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Modafinil for the Treatment of Alcohol Use Disorders

Primary Purpose

Alcohol Use Disorder

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Modafinil
Placebo
Sponsored by
The Mind Research Network
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcohol Use Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males and females age 18-65 meeting Diagnostic and Statistical Manual V criteria for moderate or severe AUD in the past year
  • Interested in cutting down or quitting
  • Able to provide voluntary informed consent
  • Have at least 4 heavy drinking days (≥ 5 drinks per day for men, and 4 for women) in the past 60 days
  • Stop signal reaction time on a stop signal task>233

Exclusion Criteria:

  • Severe neurological conditions (severe traumatic brain injury/stroke/active seizure disorder)
  • Heart disease [mitral valve prolapse, left ventricular hypertrophy, cardiac arrhythmias, angina, myocardial infarction, unstable angina, cardiac syncope or pre-syncope, any electrocardiogram (ECG) finding that suggests the presence of one of these conditions]
  • Uncontrolled hypertension (systolic blood pressure >160, diastolic blood pressure >100)
  • Heart rate greater than 70% of the maximum expected for age [0.70(220-age)]
  • Chronic renal or hepatic failure
  • Recent pancreatitis
  • Insulin-dependent diabetes
  • Other urgent medical problems
  • Elevated liver function tests (AST or ALT greater than 4 times normal; modafinil is metabolized primarily by the liver)
  • Schizophrenia, schizoaffective disorder, Bipolar I disorder, suicidal thoughts in the last month
  • Current moderate or severe other substance use disorder (SUD) (except nicotine or marijuana)
  • Active legal problems with the potential to result in incarceration
  • Pregnancy or lactation, or child bearing age and not on birth control
  • Current daily use of anti-craving medications, stimulants, benzodiazepines, opiates, anti-psychotics; current daily use of tricyclic antidepressants, bupropion, monoamine oxidase inhibitors, serotonin and norepinephrine reuptake inhibitors, or therapeutic doses (for bipolar disorder) of mood stabilizers
  • Taking a medication contraindicated for use with modafinil

Sites / Locations

  • Mind Research Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Modafinil

Placebo

Arm Description

Modafinil 300 mg by mouth each day

Identical looking capsule/number of capsules by mouth each day without active medication

Outcomes

Primary Outcome Measures

Time to Relapse
Time to relapse, starting 7 days after treatment initiation (after medication has reached maximum tolerated dose), to heavy drinking days (>4 standard drinks for men, >3 standard drinks for women); abstinent is coded as 9*7=63; dropout not included

Secondary Outcome Measures

Drinks Per Drinking Day
drinks per drinking day weeks 4-6
Drinks Per Week
drinks per week weeks 4-6
Percent Days Abstinent
percent days abstinent weeks 4-6

Full Information

First Posted
January 4, 2018
Last Updated
May 8, 2020
Sponsor
The Mind Research Network
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1. Study Identification

Unique Protocol Identification Number
NCT03424681
Brief Title
Modafinil for the Treatment of Alcohol Use Disorders
Official Title
Modafinil for the Treatment of Alcohol Use Disorders: Targeting Impaired Response Inhibition
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
December 11, 2017 (Actual)
Primary Completion Date
August 31, 2018 (Actual)
Study Completion Date
August 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Mind Research Network

