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Measurement Of Endotracheal Tube Cuff Pressure In Emergency Department Patients

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ClinicalTrials.gov Identifier: NCT01252173
Recruitment Status : Withdrawn
First Posted : December 2, 2010
Last Update Posted : April 21, 2015
Sponsor:
Information provided by (Responsible Party):
Beth Israel Medical Center

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
Intubation, Intratracheal

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 : October 2005
Actual Primary Completion Date : September 2006
Actual Study Completion Date : September 2006




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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
All emergency department patients, and all patients admitted from the ED
Criteria

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01252173


Sponsors and Collaborators
Beth Israel Medical Center
Investigators
Principal Investigator: Robert Hoffman, MD Beth Israel Medical Center

Responsible Party: Beth Israel Medical Center
ClinicalTrials.gov Identifier: NCT01252173     History of Changes
Other Study ID Numbers: 120-05
First Posted: December 2, 2010    Key Record Dates
Last Update Posted: April 21, 2015
Last Verified: April 2015

Keywords provided by Beth Israel Medical Center:
endotracheal
intubation
tracheal
pressure
cufflator

Additional relevant MeSH terms:
Emergencies
Disease Attributes
Pathologic Processes