Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05024344

ESP Block vs Control for Pain Control Following Percutaneous Nephrolithotomy

Led by University of Tennessee Medical Center · Updated on 2026-04-28

128

Participants Needed

1

Research Sites

359 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to investigate the use of the erector spinae (ESP) block in reducing the morphine milligram equivalent (MME) consumption post percutaneous nephrolithotomy. Objectives: 1. \- Determine if there is a significant effect on post percutaneous nephrolithotomy MME consumption with the usage of an ESP block vs. saline control. 2. \- Determine if there is a significant effect on reported pain levels with the use of an ESP block vs. saline control in post percutaneous nephrolithotomies.

CONDITIONS

Official Title

ESP Block vs Control for Pain Control Following Percutaneous Nephrolithotomy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years or older undergoing non-emergency percutaneous nephrolithotomy Monday through Friday between 6:00 AM and 4:00 PM
  • Female participants of childbearing potential must provide a negative pregnancy test
  • Ability to understand and explain the consent for the procedure
  • Willingness to sign consent for the procedure
  • English speaking
Not Eligible

You will not qualify if you...

  • Emergency surgery status
  • Local infection
  • Allergy to local anesthetics
  • Recreational drug use
  • Inability to provide informed consent
  • Pregnancy or breastfeeding
  • History of Guillain-Barre' Syndrome
  • Significant underlying medical conditions that pose risk
  • Opioid use greater than 90 days in the year prior to surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Tennessee Medical Center

Knoxville, Tennessee, United States, 37920

Actively Recruiting

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Research Team

J

Jason Buehler, MD

CONTACT

A

Aimee Pehrson

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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