Erector Spinae Plane Blocks (ESP) for Postoperative Pain in Lumbo-sacral Spine Surgery

Erector Spinae Plane Block Clinical Trial

Official title: Bilateral Erector Spinae Plane Blocks (ESP) for Postoperative Pain in Lumbo-sacral Spine Surgery: A Double-blinded Randomized Controlled Trial

Status Recruiting

Clinical Trial Summary

The goal of this study is to evaluate the analgesic efficacy of bilateral erector spinae plane (ESP) blocks after lumbar and lumbo-sacral spine surgery by assessing postoperative pain scores and opiate requirements as the primary outcome measures. We are aiming to investigate how ESP blocks, performed under ultrasound guidance at the T12 vertebral level, contribute to postoperative pain control. This will be determined by measuring numerical rating pain scores repeatedly following surgery and opiate consumption until patient discharge from hospital. These primary outcome measures will be compared between a treatment group of participants, who will receive ESP blocks and a control group who will receive a sham block. Our primary hypothesis is that ESP blocks significantly reduce postoperative pain and opiate requirements

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Erector Spinae Plane Block
• Lumbar Spine Surgery
• Pain, Postoperative

• NCT number: NCT04233736
• Study type: Interventional
• Source: University of California, San Francisco
• Contact: Claas Siegmueller, MD PhD MBA
• Phone: 415-443-0155
• Email: siegmuellerc@anesthesia.ucsf.edu
• Status: Recruiting
• Phase: N/A
• Start date: July 1, 2021
• Completion date: January 1, 2022