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Recruiting NCT07348419

NCT07348419 Quadro-Iliac vs Thoracolumbar Interfascial Plane Block for Analgesia After Single-Level Lumbar Disc Surgery

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Clinical Trial Summary
NCT ID NCT07348419
Status Recruiting
Phase
Sponsor Samsun University
Condition Acute Pain
Study Type INTERVENTIONAL
Enrollment 70 participants
Start Date 2026-01-06
Primary Completion 2026-07-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Quadro-iliac plane blockClassical thoracolumbar interfascial plane block

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 70 participants in total. It began in 2026-01-06 with a primary completion date of 2026-07-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

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

Contact & Investigator

Central Contact

HALE KEFELİ ÇELİK

✉ ck_hale@hotmail.com

📞 5057242409

Frequently Asked Questions

Who can join the NCT07348419 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Acute Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07348419 currently recruiting?

Yes, NCT07348419 is actively recruiting participants. Contact the research team at ck_hale@hotmail.com for enrollment information.

Where is the NCT07348419 trial being conducted?

This trial is being conducted at Samsun, Turkey (Türkiye).

Who is sponsoring the NCT07348419 clinical trial?

NCT07348419 is sponsored by Samsun University. The trial plans to enroll 70 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology