Comparison of the Intraoperative and Postoperative Effects of Ultrasound-guided Erector Spina Plane Block and Posterior Quadratus Lumborum Block in Patients Undergoing Lumbar Stabilization Surgery
1 other identifier
observational
62
1 country
1
Brief Summary
The investigators aimed to compare the effects of ultrasound guided erector spina plan block and posterior quadratus lumborum block on intraoperative and postoperative opioid consumption in patients who will undergo short segment lumbar stabilization surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 9, 2023
CompletedStudy Start
First participant enrolled
April 15, 2023
CompletedFirst Posted
Study publicly available on registry
May 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 2, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 2, 2023
CompletedNovember 2, 2023
October 1, 2023
4 months
March 9, 2023
October 31, 2023
Conditions
Outcome Measures
Primary Outcomes (7)
İntraoperative remifentanil consumption
The investigators aimed to compare intraoperative remifentanil consumption of two groups
At the end of the intraoperative period
Postoperative tramadol consumption
The investigators aimed to compare postoperative tramadol consumption of two groups
The investigators will record at postoperative 0. hour
Postoperative tramadol consumption
The investigators aimed to compare postoperative tramadol consumption of two groups
The investigators will record at postoperative 1. hour
Postoperative tramadol consumption
The investigators aimed to compare postoperative tramadol consumption of two groups
The investigators will record at postoperative 2. hour
Postoperative tramadol consumption
The investigators aimed to compare postoperative tramadol consumption of two groups
The investigators will record at postoperative 6. hour
Postoperative tramadol consumption
The investigators aimed to compare postoperative tramadol consumption of two groups
The investigators will record at postoperative 12. hour
Postoperative tramadol consumption
The investigators aimed to compare postoperative tramadol consumption of two groups
The investigators will record at postoperative 24. hour
Secondary Outcomes (8)
Postoperative nausea and vomiting
The investigators will record within 24 hours postoperatively.
Postoperative pruritus
The investigators will record within 24 hours postoperatively.
Postoperative visual analog scale
The investigators will record at postoperative 0. hour
Postoperative visual analog scale
We will record at postoperative 1. hour
Postoperative visual analog scale
The investigators will record at postoperative 2. hour
- +3 more secondary outcomes
Other Outcomes (21)
Postoperative pulse rate
The investigators will record at postoperative 0. hour
Postoperative pulse rate
The investigators will record at postoperative 1. hour
Postoperative pulse rate
The investigators will record at postoperative 2. hour
- +18 more other outcomes
Study Arms (2)
Erector Spina Plan Block Group (Group E)
Patients who underwent erector spina plane block before initiation of surgery after induction of anesthesia
Posterior Quadratus Lumborum Block Group ( Group Q)
Patients who underwent posterior quadratus lumborum block block before initiation of surgery after induction of anesthesia
Interventions
Ultrasound guided peripheral nerve block
Eligibility Criteria
Patients who will undergo lumbar stabilization operation under general anesthesia in Ankara Bilkent City Hospital Operating Room, between the ages of 18-65, both genders, and in the ASA I-III risk group will be included in the study.
You may qualify if:
- Patients who will undergo lumbar stabilization operation
- Between the ages of 18-65
- Both genders
- ASA I-III risk group
You may not qualify if:
- Patients who did not accept the study
- Patients younger than 18 years old
- Patients older than 65 years
- Patients with an ASA score greater than III
- Patients with an active infection in the area to be blocked
- Patients with a long bleeding time
- Those who are pregnant
- Patients with kidney failure
- Patients with liver failure
- Patients with BMI\<18 and BMI\>30
- Those who are allergic to local anesthetics
- Patients who have had previous lumbar surgery
- Uncooperative or mentally retarded patients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara City Hospital, Bilkent
Ankara, Cankaya, Turkey (Türkiye)
Related Publications (4)
Qiu Y, Zhang TJ, Hua Z. Erector Spinae Plane Block for Lumbar Spinal Surgery: A Systematic Review. J Pain Res. 2020 Jul 1;13:1611-1619. doi: 10.2147/JPR.S256205. eCollection 2020.
PMID: 32669870BACKGROUNDDhanjal ST, Tonder S. Quadratus Lumborum Block. 2023 Aug 14. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK537212/
PMID: 30725897BACKGROUNDElsharkawy H, El-Boghdadly K, Barrington M. Quadratus Lumborum Block: Anatomical Concepts, Mechanisms, and Techniques. Anesthesiology. 2019 Feb;130(2):322-335. doi: 10.1097/ALN.0000000000002524. No abstract available.
PMID: 30688787BACKGROUNDKang R, Lee S, Kim GS, Jeong JS, Gwak MS, Kim JM, Choi GS, Cho YJ, Ko JS. Comparison of Analgesic Efficacy of Erector Spinae Plane Block and Posterior Quadratus Lumborum Block in Laparoscopic Liver Resection: A Randomized Controlled Trial. J Pain Res. 2021 Dec 11;14:3791-3800. doi: 10.2147/JPR.S343366. eCollection 2021.
PMID: 34924770BACKGROUND
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 9, 2023
First Posted
May 6, 2023
Study Start
April 15, 2023
Primary Completion
August 2, 2023
Study Completion
August 2, 2023
Last Updated
November 2, 2023
Record last verified: 2023-10
Data Sharing
- IPD Sharing
- Will not share