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Clinical Trial Summary

The primary objective of this study is to evaluate the abuse potential of dronabinol oral solution in recreational cannabinoid users.


Clinical Trial Description

Following a four-day period for screening and qualification, there are five treatment visits with a minimum 8-day washout between treatments. Each participant will receive all treatments in a 5-way crossover design. ;


Study Design

Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor)


Related Conditions & MeSH terms


NCT number NCT02094599
Study type Interventional
Source INSYS Therapeutics Inc
Contact
Status Completed
Phase Phase 1
Start date February 2014
Completion date May 2014