Nicotine Analogs for Addiction

(CENA Trial)

TO
Overseen ByThe Ohio State University Comprehensive Cancer Center
Age: 18+
Sex: Any
Trial Phase: Phase 1
Sponsor: Ohio State University Comprehensive Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This phase I trial compares electronic cigarette (EC) user preferences and smoking behaviors of nicotine analogs to nicotine to improve the understanding of nicotine analog addictiveness. Over the last ten years, EC use has become a major concern due to its increased use among adolescents and young adults. Though progress has been made in regulating nicotine containing products, some companies have shifted toward producing products containing nicotine analogs. ECs are battery-powered electronic devices designed to atomize a nicotine (the poisonous chemical found in tobacco)-containing liquid solution for inhalation in a manner that simulates smoking a tobacco cigarette. When nicotine enters the body, it causes an increased heart rate and use of oxygen by the heart, and a sense of well-being and relaxation. Nicotine analogs are compounds that are similar to nicotine in their chemical structure. Some nicotine analogs have been shown to have nicotine-like effects; however, more research is needed to prove they function similarly to nicotine and/or have similar effects. Comparing EC user preferences and smoking behaviors of nicotine analogs to nicotine may help improve the understanding of nicotine analog addictiveness.

Who Is on the Research Team?

TL

Theodore L Wagener, PhD

Principal Investigator

Ohio State University Comprehensive Cancer Center

Are You a Good Fit for This Trial?

This trial is for adults aged 21 or older who have used electronic cigarettes (ECs) regularly for at least the past 3 months. Participants must be able to read, write, and speak English, provide consent, and agree not to use nicotine, tobacco, or marijuana products for at least 12 hours before each lab visit.

Inclusion Criteria

I am willing and able to give my consent to join the study.
I can read, write, and speak English.
I am 21 years old or older.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks
1 visit (in-person)

Treatment

Participants are randomized to different sequences of nicotine and nicotine analogs, with each sequence involving three visits where participants take puffs of ECs and are monitored for subjective effects and pharmacokinetics.

3 weeks
3 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment, with follow-up visits at 4 and 12 weeks.

12 weeks
2 visits (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • 6-Methyl Nicotine
  • nicotinamide
  • Nicotine

Trial Overview

The study compares how EC users respond to nicotine analogs versus regular nicotine by observing their preferences and smoking behaviors. It involves using different substances in EC devices and collecting data through surveys and biospecimen samples during several lab visits.

How Is the Trial Designed?

6

Treatment groups

Experimental Treatment

Group I: Sequence 6 (6-MN, nicotinamide, nicotine)Experimental Treatment6 Interventions
Group II: Sequence 5 (6-MN, nicotine, nicotinamide)Experimental Treatment6 Interventions
Group III: Sequence 4 (nicotinamide, nicotine, 6-MN)Experimental Treatment6 Interventions
Group IV: Sequence 3 (nicotinamide, 6-MN, nicotine)Experimental Treatment6 Interventions
Group V: Sequence 2 (nicotine, nicotinamide, 6-MN)Experimental Treatment6 Interventions
Group VI: Sequence 1 (nicotine, 6-MN, nicotinamide)Experimental Treatment6 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Ohio State University Comprehensive Cancer Center

Lead Sponsor

Trials
350
Recruited
295,000+