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Effect of High Flow Nasal Cannula on Oxygenation During Urodynamic Study in Pediatric Population

Effect of High Flow Nasal Cannula on Oxygenation During Urodynamic Study in Pediatric Population

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04152733
Enrollment
82
Registered
2019-11-05
Start date
2020-03-23
Completion date
2021-12-30
Last updated
2020-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Desaturation

Brief summary

To evaluate the effect of high flow nasal cannula for prevention of hypoxia during deep sedation in pediatric population

Interventions

DEVICEHigh flow nasal cannula

Oxygen is supplied via high flow nasal cannula. Heated air (2L/kg/min) is administered using Optiflow device (Fisher and Paykel Healthcare, Auckland, New Zealand).

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
No minimum to 6 Years
Healthy volunteers
No

Inclusion criteria

* Children aged \<7 years * ASA class I, II

Exclusion criteria

* Respiratory disease * Pneumothorax * Increased ICP * Nasal bleeding * Previous airway surgery * Trauma * Pulmonary hypertension

Design outcomes

Primary

MeasureTime frameDescription
Incidence of desaturationDuring deep sedation (during approximately 1 hour after propofol infusion)Incidence of peripheral pulse oximeter value lower than 95%

Secondary

MeasureTime frame
Incidence of peripheral pulse oximeter value lower than 90%During deep sedation (during approximately 1 hour after propofol infusion)
Incidence of changes in oxygen flow (control group) or FiO2 (HF group)During deep sedation (during approximately 1 hour after propofol infusion)
Minimum pulse oximeter valueDuring deep sedation (during approximately 1 hour after propofol infusion)
Oxygen reserve index valueDuring deep sedation (during approximately 1 hour after propofol infusion)
Incidence of manual ventilationDuring deep sedation (during approximately 1 hour after propofol infusion)
percutaneous CO2 valueDuring deep sedation (during approximately 1 hour after propofol infusion)

Countries

South Korea

Contacts

Primary ContactJin-Tae Kim, MD, PhD
jintae73@gmail.com82-2-2072-3661

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026