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Clinical Trial Summary

Investigating the effect of multimodal pain treatment after hernia repair


Clinical Trial Description

This is a randomized, non-blinded study comparing the effects of multimodal pain management (ibuprofen, tylenol, and narcotics/oxycodone as needed) for relief of post-operative pain in patients who undergo hernia repair. Patients who present for elective hernia surgery will be randomized in a 1:1 fashion by pre-operative pain score into a multimodal pain treatment group or conventional opiod treatment group for post-operative pain management. They will be followed up after their surgery to evaluate their pain scores and narcotic use. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03792295
Study type Interventional
Source George Washington University
Contact
Status Withdrawn
Phase Phase 2
Start date July 1, 2021
Completion date July 1, 2022

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