9
Participants
Start Date
September 30, 2012
Primary Completion Date
December 31, 2014
Study Completion Date
December 31, 2014
Buspirone
Subjects will be maintained on oral buspirone (10 mg administered 3 times daily) for 6 days each during the study in random order.
Placebo
Subjects will be maintained on oral placebo (0 mg administered 3 times daily) for 6 days each during the study in random order.
University of Kentucky Medical Center, Lexington
National Institute on Drug Abuse (NIDA)
NIH
William Stoops
OTHER