This study is designed to assess the acceptability and usability of a new Endotracheal Tube (ET) holding device for an orally intubated patient.
This is a multiple site prospective assessment of the study product in ICU settings. The study is comprised of each intubated subject wearing one study product until the device either needs to be changed or is no longer required by the subject. The study product is designed to hold a standard or subglottic ET tube and help reduce the potential for occlusion (blockage) of the tube.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
34
The single arm study product is designed to hold a standard or subglottic ET tube.
Community Regional Medical Center
Fresno, California, United States
Legacy Mount Hood Medical Center
Gresham, Oregon, United States
Legacy Good Samaritan Medical Center
Portland, Oregon, United States
Legacy Emanuel Hospital & Health Center
Portland, Oregon, United States
Overall Acceptability With Study Product
The overall acceptability relating to general experience with the study product during use will be rated with a 5-point Likert scale ranging from 1=Very Unacceptable to 5=Very Acceptable
Time frame: At product removal (maximum 29 days of patient wearing product)
Usability of Study Product
The usability of the study product at application and at removal.
Time frame: At application and product removal (maximum 29 days of patient wearing product)
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