Status:

COMPLETED

Does a Non-Opioid Multimodal Pain (NOMO) Protocol Decrease Narcotic Use

Lead Sponsor:

Prisma Health-Upstate

Conditions:

Opioid Use

Eligibility:

FEMALE

18+ years

Phase:

PHASE3

Brief Summary

The objective of this study is to evaluate narcotic use after implementation of a Non-Opioid Multimodal Pain (NOMO) protocol in patients who are undergoing a urogynecologic procedure. The study will a...

Detailed Description

The objective of this study is to evaluate narcotic use after implementation of a Non-Opioid Multimodal Pain (NOMO) protocol in patients who are undergoing a urogynecologic procedure. NOMO protocols s...

Eligibility Criteria

Inclusion

  • English-speaking females
  • greater than or equal to 18 years old
  • scheduled for a urogynecologic procedure at GHS requiring inpatient stay or extended observation.

Exclusion

  • less than 18 years of age
  • non-English speaking patients
  • unscheduled urogynecologic surgeries
  • patients expected to undergo a simple reconstructive surgery with same-day discharge,
  • history of chronic pain
  • chronic Lyrica or Celebrex use
  • psychiatric disorder, narcotic dependence or narcotic prescription in the past six weeks
  • current liver disease
  • kidney disease (defined as GFR \<60)
  • malignancy
  • sulfa allergy

Key Trial Info

Start Date :

November 15 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2021

Estimated Enrollment :

10 Patients enrolled

Trial Details

Trial ID

NCT05386069

Start Date

November 15 2019

End Date

June 1 2021

Last Update

May 23 2025

Active Locations (1)

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Prisma Health - Upstate

Greenville, South Carolina, United States, 29615