Measurement Of Endotracheal Tube Cuff Pressure In Emergency Department Patients
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
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 |
|---|
|
Intubation, Intratracheal |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | MEASUREMENT OF ENDOTRACHEAL TUBE CUFF PRESSURE IN EMERGENCY DEPARTMENT PATIENTS |
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
All emergency department patients, and all patients admitted from the ED
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
More Information
No publications provided
| Responsible Party: | Robert Hoffman, Beth Israel Medical Center |
| ClinicalTrials.gov Identifier: | NCT01252173 History of Changes |
| Other Study ID Numbers: | 120-05 |
| Study First Received: | December 1, 2010 |
| Last Updated: | December 1, 2010 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Beth Israel Medical Center:
|
endotracheal intubation tracheal pressure cufflator |
Additional relevant MeSH terms:
|
Emergencies Disease Attributes Pathologic Processes |
ClinicalTrials.gov processed this record on May 19, 2013