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

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-06

Study Completion Date

2026-07-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Acute Pain Spinal Stenosis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Active Comparator: Group QİPB

The Quadro-iliac plane block will be performed 30 minutes before lumbar spine surgery

Group Type OTHER

Quadro-iliac plane block

Intervention Type OTHER

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.

Group Type OTHER

Classical thoracolumbar interfascial plane block

Intervention Type OTHER

Classical thoracolumbar interfascial plane block will be performed under ultrasound guidance before the induction of general anesthesia.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Quadro-iliac plane block

Quadro-iliac plane block will be performed under ultrasound guidance before the induction of general anesthesia.

Intervention Type OTHER

Classical thoracolumbar interfascial plane block

Classical thoracolumbar interfascial plane block will be performed under ultrasound guidance before the induction of general anesthesia.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Samsun University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Samsun University

Samsun, , Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

HALE KEFELİ ÇELİK

Role: CONTACT

5057242409

BETÜL ÇİFTÇİ KURT

Role: CONTACT

5301785995

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

HALE KEFELİ ÇELİK

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

OMUKAEK 2025/279

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

mTLIP vs. ITP Blocks in Lumbar Disc Surgery
NCT06391541 ACTIVE_NOT_RECRUITING NA