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Wiley InterScience

Addiction

Addiction

Volume 101 Issue 10, Pages 1451 - 1462

Published Online: 10 Aug 2006

Journal compilation © 2010 Society for the Study of Addiction



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RESEARCH REPORT
Naltrexone versus acamprosate in the treatment of alcohol dependence: a multi-centre, randomized, double-blind, placebo-controlled trial
Kirsten C. Morley 1 , Maree Teesson 3 , Sophie C. Reid 6 , Claudia Sannibale 3,6 , Clare Thomson 6 , Nghi Phung 4 , Martin Weltman 2,4 , James R. Bell 3,5 , Kylie Richardson 1 & Paul S. Haber 1,3,6
  1 Central and   2 Western   3 Clinical School of Medicine, University of Sydney, NSW, Australia, National Drug and Alcohol Research Centre, University of New South Wales, NSW, Australia,   4 Department of Drug and Alcohol Medicine, Nepean Hospital, NSW, Australia,   5 Drug and Alcohol Unit, Prince of Wales Hospital, NSW, Australia and   6 Drug Health Services, Royal Prince Alfred Hospital, Camperdown, NSW, Australia
Correspondence to  Paul S. Haber, Drug Health Services, Royal Prince Alfred Hospital, Camperdown NSW 2050, Australia.
E-mail: phaber@mail.usyd.edu.au
Copyright © 2006 The Authors. Journal compilation © 2006 Society for the Study of Addiction
KEYWORDS
Acamprosate • alcohol dependence • compliance therapy • naltrexone • pharmacotherapy

ABSTRACT

Aim  To compare the efficacy of acamprosate and naltrexone in the treatment of alcohol dependence.

Design  A double-blind, placebo-controlled trial.

Setting  Three treatment centres in Australia.

Participants  A total of 169 alcohol dependent subjects were given naltrexone (50 mg/day), acamprosate (1998 mg/day) or placebo for 12 weeks.

Intervention  All subjects were offered manualized compliance therapy, a brief intervention that targets problems that may affect treatment compliance such as ambivalence and misperceptions about medication.

Measurements  Time to the first drink, time to first relapse, drinks per drinking day and cumulative abstinence.

Findings  In intention-to-treat analyses, there were no differences between groups on outcome measures of drinking, craving or biochemical markers. Similarly, analyses of the 94 subjects that completed the study in full and demonstrated 80% compliance, revealed no significant treatment effects. Differential treatment effects were identified after stratification according to scores on the Alcohol Dependence Scale (ADS) and Depression Anxiety and Stress Scale (DASS). A significant beneficial treatment effect on time to first relapse was revealed for subjects with 'no depression' allocated to naltrexone (n = 56; P < 0.01). In addition, a significant beneficial treatment effect was revealed in subjects with 'low dependence' allocated to naltrexone (n = 34; P < 0.05).

Conclusions  The results of this study support the efficacy of naltrexone in the relapse prevention of alcoholism amongst those with low levels of clinical depression and alcohol dependence severity. No effect of acamprosate was found in our sample.


Submitted 14 December 2005; initial review completed 17 February 2006; final version accepted 24 April 2006

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1360-0443.2006.01555.x About DOI

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