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Alcohol use disorder (AUD) is a major cause of morbidity and mortality and more treatments are needed, especially pharmacotherapies. There are a variety of efficacious treatments for AUD, but effect sizes are small, and vary from study to study. Medications may be more effective if particular subgroups of AUD are targeted. Identifying the mechanisms of action of a particular medication will help identify the subtypes more likely to respond to therapy. Global impulse control is a rational treatment target, and improving it is a likely mechanisms by which some medications for AUD work, especially in subtypes of AUD with impaired impulse control at baseline. Modafinil is a medication that is FDA approved for the treatment of narcolepsy, and is relatively safe and tolerable. There is reason to believe it may improve impulse control, and underlying neural circuitry, and may work best to improve alcohol use outcomes in AUD with poor impulse control. The overall aim of this study is to investigate the effects of modafinil on task performance and the integrity of neural circuits mediating response inhibition in treatment-seeking AUD with poor response inhibition, to establish target engagement. Secondary aims are to measure whether target engagement mediates improvement in alcohol use outcomes, and to utilize machine learning to identify neural and behavioral markers which best predict treatment outcomes. Twenty-four individuals with AUD and impaired response inhibition will be enrolled in the study, randomized to modafinil or placebo, and treated for 6 weeks. Functional magnetic resonance imaging brain scans during a response inhibition task and during rest will be obtained at baseline and 2 weeks. Aversive stimuli will be included in the response inhibition task to assure that efficacy generalizes to several conditions. Diffusion imaging and arterial spin labeling sequences will also be obtained. Investigators predict that modafinil will significantly increase brain activity in the medial and lateral prefrontal cortex during response inhibition, thereby establishing target engagement, and that it will improve alcohol use outcomes. Findings will provide information about whether or not a larger R01 trial investigating the efficacy of modafinil for individuals with AUD and impaired response inhibition is warranted.
Detailed Description
see above.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Use Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modafinil
Arm Type
Experimental
Arm Description
Modafinil 300 mg by mouth each day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Identical looking capsule/number of capsules by mouth each day without active medication
Intervention Type
Drug
Intervention Name(s)
Modafinil
Other Intervention Name(s)
Provigil
Intervention Description
Modafinil 300 mg by mouth daily
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Time to Relapse
Description
Time to relapse, starting 7 days after treatment initiation (after medication has reached maximum tolerated dose), to heavy drinking days (>4 standard drinks for men, >3 standard drinks for women); abstinent is coded as 9*7=63; dropout not included
Time Frame
over 9 weeks
Secondary Outcome Measure Information:
Title
Drinks Per Drinking Day
Description
drinks per drinking day weeks 4-6
Time Frame
Weeks 4-6
Title
Drinks Per Week
Description
drinks per week weeks 4-6
Time Frame
Weeks 4-6
Title
Percent Days Abstinent
Description
percent days abstinent weeks 4-6
Time Frame
Weeks 4-6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females age 18-65 meeting Diagnostic and Statistical Manual V criteria for moderate or severe AUD in the past year Interested in cutting down or quitting Able to provide voluntary informed consent Have at least 4 heavy drinking days (≥ 5 drinks per day for men, and 4 for women) in the past 60 days Stop signal reaction time on a stop signal task>233 Exclusion Criteria: Severe neurological conditions (severe traumatic brain injury/stroke/active seizure disorder) Heart disease [mitral valve prolapse, left ventricular hypertrophy, cardiac arrhythmias, angina, myocardial infarction, unstable angina, cardiac syncope or pre-syncope, any electrocardiogram (ECG) finding that suggests the presence of one of these conditions] Uncontrolled hypertension (systolic blood pressure >160, diastolic blood pressure >100) Heart rate greater than 70% of the maximum expected for age [0.70(220-age)] Chronic renal or hepatic failure Recent pancreatitis Insulin-dependent diabetes Other urgent medical problems Elevated liver function tests (AST or ALT greater than 4 times normal; modafinil is metabolized primarily by the liver) Schizophrenia, schizoaffective disorder, Bipolar I disorder, suicidal thoughts in the last month Current moderate or severe other substance use disorder (SUD) (except nicotine or marijuana) Active legal problems with the potential to result in incarceration Pregnancy or lactation, or child bearing age and not on birth control Current daily use of anti-craving medications, stimulants, benzodiazepines, opiates, anti-psychotics; current daily use of tricyclic antidepressants, bupropion, monoamine oxidase inhibitors, serotonin and norepinephrine reuptake inhibitors, or therapeutic doses (for bipolar disorder) of mood stabilizers Taking a medication contraindicated for use with modafinil
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claire Wilcox, MD
Organizational Affiliation
Mind Research Network
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mind Research Network
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87106
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Modafinil for the Treatment of Alcohol Use Disorders

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