Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT03792295

Multimodal Pain Therapy After Hernia Repair

The Effect of Multimodal Pain Therapy After Hernia Repair

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Khashayar Vaziri · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Accepted

Summary

Investigating the effect of multimodal pain treatment after hernia repair

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGacetominophen, ibuprofen, oxycodoneMultimodal pain treatment group
DRUGOxycodoneClassic opiod pain treatment group

Timeline

Start date
2021-07-01
Primary completion
2021-12-01
Completion
2022-07-01
First posted
2019-01-03
Last updated
2021-08-04

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03792295. Inclusion in this directory is not an endorsement.