跳至主要内容
临床试验/NCT00425711
NCT00425711终止不适用

An Open-Label Study of Acamprosate in DUI Court Participants

University of Oklahoma2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2007年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
4
试验地点
2
主要终点
time until relapse, i.e. any alcohol consumption

研究概览

简要总结

Acamprosate will be given to approximately 30 DUI Court participants for 3 months and outcomes will be monitored. The hypothesis is that acamprosate will be safe and well-tolerated and that subjects' craving and other symptoms related to addiction will improve over time.

详细描述

Purpose: The study is a 13 week open-label study of the use of acamprosate in subjects who have elected to participate in the DUI Court program in Tulsa County. Admission to the DUI Court is completely voluntary. Participants must apply for admission, undergo an initial evaluation, and receive approval by the District Attorney's office and the presiding judge. The four-phase program requires a minimum of 1 year to complete. Each phase requires counseling, mandatory random urine drug screens, mandatory daily breathalyzer tests, a nightly curfew and that the participant be gainfully employed or in school. Currently, approximately 10% of the participants are able to complete the program in the minimum 12 month requirement. The main objective of the study is to evaluate the duration of alcohol abstinence in DUI Court participants receiving acamprosate.

Design: Thirty subjects will be enrolled in the study. New DUI court participants, within 3 months of enrollment, will be invited to participate in the trial. Qualified subjects will receive, in addition to the required DUI court assessments and treatments, a physical examination, baseline safety laboratory, study drug, psychiatric evaluation, depressive and anxiety rating scales, a personality disorder questionnaire and vital signs taken at each visit. Alcohol and substance use will be assessed by self-report and validated with review of the court-ordered laboratory and breathalyzer tests.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adult males and females age 18 - 64 years of age
  • District Attorney-approved DUI Court participants within 3 months of enrollment into DUI Court
  • Currently meets DSM-IV criteria for alcohol dependence
  • Subject agrees to alcohol abstinence as a goal
  • Women must agree to use an approved method of birth control (tubal ligation, birth control pills, IUD)
  • Negative UCG (females only)
  • Treatment with an MAOI, other antidepressants, antipsychotics, anticonvulsants, mood stabilizers, or Saint John's Wort are permissible if subject has been on a stable dose for 3 months
  • Must have the ability to comprehend key components of the informed consent and provide consent
  • Current score of 15 or less on the Beck Depression Inventory II
  • Subject has undergone detoxification and is currently abstinent from alcohol

排除标准

  • History of allergy to acamprosate
  • Previously failed trial of acamprosate
  • Pregnancy, lactation, or unprotected intercourse during study period
  • Lifetime diagnosis of schizophrenia or schizoaffective disorder
  • Creatinine clearance <30 mL/minute. If serum creatinine is greater than 1.4 mg/dL then the Cockcroft-Gault equation will be used to estimate creatinine clearance
  • Active suicidality, a Beck Depression Inventory II suicide item score of > 2, or a Beck Depression Inventory II total score > 15
  • Any unstable medical condition which, in the opinion of the investigator, is considered clinically significant or could affect the subject's safety or ability to complete the study
  • Use of a benzodiazepine or other sedative-hypnotic agent (including kava kava or valerian), except for eszopiclone, zaleplon, or zolpidem < 3 times weekly over the last 4 weeks

研究组 & 干预措施

DUI Court Participants

Experimental

Individuals enrolled in the DUI Court treatment site will be recruited for the 13 week open-label trial of acamprosate.

干预措施: Acamprosate (Drug)

结局指标

主要结局

time until relapse, i.e. any alcohol consumption

时间窗: Baseline and weeks 2, 4, 8, and 12

次要结局

  • Proportion of days on which alcohol was consumed(baseline and weeks 2, 4, 8, and 12)
  • Obsessive Compulsive Drinking Scale scores(baseline and weeks 2, 4, 8, and 12)
  • Adverse events(baseline and weeks 2, 4, 8, and 12)
  • Admission to residential treatment or jail(baseline and weeks 2, 4, 8, and 12)
  • Depressive symptoms as measured by the Beck Depression Inventory II(baseline and weeks 2, 4, 8, and 12)
  • Anxiety symptoms as measured by the Beck Anxiety Inventory(baseline and weeks 2, 4, 8, and 12)
  • Penn Alcohol Craving Scale scores(baseline and weeks 2, 4, 8, and 12)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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