Nicotine DependenceNCT02724241
E-Cigarettes and SNA
A study testing one time exposure to e-cig with nicotine, One time exposure to e-cigarette without nicotine and one time exposure to empty e-cigarette in people with Nicotine Dependence, run by University of California, Los Angeles at 1 site in United States.
Trial summary
Randomized controlled trial of electronic cigarettes with nicotine, without nicotine, and sham control, on sympathetic nerve activity and markers of oxidative stress. Read more about this study
- Who is it for?
- Ages 21 to 45 yearsHealthy volunteers can take part
- Conditions the study is for
- Nicotine Dependence
- What is being tested?
- one time exposure to e-cig with nicotine, One time exposure to e-cigarette without nicotine and one time exposure to empty e-cigarette
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 100 participants
- Where
- 1 siteUnited States
- Study dates
- Apr 2015to Dec 2021
- Phase
- Interventional
- 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 21 to 45 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Healthy
Who cannot join
- Cardiac disease
- Respiratory disease
- Diabetes mellitus
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effects of Electronic Cigarettes on Sympathetic Nerve Activity and Oxidative Stress
Randomized controlled trial of electronic cigarettes with nicotine, without nicotine, and sham control, on sympathetic nerve activity and markers of oxidative stress.
Read the detailed description
Participants will use an electronic cigarette on 3 occasions: 1) with nicotine, 2) without nicotine, 3) sham control, and measures of autonomic tone, including heart rate variability (HRV) and sympathetic nerve activity (MSNA: microneurography), and oxidative stress will be measured pre and post exposure.
- Conditions
- Nicotine Dependence
- Being tested
- one time exposure to e-cig with nicotine, One time exposure to e-cigarette without nicotine, one time exposure to empty e-cigarette
- Keywords
- nicotine, autonomic tone, oxidative stress
- Medical subject headings
- Tobacco Use Disorder
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
one time exposure to e-cig with nicotineOther
one time exposure to e-cigarette vapor with nicotine
One time exposure to e-cigarette without nicotineOther
One time exposure to e-cig without nicotine
one time exposure to empty e-cigaretteOther
Also called sham control
one time exposure to empty e-cigarette (sham control)
| Study group | Role | What they receive |
|---|---|---|
| nicotine | Experimental | use of an e-cigarette filled with liquid with nicotine Receives: Other: one time exposure to e-cig with nicotine |
| no nicotine | Experimental | Use of an e-cigarette filled with liquid without nicotine Receives: Other: One time exposure to e-cigarette without nicotine |
| sham comparator | Sham comparator | Use of empty e-cigarette (sham control) Receives: Other: one time exposure to empty e-cigarette |
What is being measured
The primary outcome is the main question the study is designed to answer.
Heart Rate variability
Heart rate variability is a measure of autonomic tone
Measured: 10 minutes after exposure
Paraoxonase
plasma oxidative stress
Measured: less than 1 hour after exposure
Secondary outcomes (1)
muscle sympathetic nerve activity
Muscle sympathetic nerve activity (MSNA)
Measured: 10 minutes after exposure
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Mar 2016 (estimated)
- Study startApr 2015
- Primary completionDec 2021
- Study completionDec 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Nicotine DependenceStudies of the same condition, open and under way.
- More trials run by University of California, Los AngelesThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of California, Los Angeles
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Holly R Middlekauff, University of California, Los Angeles
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02724241
- Sponsor's protocol ID
- 14-000731
- Status last verified
- Dec 2021
- First submitted
- 17 Mar 2016
- Last updated
- 20 Dec 2021
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Dec 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effects of Electronic Cigarettes on Sympathetic Nerve Activity and Oxidative Stress
- ClinicalTrials.gov ID
- NCT02724241
- Acronym / sponsor ID
- 14-000731
- Conditions
- Nicotine Dependence
- Keywords
- nicotine, autonomic tone, oxidative stress
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- University of California, Los AngelesUniversity, hospital or other
- Study start
- Apr 2015
- Primary completion
- Dec 2021 (actual)
- Study completion
- Dec 2021 (actual)
- First posted
- 31 Mar 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Randomized controlled trial of electronic cigarettes with nicotine, without nicotine, and sham control, on sympathetic nerve activity and markers of oxidative stress.
Detailed description
Participants will use an electronic cigarette on 3 occasions: 1) with nicotine, 2) without nicotine, 3) sham control, and measures of autonomic tone, including heart rate variability (HRV) and sympathetic nerve activity (MSNA: microneurography), and oxidative stress will be measured pre and post exposure.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| nicotine | Experimental | Other: one time exposure to e-cig with nicotineuse of an e-cigarette filled with liquid with nicotine |
| no nicotine | Experimental | Other: One time exposure to e-cigarette without nicotineUse of an e-cigarette filled with liquid without nicotine |
| sham comparator | Sham comparator | Other: one time exposure to empty e-cigaretteUse of empty e-cigarette (sham control) |
Who may qualify
- Ages
- 21 to 45 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- Healthy
Key exclusion criteria (3 listed)
- Cardiac disease
- Respiratory disease
- Diabetes mellitus
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| one time exposure to e-cig with nicotineone time exposure to e-cigarette vapor with nicotine | Other | nicotine |
| One time exposure to e-cigarette without nicotineOne time exposure to e-cig without nicotine | Other | no nicotine |
| one time exposure to empty e-cigaretteAlso: sham controlone time exposure to empty e-cigarette (sham control) | Other | sham comparator |
Primary outcome
Heart Rate variability
Time frame: 10 minutes after exposure
Heart rate variability is a measure of autonomic tone
Paraoxonase
Time frame: less than 1 hour after exposure
plasma oxidative stress
1 secondary outcome
muscle sympathetic nerve activity
Time frame: 10 minutes after exposure
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Dec 2021.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing one time exposure to e-cig with nicotine, One time exposure to e-cigarette without nicotine and one time exposure to empty e-cigarette in people with Nicotine Dependence, run by University of California, Los Angeles 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 1 inclusion and 3 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 20 Dec 2021. 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. Some participants in this study may receive a placebo. 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?
Heart Rate variability (time frame: 10 minutes after exposure). 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 20 Dec 2021.