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Clinical Trials in Turkey / NCT07675798
Recruiting Not applicable

Effect of Caudal Block on Urethrocutaneous Fistula After Distal Hypospadias Repair

NCT07675798 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-01
Last updated
2026-06-30

Condition(s) studied

HypospadiasCaudal BlockPediatric Anesthesia

Investigational drug(s) / intervention(s)

Caudal BlockGeneral Anesthesia without Caudal Block

Caudal Block: General anesthesia combined with caudal block administered prior to distal hypospadias repair. Caudal block is performed using bupivacaine hydrochloride as part of standard institutional analgesic protocol.

General Anesthesia without Caudal Block: General anesthesia alone administered without caudal block for distal hypospadias repair. Intravenous analgesic agents used as per standard institutional protocol.

Study summary

Hypospadias is one of the most common congenital urogenital anomalies in males, occurring in approximately 1 in every 200-300 male births. It is characterized by abnormal positioning of the urethral meatus on the ventral surface of the penis. Surgical repair is the standard treatment; however, urethrocutaneous fistula formation remains one of the most frequent and clinically significant postoperative complications, potentially requiring reoperation and causing considerable distress to both the patient and the family.

Caudal nerve block is a widely used regional anesthesia technique in pediatric lower abdominal and genitourinary surgery, valued for its high analgesic efficacy, relative ease of application, and low complication profile. However, emerging evidence suggests that caudal block may be associated with an increased incidence of postoperative complications following hypospadias repair, including fistula formation and wound edema. Notably, Kundra et al. (2012) reported a fistula rate of 19.2% in patients who received caudal block, compared to 0% in those who received penile block, raising important questions about the routine use of caudal block in hypospadias surgery.

This prospective, multicenter, randomized controlled trial aims to evaluate the effect of caudal block on the incidence of urethrocutaneous fistula following distal hypospadias repair. A total of 80 male patients aged 6-60 months will be randomized 1:1 to either receive general anesthesia with caudal block or general anesthesia alone. The primary outcome is the incidence of urethrocutaneous fistula. Secondary outcomes include perioperative opioid consumption, postoperative pain scores, analgesic duration, and other surgical complications such as wound dehiscence and urethral stricture. Patients will be followed up for 3-6 months postoperatively. The study will be conducted across four centers in Turkey. Results are expected to provide evidence-based guidance on the role of caudal block in pediatric hypospadias repair.

Eligibility

Sex
MALE
Min age
6 Months
Max age
60 Months
Healthy volunteers
No
Inclusion Criteria: * Male patients aged 6-60 months * Diagnosed with distal hypospadias * Scheduled for elective hypospadias repair * Written informed consent obtained from parent or legal guardian Exclusion Criteria: * Age \< 6 months or \> 60 months * Proximal or non-distal hypospadias * Previous hypospadias repair * Skin lesions at the epidural/caudal injection site * Coagulopathy * Known allergy to anesthetic agents, particularly bupivacaine hydrochloride * Spinal anomalies * Chronic granulomatous disease * Diabetes mellitus * Patients receiving corticosteroid therapy * Refusal of informed consent by parent or guardian

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Dicle University Diyarbakır Eyalet/Yerleşke Recruiting
Gazi Yaşargil Training and Research Hospital Diyarbakır Eyalet/Yerleşke Recruiting

More Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital trials in Turkey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07675798 on ClinicalTrials.gov ↗ ← All trials in Turkey