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Quadro-Iliac vs Thoracolumbar Interfascial Plane Block for Analgesia After Single-Level Lumbar Disc Surgery

S

Samsun University

Status

Enrolling

Conditions

Spinal Stenosis
Acute Pain

Treatments

Other: Quadro-iliac plane block
Other: Classical thoracolumbar interfascial plane block

Study type

Interventional

Funder types

Other

Identifiers

NCT07348419
OMUKAEK 2025/279

Details and patient eligibility

About

The investigators aim to compare the postoperative analgesic efficacy of the classical thoracolumbar interfascial plane block and the Quadro-iliac plane block for postoperative analgesia management after lumbar disc surgery.

Full description

Lumbar spinal stenosis can lead to variable signs and symptoms such as back pain, radiating pain to the lower extremities, and reduced walking capacity. Lumbar disc surgery itself causes significant pain due to extensive dissection and muscle retraction during the procedure. A multimodal analgesic approach is preferred for postoperative pain management after lumbar spine surgery. The addition of regional anesthesia techniques can reduce opioid-related side effects and is associated with earlier mobilization, shorter hospital stay, and improved patient satisfaction.

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.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18-70 years,
  • 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

  • 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 (PCA) device
  • Suspected pregnancy, confirmed pregnancy, or breastfeeding
  • Refusal to undergo the procedure or to participate in the study

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Active Comparator: Group QİPB
Other group
Description:
The Quadro-iliac plane block will be performed 30 minutes before lumbar spine surgery
Treatment:
Other: Quadro-iliac plane block
Active Comparator: Group TLİP
Other group
Description:
The classical thoracolumbar interfascial plane (TLIP) block will be performed 30 minutes before lumbar spine surgery.
Treatment:
Other: Classical thoracolumbar interfascial plane block

Trial contacts and locations

1

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Central trial contact

BETÜL ÇİFTÇİ KURT; HALE KEFELİ ÇELİK

Data sourced from clinicaltrials.gov

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