Modified Versus Conventional Heated Humidified High Flow Nasal Cannula in Children with Respiratory Distress

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20180406001

Enrollment

Unknown

Registered

2018-04-06

Start date

2016-10-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Pediatric respiratory distress

Interventions

Use commercial high flow nasal cannula (F&P) ,Use modified high flow nasal cannula

Experimental Device,Experimental Device

Standard high flow ,Modified high flow

Eligibility

Sex/Gender

All

Age

1 Months to 5 Years

Inclusion criteria

Inclusion criteria: All respiratory distress children age 1month to 5 years old who admitted at pediatric ICU and intermediate ward in Ramathibodi Hospital

Exclusion criteria

Exclusion criteria: -Hemodynamic unstable -Respiratory failure -Facial anomaly -Tracheostomy patient -DNR patient

Design outcomes

Primary

Measure	Time frame
Intubation rate 7 day intubation	—

Secondary

Measure	Time frame
hospital stay hospital length day	—

Countries

Thailand

Contacts

Public ContactNattachai Anantasit

Mahidol University

nattachai032@gmail.com0865225433

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026