64
Participants
Start Date
July 1, 2024
Primary Completion Date
January 1, 2026
Study Completion Date
January 1, 2026
open-label placebo
Placebo will be supplied as a 330mg tablet (manufactured by Consolidated Midland Corporation). Patients will take placebo with each oral opioid intake and 3 additional times per day beginning on POD 1.
Treatment as usual
Each oral opioid dose is a 5mg Oxycodone tablet. Investigator shall never prescribe ibuprofen. Investigator shall always prescribe Tylenol 625mg every 8hrs (PRN).
RECRUITING
University of California, San Francisco, San Francisco
University of California, San Francisco
OTHER