Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Scheduled for pulmonary resection surgery
- Between 18 and 90 years old
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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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