# 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

> **NCT04522206** · PHASE4 · COMPLETED · sponsor: **NYU Langone Health** · enrollment: 44 (actual)

## Conditions studied

- Pain, Postoperative
- Spine Injuries and Disorders
- Narcotic Use

## Interventions

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

## Key facts

- **NCT ID:** NCT04522206
- **Lead sponsor:** NYU Langone Health
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2020-08-20
- **Primary completion:** 2021-06-10
- **Final completion:** 2021-06-10
- **Target enrollment:** 44 (ACTUAL)
- **Last updated:** 2022-07-11


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04522206

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration 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". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT04522206. Licensed CC0.

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