Assessment of a Oral Endotracheal Tube Fastener on Patients Intubated With Oral Endotracheal Tubes

Stopped early · Not applicable

Conditions studied: Respiratory Depression, Respiratory Failure, Ventilatory Depression

In brief

Assessment of AnchorFast Guard Oral Endotracheal Tube Fastener on Patients Intubated with Oral Endotracheal Tubes with Subglottic Suction

Key facts

Study ID

NCT02760927

Run by

Hollister Incorporated

People needed

4

Starts

2016-03-01

Expected to finish

2016-05-01

Last updated by the study team

2018-09-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Is 18 years of age or older and requires oral tracheal intubation
• Has intact skin on application site
• Is qualified to participate in the opinion of the Investigator including the requirement for endotracheal tube with subglottic suction

You may not qualify if…

• Has an existing neck injury
• Has protruding upper teeth, is without teeth or is unable to wear upper dentures
• Has facial hair
• Has clinically significant skin damage, condition or disease on the application site which may contraindicate participation
• Has a known or stated allergy to adhesive bandages, or any of the product types being tested
• Uses of topical drugs, lotions, creams or oils on the application site
• Is participating in any clinical testing which may affect performance of this device
• AnchorFast Guard Oral Endotracheal Tube Fastener does not fit subject's face

Where it is running

• Legacy Mt Hood — Gresham, Oregon, United States
• Legacy Good Samaritan — Portland, Oregon, United States
• Legacy Salmon Creek Medical Center — Vancouver, Washington, United States

Full record on ClinicalTrials.gov

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