Measurement Of Endotracheal Tube Cuff Pressure In Emergency Department Patients

Sponsor
Beth Israel Medical Center (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01252173
Collaborator
(none)
0
11

Study Details

Study Description

Brief Summary

The purpose of this research is to measure the endotracheal tube cuff pressure in patients who have been endotracheally intubated emergently in the emergency department or in the field by prehospital personnel. Overinflation of ETTc pressure is associated with injury, and we seek to determine if the phenomenon of excessively inflated ETTc can be detected in endotracheally intubated patients in the ED.

There is no experimental aspect to this study, it is only descriptive. Measurement of ETTc pressure is already performed by respiratory therapy/respiratory care. We simply seek to assess these measurements to determine if any patients in fact have high ETTc pressure. If it is found that patients do have ETTc with high pressures, this might allow emergency department staff or prehospital personnel such as paramedics or EMTs to use this information to seek methods by which endotracheal intubation can be improved and patients can be intubated without excessive ETTc pressure.

This is a pilot study. We have conducted several in vitro studies, which have all demonstrated that paramedics, EMTs, and emergency department physicians practice endotracheal intubation in a method that might result in excessively inflated ETTc.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    0 participants
    Time Perspective:
    Prospective
    Official Title:
    MEASUREMENT OF ENDOTRACHEAL TUBE CUFF PRESSURE IN EMERGENCY DEPARTMENT PATIENTS
    Study Start Date :
    Oct 1, 2005
    Actual Primary Completion Date :
    Sep 1, 2006
    Actual Study Completion Date :
    Sep 1, 2006

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • Patient emergently endotracheally intubated with a cuffed endotracheal tube.
      Exclusion Criteria:
      • Endotracheal intubation procedure performed in a setting other than the prehospital (field) or emergency department of participating institution. This specifically excludes endotracheally intubated patients transferred from another hospital, chronic care facility, or other location.

      • Non-emergent or elective endotracheal intubation.

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • Beth Israel Medical Center

      Investigators

      • Principal Investigator: Robert Hoffman, MD, Beth Israel Medical Center

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Beth Israel Medical Center
      ClinicalTrials.gov Identifier:
      NCT01252173
      Other Study ID Numbers:
      • 120-05
      First Posted:
      Dec 2, 2010
      Last Update Posted:
      Apr 21, 2015
      Last Verified:
      Apr 1, 2015
      Keywords provided by Beth Israel Medical Center
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Apr 21, 2015