Comparing two pain relief techniques for children undergoing hernia repair
Comparison of the Effects of Ultrasound-Guided Erector Spinae Plane Block and Caudal Block on Postoperative Pain in Children Undergoing Unilateral Inguinal Hernia Operation
This study is testing which of two pain relief methods works better for kids having hernia surgery to help them feel less pain afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 66 (estimated) |
| Ages | 1 Year to 8 Years |
| Sex | All |
| Sponsor | Abant Izzet Baysal University Academic / other |
| Locations | 7 sites (Bolu, Merkez and 6 other locations) |
| Trial ID | NCT05896072 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of two regional anesthesia techniques, the ultrasound-guided erector spinae plane block and the caudal block, in managing postoperative pain for pediatric patients undergoing unilateral inguinal hernia repair. The research focuses on providing adequate analgesia to improve patient mobilization and reduce the risk of chronic pain development in children. A total of 60 pediatric patients aged 1-8 years, classified as ASA I-II, will be randomly assigned to receive one of the two analgesic techniques during their elective surgery. The study will utilize a simple randomization method to ensure unbiased results.
Who should consider this trial
Good fit: Ideal candidates for this study are pediatric patients aged 1-8 years scheduled for elective unilateral inguinal hernia surgery with ASA status I-II.
Not a fit: Patients who may not benefit from this study include those with contraindications to regional anesthesia, known allergies to local anesthetics, or severe underlying health conditions.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for pediatric patients undergoing hernia repairs, enhancing their recovery experience.
How similar studies have performed: Other studies have shown promising results with similar regional anesthesia techniques in pediatric populations, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Pediatric patient scheduled for unilateral elective inguinal hernia operation * ASA status 1-2 Exclusion Criteria: * Pediatric patient's parents refusal * Contraindications to regional anesthesia * Known allergy to local anesthetics, * Bleeding diathesis, * Severe kidney or liver disease * Presence of infection at the needle entry site.
Where this trial is running
Bolu, Merkez and 6 other locations
- Abant İzzet Baysal Education and Training Hospital — Bolu, Merkez, Turkey (Recruiting)
- Bolu Abant İzzet Baysal Medical School — Bolu, Turkey (Recruiting)
- Bolu Abant İzzet Baysal University Faculty of Medicine — Bolu, Turkey (Recruiting)
- Karabuk University Training and Research Hospital — Karabuk, Turkey (Recruiting)
- Karabuk University Karabuk Training and Research Hospital — Karabük, Turkey (Recruiting)
- Karabuk University Training and Research Hospital — Karabük, Turkey (Recruiting)
- Karabük University Training and Research Hospital — Karabük, Turkey (Recruiting)
Study contacts
- Principal investigator: Kenan Kart, MD — Karabuk University Training and Research Hospital
- Study coordinator: Kenan Kart, MD
- Email: kenankart@karabuk.edu.tr
- Phone: +905337723300
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.