Viewing Study NCT04107363



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Last Modification Date: 2024-10-26 @ 1:19 PM
Study NCT ID: NCT04107363
Status: COMPLETED
Last Update Posted: 2019-09-27
First Post: 2019-09-24

Brief Title: Oropharyngeal Aspiration to Reduce Ventilator-Related Pneumonia
Sponsor: Ayşe AKBIYIK
Organization: Izmir Katip Celebi University

Study Overview

Official Title: The Effect of Oropharyngeal Aspiration Before Position Change on Reducing the Incidence of Ventilator-Related Pneumonia
Status: COMPLETED
Status Verified Date: 2019-09
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: Ventilator-associated pneumonia VAP is one of the healthcare-related infections that is common in critically ill patients prolongs hospital stay significantly increases mortality and additional health care costs

Microaspiration of oropharyngeal secretions the primary pathway in the formation of VAP has led researchers to focus on the detection of applications to prevent microbial colonization Continuous or intermittent oropharyngeal aspiration open system aspiration versus closed system aspiration extensive oral care oropharyngeal aspiration prior to patient positioning are some of these applications

When the patient is turned to position the outbreak accumulated in the oral cavity is more likely to move to the lower respiratory tract In this study it is assumed that aspiration of oropharyngeal secretions prior to each position change will reduce the accumulation of oral secretion in the endotracheal tube cuff and reduce aspiration of contaminated secretion and reduce the risk of developing VIP This randomized controlled experimental study was planned to confirm the validity of this assumption

This study was a randomized controlled experimental study designed to investigate the effect of oropharyngeal aspiration on decreasing the incidence of ventilator-associated pneumonia in patients receiving mechanical ventilation The research was conducted between July 2015 and April 2019 in anesthesiology and reanimation intensive care unit The study was carried out with 20 patients who underwent oropharyngeal aspiration as needed and 20 patients with oropharyngeal aspiration prior to each change of position
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