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Oral hygiene in critically ill patients

Oral hygiene in critically ill patients - a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7p6568
Enrollment
Unknown
Registered
2019-10-08
Start date
2019-08-05
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventilator-associated pneumonia

Interventions

A randomized, double-blind, controlled trial will be conducted to evaluate the oral care of critically ill mechanically ventilated patients with different antiseptics already used in intensive care un
Drug
Procedure/surgery
N06.850.780.200.450.150.160
H02.403.720.750

Sponsors

Universidade Federal de Uberlândia
Lead Sponsor
Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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

Countries

Brazil

Contacts

Public ContactPaula Vieira

Universidade Federal de Uberlândia

drapaulacunhavieira@gmail.com+55-34-32182111

Outcome results

None listed

Source: REBEC (via WHO ICTRP)