Trials / Completed
CompletedNCT03328182
Assessment of an Oral Endotracheal Subglottic Tube Holder
Assessment of AnchorFast Guard Subglottic ET (Endotracheal) Tube
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 34 (actual)
- Sponsor
- Hollister Incorporated · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is designed to assess the acceptability and usability of a new Endotracheal Tube (ET) holding device for an orally intubated patient.
Detailed description
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | New oral endotracheal tube holder | The single arm study product is designed to hold a standard or subglottic ET tube. |
Timeline
- Start date
- 2017-10-23
- Primary completion
- 2018-06-08
- Completion
- 2018-06-15
- First posted
- 2017-11-01
- Last updated
- 2019-07-05
- Results posted
- 2019-07-05
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT03328182. Inclusion in this directory is not an endorsement.