Actively Recruiting
Comparison of the Postoperative Analgesic Efficacy of Classical and Modified Erector Spinae Plane Blocks After Lumbar Spinal Surgery
Led by Samsun University · Updated on 2026-02-03
60
Participants Needed
1
Research Sites
38 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The investigators aim to compare the postoperative analgesic efficacy of the classical erector spinae plane block and the modified erector spinae plane block in the management of postoperative analgesia after lumbar disc surgery.
CONDITIONS
Official Title
Comparison of the Postoperative Analgesic Efficacy of Classical and Modified Erector Spinae Plane Blocks After Lumbar Spinal Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-70 years
- Classified as ASA physical status I-III
- Scheduled to undergo single-level lumbar spinal surgery under general anesthesia
- Agree to participate and provide written informed consent
You will not qualify if you...
- History of bleeding diathesis or current anticoagulant therapy
- Known allergy or hypersensitivity to local anesthetics or opioid medications
- Infection at the planned block injection site
- Previous lumbar spine surgery
- History of gabapentinoid or corticosteroid use within the last 3 weeks
- Inability to use a patient-controlled analgesia device
- Suspected pregnancy, confirmed pregnancy, or breastfeeding
- Refusal to undergo the procedure or to participate in the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Samsun University
Samsun, Turkey (Türkiye)
Actively Recruiting
Research Team
H
HALE KEFELİ ÇELİK
CONTACT
B
BETÜL ÇİFTÇİ KURT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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