Comparing two types of nerve blocks for pain relief after hernia surgery in children
Ultrasound-Guided Transversalis Fascia Plane Block Versus Caudal Block for Postoperative Analgesia in Children Undergoing Inguinal Herniorrhaphy: A Randomized Controlled Non-Inferiority Trial
This study is testing which of two pain relief methods works better for kids aged 1 to 7 after hernia surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 1 Year to 7 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Trial ID | NCT06725667 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of ultrasound-guided transversalis fascia plane block (TFPB) and caudal block for providing postoperative analgesia in children undergoing inguinal herniorrhaphy. The research focuses on children aged 1 to 7 years who are scheduled for this common surgical procedure. Both techniques are evaluated for their ability to manage pain effectively, with TFPB targeting specific nerves in the lower abdomen. The study will assess pain levels and recovery outcomes in the pediatric population following surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are children aged 1 to 7 years scheduled for inguinal herniorrhaphy under general anesthesia.
Not a fit: Patients with repeated surgeries, known allergies to study drugs, infections at the injection site, bleeding disorders, or neurological disorders 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 inguinal herniorrhaphy.
How similar studies have performed: Previous studies have shown that both TFPB and caudal blocks can be effective for postoperative analgesia, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 1 to 7 years. * Both sexes. * American Society of Anesthesiology (ASA) physical status I-II. * Scheduled for inguinal herniorrhaphy under general anesthesia (GA). Exclusion Criteria: * Repeated surgeries. * Known allergic reactions to any of the study's drugs. * Infection at the site of block needle entry. * Bleeding diathesis. * Neurological disorders.
Where this trial is running
Tanta, El-Gharbia
- Tanta University — Tanta, El-Gharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Mohammed S Elsharkawy, MD
- Email: mselsharkawy@med.tanta.edu.eg
- Phone: 00201148207870
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.