Use of Duloxetine for Perioperative Pain Control After Total Hip Arthroplasty: Randomized Controlled Clinical Trial (RCT)
Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 4
SUMMARY
The primary objective of this study is to compare total narcotic intake standardized via milligram morphine equivalents between duloxetine and placebo cohorts after a total hip arthroplasty.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Patients \> 18 years of age
• Patients undergoing primary total hip arthroplasty
• Ambulatory patient prior to fracture
• Subjects must be capable of providing informed consent
• English or Spanish speaking
Locations
United States
Florida
University of Miami
RECRUITING
Miami
Contact Information
Primary
Victor Hernandez, MD
vhh1@miami.edu
3056895195
Backup
Natalia Cruz, MD
nxc971@miami.edu
3056895195
Time Frame
Start Date: 2025-03-01
Estimated Completion Date: 2026-04-01
Participants
Target number of participants: 64
Treatments
Experimental: Duloxetine group
Participants will be in this group for up to 2 hours.
Placebo_comparator: Placebo group
Participants will be in this group for up to 2 hours.
Related Therapeutic Areas
Sponsors
Leads: University of Miami