Nicotine for Marijuana Withdrawal
Information source: Southern Illinois University Carbondale
Information obtained from ClinicalTrials.gov on February 07, 2013 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Marijuana Dependence
Intervention: Nicotine (Drug); Placebo Patch (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: Southern Illinois University Carbondale Official(s) and/or principal investigator(s): David G Gilbert, PhD, Principal Investigator, Affiliation: Southern Illinois University Carbondale
Overall contact: Norka E Rabinovich, B.A., Phone: 618-453-3527, Email: norkar@siu.edu
Summary
The purpose of this 3-year trial is to test the efficacy of transdermal nicotine patch
versus placebo patch on marijuana withdrawal symptoms in cannabis-dependent individuals,
using a randomized, double-blind, and placebo-controlled design. This proposal is in
response to RFA-DA-10-016(R01) Medications Development for Cannabis-Related Disorders.
Consistent with the goals of this RFA, the overall goal of the proposed project is to assess
the impact of transdermal nicotine patch (TNP) on marijuana (MJ) withdrawal (negative affect
and craving motivated by negative affect) symptoms in MJ-dependent individuals.
Clinical Details
Official title: Nicotine for Marijuana Withdrawal
Study design: Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science
Primary outcome: Marijuana withdrawal symptoms (mood, use, and urge to use marijuana)
Secondary outcome: Patch Guess and Attributions QuestionnaireBlood Pressure Tobacco dependence. Tobacco and nicotine intake Body Weight THC Intake Heart Rate
Detailed description:
The aim of this proposal is to accurately assess the effects of TNP on MJ withdrawal
symptoms across 15 days of biochemically confirmed MJ abstinence using a placebo-controlled,
double-blind, randomly assigned treatment design, while closely monitoring any potential
adverse effects, including changes in nicotine use and dependence.
To achieve these goals, 116 carefully screened cannabis-dependent individuals (58 female)
will be randomly assigned to one of two doses (0 mg or 7mg nicotine) of TNP while they
abstain from MJ for 15 days. Subjects will be administered a follow-up phone interview 30
days after the termination of treatment to assess the effects of nicotine-patch treatment
on: 1) frequency of nicotine and tobacco smoking intake, 2) FTND-assessed nicotine
dependence, 3) new use of nicotine during the time since completion of the study, and 4)
marijuana and other drug use patterns. Large financial contingencies will be used to provide
a high degree of abstinence and study completion. This will be the first adequately powered
study to assess the effects of TNP on MJ negative affect-related withdrawal symptoms and
urges to use MJ. Withdrawal patterns and abstinence will be assessed in two groups of
MJ-dependent individuals: 1) those who rarely or never smoke tobacco, and 2) those who smoke
four or fewer tobacco cigarettes per day (very-light tobacco smokers). A stratified
randomization method will be used to control for gender and tobacco-smoker status. It is
hypothesized that MJ withdrawal symptoms will be less severe in the group assigned to the 7
mg patch than in the group assigned to the placebo. It is also hypothesized that individuals
high in anxiety/neuroticism and those high in aggression/hostility will exhibit greater
benefits from TNP than those low in these traits. Given that no gender differences were
observed in our preliminary study, gender differences are not predicted. The
over-the-counter availability, minimal abuse risks, and minimal adverse side-effects
associated with TNP would make it an ideal and highly implementable treatment for MJ
dependence if it can be demonstrated to be efficacious in reducing MJ withdrawal symptoms.
Eligibility
Minimum age: 18 Years.
Maximum age: 50 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria: Female and male cannabis-dependent MJ smokers aged 18 years or older
will be recruited. Inclusion criteria include cannabis dependence as assessed by a
DSM-IV-based structured interview and MJ use on 10-28 occasions per week and be willing to
abstain for 15 days. Only individuals who are in good mental and physical health, with a
BMI of 17-30 kg/m2, as verified by health questionnaires and the Structured Clinical
Interview for DSM-IV (SCID), will participate in this study. Potential subjects will be
asked to indicate, on a scale of 1-10, how strong they currently want to quit smoking MJ
(from "1" = "not at all" to "10" = "very strong") and will also be assessed with the
four-item MJ Stages of Change. Additionally, subjects will fulfill one of two criteria: 1)
not smoke or use other tobacco products or 2) smoke tobacco cigarettes or use other
nicotine delivery systems (e. g., hookah, cigars, chewing tobacco) fewer than 5 times per
day (on average) for the past year. Current use of MJ and tobacco will be verified by
detectable urine THC and nicotine metabolites. All subjects will be required to provide
four pre-quit baseline urine samples. The mean creatinine-normalized THC concentration
across these samples must be of 175 ng/ml or greater based. -
Exclusion Criteria:
Criteria include meeting DSM-IV criteria for current abuse or dependence on a substance
other than MJ, nicotine, or caffeine, using psychoactive substances (other than MJ,
alcohol, nicotine, & caffeine) 6+ times/month, testing positive for stimulants,
antidepressants, anxiolytics, and/or opiates (10-panel urine drug test), testing above a
salivary cotinine concentration of 150 ng/ml during the initial screening, using
creatinine or creatinine-containing supplements, testing positive for adulteration of
urine samples, consuming more than 6 alcoholic drinks per day continuously for a month,
mental disorders including bipolar disorder, schizophrenia, psychotic symptoms, currently,
recently, or ever chronically at significant suicidal risk or experiencing violent
thoughts or current major depression. Others that will be excluded include women who are
pregnant, lactating, not taking precautions to avoid pregnancy, individuals with
significant physical disorders or unstable physical disorders that may represent a severe
untreated condition, such as hypertension, as well as those with less than a high school
education or equivalent, primary language other than English, and those with significant
cognitive impairment.
Locations and Contacts
Norka E Rabinovich, B.A., Phone: 618-453-3527, Email: norkar@siu.edu
Southern Illinois University, Carbondale, Illinois 62901, United States; Recruiting Norka E Rabinovich, B.A., Phone: 618-453-3527, Email: norkar@siu.edu David G Gilbert, PhD, Phone: 618-453-3558, Email: dgilbert@siu.edu David G Gilbert, PhD, Principal Investigator
Additional Information
Starting date: April 2011
Last updated: March 19, 2012
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