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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.

The primary objective of the study is to compare patients' reported pain and narcotic use following meniscectomy, and determine if NSAIDs can provide adequate pain relief.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02915055
Study type Observational
Source New York University School of Medicine
Contact
Status Completed
Phase N/A
Start date September 1, 2016
Completion date March 1, 2017

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