Oral vs. Injectable Naltrexone for Hospitalized Veterans With Alcohol Dependence

Completed · Phase 3

Conditions studied: Alcohol Dependence

In brief

The over-arching goal of the proposed project is to understand the impact of medication adherence upon engagement in behavioral treatment for alcohol use disorders. The proposed project is a pilot feasibility study of inpatient veterans with problem alcohol use at the William S. Middleton VA Hospital (Madison, WI). Participants will be randomized to one of two parallel study conditions: (1) an initial 50 mg oral dose of naltrexone prior to hospital discharge plus a 30-day prescription for oral naltrexone, or (2) a single 380 mg intramuscular injection of naltrexone administered prior to discharge and a second injection one month later. The central hypothesis is that hospital-administered injectable naltrexone, when compared to daily oral naltrexone taken at home, will reduce alcohol use in the days immediately following hospitalization. Injectable naltrexone has been efficacious vs. placebo in addition to behavioral treatment in several studies. However, it has yet to be examined in head-to-head comparison with oral naltrexone, or in the hospital setting as an intervention that might facilitate behavioral treatment follow up after discharge.

Key facts

Study ID

NCT01856712

Run by

University of Wisconsin, Madison

People needed

54

Starts

2013-05-01

Expected to finish

2016-01-01

Last updated by the study team

2019-03-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years or older
• diagnostic criteria for alcohol dependence or abuse
• women of childbearing potential who have a negative screening urine pregnancy test and are willing to use reliable birth control methods throughout the duration of the study

You may not qualify if…

• active or recently active (less than 1 year) opioid dependence or daily use of opioid analgesics
• acute hepatitis or liver failure
• pregnancy
• women who are currently breastfeeding
• active suicidality
• inability to provide written informed consent as determined by study comprehension questions

Where it is running

• University of Wisconsin - Department of Family Medicine — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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