Trials / Unknown
UnknownNCT04852432
Evaluation of the Efficacy of Oxygen Therapy and Clinical Feasibility of High Flow Nasal Cannula During Moderate and Deep Sedation in Pediatric Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 258 (estimated)
- Sponsor
- Seoul National University Hospital · Academic / Other
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Not accepted
Summary
The investigators evaluate the efficacy and safety of routine administration of oxygen during moderate or deep sedation in pediatric patients. In addition, in terms of efficacy and safety, oxygen administration via nasal prong and high flow nasal cannula will be compared.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | high flow nasal cannula | The heated air is administered at a rate of 2L/kg/min using an Optiflow device (Fisher and Paykel Healthcare, Auckland, New Zealand). Inhalation oxygen concentration starts with 50%. |
| DEVICE | nasal prong | Oxygen is administered via nasal prong |
Timeline
- Start date
- 2021-07-27
- Primary completion
- 2024-04-30
- Completion
- 2024-12-30
- First posted
- 2021-04-21
- Last updated
- 2024-02-23
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT04852432. Inclusion in this directory is not an endorsement.