An Analysis of the Efficacy of a Pre-Emptive Multimodal Pain Regimen in Reducing Acute Post-Operative Pain and Narcotic Pain Medication Requirements in Spine Surgery

PHASE4CompletedINTERVENTIONAL
Enrollment

44

Participants

Timeline

Start Date

August 20, 2020

Primary Completion Date

June 10, 2021

Study Completion Date

June 10, 2021

Conditions
Pain, PostoperativeSpine Injuries and DisordersNarcotic Use
Interventions
DRUG

Pre-op Multimodal analgesia (MMA) regimen + standard post-op oxycodone

"The study subjects will be assigned to the defined pre-op MMA regimen with standard postop oxycodone based pain control regimen given on an as needed basis. The treatment group outcomes will be compared to patients outside of the study including a historical control group (receiving only post-op pain regimen) prior to the implementation of the new regimen. The studied treatment group will receive within 3 hours before surgery an oral MMA regimen consisting of:~Acetaminophen 975 mg Celecoxib 200 mg Gabapentin 300 mg Oxycodone 10 mg Extended Release"

Trial Locations (1)

10016

NYU Langone Health, New York

All Listed Sponsors
lead

NYU Langone Health

OTHER

NCT04522206 - An Analysis of the Efficacy of a Pre-Emptive Multimodal Pain Regimen in Reducing Acute Post-Operative Pain and Narcotic Pain Medication Requirements in Spine Surgery | Biotech Hunter | Biotech Hunter