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Clinical Trial Summary

The aim of this study was to compare the efficacy of caudal block and sacral espb used as a postoperative analgesia method in urogenital pediatric surgery cases.


Clinical Trial Description

The parents of the patients who will undergo urogenital surgery will be included in the study after being informed and written consent is obtained. They will be randomised and divided into two groups. After general anaesthesia, sacral espb will be performed in the 1st group and caudal block will be performed in the 2nd group and postoperative pain will be evaluated with Face, Leg, Activity, Cry, Consolability (FLACC) score. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06373185
Study type Interventional
Source Giresun University
Contact Bilge Olgun Keles
Phone 05317338805
Email bilge.olgun@hotmail.com
Status Recruiting
Phase N/A
Start date April 22, 2024
Completion date June 2024

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