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Pain Relief and and Peripheral Perfusion Index During Erector Spinae Block

NCT06963424 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2026-01-09

No results posted yet for this study

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

Conditions

  • Block
  • Block, Fascicular
  • Spinae

Interventions

PROCEDURE

Erector Spinae Plane Block

lumbar erectro spinae block

Sponsors & Collaborators

  • Keimyung University Dongsan Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-13
Primary Completion
2025-12-30
Completion
2025-12-30

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06963424 on ClinicalTrials.gov