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临床试验/NCT02949934
NCT02949934已完成2 期

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

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2016年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
90
试验地点
1
主要终点
Total Number of Standard Drinks Per Day Consumed During Natural (Usual Environment) Conditions

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
21 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • Current DSM-5 diagnosis of any other substance use disorder except Nicotine Use Disorder.
  • 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.
  • 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.
  • Current suicidal ideation or homicidal ideation.
  • Need for maintenance or acute treatment with any psychoactive medication, including antiepileptic medications.
  • Currently taking medication known to affect alcohol intake (e.g., disulfiram, naltrexone, acamprosate, topiramate).
  • 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).
  • Clinically significant medical problems such as cardiovascular, renal, gastrointestinal, or endocrine problems that would impair participation or limit medication ingestion.
  • Past alcohol-related medical illness, such as gastrointestinal bleeding, pancreatitis, or peptic ulcer.
  • 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.
  • Females of childbearing potential who are pregnant (by urine human chorionic gonadotropin), nursing, or who are not using a reliable form of birth control.
  • Current charges pending for a violent crime (not including drinking while intoxicated).
  • Lack of a stable living situation.
  • Presence of ferrous metal in the body, as evidenced by metal screening and self-report.
  • Severe claustrophobia or morbid obesity that preclude placement in the MRI scanner.
  • History of head injury with > 2 minutes of unconsciousness.

研究组 & 干预措施

Tolcapone/rs4680 met/met

Active Comparator

Tolcapone 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

干预措施: Tolcapone (Drug)

Placebo/rs4680 val/val

Placebo Comparator

Placebo three times per day for eight days

Individuals with the rs4680 val/val genotype

干预措施: Placebo (Drug)

Tolcapone/rs4680 val/val

Active Comparator

Tolcapone 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

干预措施: Tolcapone (Drug)

Placebo/rs4680 val/met

Placebo Comparator

Placebo three times per day for eight days

Individuals with the rs4680 val/met genotype

干预措施: Placebo (Drug)

Tolcapone/rs4680 val/met

Active Comparator

Tolcapone 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

干预措施: Tolcapone (Drug)

Placebo/rs4680 met/met

Placebo Comparator

Placebo three times per day for eight days

Individuals with the rs4680 met/met genotype

干预措施: Placebo (Drug)

结局指标

主要结局

Total Number of Standard Drinks Per Day Consumed During Natural (Usual Environment) Conditions

时间窗: 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)

时间窗: 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.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Raymond F. Anton

Distinguished University Professor

Medical University of South Carolina

研究点 (1)

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