Viewing Study NCT06089798



Ignite Creation Date: 2024-05-06 @ 7:39 PM
Last Modification Date: 2024-10-26 @ 3:11 PM
Study NCT ID: NCT06089798
Status: RECRUITING
Last Update Posted: 2023-10-18
First Post: 2023-06-11

Brief Title: Analgesic Efficacy of Ultrasound-guided Bilateral Pecto-intercostal Plane Block in Pediatric Cardiac Surgery
Sponsor: Başakşehir Çam Sakura City Hospital
Organization: Başakşehir Çam Sakura City Hospital

Study Overview

Official Title: Analgesic Efficacy of Ultrasound-guided Bilateral Pecto-intercostal Fascial Block in Pediatric Cardiac Surgery
Status: RECRUITING
Status Verified Date: 2023-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None