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Duloxetine for Perioperative Pain in Hip Arthroplasty: A RCT
Sponsor: University of Miami
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.
Official title: Use of Duloxetine for Perioperative Pain Control After Total Hip Arthroplasty: Randomized Controlled Clinical Trial (RCT)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
64
Start Date
2025-03-01
Completion Date
2026-12-01
Last Updated
2026-03-18
Healthy Volunteers
No
Conditions
Interventions
Duloxetine
Participants will come in person and receive a one time 60 mg dose by mouth.
Placebo
Participants will come in person and receive a one time 60 mg placebo pill dose by mouth.
Locations (1)
University of Miami
Miami, Florida, United States