Clinical Trial

Effect of Regional Anesthesia or Intravenous Infusion of Lidocaine on Morphine Use After Scoliosis Repair Surgery

Recruiting
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Record status
This record was last updated November 12, 2024 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
The goal of the surgical correction of scoliosis is to prevent progression of the curve or progression of restrictive lung disease. After scoliosis surgery, patients experience severe pain. The standard treatment for pain relief after scoliosis surgery is the administration of opiates. However, treatment with these substances involves side effects such as respiratory depression, nausea and vomiting, inhibition of bowel activity and itching. To lower the dose of opiates, different types of painkillers and other techniques can be added. The purpose of the study is to compare the effect of instillation of lidocaine (which is an analgesic and anti-inflammatory) or regional anesthesia using Erector spinae plane on the dose of morphine consumption, the intensity of pain, the side effects and the quality of recovery during the first 48 hours after surgery to repair scoliosis.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2024-06-04; most recent amendment 2024-11-10.
Status change: Not Yet Recruiting → Recruiting 2024-08-15
Trial Details
NCT Number NCT06451562
Lead Sponsor Assaf-Harofeh Medical Center
Conditions Scoliosis
Enrollment 105 participants
Start Date 2024-09-01
Primary Completion 2026-06-30 (estimated)
Study Completion 2026-09-30 (estimated)
Updated on ClinicalTrials.gov 2024-11-12