Comparison of Erector Spinae Plane Block and Caudal block in pediatric patients

Not Applicable

• Conditions: lower abdominal surgery; Anaesthesiology - Pain management

• Registration Number: ACTRN12620000038998
• Lead Sponsor: Ali Ihsan Uysal

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-01-21
• Last Update Posted: 3 February 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1) Lower abdominal surgery
2) The age between 1-7 years
3) ASA I-II

Exclusion Criteria

1)ASA III-IV
2) The known alergy to bupivacain
3)The infection at the needle puncture area

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The FLACC score evaluation[Postoperative 15. minutes ]

Secondary Outcome Measures

Name	Time	Method
The total analgesic consumption as assessed by data linkage to medical records[postoperative 24. hours]