Comparing two pain management techniques for children undergoing hernia surgery
Analgesic Effect of Fascia Transversalis Block Versus Transversus Abdominal Plane Block in Children Undergoing Open Inguinal Hernia Surgery. A Randomized Comparative Trial.
PHASE2 · Kasr El Aini Hospital · NCT06326944
This study tests which of two pain relief methods works better for kids after they have hernia surgery.
Quick facts
| Phase | PHASE2 |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 1 Year to 6 Years |
| Sex | All |
| Sponsor | Kasr El Aini Hospital (other) |
| Locations | 1 site (Giza) |
| Trial ID | NCT06326944 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of the fascia transversalis plane block compared to the transversus abdominis plane block in managing postoperative pain in children undergoing inguinal hernia surgery. The study involves administering general anesthesia and performing ultrasound-guided nerve blocks to assess pain relief. Children will be monitored throughout the procedure, and various laboratory tests will be conducted to ensure safety and eligibility. The goal is to determine which technique provides longer-lasting pain relief.
Who should consider this trial
Good fit: Ideal candidates for this study are children classified as ASA physical status I-II who are scheduled for inguinal hernia repair.
Not a fit: Patients with coagulopathy, localized infections at the injection site, or known allergies to the medications used may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for pediatric patients undergoing hernia surgery.
How similar studies have performed: Previous studies have shown promising results with ultrasound-guided nerve blocks for pain management, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ASA physical status I-II Exclusion Criteria: * Parents' refusal to participate in the study. * Coagulopathy (i.e. Platelets ≤ 50,000 and/or INR\> 1.5). * Localized infection at the site of needle insertion. * Known hypersensitivity or allergies to any of the used drugs.
Where this trial is running
Giza
- Cairo University Hospitals — Giza, Egypt (RECRUITING)
Study contacts
- Study coordinator: Ramy m alkonaiesy, MD
- Email: ramyalkonaiesy@gmail.com
- Phone: 01224883990
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: Fascia Transversalis Plane Block, Transversus abdominis plane block, Open inguinal herniorrhaphy