Status:
COMPLETED
Screening and Intervention of Postextubation Dysphagia
Lead Sponsor:
National Taiwan University Hospital
Collaborating Sponsors:
Ministry of Science and Technology, Taiwan
Conditions:
Oropharyngeal Dysphagia
Swallowing Disorder
Eligibility:
All Genders
20+ years
Phase:
NA
Brief Summary
This clinical trial aims to test the validity of a two-item swallowing screen and to examine the effects of the Swallowing and Oral-Care (SOC) Program on resumption of oral intake, incidence of penetr...
Detailed Description
Endotracheal intubation is life-sustaining, but it may contribute to postextubation dysphagia (PED) increasing the risk of penetration, aspiration, and aspiration pneumonia. Up to 84% of extubated pat...
Eligibility Criteria
Inclusion
- Patient who is over 20 years old.
- Patient how has received over 48 hours endotracheal intubation and had been successfully extubated.
Exclusion
- Patient who has a history of neuromuscular disease (e.g., parkinsonism or stroke) or head and neck deformities.
- Patient who has preexisting difficulty swallowing.
- Patient who has received a tracheostomy.
- Patient who were unable to follow verbal instructions.
- Patient who were on contact and droplet precautions (e.g., open tuberculosis)
- Patient who were receiving continuous noninvasive ventilation after extubation that precluded the delivery of an SOC intervention
Key Trial Info
Start Date :
September 19 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 8 2020
Estimated Enrollment :
145 Patients enrolled
Trial Details
Trial ID
NCT03284892
Start Date
September 19 2017
End Date
August 8 2020
Last Update
July 20 2023
Active Locations (1)
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1
National Taiwan University Hospital
Taipei, Taiwan, 10055