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Completed Not applicable Interventional Accepts healthy volunteers

Changes in Biomarkers of Cigarette Smoke Exposure After Switching Either Exclusively or Partly to JUUL ENDS

ClinicalTrials.gov ID: NCT04107779

Public ClinicalTrials.gov record NCT04107779. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:53 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open Label, Parallel Group Study in Adult Smokers to Evaluate Changes in Biomarkers of Cigarette Smoke Exposure After Switching Either Exclusively or Partly to Using JUUL Electronic Nicotine Delivery Systems With Two Different Nicotine Concentrations

Study identification

NCT ID
NCT04107779
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Juul Labs, Inc.
Industry
Enrollment
279 participants

Conditions and interventions

Interventions

  • Switch from UB of Combustible Cigarette to JUUL 5% Virginia Tobacco ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 3% Virginia Tobacco ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 5% Mint ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 3% Mint ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 5% Menthol ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 3% Menthol ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 5% Mango ENDS Other
  • Switch from UB of Combustible Cigarette to JUUL 3% Mango ENDS Other
  • Switch to Dual-use of JUUL 5% and UB of Combustible Cigarette Other
  • Tobacco/Nicotine Abstention Other
  • Usual Brand of cigarettes Other

Other

Eligibility (public fields only)

Age range
21 Years to 65 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 16, 2019
Primary completion
Feb 16, 2020
Completion
Jun 23, 2020
Last update posted
Jul 27, 2020

2019 – 2020

United States locations

U.S. sites
5
U.S. states
4
U.S. cities
5
Facility City State ZIP Site status
Woodland International Research Group Little Rock Arkansas 72211
Woodland Research Northwest Rogers Arkansas 72758
St. Louis Clinical Trials St Louis Missouri 63141
Midwest Clinical Research Center Dayton Ohio 45417
Endeavor Clinical Trials San Antonio Texas 78229

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04107779, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 27, 2020 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04107779 live on ClinicalTrials.gov.

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