10
Participants
Start Date
October 31, 2011
Primary Completion Date
December 31, 2012
Study Completion Date
December 31, 2012
Pramipexole
Participants will receive pramipexole ER 0.375, .075, 1.5, 2.25, and 3mg/d in an ascending-dose pattern.
Placebo
Participants will receive matching placebo pills. The placebo group is included to maintain the blind, rather than as a comparison group.
Michael E. DeBakey VA Medical Center, Houston
National Institute on Drug Abuse (NIDA)
NIH
Baylor College of Medicine
OTHER