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Acetaminophen Randomized Controlled Trial

Post Operative Pain Clinical Trial

Official title:
Prospective Randomized Control Trial Assessing Effects of Pre-Operative Acetaminophen in Isolated Meniscectomy Patients

Clinical Trial Summary

Patients that are to undergo isolated meniscectomy will be randomized to 2 cohorts: one will take the FDA recommended dose of acetominophen (1000mg) 24hrs before surgery, one will be given a similarly looking placebo pill. A multitude of post-op variables will be included, mainly pain scores and morphine equivalent doses at different time points.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02737124
Study type Interventional
Source New York University School of Medicine
Contact
Status Withdrawn
Phase Phase 3
Start date February 16, 2017
Completion date March 19, 2018
View Details
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