Clinical Trial

Evaluation of the Postoperative Efficacy of Bilateral Lumbar Erector Spinae Plane Block (ESPB) in Patients Undergoing Lumbar Disc Herniation Repair Surgery

Active, Not Recruiting
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Summary
This prospective observational study aims to evaluate the efficacy of bilateral lumbar erector spinae plane (ESP) block in providing effective postoperative analgesia and its potential impact on early mobilization and length of hospital stay in patients undergoing surgical repair of lumbar disc herniation. Regional anesthesia techniques, particularly erector spinae plane blocks, have become an integral component of multimodal analgesia strategies in postoperative pain management. The ESP block has demonstrated effective analgesia across a wide spectrum of thoracic and abdominal surgeries and is increasingly utilized due to its ease of application and safety profile. By implementing multimodal analgesic techniques, this study seeks to achieve effective pain control, reduce opioid consumption and associated complications, facilitate early mobilization, decrease hospital length of stay, and enhance patient comfort.
Trial Details
NCT Number NCT07403734
Lead Sponsor Başakşehir Çam & Sakura City Hospital
Conditions Opioid Consumption, Postoperative, ESPB, Postoperative Pain, Plane Blocks, Lumbar Disc Herniation, Hospital Stay Time, Patient Satisfaction
Enrollment 78 participants
Start Date 2024-07-01
Primary Completion 2025-01-01 (estimated)
Study Completion 2026-03-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-11