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

RecruitingPhase 3

Who can join

Ages 18 to 90 · All sexes

Full eligibility criteria
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

About the study

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

What is being tested

Sponsor: George Washington University · Participants: 120 · Started: Mar 1, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06810375

Locations in the U.S.

District of ColumbiaThe George Washington University Hospital, Washington D.C.

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.