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Study identifier: NCT05024344 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

ESP Block vs Control for Pain Control Following Percutaneous Nephrolithotomy

Condition: Nephrolithotomy, Percutaneous  ·  Sponsor: University of Tennessee Medical Center

PhaseNA
Planned participants128
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Jason Buehler, MD  ·  865-305-9220  ·  jbuehler@utmck.edu

Aimee Pehrson  ·  865-305-5432  ·  apehrson@utmck.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Tennessee Medical CenterKnoxville, Tennessee, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05024344