Comparison of RAM Cannula Nasal Continuous Positive Airway Pressure Versus Infant Flow Nasal Continuous Positive Airway Pressure (NCPAP)
Terminated
- Conditions
- Acute Respiratory DeficiencyPrematurityAssisted Ventilation
- Registration Number
- NCT02032511
- Lead Sponsor
- University of Michigan
- Brief Summary
This study is designed to compare the effectiveness and ease of use of two commonly used NCPAP interfaces: the RAM NC and the Infant Flow prongs and nasal mask.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 19
Inclusion Criteria
- less than or equal to 7 kg
- order for nasal continuous positive pressure
Exclusion Criteria
- patients greater than 7kg
- patients that do not have informed consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Number of patients who achieve unassisted breathing One year
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie NCPAP efficacy in preterm infants with respiratory distress?
How does RAM cannula NCPAP compare to Infant Flow NCPAP in reducing intubation rates for acute respiratory deficiency?
Are there specific biomarkers that predict successful NCPAP weaning in premature neonates?
What adverse events are associated with nasal interfaces in neonatal respiratory support and how are they managed?
What combination therapies show promise with NCPAP for treating respiratory insufficiency in extremely low birth weight infants?