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RECRUITING
NCT06807866
PHASE4

Duloxetine for Perioperative Pain in Hip Arthroplasty: A RCT

Sponsor: University of Miami

View on ClinicalTrials.gov

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

DRUG

Duloxetine

Participants will come in person and receive a one time 60 mg dose by mouth.

OTHER

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