Comparing two types of nerve blocks for pain management after lumbar surgery
Comparison of the Effects of Thoracolumbar Interfascial Plane Block and Quadro Iliac Plane Block on Postoperative Opioid Consumption After Lumbar Microsurgery: A Randomized Controlled Trial
This study is testing two different nerve block techniques to see which one helps people have less pain and use fewer opioids after lumbar surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Medipol University Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06851533 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two regional anesthesia techniques, the Thoracolumbar Interfascial Plane (TLIP) block and the Quadro Iliac Plane Block, in reducing postoperative opioid use following lumbar microdiscectomy. The research aims to determine which method provides better pain control and fewer opioid-related side effects, such as nausea and respiratory depression. Patients aged 18 to 80 scheduled for this surgery will be included, and their postoperative pain levels will be assessed using a Numeric Rating Scale. The study seeks to enhance patient recovery by minimizing opioid consumption through effective pain management strategies.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 80 who are scheduled for lumbar microdiscectomy and have an ASA physical status of I to III.
Not a fit: Patients with known allergies to local anesthetics, significant drug allergies, or pre-existing psychiatric or neurological disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management techniques that reduce reliance on opioids after lumbar surgery.
How similar studies have performed: While there is limited evidence directly comparing these two specific nerve block techniques, regional anesthesia has shown promise in improving postoperative pain management in similar contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18 to 80 years * American Society of Anesthesiologists (ASA) physical status I to III * scheduled for lumbar microdiscectomy surgery Exclusion Criteria: * Known allergy to local anesthetics * Any other significant drug allergies related to the study interventions * Pregnancy * Pre-existing psychiatric or neurological disorders * Inability to provide informed consent
Where this trial is running
Istanbul
- Medipol University — Istanbul, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Burak Ömür
- Email: burakomur@outlook.com
- Phone: +905056215056
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.