At a glance
ClinicalIndex Comparison RecordN/ACompleted· 65 enrolled
Drug / intervention
Experimental ET Tube Securement Deviceother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Assessment of the Functionality and Performance of an Endotracheal (ET) Tube Protection Device
In Brief
A clinical study evaluating Experimental ET Tube Securement Device for Respiratory Insufficiency. Completed, enrolled 65 participants across 5 sites.
Detailed Summary
Endotracheal intubation is the translaryngeal placement of a tube into the trachea via the nose or mouth. Endotracheal tubes must be securely fixed to prevent movement, which may result in accidental slippage of the tube into a mainstream bronchus or into the pharynx. Hollister Incorporated is assessing the functionality and performance of an endotracheal tube securement device.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRespiratory Insufficiency
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartJul 2012
First PostedJul 2012
Primary CompletionFeb 2013
TodayJul 2026
First PostedJul 27, 2012
Enrollment StartJul 1, 2012
Primary CompletionFeb 1, 2013
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 13.9 years ago
Interventions
Experimental ET Tube Securement Deviceother
Experimental Hollister device with bite block was substituted for standard-of-care device during the study period.