100
Participants
Start Date
May 31, 2013
Primary Completion Date
January 31, 2018
Study Completion Date
March 12, 2019
Morphine
0.08mg/kg will be administered to participants randomly assigned to receive the drug via IV bolus during each quantitative sensory testing session (after one night of uninterrupted sleep and after 2 nights of forced awakenings).
Saline Placebo
Saline Placebo will administered to participants randomly assigned to receive the placebo via IV bolus during each quantitative sensory testing session (after one night of uninterrupted sleep and after 2 nights of forced awakenings).
Forced Awakenings
Participants will be awakened each hour during an 8 hour sleep opportunity period. One of the awakenings is for 60 minutes and randomly determined. The other 7 awakenings are for 20 minutes each, and are randomly scheduled to occur in either the first second or third tertile of each hour. The maximum total sleep time a participant will receive is 280 minutes.
Uninterrupted Sleep
Participants will receive an 8 hour period of undisturbed sleep
Johns Hopkins University Bayview Medical Center, Baltimore
National Institute on Drug Abuse (NIDA)
NIH
Johns Hopkins University
OTHER