drugset / Trial / NCT01495819

Nicotine Reinforcement and Aversion in Young Adult Light Smokers

NCT01495819

RandomizedCrossoverDouble-blindTreatment

Summary

The proposed study will examine the threshold for nicotine self-administration (NSA) using five different nicotine doses in young adult male and female non-dependent smokers (light and intermittent smokers or LITS). We propose a double-blind, placebo-controlled study that will enroll 195 individuals, targeting a total of 72 completers (36 male and 36 females). In each of the five experimental sessions, smokers will be randomly assigned to one of the five doses of nicotine (0.0125, 0.025, 0.05, 0.1 and 0.2 mg/70 kg). The highest dose, 0.2 mg/70 kg, corresponds to nicotine delivered by about one or two puffs of a cigarette. At the beginning of each experimental session, smokers will sample the assigned both the nicotine dose for that experimental session, and the placebo (saline) dose, followed by the opportunity to choose between nicotine and placebo for a total of ten choices over a 150-minute period. The main outcomes will be threshold dose (the minimum dose of nicotine that is self-administered more than placebo) and the slope of dose-response for nicotine self-administration (changes in nicotine self-administration per unit change in nicotine dose). We will also collect measures of nicotine intake (cotinine), nicotine clearance (3-hydroxycotinine (3-HC) / cotinine), and self-report drug effects

Timeline

Start
2017-01-04
Primary completion
2020-03-30
Completion
2020-03-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nicotine Unknown 0.000178571 mg/kg Intravenous
Comparator Nicotine Unknown 0.000357143 mg/kg Intravenous
Comparator Nicotine Unknown 0.000714286 mg/kg Intravenous
Comparator Nicotine Unknown 0.00142857 mg/kg Intravenous
Comparator Nicotine Unknown 0.00285714 mg/kg Intravenous

Indications