Quadro-Iliac vs Thoracolumbar Interfascial Plane Block for Analgesia After Single-Level Lumbar Disc Surgery
NCT ID: NCT07348419
Last Updated: 2026-02-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
70 participants
INTERVENTIONAL
2026-01-06
2026-07-30
Brief Summary
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Detailed Description
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For patients undergoing lumbar disc surgery, the classical thoracolumbar interfascial plane (TLIP) block and the Quadro-iliac plane block (QIPB) provide effective analgesia for postoperative pain control.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
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Active Comparator: Group QİPB
The Quadro-iliac plane block will be performed 30 minutes before lumbar spine surgery
Quadro-iliac plane block
Quadro-iliac plane block will be performed under ultrasound guidance before the induction of general anesthesia.
Active Comparator: Group TLİP
The classical thoracolumbar interfascial plane (TLIP) block will be performed 30 minutes before lumbar spine surgery.
Classical thoracolumbar interfascial plane block
Classical thoracolumbar interfascial plane block will be performed under ultrasound guidance before the induction of general anesthesia.
Interventions
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Quadro-iliac plane block
Quadro-iliac plane block will be performed under ultrasound guidance before the induction of general anesthesia.
Classical thoracolumbar interfascial plane block
Classical thoracolumbar interfascial plane block will be performed under ultrasound guidance before the induction of general anesthesia.
Eligibility Criteria
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Inclusion Criteria
* Classified as ASA physical status I-III,
* Scheduled to undergo single-level lumbar spinal surgery under general anesthesia
* Who agree to participate in the study by providing written informed consent
Exclusion Criteria
* 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 (PCA) device
* Suspected pregnancy, confirmed pregnancy, or breastfeeding
* Refusal to undergo the procedure or to participate in the study
18 Years
70 Years
ALL
No
Sponsors
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Samsun University
OTHER
Responsible Party
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Locations
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Samsun University
Samsun, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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OMUKAEK 2025/279
Identifier Type: -
Identifier Source: org_study_id
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