Comparing two types of nerve blocks for pain relief after hernia surgery in children
Ultrasound Guided Paravertebral Block Versus Erector Spinae Plane Block for Postoperative Analgesia After Inguinal Hernia Repair in Pediatric Patients: a Randomized Clinical Trial
NA · Zagazig University · NCT06752252
This study is testing which type of nerve block works better for managing pain in children after hernia surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 158 (estimated) |
| Ages | 24 Months to 12 Years |
| Sex | All |
| Sponsor | Zagazig University (other gov) |
| Locations | 2 sites (El Sharkia and 1 other locations) |
| Trial ID | NCT06752252 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of ultrasound-guided paravertebral block and erector spinae plane block for postoperative pain management in pediatric patients undergoing elective inguinal hernia repair. It will assess the total amount of rescue analgesics used in the first 24 hours post-surgery, the timing of the first analgesic request, and pain intensity during rest and movement. Additionally, the study will monitor for complications and evaluate parental satisfaction with the pain management provided.
Who should consider this trial
Good fit: Ideal candidates for this study are preschool and school-aged children between 24 months and 12 years old who are undergoing elective unilateral inguinal hernia repair.
Not a fit: Patients with contraindications to regional blocks, such as coagulopathy or local infections, or those with advanced systemic diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for children undergoing hernia repair, enhancing their recovery experience.
How similar studies have performed: Previous studies have shown promising results with similar nerve block techniques for postoperative analgesia, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1 - Parents acceptance 2\. Age: preschool and school age child (24 months-12 years old). 3\. Sex: both sex (males or females). 4\. Physical status: ASA 1\& II. 5\. Type of operation: elective unilateral inguinal hernia repair Exclusion Criteria: 1- Patient with any contraindications of regional blocks (as coagulopathy or local infection at injection site) 2\. Patients with known history of allergy to the study drugs (bupivacaine and lidocaine). 3\. Advanced hepatic, renal, cardiovascular, neurologic and respiratory diseases.
Where this trial is running
El Sharkia and 1 other locations
- faculty of human medicine, Zagazig university hospitals — El Sharkia, Egypt (RECRUITING)
- Faculty of Human Medicine, Zagazig University — El Sharkia, Egypt (RECRUITING)
Study contacts
- Study coordinator: Dina Sadek Salem, MD
- Email: dinamaghraby@yahoo.com
- Phone: 0109933513
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.
Conditions: Analgesia, Postoperative, postoperative analgesia, ultrasound guided paravertebral block, ultrasound guided erector spinae plane block, inguinal hernia repair in pediatric