Use of Naltrexone in a Clinical Setting

National Institute on Alcohol Abuse and Alcoholism (NIAAA)300 enrolled

Overview

This 12-week trial will compare individuals receiving naltrexone or placebo plus substance abuse counseling therapy versus those receiving only substance abuse counseling therapy in a rural, nonacademic setting. A followup period of 12 months is included. The effect on service utilization and the cost of the addition of naltrexone to treatment services for alcohol dependence also will be assessed. The study will expand existing research concerning the effectiveness of naltrexone in clinical trials versus a clinical setting.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

300

Conditions

Alcoholism

Interventions

naltrexone (Revia)DRUG

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Meets criteria for alcohol dependence (within the past 3 months). * Meets criteria for another substance use disorder (except narcotic dependence) but must identify alcohol as the primary substance of abuse. * Must be able to provide an informed consent. * Consent to random assignment and be willing to commit to possible medication treatment and research follow-up. * Must be eligible for treatment at the Dorchester Alcohol and Drug Commission. Exclusion Criteria: * Meets criteria for opiate dependence. * Clinically significant medical problems such as collagen-vascular disease, cardiovascular, renal, gastrointestinal or endocrine problem that would impair participation or limit medication ingestion. * Hepatocellular disease. * Women who are pregnant, nursing, or not practicing an effective means of birth control. * Currently being prescribed naltrexone. * Known sensitivity or allergy to naltrexone.

Locations (1)

Center for Drug and Alcohol Programs, Medical University of South Carolina

Charleston, South Carolina, United States

Data from ClinicalTrials.gov

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