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Assessment of an Oral Endotracheal Subglottic Tube Holder

NCT03328182 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2019-07-05

Study results available
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Summary

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

Conditions

  • Intubation

Interventions

DEVICE

New oral endotracheal tube holder

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

Sponsors & Collaborators

  • Hollister Incorporated

    lead INDUSTRY

Principal Investigators

  • Laura Vander Werff, MD · Legacy Mount Hood Medical Center

  • Brian Young, MD · 1. Legacy Emanuel Hospital & Health Center 2. Legacy Good Samaritan Medical Center

  • Arash Afshinnik, MD · Community Regional Medical Center

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-23
Primary Completion
2018-06-08
Completion
2018-06-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03328182 on ClinicalTrials.gov