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Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy: A Prospective Observational Study

Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07762339
Enrollment
84
Registered
2026-08-13
Start date
2026-06-08
Completion date
2027-01-08
Last updated
2026-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caudal Epidural Anesthesia, FLACC Scale, Orchiopexy, Sacral Erector Spinae Plane Block

Keywords

FLACC SCALE, caudal epidural anesthesia, sacral erector spinae plane block, orchiopexy

Brief summary

This study aims to compare the analgesic efficacy of ultrasound-guided erector spinae plane block and caudal block for postoperative pain management in pediatric patients undergoing orchiopexy. Postoperative pain scores, time to first rescue analgesic requirement, total analgesic consumption, and block-related adverse effects will be evaluated during the first 24 hours after surgery. The study will assess whether erector spinae plane block provides effective postoperative analgesia comparable to or superior to caudal block in pediatric orchiopexy.

Interventions

None listed

Sponsors

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
1 Years to 7 Years
Healthy volunteers
Yes

Inclusion criteria

* Children aged 1 to 7 years with ASA physical status I-II undergoing unilateral orchiopexy surgery.

Exclusion criteria

* ASA physical status ≥ III * History of prematurity (gestational age \< 37 weeks) Known coagulation disorders or bleeding tendency * Infection, inflammation, or skin lesion at the injection site * Known neurological or neuromuscular diseases * Presence of significant cardiac or pulmonary disease (e.g., congenital heart disease, active asthma) * Hepatic or renal dysfunction * Known allergy or hypersensitivity to local anesthetics (e.g., bupivacaine, lidocaine) * Developmental delay or cognitive impairment that prevents accurate pain assessment * Use of additional regional analgesia techniques (e.g., caudal block) during surgery * Block failure or intraoperative complications requiring exclusion from protocol analysis * Lack of parental consent for participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Time To First Analgesic Requirement After SurgeryFirst 24 hours postoperativelyThe time elapsed from the end of surgery to the administration of the first rescue analgesic

Secondary

MeasureTime frameDescription
FLACC Pain Scores at Specified Time Intervalsfirst 24 hours postoperativelyPain assessment using the Face, Legs, Activity, Cry, Consolability (FLACC) scale (score range: 0-10; higher scores indicate worse pain) at 30 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 12 hours and 24 hours postoperatively

Countries

Turkey (Türkiye)

Contacts

CONTACTKübra DEMİR
kubrademir01@yahoo.com.tr905355573969
PRINCIPAL_INVESTIGATORkübra demir

Prof. Dr Cemil Taşcıoğlu Şehir Hastanesi

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026