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Clinical Trial Summary

This will be a single-center, prospective observational study. The study will compare post- operative pain scores and narcotic consumption between two groups of patients - one cohort will receive ibuprofen (Motrin) and Percocet (to be used as needed) while the other cohort will receive only Percocet. Both pain management options are considered to be standard of care.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04018768
Study type Observational
Source NYU Langone Health
Contact
Status Completed
Phase
Start date December 1, 2017
Completion date February 1, 2019

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