Actively Recruiting

Phase 4
Age: 18Years - 90Years
All Genders
ID05521789

Erector Spinae Blocks for Thoracic Surgery A Study Evaluating Pain and Opioid Use After Pulmonary Resection Surgery

Led by George Washington University · Updated on 2026-02-25

70

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate whether erector spinae blocks (ESB) with bolus infusions of local anesthetic can reduce postsurgical pain and the need for opioid pain medications in patients undergoing pulmonary resection surgery. The study focuses on patients having surgery on the side of the chest, where nerve disruption often causes significant pain. ESB may be especially helpful for patients who need anticoagulation and cannot receive more invasive nerve blocks. Participants will be randomly assigned to one of two groups: one group will receive the erector spinae block with bupivacaine alongside standard care, while the other group will receive only standard care without the block. The ESB involves a local anesthetic infusion targeting nerves in the thoracic area. This approach is being studied for its potential to improve pain control while minimizing opioid use after surgery. During the study, patients will be monitored for pain levels and opioid consumption at 6, 12, and 24 hours after surgery. Researchers will assess pain using visual analogue scores and track medication use to understand the impact of the block. The study will help determine if ESB offers a safer alternative to traditional nerve blocks, especially for those on blood thinners, with the total participation time covering the immediate postoperative period.

CONDITIONS

Brief Title

Erector Spinae Block for Thoracic Surgery

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Scheduled for pulmonary resection surgery
  • Between 18 and 90 years old
Not Eligible

You will not qualify if you...

  • History of pleurodesis
  • History of decortication
  • Undergoing emergent surgery
  • Allergy to local anesthetics
  • Intraoperative complications such as inadvertent hemorrhage or conversion to open surgery
  • Bilateral pulmonary resection

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Up to 24 hours post-surgery

Participants receive pulmonary resection surgery with or without an erector spinae block involving bupivacaine to manage postoperative pain.

1 surgery visit and pain assessments at 6, 12, and 24 hours postoperatively

Trial Site Locations

Total: 1 location

1

The George Washington University

Washington D.C., District of Columbia, United States, 20037

Actively Recruiting

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Research Team

E

Eduard Shaykhinurov

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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