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Naltrexone Treatment for Alcoholic Women

Naltrexone: Consummatory Behaviors in Alcoholic Women

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000448
Enrollment
160
Registered
1999-11-03
Start date
1995-10-31
Completion date
2000-12-31
Last updated
2014-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcoholism, Eating Disorder

Brief summary

This study will assess naltrexone's effectiveness in treating alcoholism in women and provide information on its potential value in treating eating disorders common among alcoholic women. Alcoholic women with and without both eating disorders and depression will be randomly assigned to placebo or naltrexone treatment. Each group will receive behavioral therapy for 12 weeks, with followup 6 months after treatment.

Detailed description

Background: Despite important gender differences in drinking patterns, physiological effects of alcohol, and co-occurring psychiatric conditions, relatively little is known about the efficacy of naltrexone for the treatment of alcohol dependence in women. This study investigated the safety and efficacy of naltrexone in combination with Cognitive Behavioral Coping Skills Therapy (CBCST) in a sample of alcohol-dependent women, some with comorbid eating pathology. Methods: One hundred three women meeting DSM-IV criteria for alcohol dependence (29 with comorbid eating disturbances) were randomized to receive either naltrexone or placebo for 12 weeks in addition to weekly group CBCST.

Interventions

DRUGnaltrexone

Naltrexone is an opioid receptor antagonist used primarily in the management of alcohol dependence and opioid dependence.

DRUGPlacebo

A placebo is a simulated or otherwise medically ineffectual treatment for a disease or other medical condition intended to deceive the recipient.

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Meets criteria for alcohol dependence. Abstinent from alcohol for a period of at least 5 days. * Able to read English and complete study evaluations. * A stable residence and a telephone to ensure that subjects can be located during the study.

Exclusion criteria

* Meets criteria for dependence on another psychoactive substance besides alcohol or nicotine. * Regular use of psychoactive drugs except antidepressants. * Current use of disulfiram (Antabuse). * Psychotic or otherwise severely psychiatrically disabled. * Significant underlying medical conditions such as cerebral, renal, thyroid, or cardiac pathology. * Abstinent longer than 30 days prior to admission to program. * Hepatocellular disease or elevated bilirubin levels. * Individuals with present history of opiate abuse or who require the use of opioid analgesics. * Women who are pregnant, nursing, or not using a reliable method of birth control. * Women who are significantly overweight or significantly underweight.

Design outcomes

Primary

MeasureTime frameDescription
Time to first day of drinking12 week treatment period
Time to first day of heavy drinking12 weeksDefined as consuming 4 or more drinks during the 12-week period

Secondary

MeasureTime frameDescription
Percentage of heavy drinking days12 weeks of treatment
Beck Depression Index12 weeks of treatmentThe Beck Depression Inventory (BDI, BDI-1A, BDI-II), created by Dr. Aaron T. Beck, is a 21-question multiple-choice self-report inventory. Higher total scores indicate more severe depressive symptoms. This was administered bi-weekly throughout the treatment period.
Eating Disorder Examination (EDE)baseline, month 1, 2, 3The Eating Disorder Examination Interview (EDE) devised by Cooper & Fairburn (1987) is a semi-structured interview conducted by a clinician in the assessment of an eating disorder. The questions concern the frequency in which the patient engages in behaviors indicative of an eating disorder over a 28 day period. The test is scored on a 7 point scale from 0-6. With a zero score indicating not having engaged in the questioned behavior.
Obsessive Compulsive Drinking Scale (OCDS)Baseline, Month 1, 2, 3The OCDS was developed to reflect obsessionality and compulsivity related to craving and drinking behavior.
Percentage of days abstinent12 weeks of treatment

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026