Erector Spinae Plane Block for Cervical Spine Surgery

Status Not yet recruiting

Clinical Trial Summary

The study aims to assess the interfacial plane blocks' effect on pain level, course of postoperative rehabilitation, and anti-inflammatory analgesic effect.

Clinical Trial Description

This study evaluates the analgesic efficacy in adults of bilevel, bilateral erector spinae plane (ESP) blocks after posterior cervical spinal fusion surgery by assessing postoperative pain scores and opiate requirements as the primary outcome measures. We aim to investigate how ESP blocks, performed under ultrasound guidance at the two vertebral levels, contribute to postoperative pain control. This will be determined by measuring numerical rating pain scores repeatedly following surgery and opiate consumption until the patient is discharged from the hospital. These primary outcome measures will be compared between a treatment group of participants receiving ESP blocks and a control group receiving a sham block. Our primary hypothesis is that ESP blocks significantly reduce postoperative pain and opiate requirements. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06393530
Study type	Interventional
Source	Poznan University of Medical Sciences
Contact	Malgorzata Domagalska, Ph.D.
Phone	+48 61 8738303
Email	mdomagalska@ump.edu.pl
Status	Not yet recruiting
Phase	Phase 4
Start date	May 1, 2024
Completion date	June 30, 2025

View Details

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