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NCT05983393 Clinical Trial

Erector Spina Plane Block for Multilevel Major Spinal Surgery

Pain Clinical Trial

Official title:
Effect of Ultrasound-guided Bilateral Erector Spina Plan Block for Postoperative Analgesia in Patients Undergoing Multilevel Posterior Spinal Instrumentation.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05983393
Other study ID # 2020/12-04
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2021
Est. completion date August 7, 2023

Study information
Verified date October 2023
Source Kahramanmaras Sutcu Imam University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Erector spinae plane (ESP) block is an interfacial plane block with visceral and somatic analgesic activity at paraspinal muscles. This study aims to examine the postoperative analgesic efficacy of ESP block in patients undergoing posterior spinal instrumentation

Description:

Postoperative patient-controlled analgesia in the ESP group and control group will be compared with 24-hour morphine consumption and NRS scores at different time points. In addition, the need for rescue analgesics and patient satisfaction will be evaluated.

Recruitment information / eligibility
Status Completed
Enrollment 42
Est. completion date August 7, 2023
Est. primary completion date August 7, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - ASA I-III patients - Agreed to participate in the study Exclusion Criteria: - Patients with infection at the injection site - Coagulopathy Allergy to amide-type local anesthetics - History of peripheral neuropathy - Hepatic and/or renal failure - Refusing the procedure - Patients with heart disease - Patients who have previously undergone surgery from the same area

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Erector spinae plane block
Erector spinae plane block was performed
• Control
Erector spinae plane block was not applied.

Locations
Country Name City State
Turkey Kahramanmaras Sutcu Imam University Hospital Kahramanmaras

Sponsors (1)
Lead Sponsor Collaborator
Kahramanmaras Sutcu Imam University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary opioid consumption The amount of morphine consumed in milligrams in the first 24 hours was determined with a patient-controlled analgesia pump. up to 24 hour
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