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Clinical Trial Summary

The goal of this study is to compare patients outcome in two groups. the first group will be applied pecto-intercostal fascial block additional to general anesthesia and the second group will not. This is a single-center, prospective, observational trial to study the efficacy of Pecto-intercostal Fascial Block (PIFB) in patients undergoing pediatric congenital cardiac surgery requiring median sternotomy and cardiopulmonary bypass. The children are aged between 6 months to 12 years with American Society of Anesthesiologists (ASA) score 2 or 3. The main question it aims to answer are: The investigators' first question is if applying pecto-intercostal fascial block just after anesthesia induction reduces postoperative pain status. Secondly, if this pain status makes any reduction in preoperative opioid consumption. The investigators aim to find out; if there is any difference in opioid consumption during operation and postoperative 24-hour, postoperative Face, Legs, Activity, Cry, Consolability (FLACC) scale, length of intensive care unit and hospital stays, and other complications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06089798
Study type Observational
Source Basaksehir Cam & Sakura Sehir Hospital
Contact selin saglam
Phone 0905557198756
Email selinsaglams@gmail.com
Status Recruiting
Phase
Start date November 1, 2023
Completion date November 1, 2025

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