Caudal Block for Inguinal Hernioplasty in Children

Status Recruiting

Clinical Trial Summary

This is a prospective, randomized, controlled clinical study designed to determine the effectiveness of caudal block combined with general anesthesia in providing intra- and postoperative analgesia, and its effect on hemodynamic stability and drug consumption.

Clinical Trial Description

This prospective, randomized, controlled clinical study will include 70 boys aged 3-5 years scheduled for inguinal herniorrhaphy. Participants will be randomized in 1:1 ratio into two groups. The first group will receive general anesthesia for surgery, while the second group will receive general anesthesia in combination with caudal block. Postoperative pain, hemodynamic parameters and total consumption of all medicaments in the perioperative period will be monitored. Complications and side effects of drugs will be observed as well. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05958589
Study type	Interventional
Source	University of Novi Sad
Contact	Marina Pandurov, MD, PhD
Phone	+381641914714
Email	marina.pandurov@mf.uns.ac.rs
Status	Recruiting
Phase	Phase 3
Start date	January 8, 2022
Completion date	December 2025

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