Modified TLIP vs Retrolaminar block for pain after two-level lumbar spine surgery
Official title: Effect of Modified Thoracolumbar Interfascial Plane Block Versus Retrolaminar Block for Pain Control in Postoperative Lumbar Spine Surgeries: A Prospective Randomized Double-Blind Clinical Study
Run by Zagazig University · NCT07883616 · Data updated 2026-11-12
This randomized trial tests whether the modified TLIP block provides better early pain control and less opioid use than the retrolaminar block after two-level lumbar spine surgery, in adults aged 21–65.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 21 Years to 65 Years |
| Sex | All |
| Enrollment | 42 (estimated) |
| Sponsor | Zagazig University Government |
| Locations | 1 site (Zagazig, Sharqia Province) |
| Status | Recruiting |
| Started | October 1, 2025 |
| Main results expected | December 1, 2026 |
| Study ends | January 1, 2027 |
| Registry record updated | October 20, 2026 |
| Trial ID | NCT07883616 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 21–65 with ASA I–II undergoing elective two-level lumbar spine surgery (discectomy/decompression) and who consent to participate.
✕Probably not a fit
Patients whose pain control relies more on systemic analgesia or who have contraindications to regional blocks may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective, randomized, double-blind study compares two regional anesthesia techniques—modified Thoracolumbar Interfascial Plane (mTLIP) block and Retrolaminar block—for managing postoperative pain in adults undergoing elective two-level lumbar spine procedures. The primary outcome is total morphine consumption in the first 24 hours after surgery. Secondary outcomes include pain scores, time to first rescue analgesia, block performance metrics, side effects, functional recovery, and patient satisfaction. Local anesthetic is administered with adjuncts and the approach targets dorsal rami to reduce opioid needs while facilitating recovery. The trial will help determine which block offers more effective analgesia with potentially fewer opioid-related adverse effects.
Why it matters
Potential benefit: If successful, the preferred block could reduce opioid requirements and improve early postoperative comfort after lumbar spine surgery.
How similar studies have gone: Regional block comparisons for lumbar surgery have shown potential for opioid-sparing effects, though direct head-to-head data on mTLIP versus retrolaminar is limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age between 21 and 65 years * ASA physical status I or II * BMI \< 30 kg/m² * Scheduled for elective two-level lumbar spine surgery (discectomy/decompression) * Expected duration of surgery less than 3 hours * Patient's acceptance and written informed consent Exclusion Criteria: * Infection at block site * Known allergy to used drugs * Coagulation disorder * History of psychiatric illness * Pre-existing neurological deficits * Presence of any metastasis * Previous lumbar spine surgeries * Patients on previous opioid therapy
Where it's running
-
Zagazig University Hospitals, Anesthesia, Intensive Care and Pain Management Department
Zagazig, Sharqia Province, Egypt Recruiting
Study contacts
- Principal investigator: Mohamed Shehta Mohamed Ali, M.B.B.CH — Zagazig University
- Study coordinator: Mohamed Shehta Mohamed Ali
- Email: m.shehta025@medicine.zu.edu.eg
- Phone: +2001014634299
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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.