Vape study tests nicotine salts vs. Free-Base: which hits harder?
NCT ID NCT04231539
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study looked at how nicotine salt-based vaping products compare to free-base nicotine e-liquids. Fifteen daily vapers tried different flavors and nicotine levels, and researchers measured nicotine levels in their blood and asked about harshness and satisfaction. The goal was to understand the abuse potential of these products.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Nicotine (salt-based and free-base e-liquids)
- What this could lead to
- If successful, this could help regulators understand how different nicotine formulations affect addiction potential and user experience.
- What could go wrong
- This is a small, early-stage study with only 15 participants, so results may not apply to all vapers. It measures short-term effects, not long-term health outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
15 people
The number who actually took part.
- Started
-
Feb 2020
- Finished
-
Jul 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
21 to 55 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Willingness to abstain from using ENDS product for 8-10 hours (overnight abstinence) prior to study visits * Current daily ENDS user as determined by * Has used ENDS product every day for the past 6 months (by history) * Has used ENDS product or e-liquid containing nicotine (by history) * Participant or legal representative must understand the investigational nature of this study and sign and Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure Exclusion Criteria: * Smoked cigarettes in the past 7 days * Currently smokes \>= 5 cigarettes per month * Unstable medical conditions (such as unstable heart disease, uncontrolled hypertension, thyroid disease, diabetes, renal or liver impairment, or glaucoma) or psychiatric condition (such as current major depression, history of schizophrenia or bipolar disorder) or current regular use of psychiatric medications (such as major tranquilizers and antidepressants) * History of serious side effects from nicotine or from any nicotine replacement therapies * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements * Pregnant or nursing females * Concurrent participation in another clinical trial * Unwilling or unable to follow protocol requirements * Any condition which in the investigator's opinion deems the participant an unsuitable candidate
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Roswell Park Cancer Institute
Buffalo, New York, 14263, United States
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