Effects of Cortical Dopamine Regulation on Drinking, Craving, and Cognitive Control

NCT02949934 — Phase 2, Completed, 90 participants, Medical University of South Carolina

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RegistryNCT02949934
StatusCompleted
PhasePhase 2
Study typeInterventional; randomized, parallel, masking: double, treatment
Enrollment90 (Actual)
SponsorMedical University of South Carolina (Other); collaborators: National Institute on Alcohol Abuse and Alcoholism (NIAAA)
ConditionsAlcohol Use Disorder
InterventionsTolcapone, Placebo (Drug)
Datesstart 2016-05-01, primary completion 2021-04-13, completion 2021-04-13, first posted 2016-10-31, last updated 2023-06-09
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Alcohol Use Disorder All trials of Tolcapone All trials of Placebo

-Summary

The purpose of this study is to determine whether the catechol-O-methyltransferase (COMT) inhibitor tolcapone, relative to placebo, reduces alcohol drinking and alcohol cue-elicited brain activation and increases brain activation associated with cognitive control as a function of a participant's genotype at a polymorphism in the COMT gene.

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+Arms and interventions

ArmTypeInterventionsDescription
Placebo/rs4680 val/valPlacebo comparatorDrug: PlaceboPlacebo three times per day for eight days Individuals with the rs4680 val/val genotype
Tolcapone/rs4680 val/valActive comparatorDrug: TolcaponeTolcapone 100 mg three times per day for three days Tolcapone 200 mg three times per day for five days Individuals with the rs4680 val/val genotype
Placebo/rs4680 val/metPlacebo comparatorDrug: PlaceboPlacebo three times per day for eight days Individuals with the rs4680 val/met genotype
Tolcapone/rs4680 val/metActive comparatorDrug: TolcaponeTolcapone 100 mg three times per day for three days Tolcapone 200 mg three times per day for five days Individuals with the rs4680 val/met genotype
Placebo/rs4680 met/metPlacebo comparatorDrug: PlaceboPlacebo three times per day for eight days Individuals with the rs4680 met/met genotype
Tolcapone/rs4680 met/metActive comparatorDrug: TolcaponeTolcapone 100 mg three times per day for three days Tolcapone 200 mg three times per day for five days Individuals with the rs4680 met/met genotype
  • Tolcapone (Drug), also known as Tasmar
  • Placebo (Drug)

+Outcome measures

Primary outcomes

  • Total Number of Standard Drinks Per Day Consumed During Natural (Usual Environment) Conditions [Days 1-6 of study medication ingestion]: Number of standard alcoholic drinks per day that participants reported consuming, as assessed by the Timeline Follow-back method.
  • Total Number of Drinks Under Controlled Conditions (Bar Lab) [2 hours during the alcohol challenge procedure]: Total number of drinks, out of 8 possible, that participants chose to consume in the bar laboratory after receipt of a priming drink, targeted by sex and body weight to produce a breath alcohol concentration of 0.03 g/dL. Each of the drinks that participants chose to consume was targeted to produce a breath alcohol concentration of 0.015 g/dL. Participants were given a "bar credit" of $16 with which to "purchase" drinks, at the cost of $2/drink, and were told that any money they did not spend would be given to them the following day.

Other outcomes

  • Cognitive-control-associated Brain Activation (fMRI) [7 days--change between baseline and scan on day 7]: Magnitude of change between baseline and day 7 scan in the BOLD signal in the right inferior frontal gyrus to spatial working memory
  • Alcohol Cue-elicited Brain Activation (fMRI) [7 days--change between baseline and scan on day 7]: Magnitude of change between baseline and day 7 scan in the right inferior frontal gyrus blood oxygenation level dependent (BOLD) signal to alcohol cues, relative to neutral beverage cues (alcohol cue reactivity task described in Schacht et al., 2013, Neuropsychopharmacology)

+Eligibility

Sex: All, ages: 21 Years to 40 Years

Inclusion Criteria:

1. Age 21-40 (to focus on an age group still on a trajectory of increasing alcohol consumption).
2. Meets Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria for current Alcohol Use Disorder.
3. Currently not engaged in, and does not want treatment for, alcohol-related problems.
4. Able to read and understand questionnaires and informed consent.
5. Lives within 50 miles of the study site.
6. Able to maintain abstinence from alcohol for two days (without the aid of detoxification medications), as determined by self report and breathalyzer measurements.

Exclusion Criteria:

1. Current DSM-5 diagnosis of any other substance use disorder except Nicotine Use Disorder.
2. Any psychoactive substance use (except marijuana and nicotine) within the last 30 days, as indicated by self-report and urine drug screen. For marijuana, no use within the last seven days by verbal report and negative (or decreasing) urine tetrahydrocannibinol (THC) levels.
3. Current DSM-5 Axis I diagnosis, including major depression, panic disorder, obsessive-compulsive disorder, post-traumatic stress disorder, bipolar affective disorder, schizophrenia, dissociative disorders, eating disorders, or any other psychotic or organic mental disorder.
4. Current suicidal ideation or homicidal ideation.
5. Need for maintenance or acute treatment with any psychoactive medication, including antiepileptic medications.
6. Currently taking medication known to affect alcohol intake (e.g., disulfiram, naltrexone, acamprosate, topiramate).
7. History of severe alcohol withdrawal (e.g., seizure, delirium tremens), as evidenced by self-report and assessment with Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-Ar).
8. Clinically significant medical problems such as cardiovascular, renal, gastrointestinal, or endocrine problems that would impair participation or limit medication ingestion.
9. Past alcohol-related medical illness, such as gastrointestinal bleeding, pancreatitis, or peptic ulcer.
10. Current or past hepatocellular disease, as indicated by verbal report or elevations of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) greater than the upper limit of the normal range at screening.
11. Females of childbearing potential who are pregnant (by urine human chorionic gonadotropin), nursing, or who are not using a reliable form of birth control.
12. Current charges pending for a violent crime (not including drinking while intoxicated).
13. Lack of a stable living situation.
14. Presence of ferrous metal in the body, as evidenced by metal screening and self-report.
15. Severe claustrophobia or morbid obesity that preclude placement in the MRI scanner.
16. History of head injury with > 2 minutes of unconsciousness.

