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The Effect of Nicotine Delivery Rate on Reinforcement

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Yale University

Status and phase

Completed
Early Phase 1

Conditions

Nicotine

Treatments

Drug: Nicotine 0.024 mcg/kg/s
Drug: Nicotine 0.048 mcg/kg/s
Drug: Nicotine 0.24 mcg/kg/s
Drug: Nicotine saline 0.00mcg/kg/s

Study type

Interventional

Funder types

Other

Identifiers

NCT03134339
1609018390

Details and patient eligibility

About

The dose-effect curve to estimate a threshold delivery rate for reinforcement. The project addresses the FDA Center for Tobacco Products (CTP) interest #1: Nicotine dependence threshold among youth and adults and impact of nicotine reduction on tobacco product use behavior (e.g., topography, compensation, switching, multiple use, initiation, cessation and relapse). IV nicotine, in contrast to ECs, can deliver precise, reproducible dosing, which is necessary for accurately assessing dose-response and threshold effects. The estimated threshold for reinforcement will establish a benchmark for evaluating the addictive potential of ECs and other inhaled nicotine products.

Full description

A placebo-controlled study that will recruit male and female nicotine dependent smokers/EC users (n=18) to complete four separate experimental sessions. Each session will include one randomly assigned infusion that will be either saline or a single dose of nicotine (1 mg per 70 kg body weight) delivered at three different infusion rates, rapid, moderate or slow (0.24, 0.048 or 0.024 mcg per kg body weight per second). A total infusion duration of 10 min will be maintained during each session by adding saline infusions of variable duration after nicotine delivery. This will be achieved by two separate infusion pumps, one for saline and one for nicotine. For example, the rapid 0.24 mcg/kg/s condition will include a 1 min infusion of nicotine followed by a 9 min infusion of saline. The subjects will be blinded to the infusion pump procedures. The rapid delivery rate, which we have used in our prior studies, induces positive subjective drug effects and suppresses symptoms of nicotine withdrawal. The moderate delivery rate,0.048 mcg/kg/s, approximates the rate of nicotine intake encountered while smoking a typical cigarette over 5 min (4). The slowest nicotine delivery rate, 0.024mcg/kg/s, was chosen to approximate the rate of nicotine intake encountered while using a newer EC (5).

Enrollment

18 patients

Sex

All

Ages

18 to 30 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Female and male smokers that smoke ≥ 5 cigarettes per day for the past year
  2. aged 18 to 30 years
  3. urine cotinine levels > 100 ng/mL consistent with nicotine intake of an active smoker (23)
  4. not seeking treatment at the time of the study for nicotine dependence
  5. in good health as verified by medical history, screening examination, and screening laboratory tests
  6. for women, not pregnant as determined by pregnancy screening, nor breast feeding, and using acceptable birth control methods.

Exclusion criteria

  1. history of major medical or psychiatric disorders that the physician investigator deems as contraindicated for the subject to be in the study
  2. regular use of psychotropic medication (antidepressants, antipsychotics, or anxiolytics)
  3. current alcohol or substance dependence for any other recreational or prescription drugs other than nicotine
  4. urine drug screening indicating recent illicit drugs use (with the exception of marijuana).

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

18 participants in 4 patient groups

saline 0.00mcg/kg/s
Experimental group
Description:
0.00 mcg/kg/s The day order will be randomized per day
Treatment:
Drug: Nicotine saline 0.00mcg/kg/s
0.24mcg/kg/s
Experimental group
Description:
0.24 mcg/kg/s The day order will be randomized per day
Treatment:
Drug: Nicotine 0.24 mcg/kg/s
0.048mcg/kg/s
Experimental group
Description:
0.048 mcg/kg/s The day order will be randomized per day
Treatment:
Drug: Nicotine 0.048 mcg/kg/s
0.024 mcg/kg/s
Experimental group
Description:
0.024 mcg/kg/s The day order will be randomized per day
Treatment:
Drug: Nicotine 0.024 mcg/kg/s

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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