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Optimizing High Flow Nasal Cannula Oxygenation in Pediatric Airway Procedures

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Begins enrollment this month

Conditions

Airway Disorder

Treatments

Device: High flow
Device: Low Flow

Study type

Interventional

Funder types

Other

Identifiers

NCT06947902
HSC-MS-25-0028

Details and patient eligibility

About

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

Enrollment

80 estimated patients

Sex

All

Ages

Under 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • undergoing laryngoscopy and bronchoscopy procedures at Children's Memorial Hermann Hospital (CMHH)
  • weight greater than or equal to 5 kilograms and using flow rates between 5 to 45 liters per minute (BTPS)

Exclusion criteria

  • Emergency type cases, tracheostomy patients, unrepaired cyanotic heart disease, nasal deformity/choanal atresia, or cautery/laser type procedures

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

High flow
Experimental group
Treatment:
Device: High flow
Low Flow
Experimental group
Treatment:
Device: Low Flow

Trial contacts and locations

1

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Central trial contact

Zhen Huang, MD; Candace Hernandez

Data sourced from clinicaltrials.gov

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