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Clinical Trial Summary

The principal aim of this exploratory study is to examine whether the addition of aripiprazole to naltrexone will enhance efficacy over naltrexone alone in a 16-week randomized, placebo-controlled clinical trial, in which all subjects will be provided medical management as delivered in the COMBINE Study (Anton et al, 2006). To test whether medication treatment will reduce drinking compared to placebo treatment alone in the context of medical management and whether naltrexone plus aripiprazole will reduce drinking compared to naltrexone treatment alone in the context of medical management.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00667875
Study type Interventional
Source Medical University of South Carolina
Contact
Status Completed
Phase Phase 2
Start date April 2008
Completion date May 2011

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