Status:
TERMINATED
Comparing Nasal Suction Devices in Children With Bronchiolitis: A Pilot Study
Lead Sponsor:
Baylor College of Medicine
Conditions:
Bronchiolitis
Eligibility:
All Genders
2-2 years
Phase:
NA
Brief Summary
The purpose of our study is to determine the safety, efficacy, length of stay and parental satisfaction of the NoseFrida in comparison to a suction device used in the hospital setting in patients with...
Detailed Description
Bronchiolitis is a viral illness and a common cause for admission to the hospital. Most patients with bronchiolitis are managed at home. The indications of hospitalization are poor feeding (due to inc...
Eligibility Criteria
Inclusion
- patients above the age of 2 months and post-gestational age to 44 weeks and less than or equal to 2 years with signs and symptoms of bronchiolitis
- clinical respiratory score (CRS) of less than or equal to 4
- principle diagnosis of bronchiolitis (International Classification of Diseases-9: 466, 466.11 and 466.19)
- Patient admitted to the Pediatric Hospitalist Medicine (PHM) group
- Patient with associated hypoxemia and/or respiratory distress requiring low flow O2 nasal cannula (NC) management (2L/min or less)
Exclusion
- age less than 2 months
- age less than post-gestational age 44 weeks
- CRS greater than 4
- associated hypoxia
- already using NoseFrida at home
- chronic lung disease
- oro-facial abnormalities
- cardiac abnormalities
Key Trial Info
Start Date :
September 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2019
Estimated Enrollment :
55 Patients enrolled
Trial Details
Trial ID
NCT02219334
Start Date
September 1 2014
End Date
May 1 2019
Last Update
September 3 2020
Active Locations (1)
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1
Texas Children's Hospital
Houston, Texas, United States, 77030