Oral hygiene in critically ill patients

Not Applicable

Recruiting

• Conditions: Ventilator-associated pneumonia; ventilator-induced lung injury; mortality; severe acute respiratory syndrome; primary prevention; C01.539.248.500; C08.381.677; C08.381.520.750; E05.318.308.985.550; C02.782.600.550.200.750

• Registration Number: RBR-7p6568
• Lead Sponsor: niversidade Federal de Uberlândia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-08
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients admitted to the Intensive Care Unit of the Federal University of Uberlândia Hospital das Clínicas from 2019 to 2020; dependent on mechanical ventilation for more than 48 hours; regardless of gender; over 18 years old; head trauma victim

Exclusion Criteria

Patients under 18 years of age; undergoing endotracheal intubation 48 hours before admission; mechanical ventilation dependents before 48 hours; diagnosis of pneumonia prior to admission; burns; pregnant women; patient in palliative care; patients with restrictive measures; brain death at presentation; if the research participant is identified

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluate the number of participants who died during hospitalization in each of the three groups in order to compare the all-cause mortality rate in each group;To assess the presence or absence of ventilator-associated pneumonia during intensive care unit admission to compare which antiseptic prevented this outcome further

Secondary Outcome Measures

Name	Time	Method
To assess costs by collecting data on days of extubation time, length of stay in the intensive care unit and length of hospital stay, in addition to the proportion of discharge to home and rehabilitation clinic;Assess if there were mechanical ventilation events during the patient's hospitalization, collecting data from the physical examination chart and complementary exams that indicate and diagnose lung lesions, respiratory distress syndrome and infections;Assess if any of the antiseptics caused more local damage by identifying data recorded in medical or nursing evolution of oral ulcers, tooth damage, allergic reactions, or bleeding