Pilot Study for Verifying Endotracheal Tube Repositioning Using Ultrasound

NCT02407158 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2018-01-11

No results posted yet for this study

Summary

The investigators will compare the response to oral endotracheal tube repositioning as measured by chest x-ray and measured by the air-wave device.

Conditions

  • Endotracheal Tube Position

Interventions

DEVICE

SonarMed Airwave Device

Measure the concordance of chest x-ray and the Airwave device for measuring the change of position of an endotracheal tube.

Sponsors & Collaborators

  • Yale University

    lead OTHER

Principal Investigators

  • Kimberly A Davis, MD, MBA · Yale University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2018-01-05
Completion
2018-01-05

Countries

  • United States

Study Locations

More Related Trials

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 NCT02407158 on ClinicalTrials.gov