Switching to E-cigarettes in Smokers Not Interested in Quitting
University of Kansas Medical Center · NCT05703672
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 21+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 3
- Target enrollment
- 500
- US sites recruiting
- 2
- Study start
- July 17, 2023
- Record last updated
- October 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The objectives of this application are to 1) compare short- and long-term harm reduction and abuse liability potential of a nicotine salt pod-based electronic cigarettes (EC) in adult (AA) exclusive EC, dual cig-EC, and exclusive cig users, 2) characterize factors that predict who switches fully, partially, or not at all, and 3) examine if harm reduction can be further enhanced by treating dual users with varenicline (VAR) to eliminate cigarette smoking.
Being studied: Varenicline Tartrate; Placebo; Electronic cigarette
Conditions: Smoking Reduction
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- ≥ 21 years of age
- Smoke >5 cigarettes per day
- Smoked cigarettes for > 6 months
- Verified smoker (CO > 5 ppm)
- Functioning telephone
- Interested in switching to EC
- Willing to take varenicline and complete all study visits
Exclusion Criteria
- Interested in quitting smoking
- Use of smoking cessation pharmacotherapy in the month prior to enrollment
- Use of other tobacco products in past 30 days (i.e., cigarillos, cigars, hookah, smokeless tobacco, pipes)
- EC use on > 4 of the past 30 days
- Uncontrolled hypertension: BP > 180 (systolic) or > 105 (diastolic)
- Heart-related event in the past 30 days
- Medical contraindications to VAR: unstable cardiac condition (e.g., unstable angina or AMI) cardiac event, or stroke in the past 4 weeks; renal impairment; history of clinically significant allergic reactions; history of epilepsy or seizure disorder; hospitalized for psychiatric issue in past 30 days; active suicidal ideation
- Pregnant, contemplating getting pregnant, or breastfeeding
- Plans to move from Kansas City metro area during the treatment and follow-up phase
- Another household member enrolled in the study
Recruiting US locations
Swope Health Central
Kansas City, MO 64130
Site contact: Tricia Snow · 816-599-5311 · psnow@kumc.edu
University of Kansas Medical Center
Kansas City, MO 64130
Site contact: Tricia Snow, MPH · 816-398-8960 · psnow@kumc.edu
Study contacts (from the official record)
- Tricia Snow, MPH · 816-398-8960 · psnow@kumc.edu
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