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Tongue Brush (Orabrush) for Reducing Aspiration Pneumonia in Stroke Patients

Tongue Brush (Orabrush) for Reducing Aspiration Pneumonia in Stroke Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06765018
Acronym
StrOra
Enrollment
252
Registered
2025-01-09
Start date
2024-11-01
Completion date
2026-01-31
Last updated
2026-03-17

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

Conditions

Aspiration Pneumonias, Dysphagia After Stroke, Ischemic Stroke

Keywords

Dysphagia after stroke, Aspiration Pneumonias, Tongue Coating Index, Bacterial Tongue Colonization, Ischemic Stroke

Brief summary

The investigators conduct a controlled prospective experimental intervention study to examine whether the use of a tongue brush (Orabrush) can improve the rate of aspiration pneumonia and dysphagia in patients with ischemic stroke. Secondary outcomes include the impact on bacterial tongue colonization, the Tongue Coating Index, and the length of stay of the patients.The patients will be recruited in the Stroke Unit of the Department of Neurology from November 2024 until approximately October 2026.

Detailed description

As part of a prospective controlled experimental intervention study, patients with ischemic stroke will be recruited in the Stroke Unit of the University Hospital Marburg, who are admitted between November 2024 and approximately October 2026. The primary objective of this study is to investigate the impact of a tongue brush (Orabrush) on the rate of aspiration pneumonia and dysphagia. Secondary outcomes include the analysis of bacterial tongue colonization, the Tongue Coating Index, and the length of stay of the patients. Key study parameters include the aspiration rate, the EAT-10, the GUSS, a tongue swab, and a photograph of the tongue to determine the Tongue Coating Index. Data will be collected on the day of admission and after a duration of 3-5 days. The study has been approved by the relevant ethics committee.

Interventions

DEVICETongue Brush (Orabrush)

Patients in this group uses the Tongue Brush (Orabrush) 2 times a day for a duration for 3-5 days until the follow-up-screening takes place.

Sponsors

University Hospital Marburg
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* ischemic stroke and admission on the stroke unit at the University Hospital Marburg * minimum age: 18 years * patient is able to consent * consent has been obtained

Exclusion criteria

* surgery in the oral-pharyngeal region * irradiated patient with a history of tumor in the head and neck region * missing compliance * intake of medications with saliva-altering side effects, existing desire to have children, or pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Rate of Aspiration PneumoniasFrom the date of first admission until discharge, with the occurrence of aspiration, within max. 4 weeks pneumonia documented at any point during the inpatient stay.Evaluation of the Impact of a Tongue Brush on the Incidence of Aspiration Pneumonia in Patients with Ischemic Stroke.
Severity of dysphagia measured by EAT-10 [score from 0-40]EAT-10 is assessed on the day of admission and after a period of 3-5 days.This study aims to investigate whether the use of a tongue brush has an effect on the severity of dysphagia in ischemic stroke patients compared to the control group. The severity of dysphagia is quantified using the dysphagia screening tool EAT-10. The EAT-10 can have a score ranging from 0 to 40, with the severity of dysphagia increasing as the score rises.
Severity of dysphagia measured by GUSS [score from 0-20]GUSS is assessed on the day of admission and after a period of 3-5 days.This study aims to investigate whether the use of a tongue brush has an effect on the severity of dysphagia in ischemic stroke patients compared to the control group. The severity of dysphagia is quantified using the dysphagia screening tool GUSS. The GUSS can have a score ranging from 0 to 20, with the severity of dysphagia increasing as the score decreases.

Secondary

MeasureTime frameDescription
Winkel Tongue Coating Index [Score from 0 to 12]The WTCI of the patients is determined on the day of admission and after 3-5 days.Determination of the Winkel Tongue Coating Index (WTCI) in ischemic stroke patients. For this purpose, the tongue is divided into six equal-sized quadrants, and each quadrant is assigned a score from 0 to 2, depending on the severity of tongue coating. In total, a score ranging from a minimum of 0 to a maximum of 12 points can be achieved across the six quadrants. A low score indicates very little tongue coating, while a high score reflects a significant amount of tongue coating.
Microbiological quantification of the tongue's bacterial load through the determination of colony-forming units (CFU)Bacterial tongue colonization is assessed in the patients through swabbing on the day of admission and after 3-5 days.A swab of the tongue is taken from patients with ischemic stroke, and a microbiological quantification of the bacterial load is performed. Depending on the level of CFU, the bacterial load is categorized into the semiquantitative parameters 'low,' 'moderate,' and 'high'.
Length of in-hospital stay in daysDuration of in-hospital stay, measured from the admission date to the discharge date, during the inpatient treatment period. The average length of stay is approximately 6 days, so a maximum time frame of 30 days is chosen for the survey.It is investigated how many days patients with ischemic stroke stay in the hospital and whether there is a significant difference in the length of stay between the control and intervention groups.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026