mTLIP versus QIPB for pain relief after lumbar microdiscectomy
Official title: Comparison of Ultrasound-Guided Modified Thoracolumbar Interfascial Plane Block Versus Quadro-Iliac Plane Block for Postoperative Analgesia in Patients Undergoing Lumbar Microdiscectomy
Run by Bursa City Hospital · NCT07480278 · Data updated 2026-11-12
This study will test whether the modified thoracolumbar interfascial plane block (mTLIP) or the quadro-iliac plane block (QIPB) provides better pain relief for adults having lumbar microdiscectomy surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Bursa City Hospital Government |
| Locations | 1 site (Bursa, Nilüfer) |
| Status | Recruiting |
| Started | March 25, 2026 |
| Main results expected | July 25, 2026 |
| Study ends | September 1, 2026 |
| Registry record updated | March 27, 2026 |
| Trial ID | NCT07480278 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–65 with ASA physical status I–III scheduled for elective lumbar microdiscectomy who can provide informed consent.
✕Probably not a fit
Patients with prior lumbar spine surgery, diabetes, significant renal or hepatic impairment, bleeding risk, allergy to local anesthetics, pregnancy, or inability to reliably report pain are excluded and unlikely to benefit from this protocol.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized clinical trial will enroll 80 adults (18–65 years, ASA I–III) undergoing elective lumbar microdiscectomy and randomize 40 patients to bilateral ultrasound-guided mTLIP and 40 to bilateral QIPB performed before surgery. The primary outcome is patient-controlled opioid consumption during the first 48 postoperative hours; secondary outcomes include QoR-15 recovery score, static and dynamic NRS pain scores, total rescue analgesic use and time to first rescue, length of hospital stay, perioperative remifentanil dose, and block- or opioid-related side effects. All participants will receive standardized general anesthesia and perioperative care with prospective outcome collection through hospitalization. The trial directly compares an established fascial plane block (mTLIP) with a recently described alternative (QIPB) to determine relative safety and analgesic effectiveness.
Why it matters
Potential benefit: If successful, the trial could identify a nerve block technique that reduces opioid use and improves recovery after lumbar microdiscectomy.
How similar studies have gone: Previous studies have shown mTLIP can provide effective postoperative analgesia after lumbar spine surgery, while QIPB is newly described and has limited comparative evidence.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age between 18 and 65 years * Classified as American Society of Anesthesiologists physical status I-III * Scheduled for elective lumbar microdiscectomy surgery under general anesthesia * Provision of written informed consent Exclusion Criteria: * Use of anticoagulant medications or presence of bleeding diathesis * Known allergy or hypersensitivity to local anesthetics or opioid drugs * Infection at the planned block site * Alcohol or drug dependence * Cognitive impairment preventing reliable pain assessment * Pregnancy or lactation * History of previous lumbar spine surgery * Diabetes mellitus * Renal or hepatic insufficiency
Where it's running
-
Bursa City Hospital
Bursa, Nilüfer, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Merih Yildiz Eglen, MD
- Email: meriheg@yahoo.com
- Phone: +905059340629
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.