Acamprosate is approved by the Food and Drug Administration (FDA) for the treatment of alcoholism. The purpose of this study is to see if initiating acamprosate early in alcohol detoxification instead of waiting until detoxification has been completed effects the course of detoxification, adverse events during detoxification, drop out rate during the rehabilitative treatment phase, or overall efficacy of acamprosate for those with alcohol dependence who plan to receive at least two months of rehabilitative pharmacotherapy with acamprosate.
Primary Outcome Measures:
- 1) the mean number of adverse events rated moderate to severe; [ Time Frame: Phase I: up to 2 weeks ] [ Designated as safety issue: No ]
- 2) the week of detoxification treatment discontinuation; [ Time Frame: Phase I: up to 2 weeks ] [ Designated as safety issue: No ]
- 3) the total amount of oxazepam given; [ Time Frame: Phase I: up to 2 weeks ] [ Designated as safety issue: No ]
- 4) the rate of change in CIWA scores. [ Time Frame: Phase I: up to 2 weeks ] [ Designated as safety issue: No ]
- 1) the mean number of adverse events rated moderate to severe; [ Time Frame: Phase II: 10 weeks ] [ Designated as safety issue: No ]
- 2) the week of open-label treatment discontinuation; [ Time Frame: Phase II: 10 weeks ] [ Designated as safety issue: No ]
- 3) any reemergence of detoxification symptoms; [ Time Frame: Phase II: 10 weeks ] [ Designated as safety issue: No ]
- 4) % pills taken over what was proposed to be prescribed (medication exposure); [ Time Frame: Phase II: 10 weeks ] [ Designated as safety issue: No ]
- 5) % days abstinent; [ Time Frame: Phase II: 10 weeks ] [ Designated as safety issue: No ]
- 6) % days heavy drinking. [ Time Frame: Phase II: 10 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Changes in alcohol craving will be measured by Penn Alcohol Craving Scale (PACS; Flannery et al, 1999) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- Changes in anxiety symptoms will be measured by the Structured Interview Guide for the Hamilton Anxiety Rating Scale (SIGH-A; Hamilton, 1969) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- Changes in depressive symptoms will be measured by the Structured Interview Guide for the Hamilton Depression Rating Scale (SIGH-D; Hamilton 1967) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- Changes in social functioning will be measured by several of the subscales of the Addiction Severity Index (ASI; McLellan et al, 1992); namely, medical, legal, psychiatric, and family/social. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- Quality of Life, measured by the Short Form-36 Health Status Questionnaire (SF-36; Ware & Sherbourne, 1999) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- Overall clinical impression of improvement will be measured by the Clinical Global Impression Scale (CGI) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
| Enrollment: |
40 |
| Study Start Date: |
October 2006 |
| Study Completion Date: |
November 2007 |
| Primary Completion Date: |
September 2007 (Final data collection date for primary outcome measure) |
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1: Experimental
Acamprosate
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Drug: Acamprosate
3 pills (666 mg) for 1998mg/day
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2: Placebo Comparator
Placebo
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Drug: Placebo
3 pills (666mg) for 1998mg/day
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Biphasic clinical trial, consisting of a randomized, double-blind, placebo-controlled detoxification treatment phase (DP), followed by 9-week open-label rehabilitative treatment phase (RP).