Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
57 participants
INTERVENTIONAL
2019-09-01
2020-02-05
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
CROSSOVER
PREVENTION
NONE
Study Groups
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One group received standard oral care.
One group received standard oral care.
the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.
It was applied to the other group by aspiration.
the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.
It was applied to the other group by aspiration.
One group received standard oral care.
the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.
It was applied to the other group by aspiration.
the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.
Interventions
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One group received standard oral care.
the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.
It was applied to the other group by aspiration.
the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.
Eligibility Criteria
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Inclusion Criteria
* Patients without thrombocytopenia, leukopenia and oral stomatitis, aphthae, candiasis, gingivitis
* Patients whose respiratory support is provided by a mechanical ventilator
* Patients who are considered to be able to provide mechanical ventilator support for 7 days
* Patients without any respiratory-related infectious pathogens
* Obtaining informed consent from the patient if he/she can give consent or from his/her guardian if he/she is unable to give consent.
* It was determined as patients who did not undergo any intraoral surgical intervention.
Exclusion Criteria
18 Years
90 Years
FEMALE
No
Sponsors
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Ataturk University
OTHER
Responsible Party
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ASENA KÖSE
research assistant
Locations
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Atatürk University
Erzurum, , Turkey (Türkiye)
Countries
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Other Identifiers
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AtaturkU-001
Identifier Type: -
Identifier Source: org_study_id