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Effect of Memantine Versus Bupropion on Smoking Relapse in Nicotine-Dependent Individuals - 3

Primary Purpose

Tobacco Use Disorder

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Memantine
Sponsored by
New York State Psychiatric Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tobacco Use Disorder focused on measuring tobacco use

Eligibility Criteria

21 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: DSM-IV diagnosis of nicotine dependence with psychological dependence Smokes at least 15 cigarettes per day for the three months prior to enrollment Currently not seeking treatment for nicotine dependence Medically healthy on the basis of physical examination and medical history, vital signs, EKG, and laboratory tests Females must use an effective method of contraception for the duration of the study Exclusion Criteria: DSM-IV diagnosis of abuse or dependence on alcohol or drugs other than nicotine Current Axis I diagnosis or current treatment with psychotropic medications within the three months prior to enrollment History of schizophrenia or other psychotic disorders, bipolar disorder, or anxiety disorders Currently seeking treatment for nicotine disorders On parole or probation History of seizures or head trauma with loss of consciousness, brain contusion, or fracture History of significant recent violent behavior Blood pressure greater than 150/90 History of eating disorders History of allergic reaction to any of the study medications Pregnant

Sites / Locations

  • New York State Psychiatric Institute

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Placebo Comparator

Placebo Comparator

Arm Label

Intervention 1

Intervention 2

Intervention 3

Arm Description

Each participant receives three consecutive interventions. Placebo Bupropion Memantine

Bupropion Memantine Placebo

Memantine Placebo Bupropion

Outcomes

Primary Outcome Measures

Use of cigarettes

Secondary Outcome Measures

Full Information

First Posted
August 25, 2005
Last Updated
May 17, 2018
Sponsor
New York State Psychiatric Institute
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00136786
Brief Title
Effect of Memantine Versus Bupropion on Smoking Relapse in Nicotine-Dependent Individuals - 3
Official Title
Effect of Memantine Versus Bupropion on Smoking Relapse in Nicotine-Dependent Individuals
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

5. Study Description

Brief Summary
One of nicotine's effects on the body is at the level of the NMDA receptors in the brain. Memantine is a drug that also affects NMDA receptors, making it a candidate for the treatment of nicotine addiction. The purpose of this study is to evaluate the effectiveness of memantine using a laboratory model of smoking relapse in nicotine dependent volunteers. Investigators will compare the effects of memantine with bupropion, medication currently used to facilitate smoking cessation.
Detailed Description
Tobacco use is the leading preventable cause of death in the United States. Recent research on the effects of nicotine on the brain and behavior presents an opportunity to advance medication development. Neurotransmission at NMDA receptors in the brain is associated with learning and memory and has been linked to many of nicotine's effects on humans. It is possible that altering NMDA neurotransmission may be helpful in treating nicotine addiction. The goal of this study is to evaluate the effects of memantine, an NMDA receptor antagonist, using the laboratory model of smoking relapse in nicotine dependent volunteers. The effects of memantine used in combination with bupropion, a medication currently used to facilitate smoking cessation, will be compared to a placebo. This double-blind study will consist of three phases (placebo, bupropion, and memantine). Each phase will include 10 days of outpatient medication maintenance, followed by 5 days of inpatient testing. During the outpatient phase, study visits will occur every 2 to 3 days. During the first portion of inpatient stay, participants will not be permitted to smoke. During the second portion of inpatient stay, smoking reinstatement will be modeled, as participant will have opportunity to smoke. A variety of behavioral, subjective, physiological, and performance measures will be assessed throughout the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Disorder
Keywords
tobacco use

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention 1
Arm Type
Placebo Comparator
Arm Description
Each participant receives three consecutive interventions. Placebo Bupropion Memantine
Arm Title
Intervention 2
Arm Type
Placebo Comparator
Arm Description
Bupropion Memantine Placebo
Arm Title
Intervention 3
Arm Type
Placebo Comparator
Arm Description
Memantine Placebo Bupropion
Intervention Type
Drug
Intervention Name(s)
Memantine
Primary Outcome Measure Information:
Title
Use of cigarettes
Time Frame
Day 15

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: DSM-IV diagnosis of nicotine dependence with psychological dependence Smokes at least 15 cigarettes per day for the three months prior to enrollment Currently not seeking treatment for nicotine dependence Medically healthy on the basis of physical examination and medical history, vital signs, EKG, and laboratory tests Females must use an effective method of contraception for the duration of the study Exclusion Criteria: DSM-IV diagnosis of abuse or dependence on alcohol or drugs other than nicotine Current Axis I diagnosis or current treatment with psychotropic medications within the three months prior to enrollment History of schizophrenia or other psychotic disorders, bipolar disorder, or anxiety disorders Currently seeking treatment for nicotine disorders On parole or probation History of seizures or head trauma with loss of consciousness, brain contusion, or fracture History of significant recent violent behavior Blood pressure greater than 150/90 History of eating disorders History of allergic reaction to any of the study medications Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adam Bisaga, M.D.
Organizational Affiliation
New York State Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Effect of Memantine Versus Bupropion on Smoking Relapse in Nicotine-Dependent Individuals - 3

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