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Effects of Oral Care in the Neuroscience ICU

Comprehensive Oral Care for the Intubated Neuroscience ICU Patient: A Comparison of the Safety and Efficacy Between 2 Protocols

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00518752
Enrollment
113
Registered
2007-08-21
Start date
2007-05-31
Completion date
2011-11-30
Last updated
2013-01-16

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

Conditions

Oral Hygiene, Ventilator Associated Pneumonia

Keywords

Ventilator Acquired Pneumonia, Oral Hygiene, Oral Care, Xerostomia

Brief summary

The purpose of this study is to compare how effective different ways of mouth cleaning are for patients in a neuroscience intensive care unit with a breathing tube in their mouth.

Detailed description

Patients with neurological dysfunction requiring intubation and ventilation are at risk for developing ventilator acquired pneumonia. Several studies have suggested that oral hygiene plays a role in the subsequent development of pneumonia for patients in the intensive care unit requiring intubation and mechanical ventilation.

Interventions

Patients in this arm will receive standard oral care with manual brushes and routine oral hygiene products twice a day

Patients will receive a comprehensive oral care protocol using mechanical brushes and oral care products formulated for patients with a dry mouth twice a day

Sponsors

Lund University
CollaboratorOTHER
St. Joseph's Hospital and Medical Center, Phoenix
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \> or equal 18 years old * Intubated within 24hours of admission to the Neuroscience ICU * Intubation anticipated to continue for approximately 72 hours

Exclusion criteria

* Minors * Pregnancy * Acute cervical spinal cord injury * Severe facial trauma * Family not present for consent

Design outcomes

Primary

MeasureTime frame
Development of Ventilator Acquired PneumoniaDuring the period of intubation

Secondary

MeasureTime frame
Improved Oral HealthDuring the period of intubation and 48 hours following extubation

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026