NCT04003805.
Study name | Biomarkers of exposure and effect in standardized research e‐cigarette (SREC) users |
Methods | Design: RCT Setting: USA |
Participants | Estimated enrolment: 125 Inclusion criteria:
Exclusion criteria:
For a full list see NCT record. |
Interventions | EC: Standardized Research E‐cigarette (SREC) Arm 1: Experimental: Switching from Smoking Cigarettes to E (SREC) The device operates at a single output voltage (3.30 ± 0.05 V) and uses sealed disposable 3 mL cartridges with tobacco‐flavoured e‐liquid (~350 puffs/cartridge). The concentration of nicotine in e‐liquid is 15 mg/mL, and the vehicle composition is 50:50 propylene glycol and glycerin. The device uses a battery that can be recharged via a micro USB port. Arm 2: Experimental: Switching from smoking cigarettes to nicotine mini‐lozenge We will use commercially available nicotine mini‐lozenges containing 2 or 4 mg nicotine/lozenge (Nicorette, manufactured by GlaxoSmithKline). Dose will be determined per instructions on the package (e.g. if smoking within 30 minutes upon awakening, then 4 mg dose will be prescribed). |
Outcomes | 1 year 4 & 8 weeks for formaldehyde‐DNA adducts & oxidative DNA adduct 8‐oxo‐dG in DNA Biomarkers: TNE, NNAL, NNN, PneT, mercapturic acids HMPMA, 2‐HPMA, 3‐HPMA, formaldehyde‐DNA adducts, oxidative DNA adduct 8‐oxo‐dG in DNA, NNN and nornicotine, HPB‐releasing DNA adducts cpd, product use (EC & nicotine lozenges), CC avoidance |
Starting date | Actual start date: May 11 2022. Estimated study completion date: January 15 2023 |
Contact information | Hanna Vanderloo, RN, MSN 612.624.4983, hannav@umn.edu |
Notes | New to 2022 update |