Viewing Study NCT06306820



Ignite Creation Date: 2024-05-06 @ 8:15 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06306820
Status: RECRUITING
Last Update Posted: 2024-03-13
First Post: 2024-03-02

Brief Title: Ultrasound Guided Recruitment Manauvere Versus Individualized Positive End Expiratory Pressure in Pediatric Patients Undergoing Laparoscopic Abdominal Surgery
Sponsor: Tanta University
Organization: Tanta University

Study Overview

Official Title: Ultrasound Guided Recruitment Manauvere Versus Individualized Positive End Expiratory Pressure in Pediatric Patients Undergoing Laparoscopic Abdominal Surgery A Prospective Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-03
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 aim of this prospective randomized controlled study is to compare the effect of US-guided Recruitment Manauvere RM versus individualized positive end-expiratory pressure PEEP on oxygenation and preventing respiratory complications in pediatric patients undergoing laparoscopic abdominal surgeries
Detailed Description: Atelectasis is among the most frequent postoperative pulmonary complications PPCs of general anesthesia with an incidence of between 68 and 100 in children Atelectasis impairs gas exchange thus causing hypoxemia and other respiratory disorders such as acute lung injury and pneumonia

Pneumoperitoneum is another risk factor for perioperative atelectasis It elevates the diaphragm and intra-abdominal pressure In order to prevent atelectasis applying positive end-expiratory pressure PEEP or an alveolar recruitment Maneuvere RM have shown beneficial effects

Lung ultrasound US is a noninvasive radiation-free convenient and reproducible bedside imaging modality for anesthesia-induced atelectasis in children

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