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

Last updated: July 16, 2021
Sponsor: University of California, San Francisco
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT04233736
19-28625
  • Ages > 18
  • All Genders

Study 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

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Spine surgery at or below the L1 vertebral level
  • Midline surgical approach

Exclusion

Exclusion Criteria:

  • Previous lumbar or lumbo-sacral surgery with or without hardware placement
  • Evidence of dura pathology (including CSF leak)
  • Spine tumor
  • Non-English speaking

Study Design

Total Participants: 160
Study Start date:
July 01, 2021
Estimated Completion Date:
January 01, 2022

Connect with a study center

  • University of California San Francisco

    San Francisco, California 94143
    United States

    Active - Recruiting

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