Actively Recruiting
Erector Spinae Versus Intercostal Nerve Blocks With Liposomal Bupivacaine for Analgesia in Thoracic Surgery
Led by George Washington University · Updated on 2026-04-09
120
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial compares efficacy in postoperative pain management in thoracic surgery between erector spinae block versus liposomal bupivacaine injections.
CONDITIONS
Official Title
Erector Spinae Versus Intercostal Nerve Blocks With Liposomal Bupivacaine for Analgesia in Thoracic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Video assisted pulmonary resection, pleurodesis or decortication
You will not qualify if you...
- Allergy to local anesthetics
- Patient undergoing bilateral surgery
- Surgery is emergent as deemed by the principal investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The George Washington University Hospital
Washington D.C., District of Columbia, United States, 20037
Actively Recruiting
Research Team
E
Eduard Shaykhinurov, MS
CONTACT
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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