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Clinical Trial Summary

The purpose of this proposed study is to evaluate the efficacy of a multimodal approach to analgesia for patient's pain after hip arthroscopy and to also assess if this new approach will result in a reduction in post-operative narcotic use. This study is a single-center, randomized prospective study comparing post-operative pain scores and narcotic consumption between individuals receiving acetaminophen along with a reduced quantity of Percocet (to be used as needed for breakthrough pain) and individuals receiving Percocet only. Both pain management options are considered to be standard of care. Both cohorts will receive aspirin for DVT prophylaxis and celecoxib for heterotopic ossification prophylaxis. The primary objective of the study are to compare patients' narcotic consumption and reported pain following arthroscopic hip surgery, and determine if acetaminophen can provide adequate pain relief compared to a narcotic medication.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03510910
Study type Interventional
Source NYU Langone Health
Contact
Status Completed
Phase Phase 4
Start date April 10, 2018
Completion date December 1, 2019

See also
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Active, not recruiting NCT03909178 - Arthroscopic Labral Repair Versus Physical Therapy for Tears of the Acetabular Labrum N/A
Active, not recruiting NCT03372564 - CREST: Capsular Repair During Hip Arthroscopy N/A
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Recruiting NCT05746533 - An Evaluation of Hip Preservation Outcomes
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