Measurement Of Endotracheal Tube Cuff Pressure In Emergency Department Patients

This study has been withdrawn prior to enrollment.
Sponsor:
Information provided by (Responsible Party):
Beth Israel Medical Center
ClinicalTrials.gov Identifier:
NCT01252173
First received: December 1, 2010
Last updated: April 20, 2015
Last verified: April 2015

December 1, 2010
April 20, 2015
October 2005
September 2006   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT01252173 on ClinicalTrials.gov Archive Site
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Measurement Of Endotracheal Tube Cuff Pressure In Emergency Department Patients
MEASUREMENT OF ENDOTRACHEAL TUBE CUFF PRESSURE IN EMERGENCY DEPARTMENT PATIENTS

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.

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Observational
Time Perspective: Prospective
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Probability Sample

All emergency department patients, and all patients admitted from the ED

Intubation, Intratracheal
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
September 2006
September 2006   (final data collection date for primary outcome measure)

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.
Both
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Contact information is only displayed when the study is recruiting subjects
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NCT01252173
120-05
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Beth Israel Medical Center
Beth Israel Medical Center
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Principal Investigator: Robert Hoffman, MD Beth Israel Medical Center
Beth Israel Medical Center
April 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP