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

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Seoul National University

Status

Unknown

Conditions

Desaturation

Treatments

Device: High flow nasal cannula

Study type

Interventional

Funder types

Other

Identifiers

NCT04152733
H1910-038-1068

Details and patient eligibility

About

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

Enrollment

82 estimated patients

Sex

All

Ages

Under 6 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

82 participants in 2 patient groups

Control group
No Intervention group
Description:
Children in the control group receive oxygen via conventional nasal cannula during deep sedation. Oxygen flow is determined to set the fraction of inspired oxygen of 50%.
High flow (HF) group
Experimental group
Description:
Children in the HF group receive oxygen via high flow nasal cannula during deep sedation. Fraction of inspired oxygen is set to 50%.
Treatment:
Device: High flow nasal cannula

Trial contacts and locations

1

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Central trial contact

Jin-Tae Kim, MD, PhD

Data sourced from clinicaltrials.gov

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