many people
41 participants
Where
1 siteUnited States
Study dates
14 Jul 2023to 2 Jun 2025
Phase
Observational
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 to 29 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Chronic e-cigs users and never users that are between 18 and 29 years of age.

Who may be able to join

  • Between 18 and 29 years of age
  • Used e-cigarettes with nicotine (≥3 times/week for ≥6 months)
  • Between 18 and 29 years of age

Who cannot join

  • 17 years old and younger or 30 years old or older.
  • Former combustible tobacco user/ former smoker
  • Use of cigarettes for 15 days or more in the past 60 days
  • Use of other tobacco products (cigars, hookah, smokeless), marijuana and/or illicit or prescription drugs weekly or more frequently in the past 60 days
  • Evidence of cardiovascular, pulmonary, renal, hepatic, metabolic, cerebral diseases or sleep disorders
  • Disorder or use of medication that affects cardiopulmonary health
Show all 13Show fewer
  • Evidence of pregnancy or current nursing
  • Non e-Cig using arm
  • 17 years old and younger or 30 years old and older
  • Use of cigarettes or other tobacco products more than 50 times in their lifetime.
  • Evidence of cardiovascular, pulmonary, renal, hepatic, metabolic, cerebral diseases or sleep disorders
  • Disorder or use of medication that affects cardiopulmonary health
  • Evidence of pregnancy or current nursing

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Virginia Commonwealth University

    Richmond, Virginia, 23298

Other trials in United States

About this study

The study is focused on investigating the mechanisms involved in microvascular health in subjects that use e-cigarettes frequently. To explore microvascular health, different techniques and compounds. For one of the tests, iontophoresis, the drug's use will be stored and handled as described by the approved IND and non-IDS plan.

Read the detailed description

Electronic cigarettes or e-cigarettes have become increasingly popular, due to their promotion as a healthy alternative to traditional tobacco cigarettes. However, there are large discrepancies of knowledge in understanding how these e-cigarettes affect the subjects health and the way their body uses oxygen. The overall goal of this study is to evaluate e-cigarettes usage on subjects health.

Conditions
E-Cig Use
Being tested
E-cig use
Keywords
Microvascular Health
Medical subject headings
Vaping

What participants receive

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

  • E-cig useOther

    Based on e-cigarette usage, participants will be divided into those who used e-cigarettes and those who did not use e-cigarettes

Study groups in NCT06860698
Study groupRoleWhat they receive
Chronic e-cigs usersUsed e-cigarettes with nicotine (≥3 times/week for ≥6 months)
Receives: Other: E-cig use
Never UsersUse of cigarettes or other tobacco products less than 50 times in their lifetime.
Receives: Other: E-cig use

What is being measured

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

  1. Endothelial dependent dilation

    Endothelial-dependent dilation will be assessed using laser doppler speckle contrast in both groups through the intervention

    Measured: Participation is one week

  2. Neurogenic response

    Neurogenic response will be assessed using axon reflex in both groups through the intervention

    Measured: Participation is one week

Timeline

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

  1. First posted6 Mar 2025
  2. Study start14 Jul 2023
  3. Primary completion2 Jun 2025
  4. Study completion2 Jun 2025

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
41 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06860698
Sponsor's protocol ID
HM20029023
Status last verified
Sep 2026
First submitted
24 Feb 2025
Last updated
14 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of E-Cig Use, run by Virginia Commonwealth University 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 3 inclusion and 13 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: finished, as of the sponsor's last update on 14 Sep 2026. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Endothelial dependent dilation (time frame: Participation is one week). The study lists 2 primary outcomes in all. 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 Sep 2026.

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