Stopped: Major study re-design prior to participant enrollment
This is an observational, crossover study that will be examine use behaviors, chemical exposures, and biological effects of SREC compared to TC use in subjects confined to a research ward setting.
Age range
21 Years – 70 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Peak Nicotine Concentration
Timeframe: Up to 2 years
Time of Peak Nicotine Concentration
Timeframe: Up to 2 years
Mean overall systemic nicotine exposure
Timeframe: Baseline through study completion, approximately 2 years
Change in Mean score on the Modified Cigarette Evaluation Questionnaire (mCEQ)
Timeframe: Baseline through study completion, approximately 2 years
Patterns of puffing
Timeframe: Baseline through study completion, approximately 2 years
Change in Mean score on the Minnesota Tobacco Withdrawal Scale-Revised (MTWS-R)
Timeframe: Baseline through study completion, approximately 2 years
Change in Mean score on the Questionnaire on Smoking Urges (QSU-Brief)
Timeframe: Baseline through study completion, approximately 2 years
Change in Mean score on the Positive and Negative Affect Scale (PANAS)
Timeframe: Baseline through study completion, approximately 2 years