CompletedNot Applicable

Pain Relief and and Peripheral Perfusion Index During Erector Spinae Block

South Korea90 participantsStarted 2025-05-13

Plain-language 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

Who can participate

Age range20 Years – 80 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * lumbar disc herniation * lumbar foraminal stenosis * lumbar central stenosis * lumbar spondylolisthesis * numerical rating scale \> 4 * back pain functional scale \< 45 * duration of pain \> 1 mon * patients who can fully understand all items described in back pain functional scale Exclusion Criteria: * Allergy to local anesthetics or contrast medium * Pregnancy * Spine deformity * Prior history of lumbar spine surgery * No previous lumbar MRI or CT * Patients with coagulation abnormality

What they're measuring

Numerical rating scale changes among 5 times period

Timeframe: Baseline, 2 weeks, 4 weeks, 8 weeks after the completion of erector spine plane block

Trial details

NCT IDNCT06963424

SponsorKeimyung University Dongsan Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-30

View on ClinicalTrials.gov More Block trials