RecruitingPhase 3

Erector Spinae Versus Intercostal Nerve Blocks With Liposomal Bupivacaine for Analgesia in Thoracic Surgery

United States120 participantsStarted 2025-03-01

Plain-language summary

This clinical trial compares efficacy in postoperative pain management in thoracic surgery between erector spinae block versus liposomal bupivacaine injections.

Who can participate

Age range18 Years – 90 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Video assisted pulmonary resection, pleurodesis or decortication Exclusion Criteria: * Allergy to local anesthetics * Patient undergoing bilateral surgery * Surgery is emergent as deemed by the principal investigator

What they're measuring

Postoperative pain control assessment

Timeframe: Up to 48 hours postoperatively

Morphine equivalent assessment

Timeframe: Up to 72 hours postoperatively

Trial details

NCT IDNCT06810375

SponsorGeorge Washington University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-02-28

Contact for this trial

Eduard Shaykhinurov, MS

2022038960 eshaykhinurov@mfa.gwu.edu

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