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Intraoperative Placement of Superficial Erector Spinae Plane Block; A New Approach in Spine Surgery

Postoperative Pain Clinical Trial

Official title:
Intraoperative Placement of Superficial Erector Spinae Plane Block in Spine Surgery; An Effective Approach at Enhanced Recovery After Spine Surgery

Clinical Trial Summary

Major spine surgery causes severe postoperative pain. The primary objective of this randomized controlled study is to compare the effect of ultrasound (US)-guided superficial erector spinae plane (ESP) block on 48-hour postoperative cumulative opioid requirements with standard (opioid-based) analgesia.

Clinical Trial Description

46 patients (ASA I-II-III) between 18 and 65 years of age, who were to undergo spine surgery, were randomized and divided into two groups. (23 patients in each of the control and superficial ESP groups). Superficial ESP block was performed for SESP group and standard (opioid-based) analgesia performed in the control group. Postoperative analgesia was provided by intravenous morphine infusion using a patient-controlled analgesia device. Postoperative numeric rating scale values were the primary outcome measure. 24-hour total morphine consumption was secondary outcome measure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05244031
Study type Interventional
Source Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Contact
Status Completed
Phase N/A
Start date May 10, 2021
Completion date February 7, 2022
View Details
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