18
Participants
Start Date
June 4, 2024
Primary Completion Date
October 1, 2025
Study Completion Date
October 1, 2025
Buprenorphine
At each visit, the participant will receive a single dose of buprenorphine, either 0.15mg IV, 8mg PO, or 16mg PO. The order for the first dose administered will be fixed to the IV dose, and the subsequent doses will be randomized and counterbalanced to 8mg or 16mg PO.
Brigham and Women's hospital, Boston
University of Utah
OTHER
Brigham and Women's Hospital
OTHER