24
Participants
Start Date
December 15, 2022
Primary Completion Date
December 31, 2026
Study Completion Date
December 31, 2026
n-acetylcysteine
Subjects will be randomized to receive 2.4 oral n-acetylcysteine daily.
Hydromorphone
Subjects will receive up to 192 mg oral hydromorphone daily.
Placebo n-acetylcystine
Subjects will be randomized to receive placebo n-acetylcysteine daily.
Placebo hydromorphone
Prior to some experimental sessions, subjects will receive placebo hydromorphone
RECRUITING
University of Kentucky Laboratory of Human Behavioral Pharmacology, Lexington
RECRUITING
University of Kentucky Department of Behavioral Science, Lexington
National Institute on Drug Abuse (NIDA)
NIH
William Stoops
OTHER