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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00249379
Other study ID # NIAAAWEA-K23-00222-B
Secondary ID K23AA000222NIH G
Status Completed
Phase Phase 4
First received November 4, 2005
Last updated October 10, 2011
Start date June 2005
Est. completion date August 2008

Study information

Verified date October 2011
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test how tolerable and effective acamprosate is when used to prevent alcohol relapse in criminal justice supervisees (those on probation, parole, or in drug court).


Description:

Acamprosate has been an available treatment for alcohol dependence outside the United States and has recently been approved by the U.S. Food and Drug Administration as an effective therapy for alcohol dependence. In the past ten years, drug court programs have been implemented as one possible solution to reduce the burden placed on state and federal correctional systems. These programs are generally focused on non-violent drug dependent offenders and are offered as an alternative to incarceration. However, the use of acamprosate has never been examined for alcohol relapse prevention among a drug court population, or among those on probation or parole.

Comparison: Alcohol-dependent criminal justice supervisees who receive acamprosate, compared to participants who do not receive acamprosate.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- History of alcohol dependence in the year before entering criminal justice supervision

- Currently under criminal justice supervision (drug court, probation, or parole) in central Virginia

Exclusion Criteria:

- Pregnant or nursing a baby

- Known sensitivity to acamprosate

- Elevated serum creatinine level or other evidence of kidney problems

- Symptoms of severe depression or suicidal ideation

- Non-English speaking such that they cannot provide informed consent

- Cognitive impairment such that they cannot provide informed consent

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Acamprosate
Alcohol-dependent criminal justice supervisees will receive acamprosate

Locations

Country Name City State
United States Virginia Commonwealth University Medical Center Richmond Virginia

Sponsors (2)

Lead Sponsor Collaborator
Virginia Commonwealth University National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Days of drinking and other drug use Study period No
Primary Level of acceptance Study period No
Secondary Retention in drug court Study period No
Secondary Days of employment Study period No
Secondary Stable housing Study period No
Secondary Recidivism rates Study period No
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