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临床试验/NCT00183196
NCT00183196已完成3 期

Gabapentin as an Adjunct to Naltrexone for Alcoholism

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2003年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
150
试验地点
1
主要终点
Time to Relapse to Drinking

研究概览

简要总结

The purpose of this study is to determine whether, after a period of abstinence, adding 6 weeks of gabapentin (a medication approved to treat seizures) to a standard 16-week naltrexone (an opiate blocking agent approved for the treatment of alcohol dependence) treatment protocol is helpful in decreasing relapse to drinking compared to naltrexone alone or placebo. All participants will receive alcohol counseling.

详细描述

Subjects will enter the trial after maintaining 4 days of abstinence. During this period multiple assessments will be collected. After entering the double blind treatment portion of the study, they will be evaluated weekly for the first month, then bi-weekly until week 12 and again at week 16. There will be two follow-up visits at weeks 28 and 40. Urinary riboflavin and pill counts will be utilized to determine compliance with the medication regime.

Comparison(s): Naltrexone (50 mg/day) alone for 16-weeks; naltrexone (50 mg/day) for 16-weeks plus gabapentin (up to 1200 mg/day in divided doses) for the first 6 weeks, or inactive placebos. All subjects will receive up to 20 sessions of individual alcohol counseling.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Meet criteria for primary alcohol dependence including loss of control of drinking
  • No more than one previous inpatient medical detoxification
  • Consumes on average 5 standard drinks for men and 4 standard drinks for women
  • Able to maintain sobriety for 4 days (with or without detox medications).
  • Able to read and understand questionnaires and Informed Consent
  • Lives within 50 miles of the study site

排除标准

  • Currently meets DSM-IV criteria for any other psychoactive substance dependency disorder except nicotine dependence
  • Ever abused opiates
  • Any psychoactive substance abuse, except marijuana and nicotine within the last 30 days as evidenced by subject report, collateral report, or urine drug screen.
  • Meets DSM-IV criteria for current Axis I disorder of major depression, panic disorder, obsessive-compulsive disorder, post-traumatic stress syndrome, bipolar affective disorder, dissociative disorder or eating disorder, schizophrenia, or any other psychotic disorder or organic mental disorder.
  • Has current suicidal or homicidal ideation
  • Need for maintenance or acute treatment with any psychoactive medication including antiseizure medications.
  • Current use of disulfiram.
  • Clinically significant medical problems, such as cardiovascular, renal, GI or endocrine problem that would impair participation or limit medication ingestion.
  • Hepatocellular disease indicated by elevations of SGPT (ALT) and SGOT (AST) of at least 3.0 times normal at screening and/or after 5 days of abstinence.
  • Sexually active females of child bearing potential who are pregnant (by urine HCG), nursing or who are not using a reliable form of birth control.
  • Has current charges pending for a violent crime (not including DUI related offenses).
  • Does not have a stable living situation and a reliable source of collateral reporting.
  • Has taken an opiate antagonist drug in the last month.
  • Has taken gabapentin in the last month or has experienced adverse effects from it at any time in the past.

研究组 & 干预措施

1

Active Comparator

Naltrexone plus placebo

干预措施: Naltrexone (Drug)

2

Active Comparator

naltrexone + gabapentin

干预措施: Naltrexone plus Gabapentin (Drug)

3

Sham Comparator

Placebo plus placebo

干预措施: Inactive Placebo (Other)

结局指标

主要结局

Time to Relapse to Drinking

时间窗: 16 weeks

Time to relapse drinking which is 5 standard drinks perday for males and 4 standard drinks per day for females. Subjects had a minimum of 4 days of abstinence prior to being entered into the protocol.

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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