+Posted results

Participant flow

MilestonePlacebo/rs4680 Val/ValTolcapone/rs4680 Val/ValPlacebo/rs4680 Val/MetTolcapone/rs4680 Val/MetPlacebo/rs4680 Met/MetTolcapone/rs4680 Met/Met
Started161217161514
Completed151217151414
Not completed100110

Outcome results

  • Total Number of Standard Drinks Per Day Consumed During Natural (Usual Environment) Conditions (Primary), Mean, standard drinks per day: Placebo/rs4680 Val/Val 6.018 +/- 0.586; Tolcapone/rs4680 Val/Val 3.534 +/- 0.668; Placebo/rs4680 Val/Met 3.998 +/- 0.538; Tolcapone/rs4680 Val/Met 5.012 +/- 0.567; Placebo/rs4680 Met/Met 5.271 +/- 0.596; Tolcapone/rs4680 Met/Met 5.949 +/- 0.602 (p 0.013)
  • Total Number of Drinks Under Controlled Conditions (Bar Lab) (Primary), Mean, Drinks: Placebo/rs4680 Val/Val 5.353 +/- 0.721; Tolcapone/rs4680 Val/Val 3.256 +/- 0.955; Placebo/rs4680 Val/Met 5.01 +/- 0.812; Tolcapone/rs4680 Val/Met 4.964 +/- 0.752; Placebo/rs4680 Met/Met 1.68 +/- 0.935; Tolcapone/rs4680 Met/Met 4.732 +/- 0.704 (p 0.014)
  • Cognitive-control-associated Brain Activation (fMRI) (Other pre specified), Mean, Arbitrary units (Day 7 minus Baseline): Placebo/rs4680 Val/Val -0.196 +/- .086; Tolcapone/rs4680 Val/Val -0.063 +/- .082; Placebo/rs4680 Val/Met -0.178 +/- .074; Tolcapone/rs4680 Val/Met 0.076 +/- .076; Placebo/rs4680 Met/Met -0.017 +/- .082; Tolcapone/rs4680 Met/Met -0.224 +/- .086 (p 0.062)
  • Alcohol Cue-elicited Brain Activation (fMRI) (Other pre specified), Mean, Arbitrary units (Day 7 minus Baseline): Placebo/rs4680 Val/Val 0.09 +/- .070; Tolcapone/rs4680 Val/Val -0.045 +/- .070; Placebo/rs4680 Val/Met 0.066 +/- .063; Tolcapone/rs4680 Val/Met -0.164 +/- .063; Placebo/rs4680 Met/Met 0.138 +/- .070; Tolcapone/rs4680 Met/Met .006 +/- .070 (p 0.83)

Adverse events

Time frame: 8 days

ArmDeathsSerious adverse eventsOther adverse events
Placebo/rs4680 Val/Val0/16 (0.0%)0/16 (0.0%)1/16 (6.3%)
Tolcapone/rs4680 Val/Val0/12 (0.0%)0/12 (0.0%)0/12 (0.0%)
Placebo/rs4680 Val/Met0/17 (0.0%)0/17 (0.0%)0/17 (0.0%)
Tolcapone/rs4680 Val/Met0/16 (0.0%)0/16 (0.0%)1/16 (6.3%)
Placebo/rs4680 Met/Met0/15 (0.0%)0/15 (0.0%)0/15 (0.0%)
Tolcapone/rs4680 Met/Met0/14 (0.0%)0/14 (0.0%)0/14 (0.0%)

Other adverse events by term

TermOrgan systemPlacebo/rs4680 Val/ValTolcapone/rs4680 Val/ValPlacebo/rs4680 Val/MetTolcapone/rs4680 Val/MetPlacebo/rs4680 Met/MetTolcapone/rs4680 Met/Met
PregnancyPregnancy, puerperium and perinatal conditions0/160/120/171/160/150/14
RashSkin and subcutaneous tissue disorders1/160/120/170/160/150/14

+Locations (1)

FacilityCityCountryStatus
Medical University of South CarolinaCharleston, South CarolinaUnited States

+Publications

  • Results publication: Schacht JP, Yeongbin Im, Hoffman M, Voronin KE, Book SW, Anton RF. Effects of pharmacological and genetic regulation of COMT activity in alcohol use disorder: a randomized, placebo-controlled trial of tolcapone. Neuropsychopharmacology. 2022 Oct;47(11):1953-1960. doi: 10.1038/s41386-022-01335-z. Epub 2022 May 6. PMID 35523943

+Study documents

+Funding

NIH grants: P50AA010761