Clinical Trial

Pain Relief and and Peripheral Perfusion Index During Erector Spinae Block

Completed
View on ClinicalTrials.gov →
Summary
The primary endpoint of this study is to compare the pain relief and peripheral perfusion index when local anesthetics injected in different final target area during lumbar erector spinae block The secondary endpoint of this study is to compare the procedure related pain
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-05-06.
Status change: Not Yet Recruiting → Completed 2026-01-07
Trial Details
NCT Number NCT06963424
Lead Sponsor Keimyung University Dongsan Medical Center
Conditions Block, Block, Fascicular, Spinae
Enrollment 90 participants
Start Date 2025-05-13
Primary Completion 2025-12-30 (estimated)
Study Completion 2025-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-01-09