NCT03510910

Multimodal Analgesia With Acetaminophen vs. Narcotics Alone After Hip Arthroscopy

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 100 (actual)
• Sponsor: NYU Langone Health · Academic / Other
• Sex: All
• Age: 18 Years – 65 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Hip Arthroscopy

Interventions

Type	Name	Description
DRUG	Acetaminophen	acetaminophen 600 mg to be taken every 8 hours (TID)
DRUG	Percocet	Oxycodone/acetaminophen (Percocet) 5 mg/325 mg as needed for breakthrough pain for patients in Percocet+ Acetaminophen group. Percocet Group will receive standard of care Percocet 5 mg/325 mg every 6 hours PRN

Timeline

• Start date: 2018-04-10
• Primary completion: 2019-12-01
• Completion: 2019-12-01
• First posted: 2018-04-27
• Last updated: 2021-01-07
• Results posted: 2021-01-07

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated drug study