drugset / Trial / NCT05087914

Novel Non-opioid Post-surgical Pain Treatment in Females

NCT05087914

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study aims to determine if treatment with Carbidopa/Levodopa and Naproxen in females (biological sex) with acute pain after a bunionectomy or toe fusion (24hrs, 48hrs and 5 days) will reduce pain when compared with females receiving Placebo and Naproxen.

Timeline

Start
2021-11-01
Primary completion
2023-12-30
Completion
2024-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Levodopa Small molecule 25 mg Oral
Subject Levodopa Small molecule 100 mg Oral
Background Naproxen Small molecule 250 mg Oral

Indications

No indication recorded.