Comparison of the Postoperative Effects of the Erector Spinae Plane Block and Local Infiltration Analgesia in Patients Operated with Lumbotomy Surgery Incision: Randomized Clinical Study

Not Applicable

Completed

• Conditions: Kidney stone; Kidney tumor; Kidney patologies requiring unilateral surgery; Acute kidney disease; Chronic kidney disease; Anaesthesiology - Pain management; Anaesthesiology - Anaesthetics; Renal and Urogenital - Kidney disease; Renal and Urogenital - Other renal and urogenital disorders

• Registration Number: ACTRN12624000415505
• Lead Sponsor: Mustaf Kemal University Research Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-01-02
• Study Start: 2024-04-04
• Last Update Posted: 8 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patients in the ASA I-III risk group,
Aged 18-75,
Body mass index less than 35 kg/m² (BMI < 35 kg/m²),
Operated with open, unilateral, lumbotomy surgical incision were included

Exclusion Criteria

Allergy to the drugs used in our study,
Having active infection in the procedure area,
Mental defect, major vertebral anomalies,
Known blood and coagulation diseases,
Using anticoagulant drugs
Those who received medical treatment that could lead to opioid tolerance

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intraoperative remifentanyl consumption determined from device records[ Assessed by treating anesthesiologist 5 minutes after operation (Primary timepoint)];Postoperative morphine consumption was obtained from the records of the infusion device we used to provide patient-controlled analgesia.[ Total morphine and paracetamol doses consumed by the postoperative patients at the 0th, 1st, 2nd, 3rd, 4th, 6th, 8th, 12th (Primary timepoint), 16th, 20th, 24th, 32nd, 40th, 48th hours]

Secondary Outcome Measures

Name	Time	Method
Postoperative pain levels of our patients with the numerical rating scale (NRS) [ Postoperative at the 0th, 1st, 2nd, 3rd, 4th, 6th, 8th, 12th,(Primary timepoint) 16th, 20th, 24th, 32nd, 40th, 48th hours]