Pain management for children undergoing thoracoscopic sympathectomy using a specific nerve block technique
Erector Spinae Plane Block for Children Undergoing Thoracoscopic Sympathectomy: A Prospective Controlled Trial
This study tests if a special nerve block technique can help reduce pain and improve recovery for kids aged 6 to 16 after surgery to treat certain conditions.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 6 Years to 16 Years |
| Sex | All |
| Sponsor | Menoufia University Academic / other |
| Locations | 1 site (Shibīn al Kawm, Menoufia) |
| Trial ID | NCT06984874 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of ultrasound-guided erector spinae plane block (ESPB) in reducing postoperative pain and preventing diaphragmatic dysfunction in pediatric patients undergoing thoracoscopic sympathectomy. The research focuses on how ESPB can alleviate pain caused by surgical procedures, which can hinder recovery and lead to complications such as pneumonia. By administering this regional anesthesia technique, the study aims to improve recovery outcomes for children aged 6 to 16 years undergoing this type of surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are children aged 6 to 16 years scheduled for bilateral thoracoscopic sympathectomy.
Not a fit: Patients with allergies to local anesthetics, severe spinal deformities, or significant liver/kidney dysfunction may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance postoperative recovery and reduce complications in pediatric patients.
How similar studies have performed: Other studies have shown promising results with the use of erector spinae plane block for pain management, indicating a potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 6 to 16 years. * Either sexes (male or female). * American Society of Anesthesiologists (ASA) physical status I-II. * Scheduled for bilateral thoracoscopic sympathectomy under general anesthesia. Exclusion Criteria: * History of allergy to local anesthetics. * Abnormal liver/kidney function. * Severe spinal deformities. * Bleeding or coagulation disorders. * Skin damage or infection at the proposed puncture site.
Where this trial is running
Shibīn al Kawm, Menoufia
- Menoufia University — Shibīn al Kawm, Menoufia, Egypt (Recruiting)
Study contacts
- Study coordinator: Safaa M Sallam, Master
- Email: safaa.sallam@med.menofia.edu.eg
- Phone: 00201001876902
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.