Translational Neuropsychopharmacology Research of Nicotine Addiction

Phase 2

Completed

• Conditions: Nicotine Dependence, Cigarettes
• Interventions: Drug: Varenicline (VRN); Drug: N-Acetylcysteine (NAC); Drug: Placebo

• Registration Number: NCT02723162
• Lead Sponsor: Medical University of South Carolina

Brief Summary

This study will examine the effects of combining Varenicline (VRN) and N-acetylcysteine (NAC) on neural circuitry function and treating nicotine addiction. Healthy adult nicotine dependent cigarette smokers interested in quitting (n=110) will be randomized to one of four PBO-controlled conditions for 4 weeks: 1) VRN+NAC, 2) VRN+PBO, 3) NAC+PBO or 4) PBO+PBO. Following 1 week of medication, participants will be contingently reinforced for 3 days of smoking abstinence and be scanned using functional magnetic resonance imaging (fMRI) techniques, while nicotine deprived during a resting state and a cue-reactivity (CR) task. Participants will be followed over the next 3 weeks of treatment and clinical variables will be assessed.

Detailed Description

Cigarette (henceforth nicotine) addiction is a chronic, relapsing brain disorder and remains the leading preventable cause of death and disability in the US, costing nearly $200 billion each year. Although \~20% of adults in the USA currently smoke, the majority want to quit. In spite of the breadth of research focused on improving health outcomes and reducing the societal burden caused by nicotine addiction, the majority of smokers who attempt to quit will relapse. Nicotine withdrawal-related disturbances in executive function, negative affect and reward processes compel a smoker to self-administer nicotine-each in turn representing the loss of control to remain abstinent and risk factors for relapse. Thus, identifying the effects of nicotine addiction on mechanisms of self-regulation, and the value of novel medications for remediating dysregulated behavior are both needed in order to enhance interventions for treating nicotine addiction. The preliminary data, along with the extant literature, suggest that the maintenance of nicotine addiction is subserved by dysregulated neural function in limbic-striatal and corticostriatal neural circuitry. While VRN may be effective in treating limbic-striatal circuitry that is associated with promoting abstinence and reducing acute withdrawal; NAC may be effective in treating corticostriatal circuitry function that is associated with relapse vulnerability. Thus, the current proposal seeks to investigate two medications (VRN \& NAC), with potentially complementary effects on the two different brain circuits- limbic-striatal (VRN) and corticostriatal (NAC) circuitry-and that may therapeutically target two different phases in the recovery of nicotine addiction-the promotion of abstinence (VRN) and relapse prevention (NAC). The placebo (PBO)-controlled design in this proposal will allow the team to identify and translate between the neurobiological substrates and the neurocognitive underpinnings of the effects of VRN+NAC on smoking behavior in humans-thus, advancing the understanding of the pathophysiology of nicotine addiction.

Basic Information
|
Recruitment & Eligibility
|
Study & Design
|
Trial Locations

Study Timeline

• Study First Submitted: 2016-03-07
• Study First Submitted QC: 2016-03-23
• Study First Posted: 2016-03-30
• Study Start: 2016-05-04
• Primary Completion: 2020-03-09
• Study Completion: 2020-03-09
• Disposition First Submitted: 2021-02-04
• Disposition First Submitted QC: 2021-02-04
• Disposition First Posted: 2021-02-08
• Results First Submitted: 2021-09-30
• Status Verified: 2022-07
• Results First Submitted QC: 2022-07-22
• Last Update Submitted: 2022-07-22
• Results First Posted: 2022-08-18
• Last Update Posted: 2022-08-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 67

Inclusion Criteria

1. Age 18 - 55
2. Right Handed
3. English fluency
4. 20/20 vision with corrective lenses.
5. Smoke ≥ 10 cigarettes/day for a minimum of two years and have an expired carbon monoxide (CO) concentration of ≥ 10 ppm (to confirm inhalation).
6. Interest in quitting smoking or contemplating a quit attempt in the next 6 months
7. If female, agreement to use birth control

Read More

Exclusion Criteria

1. Past head injury or primary neurological disorder associated with MRI abnormalities, including dementia, MCI, brain tumors, epilepsy, Parkinson's disease, or demyelinating diseases
2. Any physical or intellectual disability affecting completion of assessments
3. Any contraindication to MRI
4. Positive urine drug screen for illicit substances (such as marijuana or cocaine).
5. Current or past psychosis
6. Electroconvulsive therapy in last 6 months
7. Use of antidepressant medications or other psychotropic medications in the last month.
8. Positive urine pregnancy test or current breast feeding status

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
VRN+ PBO	Varenicline (VRN)	Titrated VRN up to 1mg BID with NAC placebo for 28 days
NAC+ PBO	N-Acetylcysteine (NAC)	1200mg BID for 28 days plus VRN placebo for 28 days
VRN+ PBO	Placebo	Titrated VRN up to 1mg BID with NAC placebo for 28 days
PBO+PBO	Placebo	Double placebo taken for 28 days
VRN+ NAC	Varenicline (VRN)	Titrated VRN up to 1mg BID with NAC at 1200mg BID for 28 days
VRN+ NAC	N-Acetylcysteine (NAC)	Titrated VRN up to 1mg BID with NAC at 1200mg BID for 28 days
NAC+ PBO	Placebo	1200mg BID for 28 days plus VRN placebo for 28 days

Primary Outcome Measures

Name	Time	Method
Percent Change in Blood Oxygen Level Dependent (BOLD) Signal Response	10 Days	Measure the Effects of Varenicline and N-Acetylcysteine (NAC) on brain activation to smoking images while participants undergo Functional Magnetic Resonance (fMRI) Imaging. Mean percent signal change of fMRI BOLD in the insula and nucleus accumbens will be recorded during smoking images. The lower the BOLD signal response, the better the outcome, meaning reduced reactivity to smoking images.
rZ Change Score in Resting State Functional Connectivity From Baseline	Baseline to day 10	Measure the effects of Varenicline and N-Acetylcysteine on resting-state functional connectivity while participants undergo fMRI. Fisher transformed correlation (rZ) scores will be recorded between medial prefrontal cortex and ventral striatum during a resting state scan. The higher the rZ score, the better the outcome, meaning stronger functional connectivity. rZ scores range from -1 to 1. The rZ-score central value is analogous to a central value to of a Z-score of 0, representing the population mean.

Secondary Outcome Measures

Name	Time	Method
Number of Cigarettes Smoked Per Day	28 Days	Measure the effects of Varenicline and N-Acetylcysteine on smoking behavior over the course of the study

Trial Locations

Locations (1)

Medical University of South Carolina; 🇺🇸 Charleston, South Carolina, United States