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Erector Spinae Plane Block for Pediatric Idiopathic Scoliosis Surgery — ESPB  

Scoliosis Idiopathic Clinical Trial

Official title:
Erector Spinae Plane Block for Pediatric Idiopathic Scoliosis Surgery. A Prospective, Randomized, Double-blinded Clinical Trial.

Clinical Trial Summary

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

Clinical Trial Description

This study evaluates the analgesic efficacy in adolescents of bilevel, bilateral erector spinae plane (ESP) blocks after posterior 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 NCT05938959
Study type Interventional
Source Poznan University of Medical Sciences
Contact Magorzata Domagalska, Ph.D.
Phone 0048608762068
Email m.domagalska@icloud.com
Status Recruiting
Phase Phase 4
Start date May 1, 2023
Completion date September 1, 2024
View Details
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