Actively Recruiting
Comparison of the Effects of Sacral Erector Spinae Plane Block and Dorsal Penile Block on Postoperative Pain in Circumcision Operations
Led by Konya City Hospital · Updated on 2025-08-11
50
Participants Needed
1
Research Sites
1 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research investigates the effects of two different nerve block techniques on managing postoperative pain in children aged 7 to 12 undergoing circumcision surgery. Circumcision, a procedure with ancient historical roots and practiced for health, religious, or cultural reasons, often causes significant and lasting pain despite being a minor surgery. The study focuses on improving pain relief to support faster recovery and early discharge while exploring safer alternatives to opioids in pediatric anesthesia. Participants receive either a Dorsal Penile Block or a Sacral Erector Spinae Plane (ESP) Block after circumcision. Both nerve blocks are used alongside general anesthesia tailored by age and weight, including medications like sevoflurane, ketamine, fentanyl, and propofol. The study compares these two regional anesthesia methods, with the Sacral ESP Block noted for its ease of use, safety, and effectiveness. The trial uses a randomized, double-blind design to evaluate postoperative pain at various intervals and before discharge. During the study, children are monitored for pain at 0, 1, 2, 4, and 6 hours after surgery, and again before they leave the hospital. The evaluation includes pain scoring to assess relief provided by each block. The study ensures safety through anesthesia monitoring and tracks early mobilization and recovery. Participants are expected to stay in the hospital for at least 24 hours, allowing thorough observation and postoperative care until discharge.
CONDITIONS
Brief Title
Comparison of the Effects of Sacral Erector Spinae Plane Block and Dorsal Penile Block on Postoperative Pain in Circumcision Procedures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 7 and 12 years
- Undergoing circumcision surgery
- ASA Physical Status 1 or 2
- Planned hospital stay of at least 24 hours
- Receiving general anesthesia
You will not qualify if you...
- Lack of family or personal consent for the study
- ASA Physical Status 3 or higher
- Emergency surgery cases
- Serious blood, heart, liver, or kidney diseases
- Receiving anticoagulation (blood thinning) therapy
- Sensitivity to regional anesthetic agents
- Previous penile surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 24 hours
Participants undergo circumcision surgery followed by either a Dorsal Penile Block or a Sacral Erector Spinae Plane Block for postoperative pain management while receiving general anesthesia.
1 surgical visit and postoperative monitoring until discharge
Duration - Up to 6 hours post-surgery and before hospital discharge
Participants are observed for postoperative pain at multiple time points and before discharge to assess the effectiveness of the nerve blocks.
Multiple assessments during the first 6 hours post-surgery and 1 visit before discharge
Trial Site Locations
Total: 1 location
1
Yasin Tire
Konya, Meram, Turkey (Türkiye), 42140
Actively Recruiting
Research Team
Y
Yasin Tire
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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