Multimodal Pain Therapy After Hernia Repair

Status Withdrawn

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

Clinical Trial Details

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Status	Withdrawn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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