Status:
TERMINATED
Nasopharyngeal Pressure Measurement During Neonatal Nasal Respiratory Support
Lead Sponsor:
University of Utah
Conditions:
Nasopharyngeal Airway Pressure
Eligibility:
All Genders
Up to 72 years
Brief Summary
This study will measure nasopharyngeal pressure in neonates using a miniature high resolution catheter-tip pressure transducer. Any neonatal intensive care patient being treated with nasal respiratory...
Detailed Description
Non-invasive respiratory treatments are being used more frequently during neonatal intensive care. High-flow nasal cannula,1-2 nasal continuous positive airway pressure,3 nasal intermittent mandatory ...
Eligibility Criteria
Inclusion
- Any infant admitted to neonatal intensive care who is treated with a modality of non-invasive respiratory support, such as low or high flow nasal cannula; nasal prong, catheter or mask continuous distending pressure; or nasal ventilation either intermittent mandatory, synchronized or high frequency will be eligible for study.
Exclusion
- Patients with oral, nasal, or palatal deformities who can not otherwise be fitted with cannula or mask will be excluded from the study.
Key Trial Info
Start Date :
May 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2012
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00766194
Start Date
May 1 2007
End Date
December 1 2012
Last Update
September 12 2013
Active Locations (1)
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1
University of Utah / Primary Childrens Medical Center
Salt Lake City, Utah, United States, 84132