Pain relief method for scoliosis surgery in adolescents
Ultrasound Guided Bilateral Retrolaminar Block as Analgesia for Adolescent Idiopathic Scoliosis Correction
This study is testing a new pain relief method during scoliosis surgery to see if it helps teenagers feel less pain and recover better after the operation.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 10 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta) |
| Trial ID | NCT04336111 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of an ultrasound-guided bilateral retrolaminar block for providing analgesia during surgical correction of adolescent idiopathic scoliosis. The study involves preoperative assessments, including patient history and pain evaluation, followed by the administration of anesthesia and monitoring during surgery. The goal is to reduce postoperative pain and improve recovery outcomes for adolescents undergoing this invasive procedure. A total of 44 patients will be divided into two groups to assess the efficacy of the analgesic technique.
Who should consider this trial
Good fit: Ideal candidates for this study are adolescents diagnosed with idiopathic scoliosis who are scheduled for surgical correction.
Not a fit: Patients with bleeding disorders, mental dysfunction, or allergies to local anesthetics may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce postoperative pain and improve recovery for adolescents undergoing scoliosis surgery.
How similar studies have performed: Other studies have shown promising results with similar analgesic techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with idiopathic adolescent scoliosis undergoing surgical correction Exclusion Criteria: 1. Bleeding disorders (coagulopathy). 2. Mental dysfunction. 3. History of allergy to local anesthetics.
Where this trial is running
Tanta
- tarek Abdel Lattif — Tanta, Egypt (Recruiting)
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.