Pudendal vs Caudal Block for Pediatric Penile Surgery

NCT04840654 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2025-07-24

No results posted yet for this study

Summary

The study will compare recovery profile in children receiving pudendal blocks vs caudal analgesia for ambulatory circumcision or hypospadias repair in children between 6 months and 2 years. The subjects of the study will be randomized to receive either a caudal or a pudendal block.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

Caudal Block

A caudal block is a procedure that will help lessen a child's pain after an operation. 100 subjects will be randomized to this block procedure.

PROCEDURE

Pudendal Block

form of local anesthesia commonly used in the practice of obstetrics to relieve pain during the delivery of baby by forceps. 100 Subjects will be randomized to this block procedure.

Sponsors & Collaborators

  • University of Chicago

    lead OTHER

Principal Investigators

  • Leili Khorassani, MD · University of Chicago

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
6 Months
Max Age
3 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-01
Primary Completion
2024-10-02
Completion
2024-10-02

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04840654 on ClinicalTrials.gov