Trial intelligence / Profile preview

Duloxetine for Pain Control After Lateral Lumbar Interbody Fusion

NCT05611749Phase 2Terminated

Sponsor
Scripps Health
Start
May 2023
Primary completion
Mar 2024
Modality
Small Molecules
Countries
1
01

Overview

Phase 2, randomised, double-blind trial in acute postoperative pain and chronic post-surgical pain (CPSP) comparing Duloxetine Group with Placebo Group (2 arms). Primary endpoints: Change in Postoperative Pain at 10 days, Change in Postoperative Function at 10 days and 9 more. Started May 2023; status: terminated.

02

Drugs

duloxetine
03

Conditions

acute postoperative painchronic post-surgical pain (CPSP)

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