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Clinical Trial Summary

The primary aim of the supplemental study is to provide POC testing of aprepitant as a treatment for comorbid alcohol and cannabis dependence. The data analysis plan specified in the parent grant will likewise be applied to the supplemental project to test for effects of aprepitant vs placebo on measures of alcohol and cannabis use and protracted withdrawal. The primary hypothesis is that subjects treated with aprepitant will have significantly less alcohol and marijuana use than subjects treated with placebo.


Clinical Trial Description

Consistent with the scope and methods of the parent grant, this will be a randomized, double-blind, placebo-controlled, parallel groups, Phase II, single-site, 8-week clinical trial of aprepitant 125 mg/d or placebo. Participants will be 40 outpatients seeking treatment for concurrent alcohol and cannabis dependence. All participants will receive weekly protocol-specific counseling. Research assessments will occur weekly through the treatment phase of the 8-week study. Post treatment follow-up assessments will occur at Weeks 9 and 12. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02210195
Study type Interventional
Source The Scripps Research Institute
Contact
Status Completed
Phase Phase 2
Start date July 2014
Completion date December 2016

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