Comparing two methods for pain relief after circumcision in children
Comparison of the Effects of Sacral Erector Spinae Plane Block and Dorsal Penile Block on Postoperative Pain in Circumcision Operations
This study is testing which of two pain relief methods works better for kids aged 7-12 after they have a circumcision.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 7 Years to 12 Years |
| Sex | All |
| Sponsor | Konya City Hospital Academic / other |
| Locations | 1 site (Konya, Meram) |
| Trial ID | NCT06843070 on ClinicalTrials.gov |
What this trial studies
This clinical trial compares the effectiveness of two different anesthesia techniques, the Sacral Erector Spinae Plane Block and the Dorsal Penile Block, in managing postoperative pain for children undergoing circumcision. The study involves pediatric patients aged 7-12 years who will receive general anesthesia and are expected to stay in the hospital for at least 24 hours post-surgery. The aim is to evaluate which method provides better pain relief and facilitates quicker recovery. The trial is conducted at Konya City Hospital in Turkey, focusing on improving postoperative care for young patients.
Who should consider this trial
Good fit: Ideal candidates for this study are children aged 7-12 years who are scheduled for elective circumcision under general anesthesia.
Not a fit: Patients with ASA Physical Status 3 or higher, those undergoing emergency surgery, or those with significant comorbidities 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 circumcision, enhancing their recovery experience.
How similar studies have performed: Other studies have shown promising results with ultrasound-guided nerve blocks in pediatric anesthesia, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Inclusion criteria of the patients: Age between 7-12 years, ASA Physical Status 1 and 2, circumcision surgery, general anesthesia, planned hospital stay of at least 24 hours. Exclusion Criteria: * Exclusion criteria were defined as patients whose family or personal consent could not be obtained for the study, Asa 3 and above cases, patients in the study age group who will undergo emergency surgery, patients with serious hematopoietic system, cardiovascular, liver or kidney disease, patients receiving anticoagulation therapy, patients with sensitivity to regional anesthetic agents and patients who have previously undergone penile surgery.
Where this trial is running
Konya, Meram
- Yasin Tire — Konya, Meram, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Yasin Tire
- Email: dryasintire@hotmail.com
- Phone: +905055367970
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.