Comparison of Continuous ESP Versus TEA After Thoracotomy

Status Recruiting

Clinical Trial Summary

This prospective, randomized, assessor-blinded study is designed to evaluate the postoperative analgesic efficacy of the ultrasound-guided continuous erector spinae plane (ESP) block in patients undergoing thoracotomy. We hypothesize that US-guided ESP block is not inferior to thoracic epidural analgesia in terms of postoperative pain control in these patients.

Clinical Trial Description

Adult patients undergoing elective unilateral thoracotomy for lung cancer resection are randomly allocated to receive US-guided ESP block (n=31) or thoracic epidural analgesia (n=31). Both procedures are performed prior to surgery. Each patient was assessed by a blinded investigator on postoperative day (POD) 1,2 and 3. The primary outcome is pain severity evaluated by a numeric rating scale (NRS) at POD1. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05008614
Study type	Interventional
Source	Seoul National University Hospital
Contact	Hojin Lee, MD
Phone	82-2-2072-0039
Email	zenerdiode03@gmail.com
Status	Recruiting
Phase	N/A
Start date	July 22, 2021
Completion date	February 28, 2026

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