Actively Recruiting

Age: 1Year - 6Years
All Genders
NCT06855199

CAUDAL EPIDURAL BLOCK IN PEDIATRIC SURGERY CASES

Led by Cigdem Demirci · Updated on 2025-03-03

55

Participants Needed

1

Research Sites

33 weeks

Total Duration

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Sponsors

C

Cigdem Demirci

Lead Sponsor

S

sivas devlet hastanesi

Collaborating Sponsor

AI-Summary

What this Trial Is About

Caudal epidural anesthesia was reported as the first epidural anesthesia technique in 1933, but its use began to become widespread after the 1960s (1). The procedure is reliable, easy to perform, the incidence of complications is low, and the total complication rate is 1.5/1000; Serious complications occur at a rate of 1/40000. There are many methods to demonstrate the success of caudal epidural block. Some of the common traditional methods are changes in mean arterial pressure and heart rate. These methods are sometimes not objective and take time. In this study, we will examine the block success in pediatric patients who underwent caudal epidural block, which is applied in our hospital, whether the Galvanic skin response measured with a finger probe, other than traditional methods, correlates with the block success, and whether it shows faster block success compared to other traditional methods.

CONDITIONS

Official Title

CAUDAL EPIDURAL BLOCK IN PEDIATRIC SURGERY CASES

Who Can Participate

Age: 1Year - 6Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Undergoing lower abdominal, urogenital, or lower extremity surgery
  • Patients classified as ASA physical status 1 or 2
Not Eligible

You will not qualify if you...

  • Having neuromuscular disease
  • Patients classified as ASA physical status 3 or 4
  • Having cerebral palsy
  • Having mental retardation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sivas State Hospital

Sivas, Sivas, Turkey (Türkiye)

Actively Recruiting

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Research Team

Ç

ÇİĞDEM DEMİRCİ

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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