Optimizing High Flow Nasal Cannula Oxygenation in Pediatric Airway Procedures
Part of paid clinical trials in Houston, Texas.
- Sponsor
- The University of Texas Health Science Center, Houston
- Study ID
- NCT06947902
- Status
- Not Yet Recruiting
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Conditions
- Airway Disorder
Eligibility Criteria
- Sex
- ALL
- Age
- 0 Years - 17 Years
- Healthy Volunteers
- Not accepted
Interventions
- High flow — DEVICEThe High Flow Nasal Cannula (HFNC) device (Vapotherm) will be placed through the nostrils for oxygen (2L/kg per min with max of 45L)
- Low Flow — DEVICEThe High Flow Nasal Cannula (HFNC) device (Vapotherm) will be placed through the nostrils for oxygen (0.5L/kg per min with max of 5L)
Study Details
The purpose of this study is to investigate which flow rate (higher versus lower) is most effective at increasing apneic time and preventing greater than 5% drop in desaturation, as well as assessing transcutaneous carbon dioxide (CO2) levels during airway procedures in children
Key Dates
- Start date
- Aug 1, 2025
- Status verified
- Apr 2025
- Primary completion
- Sep 1, 2027
- Completion
- Sep 30, 2027
Study Design
- Enrollment
- 80 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: High flow
- Experimental: Low Flow
Primary Outcome Measure
Number of participants that show an incidence of oxygen desaturation >5 % [ Time Frame: from start of procedure to end of procedure (about 1 hour) ]
Central Contacts
- Zhen Huang, MD(713) 500-5419
- Candace Hernandez(713) 500-5410
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Texas Health Science Center at Houston | Houston | Texas | 77030 |