CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 34 enrolled
Drug / intervention
New oral endotracheal tube holderdevice
Likely dose
AnchorFast Guard Subglottic ET Tube (oral endotracheal tube holder for standard or subglottic ET tubes 6.0-8.0 mm)AI-extracted
Key inclusion· 4
  • ✓Age ≥18 years and requiring oral tracheal intubation with subglottic ET tube size 6.0-8.0 mm
  • ✓Intact skin on and around application site (cheeks, lips)
  • ✓Oral cavity free of open sores, ulcers, wounds, and lesions
  • ✓Requires bite block per hospital standard of care
Key exclusion· 6
  • ✕Loose, missing teeth, or unable to wear upper dentures
  • ✕Facial hair interfering with adhesion of skin barrier pads
  • ✕Clinically significant skin disease or condition (psoriasis, eczema, atopic dermatitis, active cancer, sores, sunburns, scars, moles)
  • ✕Known or stated allergy to adhesives

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03328182
NCT03328182N/ACompleted
CompareCT.gov

Assessment of AnchorFast Guard Subglottic ET (Endotracheal) Tube

Hollister Incorporated·interventional·Posted Nov 1, 2017·Updated Jul 5, 2019

In Brief

A clinical study evaluating New oral endotracheal tube holder for Intubation. Completed, enrolled 34 participants across 4 sites.

Detailed Summary

This study is designed to assess the acceptability and usability of a new Endotracheal Tube (ET) holding device for an orally intubated patient.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntubation
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedNov 1, 2017
Enrollment StartOct 23, 2017
Primary CompletionJun 8, 2018
Study CompletionJun 15, 2018
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 8.7 years ago

Interventions

New oral endotracheal tube holderdevice

The single arm study product is designed to hold a standard or subglottic ET tube.