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Clinical Trials/NCT03258736
NCT03258736
Completed
Not Applicable

Comparison of Caudal Block and Ultrasound Guided Ilioinguinal/Iliohypogastric Block for Bilateral Inguinal Surgery in Pediatric Patient: A Prospective Randomized Trial

Istanbul University1 site in 1 country110 target enrollmentApril 4, 2017
ConditionsSurgery

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Surgery
Sponsor
Istanbul University
Enrollment
110
Locations
1
Primary Endpoint
Analgesic requirements
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The caudal block is the most common technique for inguinal surgery. Increased use of ultrasound in regional analgesia techniques has been improved the practise of the peripheral nerve blocks. Ilioinguinal and iliohypogastric nerve blocks are possible to alternative methods to the central blocks. The aim of this study is to compare analgesic efficiency of caudal block and ultrasound guided Ilioinguinal and iliohypogastric nerve blocks for bilateral inguinal hernia in pediatric patients

Detailed Description

In this prospective randomized study, pediatric patients between 1- 10 years old who were scheduled to bilateral inguinal hernia surgery wil be enrolled the study. The patients wil randomly assign to receive an ultrasound-guided Ilioinguinal/iliohypogastric block group or caudal block group Ilioinguinal/iliohypogastric block was performed with 2 mg/kg bupivacaine as 0.25 % and total volum wil be divided equally for each side, Caudal block wil performe with bupivacaine 2 mg/kg as 0.2%. Supplemental analgesia will consist of as requred intraoperative remifentanyl, for recovery unit rescue tramadol, as requred at home ibuprofen. Patients wil be evaluated in the recovery unit for analgesia with FLACC pain scale, analgesic requirement, complications and parental satisfaction. Parents will be also called for analgesia and satisfaction after discharge of the patients in first 24 hours. The evaluation will be performed by a researcher whom does not know which participants belong to the caudal or ilioinguinal/iliohypogastric nerve block group

Registry
clinicaltrials.gov
Start Date
April 4, 2017
End Date
August 30, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ayse Cigdem Tutuncu

assoc prof

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • 1- 10 year- old who were scheduled to bilateral inguinal hernia surgery -

Exclusion Criteria

  • Patients with neurological disoder, reoperation for inguinal hernia surgery, coagulation disorder

Outcomes

Primary Outcomes

Analgesic requirements

Time Frame: up to 24 hours

FLACC score

Secondary Outcomes

  • Postoperative complications(up to 24 hours)

Study Sites (1)

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